Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4012 |
| ensemblid | ENSG00000113441.16 |
| hgncid | 6656 |
| symbol | LNPEP |
| name | leucyl and cystinyl aminopeptidase |
| refseq_nuc | NM_005575.3 |
| refseq_prot | NP_005566.2 |
| ensembl_nuc | ENST00000231368.10 |
| ensembl_prot | ENSP00000231368.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 96936080 |
| end | 97037513 |
| strand | + |
| ver | v1.2 |
| region | chr5:96936080-97037513 |
| region5000 | chr5:96931080-97042513 |
| regionname0 | LNPEP_chr5_96936080_97037513 |
| regionname5000 | LNPEP_chr5_96931080_97042513 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1025 | 242 | 67 | 46 | 103 | 6 | 19 | 88 | LNPEP_chr5_96931080_97042513 | LNPEP | MEPFT others(1020): Show |
chr5 | 96931080 | 97042513 |
| a0002 | 0/0 | 1025 | 71 | 11 | 6 | 44 | 1 | 9 | 34 | LNPEP_chr5_96931080_97042513 | LNPEP | MEPFT others(1020): Show |
chr5 | 96931080 | 97042513 |
| a0003 | 0/0 | 1025 | 17 | 0 | 7 | 0 | 6 | 4 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | MEPFT others(1020): Show |
chr5 | 96931080 | 97042513 |
| a0004 | 0/1 | 1025 | 12 | 3 | 3 | 0 | 1 | 4 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | MEPFT others(1020): Show |
chr5 | 96931080 | 97042513 |
| a0005 | 0/0 | 1025 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | LNPEP_chr5_96931080_97042513 | LNPEP | MEPFT others(1020): Show |
chr5 | 96931080 | 97042513 |
| a0006 | 0/0 | 1025 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | MEPFT others(1020): Show |
chr5 | 96931080 | 97042513 |
| a0007 | 0/0 | 1025 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | LNPEP_chr5_96931080_97042513 | LNPEP | MEPFT others(1020): Show |
chr5 | 96931080 | 97042513 |
| a0008 | 0/0 | 1025 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | MEPFT others(1020): Show |
chr5 | 96931080 | 97042513 |
| a0009 | 0/0 | 1025 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | MEPFT others(1020): Show |
chr5 | 96931080 | 97042513 |
| a0010 | 0/0 | 1025 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | MEPFT others(1020): Show |
chr5 | 96931080 | 97042513 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3075 | 204 | 48 | 44 | 88 | 6 | 17 | LNPEP_chr5_96931080_97042513 | LNPEP | ATGGA others(3070): Show |
chr5 | 96931080 | 97042513 | ||
| a0001c0003 | 0/0 | 3075 | 34 | 19 | 2 | 13 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | ATGGA others(3070): Show |
chr5 | 96931080 | 97042513 | ||
| a0001c0012 | 0/0 | 3075 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | ATGGA others(3070): Show |
chr5 | 96931080 | 97042513 | ||
| a0001c0013 | 0/0 | 3075 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | ATGGA others(3070): Show |
chr5 | 96931080 | 97042513 | ||
| a0001c0015 | 0/0 | 3075 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | ATGGA others(3070): Show |
chr5 | 96931080 | 97042513 | ||
| a0001c0016 | 0/0 | 3075 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | ATGGA others(3070): Show |
chr5 | 96931080 | 97042513 | ||
| a0002c0002 | 0/0 | 3075 | 71 | 11 | 6 | 44 | 1 | 9 | LNPEP_chr5_96931080_97042513 | LNPEP | ATGGA others(3070): Show |
chr5 | 96931080 | 97042513 | ||
| a0003c0004 | 0/0 | 3075 | 17 | 0 | 7 | 0 | 6 | 4 | LNPEP_chr5_96931080_97042513 | LNPEP | ATGGA others(3070): Show |
chr5 | 96931080 | 97042513 | ||
| a0004c0005 | 0/1 | 3075 | 10 | 3 | 3 | 0 | 1 | 2 | LNPEP_chr5_96931080_97042513 | LNPEP | ATGGA others(3070): Show |
chr5 | 96931080 | 97042513 | ||
| a0004c0008 | 0/0 | 3075 | 2 | 0 | 0 | 0 | 0 | 2 | LNPEP_chr5_96931080_97042513 | LNPEP | ATGGA others(3070): Show |
chr5 | 96931080 | 97042513 | ||
| a0005c0006 | 0/0 | 3075 | 3 | 0 | 0 | 3 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | ATGGA others(3070): Show |
chr5 | 96931080 | 97042513 | ||
| a0006c0009 | 0/0 | 3075 | 2 | 1 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | ATGGA others(3070): Show |
chr5 | 96931080 | 97042513 | ||
| a0007c0007 | 0/0 | 3075 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | ATGGA others(3070): Show |
chr5 | 96931080 | 97042513 | ||
| a0008c0011 | 0/0 | 3075 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | ATGGA others(3070): Show |
chr5 | 96931080 | 97042513 | ||
| a0009c0014 | 0/0 | 3075 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | ATGGA others(3070): Show |
chr5 | 96931080 | 97042513 | ||
| a0010c0010 | 0/0 | 3075 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | ATGGA others(3070): Show |
chr5 | 96931080 | 97042513 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 12134 | 75 | 16 | 11 | 37 | 3 | 7 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0002 | 0/0 | 12134 | 27 | 5 | 4 | 14 | 1 | 3 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0003 | 0/0 | 12133 | 17 | 3 | 7 | 3 | 2 | 2 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12128): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0005 | 0/0 | 12135 | 13 | 0 | 2 | 10 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12130): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0009 | 0/0 | 12134 | 8 | 6 | 2 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0010 | 0/0 | 12121 | 4 | 0 | 4 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12116): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0011 | 0/0 | 12134 | 5 | 4 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0012 | 0/0 | 12135 | 4 | 0 | 0 | 4 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12130): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0013 | 0/0 | 12135 | 4 | 0 | 0 | 4 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12130): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0014 | 0/0 | 12135 | 4 | 0 | 0 | 4 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12130): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0015 | 0/0 | 12134 | 4 | 0 | 4 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0016 | 0/0 | 12135 | 4 | 4 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12130): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0018 | 0/0 | 12135 | 3 | 2 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12130): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0019 | 0/0 | 12133 | 3 | 0 | 3 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12128): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0021 | 0/0 | 12134 | 3 | 0 | 0 | 3 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0022 | 0/0 | 12134 | 2 | 2 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0023 | 0/0 | 12134 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0024 | 0/0 | 12134 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0025 | 0/0 | 12134 | 2 | 1 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0029 | 0/0 | 12120 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12115): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0030 | 0/0 | 12134 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0031 | 0/0 | 12134 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0032 | 0/0 | 12134 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0033 | 0/0 | 12134 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0034 | 0/0 | 12134 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0035 | 0/0 | 12134 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0036 | 0/0 | 12134 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0037 | 0/0 | 12134 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0038 | 0/0 | 12134 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0039 | 0/0 | 12134 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0040 | 0/0 | 12135 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12130): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0047 | 0/0 | 12134 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0051 | 0/0 | 12134 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0052 | 0/0 | 12134 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0053 | 0/0 | 12134 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0054 | 0/0 | 12135 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12130): Show |
chr5 | 96931080 | 97042513 |
| a0001c0001t0055 | 0/0 | 12133 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12128): Show |
chr5 | 96931080 | 97042513 |
| a0001c0003t0006 | 0/0 | 12135 | 11 | 10 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12130): Show |
chr5 | 96931080 | 97042513 |
| a0001c0003t0007 | 0/0 | 12136 | 8 | 0 | 0 | 8 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12131): Show |
chr5 | 96931080 | 97042513 |
| a0001c0003t0017 | 0/0 | 12135 | 4 | 4 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12130): Show |
chr5 | 96931080 | 97042513 |
| a0001c0003t0020 | 0/0 | 12135 | 3 | 3 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12130): Show |
chr5 | 96931080 | 97042513 |
| a0001c0003t0027 | 0/0 | 12136 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12131): Show |
chr5 | 96931080 | 97042513 |
| a0001c0003t0043 | 0/0 | 12135 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12130): Show |
chr5 | 96931080 | 97042513 |
| a0001c0003t0045 | 0/0 | 12135 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12130): Show |
chr5 | 96931080 | 97042513 |
| a0001c0003t0046 | 0/0 | 12136 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12131): Show |
chr5 | 96931080 | 97042513 |
| a0001c0003t0048 | 0/0 | 12135 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12130): Show |
chr5 | 96931080 | 97042513 |
| a0001c0003t0049 | 0/0 | 12136 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12131): Show |
chr5 | 96931080 | 97042513 |
| a0001c0003t0050 | 0/0 | 12135 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12130): Show |
chr5 | 96931080 | 97042513 |
| a0001c0012t0010 | 0/0 | 12121 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12116): Show |
chr5 | 96931080 | 97042513 |
| a0001c0013t0001 | 0/0 | 12134 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0001c0015t0010 | 0/0 | 12121 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12116): Show |
chr5 | 96931080 | 97042513 |
| a0001c0016t0001 | 0/0 | 12134 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0002c0002t0002 | 0/0 | 12134 | 45 | 10 | 3 | 22 | 1 | 9 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0002c0002t0004 | 0/0 | 12134 | 26 | 1 | 3 | 22 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0003c0004t0003 | 0/0 | 12133 | 4 | 0 | 1 | 0 | 3 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12128): Show |
chr5 | 96931080 | 97042513 |
| a0003c0004t0008 | 0/0 | 12133 | 9 | 0 | 4 | 0 | 2 | 3 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12128): Show |
chr5 | 96931080 | 97042513 |
| a0003c0004t0041 | 0/0 | 12133 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12128): Show |
chr5 | 96931080 | 97042513 |
| a0003c0004t0042 | 0/0 | 12131 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12126): Show |
chr5 | 96931080 | 97042513 |
| a0003c0004t0056 | 0/0 | 12133 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12128): Show |
chr5 | 96931080 | 97042513 |
| a0003c0004t0057 | 0/0 | 12133 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12128): Show |
chr5 | 96931080 | 97042513 |
| a0004c0005t0003 | 0/0 | 12133 | 9 | 3 | 3 | 0 | 1 | 2 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12128): Show |
chr5 | 96931080 | 97042513 |
| a0004c0005t0044 | 0/1 | 12127 | 1 | 0 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12122): Show |
chr5 | 96931080 | 97042513 |
| a0004c0008t0026 | 0/0 | 12133 | 2 | 0 | 0 | 0 | 0 | 2 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12128): Show |
chr5 | 96931080 | 97042513 |
| a0005c0006t0001 | 0/0 | 12134 | 3 | 0 | 0 | 3 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12129): Show |
chr5 | 96931080 | 97042513 |
| a0006c0009t0028 | 0/0 | 12133 | 2 | 1 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12128): Show |
chr5 | 96931080 | 97042513 |
| a0007c0007t0005 | 0/0 | 12135 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12130): Show |
chr5 | 96931080 | 97042513 |
| a0008c0011t0007 | 0/0 | 12136 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12131): Show |
chr5 | 96931080 | 97042513 |
| a0009c0014t0003 | 0/0 | 12133 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12128): Show |
chr5 | 96931080 | 97042513 |
| a0010c0010t0007 | 0/0 | 12136 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | AGTCA others(12131): Show |
chr5 | 96931080 | 97042513 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0001g0197 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0003g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0005g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0005g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0009g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0009g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0009g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0009g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0009g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0009g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0009g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0009g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0010g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0010g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0010g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0010g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0011g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0011g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0011g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0011g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0011g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0012g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0012g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0012g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0012g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0013g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0013g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0013g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0013g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0014g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0014g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0014g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0014g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0015g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0015g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0015g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0015g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0016g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0016g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0016g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0016g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0018g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0018g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0018g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0019g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0021g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0021g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0021g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0022g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0022g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0023g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0024g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0024g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0025g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0025g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0029g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0030g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0031g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0032g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0033g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0034g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0035g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0036g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0037g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0038g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0039g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0040g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0047g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0051g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0052g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0053g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0054g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0001t0055g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0006g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0006g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0006g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0007g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0007g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0007g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0007g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0007g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0007g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0007g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0007g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0017g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0017g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0017g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0017g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0020g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0020g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0020g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0027g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0027g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0043g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0045g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0046g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0048g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0049g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0003t0050g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0012t0010g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0013t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0015t0010g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0001c0016t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0002c0002t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0003c0004t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0003c0004t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0003c0004t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0003c0004t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0003c0004t0008g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0003c0004t0008g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0003c0004t0008g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0003c0004t0008g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0003c0004t0008g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0003c0004t0008g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0003c0004t0008g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0003c0004t0008g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0003c0004t0008g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0003c0004t0041g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0003c0004t0042g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0003c0004t0056g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0003c0004t0057g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0004c0005t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0004c0005t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0004c0005t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0004c0005t0003g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0004c0005t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0004c0005t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0004c0005t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0004c0005t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0004c0005t0003g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0004c0005t0044g0303 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0004c0008t0026g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0005c0006t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0005c0006t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0005c0006t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0006c0009t0028g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0006c0009t0028g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0007c0007t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0007c0007t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0008c0011t0007g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0009c0014t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| a0010c0010t0007g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0319 | EUR | GBR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | GBR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00280 | hp1 | a0004 | c0005 | t0003 | g0335 | EUR | FIN | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0204 | EUR | FIN | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | FIN | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0332 | EUR | FIN | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00423 | hp2 | a0002 | c0002 | t0004 | g0277 | EAS | CHS | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00558 | hp1 | a0001 | c0001 | t0014 | g0163 | EAS | CHS | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0260 | EAS | CHS | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00597 | hp1 | a0008 | c0011 | t0007 | g0021 | EAS | CHS | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | CHS | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00609 | hp2 | a0001 | c0001 | t0012 | g0160 | EAS | CHS | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0312 | EAS | CHS | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00642 | hp1 | a0003 | c0004 | t0008 | g0149 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0294 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0306 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00735 | hp2 | a0003 | c0004 | t0056 | g0139 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00738 | hp1 | a0001 | c0001 | t0011 | g0239 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00738 | hp2 | a0001 | c0001 | t0010 | g0190 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01070 | hp1 | a0004 | c0005 | t0003 | g0302 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01070 | hp2 | a0001 | c0001 | t0015 | g0063 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0135 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01071 | hp2 | a0004 | c0005 | t0003 | g0284 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01074 | hp2 | a0006 | c0009 | t0028 | g0182 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01081 | hp1 | a0009 | c0014 | t0003 | g0321 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01081 | hp2 | a0001 | c0001 | t0015 | g0096 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01099 | hp2 | a0004 | c0005 | t0003 | g0282 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01109 | hp1 | a0001 | c0003 | t0006 | g0003 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01167 | hp1 | a0001 | c0001 | t0019 | g0004 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01167 | hp2 | a0001 | c0001 | t0010 | g0191 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01168 | hp2 | a0003 | c0004 | t0008 | g0141 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01169 | hp1 | a0001 | c0001 | t0019 | g0004 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01169 | hp2 | a0003 | c0004 | t0008 | g0148 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01192 | hp1 | a0001 | c0001 | t0025 | g0060 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01243 | hp1 | a0001 | c0001 | t0018 | g0174 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01243 | hp2 | a0001 | c0003 | t0043 | g0230 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01255 | hp2 | a0002 | c0002 | t0004 | g0012 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0008 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01257 | hp2 | a0001 | c0001 | t0009 | g0291 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0266 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0008 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01261 | hp1 | a0001 | c0001 | t0015 | g0108 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01261 | hp2 | a0001 | c0001 | t0019 | g0004 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01433 | hp2 | a0001 | c0001 | t0009 | g0316 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | IBS | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01515 | hp2 | a0003 | c0004 | t0003 | g0285 | EUR | IBS | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01516 | hp1 | a0003 | c0004 | t0008 | g0142 | EUR | IBS | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01516 | hp2 | a0003 | c0004 | t0003 | g0254 | EUR | IBS | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01517 | hp1 | a0003 | c0004 | t0003 | g0253 | EUR | IBS | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01517 | hp2 | a0003 | c0004 | t0008 | g0145 | EUR | IBS | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01884 | hp1 | a0001 | c0003 | t0006 | g0003 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0281 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01934 | hp2 | a0003 | c0004 | t0008 | g0150 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01943 | hp1 | a0001 | c0001 | t0032 | g0046 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01943 | hp2 | a0002 | c0002 | t0004 | g0274 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01975 | hp1 | a0001 | c0001 | t0055 | g0136 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01975 | hp2 | a0001 | c0001 | t0010 | g0189 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01978 | hp1 | a0002 | c0002 | t0004 | g0276 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01978 | hp2 | a0003 | c0004 | t0003 | g0286 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01981 | hp2 | a0001 | c0001 | t0010 | g0192 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0301 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02055 | hp1 | a0001 | c0003 | t0050 | g0187 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0235 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02056 | hp2 | a0002 | c0002 | t0004 | g0309 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0267 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02083 | hp1 | a0001 | c0003 | t0007 | g0026 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02129 | hp1 | a0001 | c0001 | t0038 | g0061 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02129 | hp2 | a0002 | c0002 | t0004 | g0278 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0310 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02135 | hp2 | a0001 | c0016 | t0001 | g0097 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0325 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0331 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0138 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02257 | hp1 | a0001 | c0001 | t0025 | g0029 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02293 | hp1 | a0001 | c0001 | t0015 | g0121 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0137 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02300 | hp1 | a0001 | c0001 | t0030 | g0053 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02451 | hp1 | a0001 | c0003 | t0017 | g0033 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02451 | hp2 | a0001 | c0003 | t0045 | g0237 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02572 | hp1 | a0004 | c0005 | t0003 | g0304 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02572 | hp2 | a0001 | c0001 | t0022 | g0089 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0323 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02622 | hp1 | a0001 | c0003 | t0006 | g0232 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02622 | hp2 | a0001 | c0003 | t0020 | g0183 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02630 | hp2 | a0001 | c0003 | t0006 | g0236 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0305 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02647 | hp2 | a0001 | c0001 | t0018 | g0176 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0249 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02738 | hp1 | a0001 | c0012 | t0010 | g0188 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02809 | hp1 | a0001 | c0003 | t0020 | g0185 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0263 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02818 | hp1 | a0001 | c0001 | t0011 | g0238 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02886 | hp1 | a0001 | c0003 | t0020 | g0184 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0287 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02895 | hp1 | a0001 | c0003 | t0006 | g0227 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02895 | hp2 | a0001 | c0001 | t0036 | g0112 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02896 | hp1 | a0001 | c0001 | t0016 | g0180 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02897 | hp1 | a0001 | c0003 | t0006 | g0233 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0264 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02976 | hp1 | a0001 | c0001 | t0016 | g0178 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03098 | hp1 | a0001 | c0003 | t0006 | g0226 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03098 | hp2 | a0001 | c0001 | t0022 | g0058 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03130 | hp1 | a0001 | c0001 | t0037 | g0051 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03130 | hp2 | a0001 | c0001 | t0018 | g0175 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0262 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0265 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03209 | hp1 | a0001 | c0001 | t0047 | g0334 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0256 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03225 | hp1 | a0001 | c0003 | t0006 | g0228 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03225 | hp2 | a0004 | c0005 | t0003 | g0257 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03239 | hp1 | a0003 | c0004 | t0008 | g0144 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03239 | hp2 | a0004 | c0005 | t0003 | g0283 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03453 | hp2 | a0004 | c0005 | t0003 | g0240 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03486 | hp2 | a0001 | c0003 | t0006 | g0231 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03491 | hp1 | a0004 | c0008 | t0026 | g0007 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0194 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03492 | hp1 | a0004 | c0008 | t0026 | g0007 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03492 | hp2 | a0001 | c0001 | t0052 | g0206 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0032 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03540 | hp1 | a0001 | c0003 | t0006 | g0234 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03540 | hp2 | a0001 | c0003 | t0017 | g0186 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03579 | hp1 | a0001 | c0001 | t0016 | g0179 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0327 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0293 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03654 | hp2 | a0001 | c0001 | t0031 | g0098 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0164 | SAS | STU | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0329 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0272 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03710 | hp1 | a0001 | c0001 | t0034 | g0054 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03710 | hp2 | a0003 | c0004 | t0008 | g0143 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0292 | SAS | BEB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03831 | hp2 | a0001 | c0015 | t0010 | g0193 | SAS | BEB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03834 | hp1 | a0001 | c0001 | t0053 | g0217 | SAS | BEB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0251 | SAS | BEB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03927 | hp2 | a0003 | c0004 | t0008 | g0151 | SAS | BEB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0290 | SAS | BEB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | STU | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0328 | SAS | STU | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG04204 | hp2 | a0003 | c0004 | t0042 | g0140 | SAS | STU | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | STU | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0250 | SAS | STU | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18522 | hp1 | a0001 | c0003 | t0017 | g0034 | AFR | YRI | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | YRI | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | CHB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0299 | EAS | CHB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0320 | EAS | CHB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18942 | hp2 | a0001 | c0003 | t0007 | g0023 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18947 | hp1 | a0001 | c0001 | t0039 | g0115 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0297 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18950 | hp1 | a0001 | c0001 | t0012 | g0156 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18950 | hp2 | a0002 | c0002 | t0004 | g0280 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18960 | hp1 | a0005 | c0006 | t0001 | g0092 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0298 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18961 | hp2 | a0001 | c0003 | t0007 | g0018 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18962 | hp1 | a0001 | c0001 | t0013 | g0157 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18962 | hp2 | a0002 | c0002 | t0004 | g0245 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0152 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18967 | hp1 | a0001 | c0001 | t0024 | g0093 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18968 | hp1 | a0001 | c0001 | t0021 | g0043 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18968 | hp2 | a0001 | c0001 | t0012 | g0172 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0271 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0317 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18973 | hp1 | a0007 | c0007 | t0005 | g0171 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18973 | hp2 | a0002 | c0002 | t0004 | g0246 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18977 | hp2 | a0001 | c0003 | t0046 | g0022 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0313 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18978 | hp2 | a0001 | c0003 | t0007 | g0025 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18979 | hp1 | a0002 | c0002 | t0004 | g0270 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18980 | hp2 | a0002 | c0002 | t0004 | g0333 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18981 | hp1 | a0002 | c0002 | t0004 | g0311 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18981 | hp2 | a0001 | c0001 | t0012 | g0173 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18982 | hp2 | a0001 | c0003 | t0027 | g0017 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18984 | hp2 | a0001 | c0001 | t0005 | g0165 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18985 | hp1 | a0001 | c0001 | t0005 | g0154 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18985 | hp2 | a0002 | c0002 | t0004 | g0307 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18986 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18987 | hp1 | a0001 | c0003 | t0007 | g0028 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18987 | hp2 | a0002 | c0002 | t0004 | g0242 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18988 | hp1 | a0002 | c0002 | t0004 | g0241 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18988 | hp2 | a0005 | c0006 | t0001 | g0073 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18990 | hp1 | a0001 | c0001 | t0029 | g0161 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18991 | hp1 | a0001 | c0001 | t0013 | g0167 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18991 | hp2 | a0001 | c0003 | t0048 | g0015 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18992 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18992 | hp2 | a0002 | c0002 | t0004 | g0010 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18994 | hp1 | a0007 | c0007 | t0005 | g0169 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18999 | hp1 | a0002 | c0002 | t0004 | g0212 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19002 | hp1 | a0001 | c0003 | t0007 | g0024 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19002 | hp2 | a0001 | c0001 | t0013 | g0158 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0177 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19005 | hp1 | a0005 | c0006 | t0001 | g0075 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19005 | hp2 | a0002 | c0002 | t0004 | g0273 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19006 | hp1 | a0001 | c0003 | t0007 | g0027 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19007 | hp2 | a0002 | c0002 | t0004 | g0010 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19009 | hp2 | a0002 | c0002 | t0004 | g0308 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19010 | hp1 | a0001 | c0001 | t0023 | g0005 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19010 | hp2 | a0001 | c0001 | t0005 | g0155 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | LWK | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19030 | hp2 | a0001 | c0001 | t0051 | g0229 | AFR | LWK | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19043 | hp2 | a0001 | c0001 | t0040 | g0030 | AFR | LWK | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19056 | hp1 | a0001 | c0001 | t0021 | g0038 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0259 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19057 | hp1 | a0001 | c0001 | t0014 | g0162 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19058 | hp2 | a0001 | c0003 | t0049 | g0020 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19060 | hp1 | a0001 | c0003 | t0007 | g0019 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19060 | hp2 | a0002 | c0002 | t0004 | g0243 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19064 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19064 | hp2 | a0001 | c0001 | t0054 | g0207 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19066 | hp1 | a0001 | c0001 | t0024 | g0045 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0295 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19068 | hp1 | a0002 | c0002 | t0004 | g0012 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19068 | hp2 | a0001 | c0001 | t0023 | g0005 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19074 | hp1 | a0001 | c0001 | t0013 | g0166 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0296 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19076 | hp2 | a0002 | c0002 | t0002 | g0314 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19077 | hp2 | a0001 | c0001 | t0014 | g0159 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19080 | hp1 | a0002 | c0002 | t0004 | g0255 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19081 | hp1 | a0001 | c0013 | t0001 | g0104 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19083 | hp1 | a0010 | c0010 | t0007 | g0014 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19083 | hp2 | a0001 | c0001 | t0021 | g0065 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0300 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19087 | hp1 | a0001 | c0001 | t0014 | g0168 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19087 | hp2 | a0002 | c0002 | t0004 | g0244 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0170 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19088 | hp2 | a0001 | c0001 | t0033 | g0095 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19090 | hp1 | a0002 | c0002 | t0004 | g0275 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19090 | hp2 | a0001 | c0001 | t0005 | g0153 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | YRI | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA19240 | hp2 | a0001 | c0003 | t0006 | g0003 | AFR | YRI | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA20129 | hp1 | a0001 | c0001 | t0011 | g0031 | AFR | ASW | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA20129 | hp2 | a0001 | c0001 | t0009 | g0324 | AFR | ASW | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA20752 | hp1 | a0003 | c0004 | t0057 | g0146 | EUR | TSI | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0322 | EUR | TSI | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0279 | SAS | GIH | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA20905 | hp2 | a0004 | c0005 | t0003 | g0289 | SAS | GIH | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01123 | hp1 | a0003 | c0004 | t0041 | g0147 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG01123 | hp2 | a0001 | c0001 | t0035 | g0069 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02559 | hp1 | a0001 | c0001 | t0016 | g0181 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG02559 | hp2 | a0001 | c0001 | t0009 | g0326 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03471 | hp1 | a0001 | c0001 | t0011 | g0318 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | USA | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| HG06807 | hp2 | a0006 | c0009 | t0028 | g0248 | AFR | USA | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0330 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA18955 | hp2 | a0001 | c0003 | t0027 | g0016 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA20300 | hp1 | a0001 | c0003 | t0017 | g0035 | AFR | USA | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA20300 | hp2 | a0002 | c0002 | t0004 | g0211 | AFR | USA | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| homoSapiens | chm13v2 | a0004 | c0005 | t0044 | g0303 | REF | REF | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0197 | REF | REF | LNPEP_chr5_96931080_97042513 | LNPEP | chr5 | 96931080 | 97042513 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:96979374 | T | C | 1 | a0007 | 2 | NA18973.hp1 NA18994.hp1 |
missense_variant | MODERATE | c.256T>C | p.Ser86Pro | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/18 | 332/12134 | 256/3078 | 86/1025 | chr5 | 96979374 | |||
| chr5:96979616 | C | G | 1 | a0006 | 2 | HG01074.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.498C>G | p.Ile166Met | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/18 | 574/12134 | 498/3078 | 166/1025 | chr5 | 96979616 | |||
| chr5:96979783 | T | G | 1 | a0010 | 1 | NA19083.hp1 | missense_variant | MODERATE | c.665T>G | p.Met222Arg | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/18 | 741/12134 | 665/3078 | 222/1025 | chr5 | 96979783 | |||
| chr5:96985198 | G | A | 1 | a0005 | 3 | NA18960.hp1 NA18988.hp2 NA19005.hp1 |
missense_variant | MODERATE | c.979G>A | p.Ala327Thr | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 3/18 | 1055/12134 | 979/3078 | 327/1025 | chr5 | 96985198 | |||
| chr5:96986656 | G | A | 1 | a0003 | 17 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(14): Show |
missense_variant | MODERATE | c.1117G>A | p.Val373Ile | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/18 | 1193/12134 | 1117/3078 | 373/1025 | chr5 | 96986656 | |||
| chr5:96993097 | A | G | 1 | a0005 | 3 | NA18960.hp1 NA18988.hp2 NA19005.hp1 |
missense_variant | MODERATE | c.1214A>G | p.Gln405Arg | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 5/18 | 1290/12134 | 1214/3078 | 405/1025 | chr5 | 96993097 | |||
| chr5:96996429 | C | A | 1 | a0008 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.1447C>A | p.Leu483Ile | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 7/18 | 1523/12134 | 1447/3078 | 483/1025 | chr5 | 96996429 | |||
| chr5:97006208 | C | T | 1 | a0009 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.1921C>T | p.Pro641Ser | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 10/18 | 1997/12134 | 1921/3078 | 641/1025 | chr5 | 97006208 | |||
| chr5:97015006 | G | A | 1 | a0002 | 71 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
missense_variant | MODERATE | c.2287G>A | p.Ala763Thr | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/18 | 2363/12134 | 2287/3078 | 763/1025 | chr5 | 97015006 | |||
| chr5:97027755 | A | G | 2 | a0004 a0009 |
12 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(9): Show |
missense_variant | MODERATE | c.2887A>G | p.Ile963Val | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 17/18 | 2963/12134 | 2887/3078 | 963/1025 | chr5 | 97027755 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:96979667 | G | A | 1 | a0004c0008 | 2 | HG03491.hp1 HG03492.hp1 |
synonymous_variant | LOW | c.549G>A | p.Pro183Pro | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/18 | 625/12134 | 549/3078 | 183/1025 | chr5 | 96979667 | |||
| chr5:96979751 | C | T | 1 | a0001c0016 | 1 | HG02135.hp2 | synonymous_variant | LOW | c.633C>T | p.Ser211Ser | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/18 | 709/12134 | 633/3078 | 211/1025 | chr5 | 96979751 | |||
| chr5:96979847 | C | T | 1 | a0001c0015 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.729C>T | p.Ile243Ile | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/18 | 805/12134 | 729/3078 | 243/1025 | chr5 | 96979847 | |||
| chr5:97022329 | A | G | 1 | a0001c0013 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.2406A>G | p.Gln802Gln | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/18 | 2482/12134 | 2406/3078 | 802/1025 | chr5 | 97022329 | |||
| chr5:97022356 | G | A | 3 | a0001c0003 a0008c0011 a0010c0010 |
36 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(33): Show |
synonymous_variant | LOW | c.2433G>A | p.Glu811Glu | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/18 | 2509/12134 | 2433/3078 | 811/1025 | chr5 | 97022356 | |||
| chr5:97022425 | C | T | 2 | a0001c0012 a0001c0015 |
2 | HG02738.hp1 HG03831.hp2 |
synonymous_variant | LOW | c.2502C>T | p.Asn834Asn | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/18 | 2578/12134 | 2502/3078 | 834/1025 | chr5 | 97022425 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:96936100 | C | T | 1 | a0006c0009t0028 | 2 | HG01074.hp2 HG06807.hp2 |
5_prime_UTR_variant | MODIFIER | c.-56C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/18 | 56 | chr5 | 96936100 | ||||||
| chr5:96936113 | A | C | 1 | a0001c0001t0021 | 3 | NA18968.hp1 NA19056.hp1 NA19083.hp2 |
5_prime_UTR_variant | MODIFIER | c.-43A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/18 | 43 | chr5 | 96936113 | ||||||
| chr5:97028667 | C | T | 2 | a0003c0004t0056 a0003c0004t0057 |
2 | HG00735.hp2 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*134C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 134 | chr5 | 97028667 | ||||||
| chr5:97028750 | C | G | 35 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(32): Show |
202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*217C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 217 | chr5 | 97028750 | ||||||
| chr5:97028920 | C | T | 1 | a0001c0003t0027 | 2 | NA18955.hp2 NA18982.hp2 |
3_prime_UTR_variant | MODIFIER | c.*387C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 387 | chr5 | 97028920 | ||||||
| chr5:97028941 | T | C | 5 | a0003c0004t0008 a0003c0004t0041 a0003c0004t0042 others(2): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*408T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 408 | chr5 | 97028941 | ||||||
| chr5:97028964 | T | A | 3 | a0001c0001t0010 a0001c0012t0010 a0001c0015t0010 |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*431T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 431 | chr5 | 97028964 | ||||||
| chr5:97029034 | T | A | 6 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0013 others(3): Show |
28 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*501T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 501 | chr5 | 97029034 | ||||||
| chr5:97029121 | T | A | 1 | a0001c0001t0029 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*588T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 588 | chr5 | 97029121 | ||||||
| chr5:97029122 | A | C | 1 | a0001c0001t0029 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*589A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 589 | chr5 | 97029122 | ||||||
| chr5:97029123 | T | G | 1 | a0001c0001t0029 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*590T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 590 | chr5 | 97029123 | ||||||
| chr5:97029124 | T | C | 1 | a0001c0001t0029 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*591T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 591 | chr5 | 97029124 | ||||||
| chr5:97029126 | T | C | 1 | a0001c0001t0029 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*593T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 593 | chr5 | 97029126 | ||||||
| chr5:97029127 | G | T | 5 | a0003c0004t0008 a0003c0004t0041 a0003c0004t0042 others(2): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*594G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 594 | chr5 | 97029127 | ||||||
| chr5:97029128 | T | C | 1 | a0001c0001t0029 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*595T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 595 | chr5 | 97029128 | ||||||
| chr5:97029130 | T | A | 1 | a0001c0001t0029 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*597T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 597 | chr5 | 97029130 | ||||||
| chr5:97029132 | T | A | 1 | a0001c0001t0029 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*599T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 599 | chr5 | 97029132 | ||||||
| chr5:97029135 | CCTGCCGA others(7): Show |
C | 1 | a0001c0001t0029 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*603_*616delCTGCCG others(8): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 603 | chr5 | 97029135 | ||||||
| chr5:97029141 | G | A | 2 | a0001c0012t0010 a0001c0015t0010 |
2 | HG02738.hp1 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*608G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 608 | chr5 | 97029141 | ||||||
| chr5:97029147 | C | T | 5 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0013 others(2): Show |
27 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*614C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 614 | chr5 | 97029147 | ||||||
| chr5:97029150 | G | A | 1 | a0001c0001t0029 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*617G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 617 | chr5 | 97029150 | ||||||
| chr5:97029693 | T | A | 1 | a0001c0003t0043 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1160T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 1160 | chr5 | 97029693 | ||||||
| chr5:97029723 | T | C | 1 | a0001c0001t0022 | 2 | HG02572.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1190T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 1190 | chr5 | 97029723 | ||||||
| chr5:97030616 | CTCTCTGT others(7): Show |
C | 3 | a0001c0001t0010 a0001c0012t0010 a0001c0015t0010 |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2085_*2098delCTCT others(10): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2085 | INFO_REALIGN_3_PRIME | chr5 | 97030616 | |||||
| chr5:97030618 | CTCTGTGT others(7): Show |
C | 1 | a0001c0001t0018 | 3 | HG01243.hp1 HG02647.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2087_*2100delCTGT others(10): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2087 | INFO_REALIGN_3_PRIME | chr5 | 97030618 | |||||
| chr5:97030620 | C | CTG | 3 | a0001c0001t0001 a0001c0001t0023 a0001c0001t0030 |
15 | HG00621.hp2 HG02027.hp1 HG02071.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2135_*2136dupGT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2137 | INFO_REALIGN_3_PRIME | chr5 | 97030620 | |||||
| chr5:97030620 | C | CTGTG | 3 | a0001c0001t0001 a0001c0001t0023 a0001c0001t0029 |
4 | HG01934.hp1 HG02615.hp2 NA18990.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2133_*2136dupGTGT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2137 | INFO_REALIGN_3_PRIME | chr5 | 97030620 | |||||
| chr5:97030620 | C | CTGTGTGT others(1): Show |
3 | a0001c0001t0001 a0001c0001t0032 a0001c0001t0039 |
4 | HG01099.hp1 HG01175.hp1 HG01943.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2129_*2136dupGTGT others(4): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2137 | INFO_REALIGN_3_PRIME | chr5 | 97030620 | |||||
| chr5:97030620 | C | G | 1 | a0001c0001t0001 | 3 | HG01255.hp1 HG03195.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2087C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2087 | chr5 | 97030620 | ||||||
| chr5:97030620 | CTG | C | 9 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(6): Show |
19 | HG01123.hp2 HG01192.hp2 HG01433.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2135_*2136delGT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2135 | INFO_REALIGN_3_PRIME | chr5 | 97030620 | |||||
| chr5:97030620 | CTGTG | C | 9 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(6): Show |
25 | HG00140.hp1 HG00558.hp2 HG00621.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2133_*2136delGTGT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2133 | INFO_REALIGN_3_PRIME | chr5 | 97030620 | |||||
| chr5:97030620 | CTGTGTG | C | 18 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(15): Show |
118 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*2131_*2136delGTGT others(2): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2131 | INFO_REALIGN_3_PRIME | chr5 | 97030620 | |||||
| chr5:97030620 | CTGTGTGT others(1): Show |
C | 10 | a0001c0001t0002 a0001c0001t0003 a0001c0003t0007 others(7): Show |
28 | HG00597.hp1 HG01884.hp2 HG02055.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2129_*2136delGTGT others(4): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2129 | INFO_REALIGN_3_PRIME | chr5 | 97030620 | |||||
| chr5:97030620 | CTGTGTGT others(3): Show |
C | 1 | a0001c0001t0016 | 4 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2127_*2136delGTGT others(6): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2127 | INFO_REALIGN_3_PRIME | chr5 | 97030620 | |||||
| chr5:97030620 | CTGTGTGT others(5): Show |
C | 5 | a0001c0003t0006 a0001c0003t0043 a0001c0003t0045 others(2): Show |
15 | HG00735.hp2 HG01109.hp1 HG01243.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2125_*2136delGTGT others(8): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2125 | INFO_REALIGN_3_PRIME | chr5 | 97030620 | |||||
| chr5:97030620 | CTGTGTGT others(7): Show |
C | 10 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0013 others(7): Show |
38 | HG00558.hp1 HG00609.hp2 HG00642.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2123_*2136delGTGT others(10): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2123 | INFO_REALIGN_3_PRIME | chr5 | 97030620 | |||||
| chr5:97030620 | CTGTGTGT others(9): Show |
C | 2 | a0001c0001t0001 a0001c0001t0005 |
3 | HG02698.hp2 HG04199.hp2 NA18986.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2121_*2136delGTGT others(12): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2121 | INFO_REALIGN_3_PRIME | chr5 | 97030620 | |||||
| chr5:97030620 | CTGTGTGT others(13): Show |
C | 1 | a0001c0001t0047 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2117_*2136delGTGT others(16): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2117 | INFO_REALIGN_3_PRIME | chr5 | 97030620 | |||||
| chr5:97030622 | G | C | 5 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2089G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2089 | chr5 | 97030622 | ||||||
| chr5:97030624 | G | C | 6 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(3): Show |
6 | HG01192.hp2 HG01975.hp1 HG02055.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2091G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2091 | chr5 | 97030624 | ||||||
| chr5:97030626 | G | C | 7 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(4): Show |
22 | HG00140.hp1 HG00558.hp2 HG00621.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2093G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2093 | chr5 | 97030626 | ||||||
| chr5:97030628 | G | C | 16 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(13): Show |
114 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*2095G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2095 | chr5 | 97030628 | ||||||
| chr5:97030630 | G | C | 11 | a0001c0001t0002 a0001c0001t0003 a0001c0003t0007 others(8): Show |
32 | HG00323.hp2 HG00597.hp1 HG01884.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2097G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2097 | chr5 | 97030630 | ||||||
| chr5:97030634 | G | C | 3 | a0001c0003t0006 a0001c0003t0043 a0001c0003t0045 |
13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2101G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2101 | chr5 | 97030634 | ||||||
| chr5:97030636 | G | C | 1 | a0001c0003t0046 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2103G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2103 | chr5 | 97030636 | ||||||
| chr5:97030642 | G | C | 1 | a0001c0001t0047 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2109G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2109 | chr5 | 97030642 | ||||||
| chr5:97030768 | T | C | 1 | a0003c0004t0041 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2235T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2235 | chr5 | 97030768 | ||||||
| chr5:97030788 | C | T | 1 | a0001c0003t0020 | 3 | HG02622.hp2 HG02809.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2255C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2255 | chr5 | 97030788 | ||||||
| chr5:97030795 | A | C | 1 | a0003c0004t0041 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2262A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2262 | chr5 | 97030795 | ||||||
| chr5:97031181 | TA | T | 8 | a0001c0001t0003 a0001c0001t0019 a0001c0001t0055 others(5): Show |
39 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*2654delA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2654 | INFO_REALIGN_3_PRIME | chr5 | 97031181 | |||||
| chr5:97031207 | G | A | 1 | a0001c0001t0030 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2674G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2674 | chr5 | 97031207 | ||||||
| chr5:97031222 | A | G | 2 | a0001c0001t0016 a0001c0001t0040 |
5 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2689A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2689 | chr5 | 97031222 | ||||||
| chr5:97031524 | G | A | 5 | a0003c0004t0008 a0003c0004t0041 a0003c0004t0042 others(2): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2991G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2991 | chr5 | 97031524 | ||||||
| chr5:97031527 | C | G | 5 | a0003c0004t0008 a0003c0004t0041 a0003c0004t0042 others(2): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2994C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 2994 | chr5 | 97031527 | ||||||
| chr5:97031617 | G | A | 3 | a0001c0003t0006 a0001c0003t0043 a0001c0003t0045 |
13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3084G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 3084 | chr5 | 97031617 | ||||||
| chr5:97031704 | G | A | 40 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(37): Show |
211 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*3171G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 3171 | chr5 | 97031704 | ||||||
| chr5:97031896 | C | CA | 7 | a0001c0003t0007 a0001c0003t0027 a0001c0003t0046 others(4): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3373dupA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 3374 | INFO_REALIGN_3_PRIME | chr5 | 97031896 | |||||
| chr5:97031896 | C | CAA | 4 | a0003c0004t0008 a0003c0004t0041 a0003c0004t0056 others(1): Show |
12 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3372_*3373dupAA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 3374 | INFO_REALIGN_3_PRIME | chr5 | 97031896 | |||||
| chr5:97031943 | T | G | 1 | a0001c0001t0015 | 4 | HG01070.hp2 HG01081.hp2 HG01261.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3410T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 3410 | chr5 | 97031943 | ||||||
| chr5:97031966 | G | A | 1 | a0001c0001t0055 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3433G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 3433 | chr5 | 97031966 | ||||||
| chr5:97032020 | T | A | 2 | a0001c0001t0016 a0001c0001t0040 |
5 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3487T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 3487 | chr5 | 97032020 | ||||||
| chr5:97032118 | T | C | 1 | a0001c0001t0023 | 2 | NA19010.hp1 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3585T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 3585 | chr5 | 97032118 | ||||||
| chr5:97032171 | A | G | 5 | a0003c0004t0008 a0003c0004t0041 a0003c0004t0042 others(2): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3638A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 3638 | chr5 | 97032171 | ||||||
| chr5:97032254 | T | C | 5 | a0003c0004t0008 a0003c0004t0041 a0003c0004t0042 others(2): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3721T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 3721 | chr5 | 97032254 | ||||||
| chr5:97032391 | C | A | 13 | a0001c0003t0006 a0001c0003t0007 a0001c0003t0017 others(10): Show |
36 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*3858C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 3858 | chr5 | 97032391 | ||||||
| chr5:97032439 | C | T | 1 | a0001c0001t0039 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3906C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 3906 | chr5 | 97032439 | ||||||
| chr5:97032671 | C | G | 5 | a0003c0004t0008 a0003c0004t0041 a0003c0004t0042 others(2): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4138C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 4138 | chr5 | 97032671 | ||||||
| chr5:97032753 | C | T | 3 | a0001c0001t0010 a0001c0012t0010 a0001c0015t0010 |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4220C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 4220 | chr5 | 97032753 | ||||||
| chr5:97032878 | G | A | 1 | a0001c0001t0018 | 3 | HG01243.hp1 HG02647.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4345G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 4345 | chr5 | 97032878 | ||||||
| chr5:97033135 | T | A | 1 | a0002c0002t0004 | 26 | HG00423.hp2 HG01255.hp2 HG01943.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4602T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 4602 | chr5 | 97033135 | ||||||
| chr5:97033369 | G | A | 1 | a0001c0001t0051 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4836G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 4836 | chr5 | 97033369 | ||||||
| chr5:97033442 | C | G | 1 | a0006c0009t0028 | 2 | HG01074.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4909C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 4909 | chr5 | 97033442 | ||||||
| chr5:97033581 | A | G | 1 | a0001c0003t0049 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5048A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 5048 | chr5 | 97033581 | ||||||
| chr5:97034076 | G | A | 1 | a0001c0001t0019 | 3 | HG01167.hp1 HG01169.hp1 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5543G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 5543 | chr5 | 97034076 | ||||||
| chr5:97034256 | C | A | 3 | a0001c0001t0010 a0001c0012t0010 a0001c0015t0010 |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5723C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 5723 | chr5 | 97034256 | ||||||
| chr5:97034344 | C | T | 1 | a0001c0001t0038 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5811C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 5811 | chr5 | 97034344 | ||||||
| chr5:97034346 | C | T | 1 | a0001c0001t0014 | 4 | HG00558.hp1 NA19057.hp1 NA19077.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5813C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 5813 | chr5 | 97034346 | ||||||
| chr5:97034397 | G | GT | 11 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0012 others(8): Show |
41 | HG00558.hp1 HG00609.hp2 HG00738.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*5871dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 5872 | INFO_REALIGN_3_PRIME | chr5 | 97034397 | |||||
| chr5:97034413 | G | GT | 13 | a0001c0001t0054 a0001c0003t0006 a0001c0003t0007 others(10): Show |
36 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*5890dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 5891 | INFO_REALIGN_3_PRIME | chr5 | 97034413 | |||||
| chr5:97034496 | T | C | 2 | a0001c0001t0024 a0001c0001t0038 |
3 | HG02129.hp1 NA18967.hp1 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5963T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 5963 | chr5 | 97034496 | ||||||
| chr5:97034541 | G | A | 1 | a0001c0001t0025 | 2 | HG01192.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6008G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 6008 | chr5 | 97034541 | ||||||
| chr5:97034558 | G | A | 5 | a0003c0004t0008 a0003c0004t0041 a0003c0004t0042 others(2): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*6025G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 6025 | chr5 | 97034558 | ||||||
| chr5:97034760 | T | A | 1 | a0001c0001t0032 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6227T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 6227 | chr5 | 97034760 | ||||||
| chr5:97034812 | A | G | 1 | a0001c0001t0037 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6279A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 6279 | chr5 | 97034812 | ||||||
| chr5:97035068 | A | G | 1 | a0001c0001t0047 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6535A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 6535 | chr5 | 97035068 | ||||||
| chr5:97035130 | A | G | 1 | a0001c0001t0053 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6597A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 6597 | chr5 | 97035130 | ||||||
| chr5:97035175 | G | A | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0009 others(14): Show |
154 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*6642G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 6642 | chr5 | 97035175 | ||||||
| chr5:97035310 | G | A | 3 | a0001c0001t0010 a0001c0012t0010 a0001c0015t0010 |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6777G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 6777 | chr5 | 97035310 | ||||||
| chr5:97035363 | C | T | 1 | a0001c0001t0040 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6830C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 6830 | chr5 | 97035363 | ||||||
| chr5:97035394 | T | C | 8 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0013 others(5): Show |
35 | HG00558.hp1 HG00609.hp2 HG01243.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*6861T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 6861 | chr5 | 97035394 | ||||||
| chr5:97035440 | A | G | 5 | a0003c0004t0008 a0003c0004t0041 a0003c0004t0042 others(2): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*6907A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 6907 | chr5 | 97035440 | ||||||
| chr5:97035472 | C | A | 1 | a0001c0001t0033 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6939C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 6939 | chr5 | 97035472 | ||||||
| chr5:97035517 | C | T | 1 | a0001c0001t0013 | 4 | NA18962.hp1 NA18991.hp1 NA19002.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6984C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 6984 | chr5 | 97035517 | ||||||
| chr5:97035553 | C | T | 1 | a0001c0001t0011 | 5 | HG00738.hp1 HG02818.hp1 HG03471.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7020C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 7020 | chr5 | 97035553 | ||||||
| chr5:97035631 | A | G | 8 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0013 others(5): Show |
35 | HG00558.hp1 HG00609.hp2 HG01243.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*7098A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 7098 | chr5 | 97035631 | ||||||
| chr5:97035678 | G | A | 1 | a0001c0001t0012 | 4 | HG00609.hp2 NA18950.hp1 NA18968.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7145G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 7145 | chr5 | 97035678 | ||||||
| chr5:97035906 | G | A | 1 | a0001c0001t0034 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7373G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 7373 | chr5 | 97035906 | ||||||
| chr5:97035940 | T | A | 7 | a0001c0003t0007 a0001c0003t0027 a0001c0003t0046 others(4): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*7407T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 7407 | chr5 | 97035940 | ||||||
| chr5:97036052 | A | T | 1 | a0001c0001t0038 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7519A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 7519 | chr5 | 97036052 | ||||||
| chr5:97036212 | G | T | 1 | a0001c0003t0050 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7679G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 7679 | chr5 | 97036212 | ||||||
| chr5:97036267 | CCCA | C | 5 | a0003c0004t0008 a0003c0004t0041 a0003c0004t0042 others(2): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*7736_*7738delCAC | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 7736 | INFO_REALIGN_3_PRIME | chr5 | 97036267 | |||||
| chr5:97036461 | G | A | 28 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(25): Show |
195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*7928G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 7928 | chr5 | 97036461 | ||||||
| chr5:97036481 | G | A | 8 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0013 others(5): Show |
35 | HG00558.hp1 HG00609.hp2 HG01243.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*7948G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 7948 | chr5 | 97036481 | ||||||
| chr5:97036852 | C | G | 1 | a0001c0001t0036 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8319C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 8319 | chr5 | 97036852 | ||||||
| chr5:97036953 | G | T | 1 | a0001c0001t0035 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8420G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 8420 | chr5 | 97036953 | ||||||
| chr5:97036998 | G | A | 2 | a0001c0001t0009 a0001c0001t0051 |
9 | HG01257.hp2 HG01433.hp2 HG02055.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*8465G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 8465 | chr5 | 97036998 | ||||||
| chr5:97037066 | A | G | 1 | a0003c0004t0057 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8533A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 8533 | chr5 | 97037066 | ||||||
| chr5:97037314 | T | C | 1 | a0001c0001t0052 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8781T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 8781 | chr5 | 97037314 | ||||||
| chr5:97037389 | G | C | 1 | a0001c0003t0045 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8856G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 8856 | chr5 | 97037389 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:96936238 | G | A | 15 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.19+64G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96936238 | |||||||
| chr5:96936302 | G | A | 1 | a0001c0001t0025g0029 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.19+128G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96936302 | |||||||
| chr5:96936325 | G | A | 1 | a0001c0001t0040g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.19+151G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96936325 | |||||||
| chr5:96936361 | G | A | 2 | a0001c0001t0011g0031 a0001c0001t0011g0032 |
2 | HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.19+187G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96936361 | |||||||
| chr5:96936362 | T | C | 3 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 |
3 | HG02451.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.19+188T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96936362 | |||||||
| chr5:96936391 | G | GCGC | 103 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(100): Show |
106 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.19+227_19+229dupCG others(1): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96936391 | ||||||
| chr5:96936408 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.19+234C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96936408 | |||||||
| chr5:96936495 | C | A | 5 | a0001c0001t0003g0001 a0001c0001t0003g0135 a0001c0001t0003g0137 others(2): Show |
7 | HG01069.hp1 HG01071.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+321C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96936495 | |||||||
| chr5:96936529 | G | C | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.19+355G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96936529 | |||||||
| chr5:96936651 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.19+477G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96936651 | |||||||
| chr5:96936716 | T | G | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+542T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96936716 | |||||||
| chr5:96936803 | A | G | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.19+629A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96936803 | |||||||
| chr5:96936824 | CAA | C | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+652_19+653delAA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96936824 | ||||||
| chr5:96936874 | G | A | 1 | a0006c0009t0028g0182 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.19+700G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96936874 | |||||||
| chr5:96936955 | A | C | 1 | a0004c0005t0003g0335 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.19+781A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96936955 | |||||||
| chr5:96937024 | T | G | 8 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.19+850T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96937024 | |||||||
| chr5:96937130 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.19+956A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96937130 | |||||||
| chr5:96937274 | T | C | 21 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(18): Show |
21 | HG00597.hp1 HG00738.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.19+1100T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96937274 | |||||||
| chr5:96937329 | A | T | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+1155A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96937329 | |||||||
| chr5:96937330 | T | C | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+1156T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96937330 | |||||||
| chr5:96937476 | G | A | 103 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(100): Show |
106 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.19+1302G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96937476 | |||||||
| chr5:96937483 | G | A | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+1309G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96937483 | |||||||
| chr5:96937594 | C | T | 137 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(134): Show |
143 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.19+1420C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96937594 | |||||||
| chr5:96937694 | C | T | 1 | a0001c0001t0047g0334 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.19+1520C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96937694 | |||||||
| chr5:96938063 | T | C | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+1889T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96938063 | |||||||
| chr5:96938365 | A | T | 4 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(1): Show |
4 | NA18970.hp1 NA18975.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+2191A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96938365 | |||||||
| chr5:96938460 | A | T | 1 | a0004c0008t0026g0007 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.19+2286A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96938460 | |||||||
| chr5:96938519 | C | T | 149 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(146): Show |
155 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.19+2345C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96938519 | |||||||
| chr5:96938565 | G | GT | 5 | a0001c0001t0001g0128 a0001c0003t0007g0026 a0001c0003t0007g0027 others(2): Show |
5 | HG02083.hp1 HG02615.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+2399dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96938565 | ||||||
| chr5:96938629 | G | T | 8 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.19+2455G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96938629 | |||||||
| chr5:96938831 | G | T | 1 | a0001c0001t0001g0127 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.19+2657G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96938831 | |||||||
| chr5:96938876 | T | G | 1 | a0003c0004t0056g0139 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.19+2702T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96938876 | |||||||
| chr5:96938963 | G | A | 1 | a0002c0002t0002g0194 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.19+2789G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96938963 | |||||||
| chr5:96938984 | CA | C | 214 | a0001c0001t0001g0036 a0001c0001t0001g0047 a0001c0001t0001g0048 others(211): Show |
224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.19+2825delA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96938984 | ||||||
| chr5:96938984 | CAA | C | 34 | a0001c0001t0001g0006 a0001c0001t0001g0117 a0001c0001t0001g0118 others(31): Show |
35 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.19+2824_19+2825del others(2): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96938984 | ||||||
| chr5:96939016 | G | T | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+2842G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96939016 | |||||||
| chr5:96939205 | A | G | 2 | a0002c0002t0002g0328 a0002c0002t0002g0329 |
2 | HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.19+3031A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96939205 | |||||||
| chr5:96939216 | C | CT | 132 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(129): Show |
138 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.19+3057dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96939216 | ||||||
| chr5:96939216 | C | CTT | 6 | a0001c0001t0005g0177 a0001c0001t0018g0174 a0001c0001t0018g0175 others(3): Show |
6 | HG01243.hp1 HG02257.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.19+3056_19+3057dup others(2): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96939216 | ||||||
| chr5:96939415 | T | C | 3 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 |
3 | HG02451.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.19+3241T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96939415 | |||||||
| chr5:96939450 | G | A | 103 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(100): Show |
106 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.19+3276G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96939450 | |||||||
| chr5:96939462 | C | T | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+3288C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96939462 | |||||||
| chr5:96939482 | C | T | 103 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(100): Show |
106 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.19+3308C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96939482 | |||||||
| chr5:96939497 | G | A | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+3323G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96939497 | |||||||
| chr5:96939597 | A | ATAATT | 191 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(188): Show |
199 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.19+3426_19+3427ins others(5): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96939597 | ||||||
| chr5:96939640 | A | G | 25 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(22): Show |
28 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.19+3466A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96939640 | |||||||
| chr5:96939709 | C | T | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+3535C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96939709 | |||||||
| chr5:96939818 | AT | A | 8 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.19+3646delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96939818 | ||||||
| chr5:96939846 | A | G | 8 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0225 others(5): Show |
8 | HG02145.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.19+3672A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96939846 | |||||||
| chr5:96939873 | TA | T | 24 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0153 others(21): Show |
27 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(24): Show |
intron_variant | MODIFIER | c.19+3708delA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96939873 | ||||||
| chr5:96939883 | T | A | 1 | a0001c0001t0040g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.19+3709T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96939883 | |||||||
| chr5:96940234 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.19+4060C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96940234 | |||||||
| chr5:96940257 | C | T | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.19+4083C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96940257 | |||||||
| chr5:96940283 | A | T | 1 | a0001c0001t0001g0036 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.19+4109A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96940283 | |||||||
| chr5:96940302 | G | A | 4 | a0001c0001t0011g0031 a0001c0001t0011g0032 a0001c0001t0011g0238 others(1): Show |
4 | HG00738.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+4128G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96940302 | |||||||
| chr5:96940635 | T | C | 2 | a0001c0001t0002g0195 a0001c0001t0002g0196 |
2 | HG00741.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.19+4461T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96940635 | |||||||
| chr5:96940682 | A | G | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+4508A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96940682 | |||||||
| chr5:96940691 | G | C | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+4517G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96940691 | |||||||
| chr5:96940926 | A | C | 2 | a0001c0012t0010g0188 a0001c0015t0010g0193 |
2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.19+4752A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96940926 | |||||||
| chr5:96941004 | A | T | 1 | a0001c0003t0050g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.19+4830A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96941004 | |||||||
| chr5:96941173 | C | T | 103 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(100): Show |
106 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.19+4999C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96941173 | |||||||
| chr5:96941175 | C | G | 2 | a0001c0001t0009g0326 a0001c0001t0009g0327 |
2 | HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.19+5001C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96941175 | |||||||
| chr5:96942017 | G | A | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+5843G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96942017 | |||||||
| chr5:96942238 | G | A | 25 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(22): Show |
28 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.19+6064G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96942238 | |||||||
| chr5:96942279 | C | T | 1 | a0001c0001t0039g0115 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.19+6105C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96942279 | |||||||
| chr5:96942498 | A | G | 1 | a0001c0001t0040g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.19+6324A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96942498 | |||||||
| chr5:96942563 | A | G | 5 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(2): Show |
5 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+6389A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96942563 | |||||||
| chr5:96942602 | C | T | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.19+6428C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96942602 | |||||||
| chr5:96942652 | C | CA | 6 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(3): Show |
6 | HG02056.hp1 HG02083.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.19+6497dupA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96942652 | ||||||
| chr5:96942652 | CA | C | 183 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0002g0009 others(180): Show |
194 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.19+6497delA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96942652 | ||||||
| chr5:96942652 | CAA | C | 6 | a0001c0001t0002g0221 a0001c0001t0002g0222 a0001c0001t0003g0322 others(3): Show |
6 | HG00323.hp2 HG01081.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.19+6496_19+6497del others(2): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96942652 | ||||||
| chr5:96942880 | AT | A | 25 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(22): Show |
28 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.19+6707delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96942880 | |||||||
| chr5:96943195 | C | T | 1 | a0001c0003t0050g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.19+7021C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96943195 | |||||||
| chr5:96943223 | TA | T | 13 | a0002c0002t0002g0319 a0002c0002t0002g0320 a0003c0004t0008g0143 others(10): Show |
13 | HG00140.hp1 HG00642.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.19+7063delA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96943223 | ||||||
| chr5:96943233 | AAAAAG | A | 30 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(27): Show |
33 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.19+7064_19+7068del others(5): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96943233 | ||||||
| chr5:96943234 | AAAAG | A | 105 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(102): Show |
108 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.19+7064_19+7067del others(4): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96943234 | ||||||
| chr5:96943244 | T | G | 103 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(100): Show |
106 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.19+7070T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96943244 | |||||||
| chr5:96943349 | C | T | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+7175C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96943349 | |||||||
| chr5:96943512 | C | G | 1 | a0001c0001t0002g0222 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.19+7338C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96943512 | |||||||
| chr5:96943578 | C | A | 1 | a0004c0005t0003g0240 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.19+7404C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96943578 | |||||||
| chr5:96943747 | G | A | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.19+7573G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96943747 | |||||||
| chr5:96943755 | C | T | 1 | a0001c0003t0017g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.19+7581C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96943755 | |||||||
| chr5:96943786 | A | G | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+7612A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96943786 | |||||||
| chr5:96943954 | T | A | 9 | a0001c0001t0002g0247 a0002c0002t0004g0010 a0002c0002t0004g0241 others(6): Show |
10 | NA18962.hp2 NA18973.hp2 NA18980.hp2 others(7): Show |
intron_variant | MODIFIER | c.19+7780T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96943954 | |||||||
| chr5:96943970 | A | C | 1 | a0001c0001t0002g0220 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.19+7796A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96943970 | |||||||
| chr5:96944033 | G | A | 4 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(1): Show |
4 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+7859G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96944033 | |||||||
| chr5:96944275 | A | T | 1 | a0001c0001t0005g0152 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.19+8101A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96944275 | |||||||
| chr5:96944303 | G | T | 2 | a0001c0001t0012g0172 a0001c0001t0012g0173 |
2 | NA18968.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.19+8129G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96944303 | |||||||
| chr5:96944537 | C | CT | 135 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(132): Show |
141 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.19+8369dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96944537 | ||||||
| chr5:96944544 | G | T | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+8370G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96944544 | |||||||
| chr5:96944560 | C | CT | 101 | a0001c0001t0001g0006 a0001c0001t0001g0039 a0001c0001t0001g0040 others(98): Show |
104 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.19+8412dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96944560 | ||||||
| chr5:96944560 | C | CTT | 51 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(48): Show |
52 | HG00423.hp1 HG00597.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.19+8411_19+8412dup others(2): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96944560 | ||||||
| chr5:96944560 | C | CTTTT | 16 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(13): Show |
19 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.19+8409_19+8412dup others(4): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96944560 | ||||||
| chr5:96944560 | C | CTTTTT | 6 | a0001c0001t0005g0170 a0001c0001t0013g0166 a0001c0001t0013g0167 others(3): Show |
6 | NA18973.hp1 NA18991.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+8408_19+8412dup others(5): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96944560 | ||||||
| chr5:96944560 | CT | C | 13 | a0001c0001t0002g0198 a0001c0001t0009g0324 a0001c0001t0009g0325 others(10): Show |
13 | HG00738.hp2 HG01516.hp2 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.19+8412delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96944560 | ||||||
| chr5:96944560 | CTT | C | 6 | a0001c0001t0009g0235 a0001c0001t0009g0323 a0001c0003t0006g0233 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.19+8411_19+8412del others(2): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96944560 | ||||||
| chr5:96944560 | CTTT | C | 15 | a0001c0001t0051g0229 a0001c0003t0006g0003 a0001c0003t0006g0226 others(12): Show |
17 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.19+8410_19+8412del others(3): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96944560 | ||||||
| chr5:96944560 | CTTTTTTT | C | 19 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(16): Show |
19 | HG00642.hp1 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.19+8406_19+8412del others(7): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96944560 | ||||||
| chr5:96944560 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0037g0051 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.19+8401_19+8412del others(12): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96944560 | ||||||
| chr5:96944588 | A | T | 1 | a0001c0001t0030g0053 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.19+8414A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96944588 | |||||||
| chr5:96944591 | C | G | 1 | a0001c0001t0030g0053 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.19+8417C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96944591 | |||||||
| chr5:96944686 | A | T | 1 | a0001c0001t0001g0132 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.19+8512A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96944686 | |||||||
| chr5:96944709 | T | C | 1 | a0002c0002t0004g0241 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.19+8535T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96944709 | |||||||
| chr5:96944768 | C | T | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.19+8594C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96944768 | |||||||
| chr5:96944792 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.19+8618G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96944792 | |||||||
| chr5:96944913 | GTTA | G | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.19+8744_19+8746del others(3): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96944913 | ||||||
| chr5:96945118 | G | T | 15 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.19+8944G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96945118 | |||||||
| chr5:96945157 | G | A | 3 | a0001c0001t0009g0323 a0001c0001t0009g0324 a0001c0001t0009g0325 |
3 | HG02145.hp1 HG02615.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.19+8983G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96945157 | |||||||
| chr5:96945249 | T | TA | 13 | a0001c0001t0009g0235 a0001c0001t0051g0229 a0001c0003t0006g0003 others(10): Show |
15 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.19+9086dupA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96945249 | ||||||
| chr5:96945249 | TA | T | 149 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(146): Show |
155 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.19+9086delA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96945249 | ||||||
| chr5:96945339 | A | T | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+9165A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96945339 | |||||||
| chr5:96945347 | A | G | 6 | a0001c0001t0001g0048 a0001c0001t0001g0086 a0001c0001t0001g0087 others(3): Show |
6 | NA18953.hp2 NA18971.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+9173A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96945347 | |||||||
| chr5:96945405 | C | CA | 12 | a0001c0001t0001g0049 a0001c0001t0001g0117 a0001c0001t0002g0210 others(9): Show |
12 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.19+9250dupA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96945405 | ||||||
| chr5:96945405 | CA | C | 20 | a0001c0001t0002g0209 a0001c0001t0002g0218 a0001c0001t0036g0112 others(17): Show |
20 | HG00597.hp1 HG01070.hp1 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.19+9250delA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96945405 | ||||||
| chr5:96945405 | CAAAAAA | C | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.19+9245_19+9250del others(6): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96945405 | ||||||
| chr5:96945435 | A | C | 1 | a0004c0008t0026g0007 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.19+9261A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96945435 | |||||||
| chr5:96945462 | CAA | C | 4 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(1): Show |
4 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+9289_19+9290del others(2): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96945462 | |||||||
| chr5:96945698 | C | T | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+9524C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96945698 | |||||||
| chr5:96945717 | A | G | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.19+9543A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96945717 | |||||||
| chr5:96945765 | C | T | 149 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(146): Show |
155 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.19+9591C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96945765 | |||||||
| chr5:96945958 | C | A | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+9784C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96945958 | |||||||
| chr5:96946133 | A | G | 3 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 |
3 | HG02451.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.19+9959A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96946133 | |||||||
| chr5:96946220 | A | T | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.19+10046A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96946220 | |||||||
| chr5:96946677 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19+10503G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96946677 | |||||||
| chr5:96946768 | A | G | 3 | a0001c0003t0006g0003 a0001c0003t0006g0231 a0001c0003t0006g0232 |
5 | HG01109.hp1 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+10594A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96946768 | |||||||
| chr5:96946879 | A | G | 1 | a0002c0002t0002g0329 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.19+10705A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96946879 | |||||||
| chr5:96946971 | A | G | 1 | a0002c0002t0002g0329 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.19+10797A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96946971 | |||||||
| chr5:96947368 | G | A | 2 | a0004c0005t0003g0257 a0004c0005t0003g0304 |
2 | HG02572.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.19+11194G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96947368 | |||||||
| chr5:96947411 | CTT | C | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.19+11240_19+11241d others(4): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96947411 | ||||||
| chr5:96947975 | A | G | 1 | a0002c0002t0002g0301 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.19+11801A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96947975 | |||||||
| chr5:96948091 | A | G | 3 | a0001c0001t0018g0174 a0001c0001t0018g0175 a0001c0001t0018g0176 |
3 | HG01243.hp1 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.19+11917A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96948091 | |||||||
| chr5:96948117 | T | C | 149 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(146): Show |
155 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.19+11943T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96948117 | |||||||
| chr5:96948120 | C | CT | 20 | a0001c0001t0005g0155 a0001c0001t0005g0165 a0001c0001t0005g0170 others(17): Show |
20 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.19+11961dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96948120 | ||||||
| chr5:96948278 | C | T | 13 | a0001c0001t0009g0235 a0001c0001t0051g0229 a0001c0003t0006g0003 others(10): Show |
15 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.19+12104C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96948278 | |||||||
| chr5:96948369 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.19+12195C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96948369 | |||||||
| chr5:96948436 | T | A | 4 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(1): Show |
4 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+12262T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96948436 | |||||||
| chr5:96948437 | G | A | 1 | a0001c0001t0012g0156 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.19+12263G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96948437 | |||||||
| chr5:96948520 | A | G | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.19+12346A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96948520 | |||||||
| chr5:96948964 | A | C | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.19+12790A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96948964 | |||||||
| chr5:96949029 | G | C | 1 | a0010c0010t0007g0014 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.19+12855G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96949029 | |||||||
| chr5:96949066 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.19+12892T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96949066 | |||||||
| chr5:96949087 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.19+12913G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96949087 | |||||||
| chr5:96949099 | G | A | 149 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(146): Show |
155 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.19+12925G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96949099 | |||||||
| chr5:96949188 | C | T | 94 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(91): Show |
97 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.19+13014C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96949188 | |||||||
| chr5:96949265 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.19+13091C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96949265 | |||||||
| chr5:96949302 | C | T | 33 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(30): Show |
36 | HG00558.hp1 HG00609.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.19+13128C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96949302 | |||||||
| chr5:96949492 | C | T | 15 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.19+13318C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96949492 | |||||||
| chr5:96949675 | T | C | 8 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.19+13501T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96949675 | |||||||
| chr5:96949756 | A | G | 2 | a0001c0001t0022g0058 a0001c0001t0022g0089 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.19+13582A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96949756 | |||||||
| chr5:96949766 | G | A | 6 | a0001c0001t0005g0153 a0001c0001t0005g0154 a0001c0001t0013g0157 others(3): Show |
6 | NA18962.hp1 NA18985.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+13592G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96949766 | |||||||
| chr5:96949877 | CTTAAA | C | 13 | a0001c0001t0009g0235 a0001c0001t0051g0229 a0001c0003t0006g0003 others(10): Show |
15 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.19+13707_19+13711d others(7): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96949877 | ||||||
| chr5:96949956 | C | T | 3 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 |
3 | HG02451.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.19+13782C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96949956 | |||||||
| chr5:96950117 | C | G | 103 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(100): Show |
106 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.19+13943C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96950117 | |||||||
| chr5:96950171 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.19+13997G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96950171 | |||||||
| chr5:96950314 | A | G | 13 | a0001c0001t0009g0235 a0001c0001t0051g0229 a0001c0003t0006g0003 others(10): Show |
15 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.19+14140A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96950314 | |||||||
| chr5:96950432 | A | G | 1 | a0001c0001t0003g0322 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.19+14258A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96950432 | |||||||
| chr5:96950581 | C | T | 3 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 |
3 | HG02451.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.19+14407C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96950581 | |||||||
| chr5:96950582 | G | A | 103 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(100): Show |
106 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.19+14408G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96950582 | |||||||
| chr5:96950962 | A | G | 1 | a0001c0001t0005g0164 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.19+14788A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96950962 | |||||||
| chr5:96951016 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.19+14842A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96951016 | |||||||
| chr5:96951030 | G | A | 13 | a0001c0001t0009g0235 a0001c0001t0051g0229 a0001c0003t0006g0003 others(10): Show |
15 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.19+14856G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96951030 | |||||||
| chr5:96951136 | A | G | 4 | a0002c0002t0002g0298 a0002c0002t0002g0299 a0002c0002t0002g0300 others(1): Show |
4 | HG02027.hp2 NA18612.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+14962A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96951136 | |||||||
| chr5:96951238 | G | A | 2 | a0001c0001t0012g0172 a0001c0001t0012g0173 |
2 | NA18968.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.19+15064G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96951238 | |||||||
| chr5:96951262 | T | G | 8 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.19+15088T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96951262 | |||||||
| chr5:96951262 | T | TG | 31 | a0001c0001t0001g0037 a0001c0001t0001g0047 a0001c0001t0001g0080 others(28): Show |
31 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.19+15090dupG | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96951262 | ||||||
| chr5:96951262 | T | TGG | 7 | a0001c0001t0001g0109 a0001c0012t0010g0188 a0001c0015t0010g0193 others(4): Show |
7 | HG00735.hp2 HG01175.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+15089_19+15090d others(4): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96951262 | ||||||
| chr5:96951263 | G | T | 5 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(2): Show |
5 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+15089G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96951263 | |||||||
| chr5:96951265 | C | G | 191 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(188): Show |
199 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(196): Show |
intron_variant | MODIFIER | c.19+15091C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96951265 | |||||||
| chr5:96951271 | G | A | 5 | a0001c0003t0006g0226 a0001c0003t0006g0227 a0001c0003t0006g0228 others(2): Show |
5 | HG02895.hp1 HG02897.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+15097G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96951271 | |||||||
| chr5:96951296 | C | T | 1 | a0002c0002t0002g0013 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.19+15122C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96951296 | |||||||
| chr5:96951315 | G | A | 25 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(22): Show |
28 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.19+15141G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96951315 | |||||||
| chr5:96951321 | C | G | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.19+15147C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96951321 | |||||||
| chr5:96951557 | G | A | 6 | a0001c0001t0003g0001 a0001c0001t0003g0135 a0001c0001t0003g0137 others(3): Show |
8 | HG01069.hp1 HG01071.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.19+15383G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96951557 | |||||||
| chr5:96951655 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.19+15481C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96951655 | |||||||
| chr5:96951796 | CA | C | 149 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(146): Show |
155 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.19+15628delA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96951796 | ||||||
| chr5:96951829 | T | C | 13 | a0001c0001t0009g0235 a0001c0001t0051g0229 a0001c0003t0006g0003 others(10): Show |
15 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.19+15655T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96951829 | |||||||
| chr5:96952008 | AT | A | 15 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.19+15842delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96952008 | ||||||
| chr5:96952434 | A | G | 189 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(186): Show |
197 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.19+16260A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96952434 | |||||||
| chr5:96952549 | C | G | 1 | a0001c0001t0002g0209 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.19+16375C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96952549 | |||||||
| chr5:96952584 | A | G | 4 | a0002c0002t0002g0295 a0002c0002t0002g0296 a0002c0002t0002g0297 others(1): Show |
4 | NA18947.hp2 NA18972.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+16410A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96952584 | |||||||
| chr5:96952802 | TAG | T | 103 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(100): Show |
106 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.19+16632_19+16633d others(4): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96952802 | ||||||
| chr5:96952808 | C | T | 1 | a0001c0001t0002g0208 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.19+16634C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96952808 | |||||||
| chr5:96952968 | T | C | 1 | a0001c0001t0040g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.19+16794T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96952968 | |||||||
| chr5:96952989 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.19+16815A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96952989 | |||||||
| chr5:96953081 | GC | G | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.19+16911delC | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96953081 | ||||||
| chr5:96953153 | T | TA | 170 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(167): Show |
176 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.19+16980dupA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96953153 | ||||||
| chr5:96953210 | TC | T | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.19+17038delC | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96953210 | ||||||
| chr5:96953251 | A | T | 2 | a0002c0002t0002g0293 a0002c0002t0002g0294 |
2 | HG00642.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.19+17077A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96953251 | |||||||
| chr5:96953256 | G | A | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+17082G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96953256 | |||||||
| chr5:96953332 | GAGAC | G | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+17161_19+17164d others(6): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96953332 | ||||||
| chr5:96953339 | G | T | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+17165G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96953339 | |||||||
| chr5:96953526 | A | T | 1 | a0001c0001t0002g0247 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.19+17352A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96953526 | |||||||
| chr5:96953894 | A | T | 1 | a0001c0001t0001g0047 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.19+17720A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96953894 | |||||||
| chr5:96953903 | A | G | 1 | a0001c0013t0001g0104 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.19+17729A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96953903 | |||||||
| chr5:96954007 | G | C | 189 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(186): Show |
197 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.19+17833G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954007 | |||||||
| chr5:96954020 | T | C | 67 | a0001c0001t0002g0247 a0002c0002t0002g0011 a0002c0002t0002g0013 others(64): Show |
71 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.19+17846T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954020 | |||||||
| chr5:96954098 | A | G | 4 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(1): Show |
4 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+17924A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954098 | |||||||
| chr5:96954274 | T | C | 8 | a0001c0001t0002g0009 a0001c0001t0002g0198 a0001c0001t0002g0200 others(5): Show |
9 | NA18946.hp2 NA18953.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+18100T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954274 | |||||||
| chr5:96954351 | A | G | 3 | a0001c0001t0003g0292 a0001c0001t0003g0331 a0001c0001t0003g0332 |
3 | HG00323.hp2 HG02145.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.19+18177A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954351 | |||||||
| chr5:96954481 | G | A | 1 | a0002c0002t0002g0301 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.19+18307G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954481 | |||||||
| chr5:96954521 | T | G | 1 | a0001c0001t0003g0258 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.19+18347T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954521 | |||||||
| chr5:96954525 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.19+18351A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954525 | |||||||
| chr5:96954526 | G | A | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+18352G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954526 | |||||||
| chr5:96954614 | CTCTCTA | C | 3 | a0001c0001t0001g0059 a0001c0001t0001g0106 a0001c0001t0001g0128 |
3 | HG02615.hp2 HG04199.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.19+18442_19+18447d others(8): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954614 | ||||||
| chr5:96954616 | CTCTA | C | 4 | a0001c0001t0001g0057 a0001c0001t0001g0088 a0001c0001t0001g0114 others(1): Show |
4 | HG01255.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+18444_19+18447d others(6): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954616 | ||||||
| chr5:96954616 | CTCTATA | C | 59 | a0001c0001t0001g0006 a0001c0001t0001g0037 a0001c0001t0001g0041 others(56): Show |
60 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.19+18444_19+18449d others(8): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954616 | ||||||
| chr5:96954618 | C | A | 4 | a0001c0003t0006g0236 a0002c0002t0002g0298 a0003c0004t0008g0150 others(1): Show |
5 | HG01934.hp2 HG02630.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+18444C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954618 | |||||||
| chr5:96954618 | C | CTCTATAT others(7): Show |
2 | a0003c0004t0008g0149 a0003c0004t0056g0139 |
2 | HG00642.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.19+18445_19+18446i others(16): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954618 | ||||||
| chr5:96954618 | C | CTCTCTAT others(7): Show |
2 | a0003c0004t0008g0141 a0003c0004t0008g0148 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.19+18445_19+18446i others(16): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954618 | ||||||
| chr5:96954620 | A | C | 139 | a0001c0001t0001g0052 a0001c0001t0002g0009 a0001c0001t0002g0195 others(136): Show |
151 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.19+18446A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954620 | |||||||
| chr5:96954622 | A | C | 12 | a0001c0001t0001g0052 a0001c0001t0002g0220 a0001c0001t0009g0291 others(9): Show |
12 | HG01243.hp1 HG01257.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.19+18448A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954622 | |||||||
| chr5:96954623 | TATATATA others(3): Show |
T | 23 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(20): Show |
26 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.19+18457_19+18466d others(12): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954623 | ||||||
| chr5:96954625 | T | C | 6 | a0001c0001t0002g0224 a0001c0001t0002g0225 a0003c0004t0008g0141 others(3): Show |
6 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.19+18451T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954625 | |||||||
| chr5:96954625 | T | TATATATA others(7): Show |
8 | a0003c0004t0008g0142 a0003c0004t0008g0143 a0003c0004t0008g0144 others(5): Show |
8 | HG01123.hp1 HG01516.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.19+18458_19+18459i others(16): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954625 | ||||||
| chr5:96954627 | TATATAC | T | 39 | a0001c0001t0001g0036 a0001c0001t0001g0039 a0001c0001t0001g0040 others(36): Show |
40 | HG00609.hp1 HG01069.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.19+18459_19+18464d others(8): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954627 | ||||||
| chr5:96954627 | TATATACA others(7): Show |
T | 2 | a0001c0001t0018g0174 a0001c0001t0018g0175 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.19+18459_19+18472d others(16): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954627 | ||||||
| chr5:96954629 | TATACATA others(39): Show |
T | 2 | a0001c0001t0005g0165 a0001c0001t0005g0177 |
2 | NA18984.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.19+18457_19+18502d others(48): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954629 | ||||||
| chr5:96954633 | C | T | 66 | a0001c0001t0001g0006 a0001c0001t0001g0037 a0001c0001t0001g0041 others(63): Show |
67 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.19+18459C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954633 | |||||||
| chr5:96954639 | T | TACATATA others(11): Show |
1 | a0001c0001t0009g0327 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.19+18529_19+18546d others(20): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954639 | ||||||
| chr5:96954639 | TACATATA others(11): Show |
T | 31 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(28): Show |
33 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.19+18529_19+18546d others(20): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954639 | ||||||
| chr5:96954651 | T | C | 1 | a0004c0008t0026g0007 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.19+18477T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954651 | |||||||
| chr5:96954652 | A | G | 3 | a0002c0002t0002g0266 a0002c0002t0002g0306 a0002c0002t0002g0319 |
3 | HG00140.hp1 HG00735.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.19+18478A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954652 | |||||||
| chr5:96954657 | C | T | 1 | a0004c0008t0026g0007 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.19+18483C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954657 | |||||||
| chr5:96954659 | C | T | 1 | a0001c0001t0018g0176 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.19+18485C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954659 | |||||||
| chr5:96954665 | T | C | 1 | a0001c0001t0018g0176 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.19+18491T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954665 | |||||||
| chr5:96954677 | C | CAT | 106 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(103): Show |
108 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.19+18509_19+18510d others(4): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954677 | ||||||
| chr5:96954677 | C | T | 1 | a0004c0008t0026g0007 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.19+18503C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954677 | |||||||
| chr5:96954679 | TATATACA others(9): Show |
T | 23 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(20): Show |
26 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.19+18511_19+18526d others(18): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954679 | ||||||
| chr5:96954685 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.19+18511C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954685 | |||||||
| chr5:96954687 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.19+18513T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954687 | |||||||
| chr5:96954693 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.19+18519C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954693 | |||||||
| chr5:96954695 | C | CATATATA others(7): Show |
1 | a0001c0001t0040g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.19+18528_19+18529i others(16): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954695 | ||||||
| chr5:96954695 | C | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0085 a0001c0001t0001g0105 |
3 | HG00423.hp1 HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.19+18521C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954695 | |||||||
| chr5:96954695 | CATATATA others(23): Show |
C | 3 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 |
3 | HG02451.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.19+18529_19+18558d others(32): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954695 | ||||||
| chr5:96954697 | TATATAC | T | 109 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(106): Show |
112 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.19+18529_19+18534d others(8): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954697 | ||||||
| chr5:96954697 | TATATACA others(45): Show |
T | 4 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(1): Show |
4 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+18529_19+18580d others(54): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954697 | ||||||
| chr5:96954699 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.19+18525T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954699 | |||||||
| chr5:96954701 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0085 |
2 | HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.19+18527T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954701 | |||||||
| chr5:96954703 | C | T | 3 | a0001c0001t0001g0105 a0001c0001t0025g0060 a0001c0001t0038g0061 |
3 | HG00423.hp1 HG01192.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.19+18529C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954703 | |||||||
| chr5:96954705 | T | C | 1 | a0001c0001t0025g0060 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.19+18531T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954705 | |||||||
| chr5:96954711 | C | T | 4 | a0001c0001t0001g0052 a0001c0001t0001g0085 a0001c0001t0001g0090 others(1): Show |
4 | HG01109.hp2 HG01192.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+18537C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954711 | |||||||
| chr5:96954713 | C | T | 112 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(109): Show |
115 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.19+18539C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954713 | |||||||
| chr5:96954715 | T | C | 103 | a0001c0001t0002g0247 a0001c0001t0003g0001 a0001c0001t0003g0135 others(100): Show |
111 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.19+18541T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954715 | |||||||
| chr5:96954717 | T | C | 1 | a0001c0001t0025g0060 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.19+18543T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954717 | |||||||
| chr5:96954723 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0025g0060 |
2 | HG01192.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.19+18549C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954723 | |||||||
| chr5:96954725 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.19+18551T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954725 | |||||||
| chr5:96954727 | T | C | 1 | a0001c0001t0025g0060 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.19+18553T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954727 | |||||||
| chr5:96954731 | T | C | 1 | a0002c0002t0002g0194 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.19+18557T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954731 | |||||||
| chr5:96954733 | T | C | 1 | a0001c0001t0003g0315 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.19+18559T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954733 | |||||||
| chr5:96954735 | C | T | 3 | a0001c0001t0001g0090 a0001c0001t0003g0315 a0001c0001t0025g0060 |
3 | HG01192.hp1 HG03688.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.19+18561C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954735 | |||||||
| chr5:96954735 | CATATATA others(3): Show |
C | 1 | a0001c0003t0007g0018 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.19+18563_19+18572d others(12): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954735 | ||||||
| chr5:96954737 | T | C | 7 | a0001c0001t0018g0174 a0001c0001t0018g0175 a0001c0001t0018g0176 others(4): Show |
7 | HG01243.hp1 HG02129.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.19+18563T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954737 | |||||||
| chr5:96954739 | T | C | 5 | a0001c0001t0001g0090 a0001c0001t0018g0174 a0001c0001t0018g0175 others(2): Show |
5 | HG01243.hp1 HG02129.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+18565T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954739 | |||||||
| chr5:96954739 | TATATATA others(3): Show |
T | 3 | a0001c0001t0010g0190 a0001c0001t0010g0191 a0001c0001t0010g0192 |
3 | HG00738.hp2 HG01167.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.19+18573_19+18582d others(12): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954739 | ||||||
| chr5:96954741 | T | C | 7 | a0001c0001t0001g0090 a0001c0001t0001g0105 a0001c0001t0018g0174 others(4): Show |
7 | HG00423.hp1 HG01192.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+18567T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954741 | |||||||
| chr5:96954743 | T | C | 6 | a0001c0001t0001g0090 a0001c0001t0001g0105 a0001c0001t0018g0174 others(3): Show |
6 | HG00423.hp1 HG01192.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+18569T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954743 | |||||||
| chr5:96954743 | TATACAC | T | 4 | a0001c0003t0007g0028 a0001c0003t0048g0015 a0001c0012t0010g0188 others(1): Show |
4 | HG02738.hp1 HG03831.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+18573_19+18578d others(8): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954743 | ||||||
| chr5:96954745 | T | C | 3 | a0001c0001t0001g0090 a0001c0001t0001g0105 a0001c0001t0025g0060 |
3 | HG00423.hp1 HG01192.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.19+18571T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954745 | |||||||
| chr5:96954745 | T | TACAC | 3 | a0001c0001t0005g0164 a0001c0001t0012g0173 a0001c0001t0014g0163 |
3 | HG00558.hp1 HG03688.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.19+18573_19+18576d others(6): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954745 | ||||||
| chr5:96954745 | T | TACACAC | 28 | a0001c0001t0001g0057 a0001c0001t0001g0062 a0001c0001t0001g0085 others(25): Show |
31 | HG00609.hp2 HG01069.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.19+18576_19+18577i others(8): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954745 | ||||||
| chr5:96954745 | T | TACACACA others(3): Show |
1 | a0001c0001t0040g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.19+18576_19+18577i others(12): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954745 | ||||||
| chr5:96954745 | T | TATACACA others(1): Show |
87 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(84): Show |
90 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.19+18572_19+18573i others(10): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954745 | ||||||
| chr5:96954747 | C | T | 4 | a0001c0001t0018g0174 a0001c0001t0018g0175 a0001c0001t0018g0176 others(1): Show |
4 | HG01243.hp1 HG02129.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+18573C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954747 | |||||||
| chr5:96954749 | C | CACACACA others(5): Show |
1 | a0001c0001t0001g0128 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.19+18576_19+18577i others(14): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954749 | ||||||
| chr5:96954749 | C | CACACACA others(3): Show |
1 | a0001c0001t0001g0116 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.19+18576_19+18577i others(12): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954749 | ||||||
| chr5:96954749 | C | T | 7 | a0001c0001t0001g0090 a0001c0001t0010g0189 a0001c0001t0018g0174 others(4): Show |
7 | HG01243.hp1 HG01975.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+18575C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954749 | |||||||
| chr5:96954749 | CAT | C | 9 | a0001c0001t0002g0223 a0001c0003t0007g0023 a0001c0003t0007g0025 others(6): Show |
9 | HG00642.hp2 HG02083.hp1 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+18598_19+18599d others(4): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954749 | ||||||
| chr5:96954749 | CATAT | C | 7 | a0001c0003t0006g0227 a0001c0003t0006g0228 a0001c0003t0006g0233 others(4): Show |
7 | HG00280.hp1 HG01243.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+18596_19+18599d others(6): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954749 | ||||||
| chr5:96954749 | CATATAT | C | 7 | a0001c0001t0003g0290 a0001c0003t0006g0236 a0003c0004t0008g0141 others(4): Show |
7 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.19+18594_19+18599d others(8): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954749 | ||||||
| chr5:96954750 | A | G | 2 | a0001c0012t0010g0188 a0001c0015t0010g0193 |
2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.19+18576A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954750 | |||||||
| chr5:96954751 | T | C | 6 | a0001c0001t0005g0164 a0001c0001t0012g0173 a0001c0001t0014g0163 others(3): Show |
6 | HG00558.hp1 HG01074.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.19+18577T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954751 | |||||||
| chr5:96954753 | T | C | 2 | a0001c0001t0002g0223 a0001c0001t0036g0112 |
2 | HG02895.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.19+18579T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954753 | |||||||
| chr5:96954754 | A | G | 3 | a0001c0001t0010g0190 a0001c0001t0010g0191 a0001c0001t0010g0192 |
3 | HG00738.hp2 HG01167.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.19+18580A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954754 | |||||||
| chr5:96954755 | T | C | 1 | a0001c0001t0036g0112 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.19+18581T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954755 | |||||||
| chr5:96954756 | A | G | 7 | a0003c0004t0008g0142 a0003c0004t0008g0143 a0003c0004t0008g0144 others(4): Show |
7 | HG01123.hp1 HG01516.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.19+18582A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954756 | |||||||
| chr5:96954757 | T | C | 4 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(1): Show |
4 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+18583T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954757 | |||||||
| chr5:96954758 | A | T | 1 | a0002c0002t0004g0278 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.19+18584A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954758 | |||||||
| chr5:96954762 | A | G | 5 | a0003c0004t0008g0141 a0003c0004t0008g0148 a0003c0004t0008g0149 others(2): Show |
5 | HG00642.hp1 HG00735.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+18588A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954762 | |||||||
| chr5:96954764 | A | G | 1 | a0003c0004t0008g0150 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.19+18590A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954764 | |||||||
| chr5:96954768 | A | ATTTTTTT | 6 | a0001c0001t0001g0077 a0001c0001t0001g0081 a0001c0001t0001g0082 others(3): Show |
6 | HG00140.hp2 HG00323.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+18595_19+18596i others(9): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954768 | ||||||
| chr5:96954768 | ATATATT | A | 6 | a0001c0003t0020g0184 a0001c0003t0020g0185 a0001c0003t0050g0187 others(3): Show |
6 | HG01074.hp2 HG02055.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+18596_19+18601d others(8): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954768 | ||||||
| chr5:96954769 | TA | T | 6 | a0001c0001t0018g0174 a0001c0001t0018g0175 a0001c0001t0018g0176 others(3): Show |
6 | HG01243.hp1 HG02647.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+18596delA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954769 | |||||||
| chr5:96954770 | A | ATTTTTTT | 6 | a0001c0001t0001g0006 a0001c0001t0001g0037 a0001c0001t0001g0055 others(3): Show |
6 | HG00741.hp1 HG01934.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+18597_19+18598i others(9): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954770 | ||||||
| chr5:96954770 | A | ATTTTTTT others(1): Show |
6 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0132 others(3): Show |
6 | HG01123.hp2 HG01993.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+18597_19+18598i others(10): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954770 | ||||||
| chr5:96954770 | A | ATTTTTTT others(2): Show |
11 | a0001c0001t0001g0047 a0001c0001t0001g0064 a0001c0001t0001g0066 others(8): Show |
11 | HG01192.hp1 HG01433.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.19+18597_19+18598i others(11): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954770 | ||||||
| chr5:96954770 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0001g0114 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.19+18597_19+18598i others(12): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954770 | ||||||
| chr5:96954770 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0039 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.19+18597_19+18598i others(13): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954770 | ||||||
| chr5:96954770 | A | T | 13 | a0001c0001t0001g0006 a0001c0001t0001g0077 a0001c0001t0001g0081 others(10): Show |
13 | HG00140.hp2 HG00323.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.19+18596A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954770 | |||||||
| chr5:96954770 | ATAT | A | 11 | a0001c0001t0002g0247 a0001c0001t0003g0001 a0001c0001t0003g0292 others(8): Show |
11 | HG01255.hp2 HG01943.hp2 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.19+18598_19+18600d others(5): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954770 | ||||||
| chr5:96954770 | ATATT | A | 26 | a0001c0001t0003g0001 a0001c0001t0003g0135 a0001c0001t0003g0137 others(23): Show |
29 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.19+18598_19+18601d others(6): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954770 | ||||||
| chr5:96954770 | ATATTT | A | 6 | a0001c0001t0003g0203 a0001c0001t0009g0291 a0001c0003t0006g0003 others(3): Show |
8 | HG01109.hp1 HG01168.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.19+18598_19+18602d others(7): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954770 | ||||||
| chr5:96954771 | TA | T | 7 | a0001c0001t0005g0002 a0001c0001t0005g0152 a0001c0001t0014g0159 others(4): Show |
9 | NA18964.hp2 NA18986.hp1 NA18987.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+18598delA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954771 | |||||||
| chr5:96954772 | A | ATATATTT others(3): Show |
2 | a0001c0001t0001g0076 a0001c0001t0001g0101 |
2 | NA18984.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.19+18599_19+18600i others(12): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954772 | ||||||
| chr5:96954772 | A | ATATATTT others(4): Show |
1 | a0001c0001t0001g0079 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.19+18599_19+18600i others(13): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954772 | ||||||
| chr5:96954772 | A | ATATATTT others(5): Show |
1 | a0001c0001t0001g0071 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.19+18599_19+18600i others(14): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954772 | ||||||
| chr5:96954772 | A | ATATATTT others(6): Show |
1 | a0001c0001t0001g0102 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.19+18599_19+18600i others(15): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954772 | ||||||
| chr5:96954772 | A | ATATTTTT others(1): Show |
7 | a0001c0001t0001g0056 a0001c0001t0001g0078 a0001c0001t0001g0124 others(4): Show |
7 | HG01081.hp2 HG01261.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+18599_19+18600i others(10): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954772 | ||||||
| chr5:96954772 | A | ATATTTTT others(3): Show |
2 | a0001c0001t0001g0050 a0001c0001t0001g0086 |
2 | NA19003.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.19+18599_19+18600i others(12): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954772 | ||||||
| chr5:96954772 | A | ATATTTTT others(4): Show |
3 | a0001c0001t0001g0044 a0001c0001t0001g0049 a0001c0001t0001g0059 |
3 | NA18993.hp1 NA19000.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.19+18599_19+18600i others(13): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954772 | ||||||
| chr5:96954772 | A | ATATTTTT others(5): Show |
2 | a0001c0001t0001g0040 a0001c0001t0033g0095 |
2 | NA18977.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.19+18599_19+18600i others(14): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954772 | ||||||
| chr5:96954772 | A | ATTTTTTT others(1): Show |
9 | a0001c0001t0001g0068 a0001c0001t0001g0070 a0001c0001t0001g0080 others(6): Show |
10 | HG01515.hp1 HG02027.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.19+18619_19+18626d others(10): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954772 | ||||||
| chr5:96954772 | A | ATTTTTTT others(2): Show |
11 | a0001c0001t0001g0036 a0001c0001t0001g0074 a0001c0001t0001g0105 others(8): Show |
11 | HG00423.hp1 HG02135.hp2 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.19+18618_19+18626d others(11): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954772 | ||||||
| chr5:96954772 | A | ATTTTTTT others(3): Show |
5 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0087 others(2): Show |
5 | HG00621.hp2 NA18953.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+18617_19+18626d others(12): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954772 | ||||||
| chr5:96954772 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0111 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.19+18616_19+18626d others(13): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954772 | ||||||
| chr5:96954772 | A | T | 60 | a0001c0001t0001g0006 a0001c0001t0001g0037 a0001c0001t0001g0039 others(57): Show |
61 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.19+18598A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954772 | |||||||
| chr5:96954772 | AT | A | 25 | a0001c0001t0002g0202 a0001c0001t0002g0213 a0001c0001t0002g0220 others(22): Show |
29 | HG00558.hp2 HG00609.hp2 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.19+18626delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954772 | ||||||
| chr5:96954772 | ATT | A | 17 | a0001c0001t0002g0219 a0001c0001t0003g0322 a0001c0001t0009g0323 others(14): Show |
17 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.19+18625_19+18626d others(4): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954772 | ||||||
| chr5:96954772 | ATTT | A | 33 | a0001c0001t0009g0324 a0001c0001t0011g0031 a0002c0002t0002g0249 others(30): Show |
33 | HG00140.hp1 HG00423.hp2 HG02027.hp2 others(30): Show |
intron_variant | MODIFIER | c.19+18624_19+18626d others(5): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96954772 | ||||||
| chr5:96954773 | T | TA | 10 | a0001c0001t0001g0052 a0001c0001t0002g0009 a0001c0001t0002g0196 others(7): Show |
11 | HG00741.hp2 NA18946.hp2 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.19+18599_19+18600i others(3): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954773 | |||||||
| chr5:96954774 | T | A | 11 | a0001c0001t0002g0195 a0001c0001t0002g0204 a0001c0001t0002g0214 others(8): Show |
11 | HG00280.hp2 HG00558.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.19+18600T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954774 | |||||||
| chr5:96954775 | T | A | 8 | a0002c0002t0002g0011 a0002c0002t0002g0013 a0002c0002t0002g0256 others(5): Show |
10 | HG00558.hp2 HG02630.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.19+18601T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954775 | |||||||
| chr5:96954776 | T | A | 7 | a0001c0001t0002g0219 a0001c0001t0009g0326 a0001c0001t0009g0327 others(4): Show |
7 | HG00735.hp1 HG01192.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.19+18602T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954776 | |||||||
| chr5:96954777 | T | A | 4 | a0002c0002t0002g0249 a0002c0002t0002g0265 a0002c0002t0002g0279 others(1): Show |
4 | HG00140.hp1 HG02698.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+18603T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954777 | |||||||
| chr5:96954778 | T | A | 1 | a0001c0001t0036g0112 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.19+18604T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954778 | |||||||
| chr5:96954779 | T | A | 2 | a0001c0003t0017g0033 a0002c0002t0002g0319 |
2 | HG00140.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.19+18605T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954779 | |||||||
| chr5:96954780 | T | A | 1 | a0001c0001t0036g0112 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.19+18606T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954780 | |||||||
| chr5:96954781 | T | A | 3 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 |
3 | HG02451.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.19+18607T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954781 | |||||||
| chr5:96954783 | T | A | 2 | a0001c0003t0017g0033 a0001c0003t0017g0034 |
2 | HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.19+18609T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954783 | |||||||
| chr5:96954846 | G | C | 3 | a0001c0003t0020g0183 a0001c0003t0020g0184 a0001c0003t0020g0185 |
3 | HG02622.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.19+18672G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954846 | |||||||
| chr5:96954851 | C | T | 15 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.19+18677C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954851 | |||||||
| chr5:96954925 | G | A | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.19+18751G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954925 | |||||||
| chr5:96954943 | C | T | 137 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(134): Show |
143 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.19+18769C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954943 | |||||||
| chr5:96955052 | G | C | 3 | a0001c0001t0018g0174 a0001c0001t0018g0175 a0001c0001t0018g0176 |
3 | HG01243.hp1 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.19+18878G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96955052 | |||||||
| chr5:96955077 | C | T | 1 | a0002c0002t0004g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.19+18903C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96955077 | |||||||
| chr5:96955396 | C | G | 1 | a0001c0001t0038g0061 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.19+19222C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96955396 | |||||||
| chr5:96955474 | A | T | 15 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.19+19300A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96955474 | |||||||
| chr5:96955689 | A | G | 15 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.19+19515A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96955689 | |||||||
| chr5:96955733 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.19+19559C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96955733 | |||||||
| chr5:96955841 | T | TAAGTTTT others(340): Show |
1 | a0001c0001t0001g0079 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.19+19682_19+19683i others(349): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96955841 | ||||||
| chr5:96956092 | CTGTTTAA others(1): Show |
C | 170 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(167): Show |
176 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.19+19928_19+19935d others(10): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96956092 | ||||||
| chr5:96956300 | T | A | 35 | a0001c0001t0003g0001 a0001c0001t0003g0135 a0001c0001t0003g0137 others(32): Show |
39 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.19+20126T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96956300 | |||||||
| chr5:96956434 | C | T | 4 | a0001c0001t0002g0247 a0002c0002t0004g0241 a0002c0002t0004g0245 others(1): Show |
4 | NA18962.hp2 NA18973.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.19+20260C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96956434 | |||||||
| chr5:96956614 | G | A | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.19+20440G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96956614 | |||||||
| chr5:96956628 | G | A | 2 | a0001c0001t0009g0235 a0001c0001t0051g0229 |
2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.19+20454G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96956628 | |||||||
| chr5:96956809 | C | T | 1 | a0001c0001t0036g0112 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.19+20635C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96956809 | |||||||
| chr5:96956810 | G | A | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.19+20636G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96956810 | |||||||
| chr5:96956919 | T | G | 1 | a0001c0001t0040g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.19+20745T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96956919 | |||||||
| chr5:96957049 | C | A | 1 | a0002c0002t0002g0250 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.19+20875C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96957049 | |||||||
| chr5:96957177 | T | G | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.19+21003T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96957177 | |||||||
| chr5:96957263 | G | A | 1 | a0001c0003t0017g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.19+21089G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96957263 | |||||||
| chr5:96957302 | C | A | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+21128C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96957302 | |||||||
| chr5:96957317 | G | A | 35 | a0001c0001t0003g0001 a0001c0001t0003g0135 a0001c0001t0003g0137 others(32): Show |
39 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.19+21143G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96957317 | |||||||
| chr5:96957339 | C | T | 1 | a0001c0001t0002g0209 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.19+21165C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96957339 | |||||||
| chr5:96957340 | C | T | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.19+21166C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96957340 | |||||||
| chr5:96957346 | T | A | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.19+21172T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96957346 | |||||||
| chr5:96957396 | C | T | 3 | a0002c0002t0002g0249 a0002c0002t0002g0250 a0002c0002t0002g0251 |
3 | HG02698.hp1 HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.19+21222C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96957396 | |||||||
| chr5:96957449 | A | G | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.19+21275A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96957449 | |||||||
| chr5:96957647 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.19+21473A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96957647 | |||||||
| chr5:96957862 | A | G | 1 | a0002c0002t0002g0314 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.20-21276A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96957862 | |||||||
| chr5:96957972 | G | A | 11 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(8): Show |
13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.20-21166G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96957972 | |||||||
| chr5:96957982 | C | G | 3 | a0001c0001t0018g0174 a0001c0001t0018g0175 a0001c0001t0018g0176 |
3 | HG01243.hp1 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.20-21156C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96957982 | |||||||
| chr5:96958053 | C | G | 1 | a0001c0001t0001g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.20-21085C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96958053 | |||||||
| chr5:96958112 | A | G | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.20-21026A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96958112 | |||||||
| chr5:96958170 | T | G | 25 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(22): Show |
28 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.20-20968T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96958170 | |||||||
| chr5:96958224 | C | T | 1 | a0001c0001t0003g0288 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.20-20914C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96958224 | |||||||
| chr5:96958225 | G | A | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.20-20913G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96958225 | |||||||
| chr5:96958460 | TCCACTAA others(14): Show |
T | 1 | a0001c0003t0050g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.20-20675_20-20655d others(23): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96958460 | ||||||
| chr5:96958673 | G | A | 11 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(8): Show |
13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.20-20465G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96958673 | |||||||
| chr5:96958729 | C | T | 1 | a0002c0002t0004g0277 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.20-20409C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96958729 | |||||||
| chr5:96958733 | C | T | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.20-20405C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96958733 | |||||||
| chr5:96958823 | C | CT | 57 | a0001c0001t0001g0047 a0001c0001t0001g0077 a0001c0001t0001g0078 others(54): Show |
60 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.20-20291dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96958823 | ||||||
| chr5:96958823 | CT | C | 22 | a0001c0001t0001g0086 a0001c0001t0001g0118 a0001c0001t0010g0189 others(19): Show |
24 | HG00738.hp2 HG01070.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.20-20291delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96958823 | ||||||
| chr5:96958898 | G | T | 8 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.20-20240G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96958898 | |||||||
| chr5:96958973 | C | T | 1 | a0001c0001t0053g0217 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.20-20165C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96958973 | |||||||
| chr5:96959126 | C | T | 3 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 |
3 | HG02451.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.20-20012C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96959126 | |||||||
| chr5:96959127 | G | A | 1 | a0001c0003t0007g0019 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.20-20011G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96959127 | |||||||
| chr5:96959163 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.20-19975G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96959163 | |||||||
| chr5:96959417 | G | T | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.20-19721G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96959417 | |||||||
| chr5:96959418 | T | C | 4 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(1): Show |
4 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-19720T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96959418 | |||||||
| chr5:96959690 | G | A | 1 | a0001c0001t0003g0292 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.20-19448G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96959690 | |||||||
| chr5:96959933 | C | CT | 25 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0076 others(22): Show |
25 | HG00738.hp2 HG01167.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.20-19182dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96959933 | ||||||
| chr5:96959933 | CT | C | 28 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0123 others(25): Show |
28 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.20-19182delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96959933 | ||||||
| chr5:96959933 | CTT | C | 9 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(6): Show |
11 | HG01109.hp1 HG01884.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.20-19183_20-19182d others(4): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96959933 | ||||||
| chr5:96960106 | T | C | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.20-19032T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96960106 | |||||||
| chr5:96960158 | G | A | 1 | a0001c0001t0015g0063 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.20-18980G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96960158 | |||||||
| chr5:96960217 | C | G | 1 | a0001c0001t0002g0218 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.20-18921C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96960217 | |||||||
| chr5:96960236 | C | A | 1 | a0003c0004t0056g0139 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.20-18902C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96960236 | |||||||
| chr5:96960880 | GT | G | 147 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(144): Show |
153 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.20-18248delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96960880 | ||||||
| chr5:96960904 | T | C | 3 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 |
3 | HG02451.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.20-18234T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96960904 | |||||||
| chr5:96960920 | A | T | 1 | a0001c0001t0001g0091 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.20-18218A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96960920 | |||||||
| chr5:96961176 | AAAAAC | A | 3 | a0002c0002t0002g0266 a0002c0002t0002g0306 a0002c0002t0002g0319 |
3 | HG00140.hp1 HG00735.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.20-17952_20-17948d others(7): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96961176 | ||||||
| chr5:96961295 | G | A | 4 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(1): Show |
4 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-17843G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96961295 | |||||||
| chr5:96961348 | C | G | 1 | a0001c0001t0047g0334 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.20-17790C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96961348 | |||||||
| chr5:96961442 | T | C | 1 | a0001c0001t0016g0181 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.20-17696T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96961442 | |||||||
| chr5:96961628 | A | G | 3 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 |
3 | HG02451.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.20-17510A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96961628 | |||||||
| chr5:96961630 | T | G | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-17508T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96961630 | |||||||
| chr5:96961651 | C | A | 1 | a0001c0001t0001g0106 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.20-17487C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96961651 | |||||||
| chr5:96961705 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.20-17433C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96961705 | |||||||
| chr5:96961707 | C | T | 1 | a0003c0004t0008g0144 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.20-17431C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96961707 | |||||||
| chr5:96961823 | T | A | 103 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(100): Show |
106 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.20-17315T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96961823 | |||||||
| chr5:96961873 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.20-17265T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96961873 | |||||||
| chr5:96962277 | G | A | 3 | a0001c0001t0018g0174 a0001c0001t0018g0175 a0001c0001t0018g0176 |
3 | HG01243.hp1 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.20-16861G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96962277 | |||||||
| chr5:96962596 | C | A | 1 | a0001c0003t0017g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.20-16542C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96962596 | |||||||
| chr5:96962642 | C | CTT | 34 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(31): Show |
34 | HG00597.hp1 HG00642.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.20-16482_20-16481d others(4): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96962642 | ||||||
| chr5:96962642 | CT | C | 99 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(96): Show |
102 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.20-16481delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96962642 | ||||||
| chr5:96962658 | C | A | 1 | a0001c0003t0050g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.20-16480C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96962658 | |||||||
| chr5:96962790 | G | A | 21 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(18): Show |
21 | HG00597.hp1 HG00738.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.20-16348G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96962790 | |||||||
| chr5:96962836 | T | TGAATGTT others(306): Show |
6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-16288_20-16287i others(315): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96962836 | ||||||
| chr5:96962913 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.20-16225C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96962913 | |||||||
| chr5:96962959 | G | C | 1 | a0001c0003t0007g0019 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.20-16179G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96962959 | |||||||
| chr5:96963054 | T | A | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.20-16084T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96963054 | |||||||
| chr5:96963067 | C | T | 15 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.20-16071C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96963067 | |||||||
| chr5:96963367 | C | T | 14 | a0001c0001t0002g0215 a0003c0004t0008g0141 a0003c0004t0008g0142 others(11): Show |
14 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.20-15771C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96963367 | |||||||
| chr5:96963647 | T | A | 5 | a0002c0002t0002g0266 a0002c0002t0002g0293 a0002c0002t0002g0294 others(2): Show |
5 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-15491T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96963647 | |||||||
| chr5:96963765 | A | T | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.20-15373A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96963765 | |||||||
| chr5:96963877 | T | G | 3 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 |
3 | HG02451.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.20-15261T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96963877 | |||||||
| chr5:96963970 | C | CAATA | 21 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(18): Show |
21 | HG00597.hp1 HG00738.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.20-15167_20-15164d others(6): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96963970 | ||||||
| chr5:96964112 | CT | C | 22 | a0001c0001t0001g0129 a0001c0001t0002g0200 a0001c0001t0010g0189 others(19): Show |
22 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.20-15012delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96964112 | ||||||
| chr5:96964279 | T | G | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.20-14859T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96964279 | |||||||
| chr5:96964375 | C | A | 1 | a0001c0001t0047g0334 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.20-14763C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96964375 | |||||||
| chr5:96964613 | A | G | 4 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(1): Show |
4 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-14525A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96964613 | |||||||
| chr5:96964718 | G | C | 15 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.20-14420G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96964718 | |||||||
| chr5:96964769 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.20-14369G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96964769 | |||||||
| chr5:96965006 | A | G | 3 | a0001c0003t0007g0023 a0001c0003t0007g0024 a0001c0003t0007g0025 |
3 | NA18942.hp2 NA18978.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.20-14132A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96965006 | |||||||
| chr5:96965438 | G | C | 189 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(186): Show |
197 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.20-13700G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96965438 | |||||||
| chr5:96965496 | A | G | 21 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(18): Show |
21 | HG00597.hp1 HG00738.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.20-13642A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96965496 | |||||||
| chr5:96965585 | T | A | 1 | a0001c0001t0009g0326 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.20-13553T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96965585 | |||||||
| chr5:96965628 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.20-13510A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96965628 | |||||||
| chr5:96965706 | A | C | 3 | a0001c0001t0018g0174 a0001c0001t0018g0175 a0001c0001t0018g0176 |
3 | HG01243.hp1 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.20-13432A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96965706 | |||||||
| chr5:96965885 | A | G | 14 | a0001c0001t0001g0036 a0001c0001t0001g0039 a0001c0001t0001g0040 others(11): Show |
14 | HG00609.hp1 HG01993.hp1 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.20-13253A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96965885 | |||||||
| chr5:96966031 | A | C | 21 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(18): Show |
21 | HG00597.hp1 HG00738.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.20-13107A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96966031 | |||||||
| chr5:96966043 | T | C | 3 | a0002c0002t0002g0266 a0002c0002t0002g0306 a0002c0002t0002g0319 |
3 | HG00140.hp1 HG00735.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.20-13095T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96966043 | |||||||
| chr5:96966189 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.20-12949G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96966189 | |||||||
| chr5:96966279 | A | G | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.20-12859A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96966279 | |||||||
| chr5:96966379 | A | G | 5 | a0001c0001t0009g0235 a0001c0001t0009g0323 a0001c0001t0009g0324 others(2): Show |
5 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-12759A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96966379 | |||||||
| chr5:96966506 | A | ATT | 3 | a0001c0003t0017g0186 a0001c0003t0043g0230 a0001c0003t0045g0237 |
3 | HG01243.hp2 HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.20-12630_20-12629d others(4): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96966506 | ||||||
| chr5:96966506 | AT | A | 3 | a0001c0001t0001g0064 a0001c0001t0003g0135 a0003c0004t0008g0141 |
3 | HG01071.hp1 HG01168.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.20-12629delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96966506 | ||||||
| chr5:96966508 | T | G | 1 | a0002c0002t0004g0212 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.20-12630T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96966508 | |||||||
| chr5:96966508 | T | TTG | 20 | a0001c0001t0001g0006 a0001c0001t0001g0059 a0001c0001t0001g0071 others(17): Show |
21 | HG00597.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.20-12586_20-12585d others(4): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96966508 | ||||||
| chr5:96966508 | T | TTGTG | 20 | a0001c0001t0001g0118 a0001c0001t0002g0009 a0001c0001t0002g0195 others(17): Show |
21 | HG00280.hp2 HG01192.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.20-12588_20-12585d others(6): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96966508 | ||||||
| chr5:96966508 | T | TTTTG | 9 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0228 others(6): Show |
11 | HG01109.hp1 HG01884.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.20-12629_20-12628i others(6): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96966508 | ||||||
| chr5:96966508 | TTG | T | 171 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0040 others(168): Show |
179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.20-12586_20-12585d others(4): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96966508 | ||||||
| chr5:96966508 | TTGTG | T | 10 | a0001c0001t0001g0039 a0001c0001t0001g0066 a0001c0001t0005g0154 others(7): Show |
10 | HG00558.hp2 HG00609.hp1 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.20-12588_20-12585d others(6): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96966508 | ||||||
| chr5:96966508 | TTGTGTG | T | 40 | a0001c0001t0001g0072 a0001c0001t0003g0331 a0001c0001t0003g0332 others(37): Show |
43 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.20-12590_20-12585d others(8): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96966508 | ||||||
| chr5:96966508 | TTGTGTGT others(3): Show |
T | 1 | a0001c0001t0040g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.20-12594_20-12585d others(12): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96966508 | ||||||
| chr5:96966508 | TTGTGTGT others(5): Show |
T | 4 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(1): Show |
4 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-12596_20-12585d others(14): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96966508 | ||||||
| chr5:96966508 | TTGTGTGT others(7): Show |
T | 2 | a0001c0012t0010g0188 a0001c0015t0010g0193 |
2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.20-12598_20-12585d others(16): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96966508 | ||||||
| chr5:96966508 | TTGTGTGT others(13): Show |
T | 1 | a0001c0003t0050g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.20-12604_20-12585d others(22): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96966508 | ||||||
| chr5:96966508 | TTGTGTGT others(15): Show |
T | 1 | a0001c0001t0018g0174 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.20-12606_20-12585d others(24): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96966508 | ||||||
| chr5:96966530 | G | T | 1 | a0001c0003t0050g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.20-12608G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96966530 | |||||||
| chr5:96966576 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.20-12562C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96966576 | |||||||
| chr5:96966868 | C | T | 2 | a0001c0001t0025g0029 a0001c0001t0025g0060 |
2 | HG01192.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.20-12270C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96966868 | |||||||
| chr5:96966939 | A | G | 19 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(16): Show |
21 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.20-12199A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96966939 | |||||||
| chr5:96967110 | A | G | 2 | a0004c0005t0003g0289 a0004c0005t0003g0335 |
2 | HG00280.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.20-12028A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96967110 | |||||||
| chr5:96967269 | G | A | 15 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.20-11869G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96967269 | |||||||
| chr5:96967312 | AT | A | 34 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(31): Show |
34 | HG00597.hp1 HG00642.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.20-11814delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96967312 | ||||||
| chr5:96967315 | T | A | 294 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(291): Show |
311 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(308): Show |
intron_variant | MODIFIER | c.20-11823T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96967315 | |||||||
| chr5:96967444 | G | C | 189 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(186): Show |
197 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.20-11694G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96967444 | |||||||
| chr5:96967462 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.20-11676G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96967462 | |||||||
| chr5:96967530 | A | T | 21 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(18): Show |
21 | HG00597.hp1 HG00738.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.20-11608A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96967530 | |||||||
| chr5:96967669 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.20-11469C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96967669 | |||||||
| chr5:96967752 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.20-11386A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96967752 | |||||||
| chr5:96967994 | A | T | 189 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(186): Show |
197 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.20-11144A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96967994 | |||||||
| chr5:96968091 | A | G | 1 | a0003c0004t0008g0149 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.20-11047A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96968091 | |||||||
| chr5:96968114 | A | T | 2 | a0001c0001t0002g0224 a0001c0001t0002g0225 |
2 | HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.20-11024A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96968114 | |||||||
| chr5:96968134 | G | A | 1 | a0002c0002t0002g0306 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.20-11004G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96968134 | |||||||
| chr5:96968604 | A | G | 3 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 |
3 | HG02451.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.20-10534A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96968604 | |||||||
| chr5:96968702 | C | T | 1 | a0001c0001t0025g0060 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.20-10436C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96968702 | |||||||
| chr5:96968772 | A | G | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.20-10366A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96968772 | |||||||
| chr5:96968872 | G | A | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-10266G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96968872 | |||||||
| chr5:96968910 | G | A | 1 | a0001c0001t0009g0235 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.20-10228G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96968910 | |||||||
| chr5:96968943 | A | C | 1 | a0001c0001t0001g0101 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.20-10195A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96968943 | |||||||
| chr5:96969041 | T | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0122 a0001c0001t0001g0125 others(1): Show |
5 | HG00741.hp1 HG02965.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-10097T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96969041 | |||||||
| chr5:96969253 | C | CT | 45 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(42): Show |
50 | HG00558.hp1 HG00609.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.20-9872dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96969253 | ||||||
| chr5:96969253 | CT | C | 24 | a0001c0001t0001g0128 a0001c0001t0010g0189 a0001c0001t0010g0190 others(21): Show |
24 | HG00597.hp1 HG00738.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.20-9872delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96969253 | ||||||
| chr5:96969337 | T | A | 1 | a0001c0001t0001g0129 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.20-9801T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96969337 | |||||||
| chr5:96969338 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.20-9800A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96969338 | |||||||
| chr5:96969481 | C | T | 1 | a0001c0001t0016g0180 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.20-9657C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96969481 | |||||||
| chr5:96969586 | G | A | 2 | a0001c0001t0011g0031 a0001c0001t0011g0032 |
2 | HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.20-9552G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96969586 | |||||||
| chr5:96969627 | G | C | 21 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(18): Show |
21 | HG00597.hp1 HG00738.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.20-9511G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96969627 | |||||||
| chr5:96969651 | G | C | 3 | a0001c0001t0001g0057 a0001c0001t0001g0088 a0001c0001t0001g0116 |
3 | HG01255.hp1 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.20-9487G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96969651 | |||||||
| chr5:96969654 | G | A | 19 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(16): Show |
21 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.20-9484G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96969654 | |||||||
| chr5:96969742 | G | GT | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.20-9386dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96969742 | ||||||
| chr5:96969812 | G | A | 11 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(8): Show |
13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.20-9326G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96969812 | |||||||
| chr5:96970128 | G | A | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.20-9010G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96970128 | |||||||
| chr5:96970298 | A | G | 3 | a0001c0003t0020g0183 a0001c0003t0020g0184 a0001c0003t0020g0185 |
3 | HG02622.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.20-8840A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96970298 | |||||||
| chr5:96970312 | A | T | 2 | a0001c0001t0003g0331 a0001c0001t0003g0332 |
2 | HG00323.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.20-8826A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96970312 | |||||||
| chr5:96970393 | T | C | 1 | a0001c0003t0043g0230 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.20-8745T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96970393 | |||||||
| chr5:96970451 | G | A | 1 | a0001c0003t0017g0033 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.20-8687G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96970451 | |||||||
| chr5:96970610 | A | AT | 103 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(100): Show |
106 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.20-8520dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96970610 | ||||||
| chr5:96970681 | C | A | 1 | a0006c0009t0028g0182 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.20-8457C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96970681 | |||||||
| chr5:96970937 | A | G | 1 | a0001c0001t0029g0161 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.20-8201A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96970937 | |||||||
| chr5:96971046 | C | T | 1 | a0001c0003t0020g0185 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.20-8092C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96971046 | |||||||
| chr5:96971156 | G | T | 1 | a0002c0002t0002g0272 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.20-7982G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96971156 | |||||||
| chr5:96971221 | G | A | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.20-7917G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96971221 | |||||||
| chr5:96971226 | G | A | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-7912G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96971226 | |||||||
| chr5:96971345 | T | G | 1 | a0002c0002t0002g0251 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.20-7793T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96971345 | |||||||
| chr5:96971345 | T | TTG | 107 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(104): Show |
110 | HG00423.hp1 HG00609.hp1 HG00621.hp2 others(107): Show |
intron_variant | MODIFIER | c.20-7755_20-7754dup others(2): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96971345 | ||||||
| chr5:96971345 | T | TTGTG | 31 | a0001c0001t0001g0077 a0001c0001t0001g0082 a0001c0001t0001g0083 others(28): Show |
32 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.20-7757_20-7754dup others(4): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96971345 | ||||||
| chr5:96971345 | T | TTGTGTG | 16 | a0001c0001t0001g0052 a0001c0001t0001g0059 a0001c0001t0001g0064 others(13): Show |
16 | HG01123.hp2 HG01433.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.20-7759_20-7754dup others(6): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96971345 | ||||||
| chr5:96971345 | T | TTGTGTGT others(1): Show |
1 | a0001c0001t0005g0002 | 3 | NA18986.hp1 NA18992.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.20-7761_20-7754dup others(8): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96971345 | ||||||
| chr5:96971345 | T | TTGTGTGT others(3): Show |
1 | a0001c0015t0010g0193 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.20-7763_20-7754dup others(10): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96971345 | ||||||
| chr5:96971345 | T | TTGTGTGT others(7): Show |
1 | a0001c0012t0010g0188 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.20-7767_20-7754dup others(14): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96971345 | ||||||
| chr5:96971345 | TTG | T | 8 | a0001c0001t0016g0178 a0001c0001t0016g0180 a0001c0001t0016g0181 others(5): Show |
8 | HG02083.hp1 HG02559.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.20-7755_20-7754del others(2): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96971345 | ||||||
| chr5:96971345 | TTGTG | T | 14 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(11): Show |
14 | HG00597.hp1 NA18942.hp2 NA18955.hp2 others(11): Show |
intron_variant | MODIFIER | c.20-7757_20-7754del others(4): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96971345 | ||||||
| chr5:96971345 | TTGTGTG | T | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.20-7759_20-7754del others(6): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96971345 | ||||||
| chr5:96971454 | T | A | 170 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(167): Show |
176 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.20-7684T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96971454 | |||||||
| chr5:96971577 | T | C | 34 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(31): Show |
34 | HG00597.hp1 HG00642.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.20-7561T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96971577 | |||||||
| chr5:96971650 | T | C | 4 | a0001c0001t0012g0156 a0001c0001t0012g0172 a0001c0001t0012g0173 others(1): Show |
4 | NA18950.hp1 NA18968.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-7488T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96971650 | |||||||
| chr5:96971655 | T | C | 34 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(31): Show |
34 | HG00597.hp1 HG00642.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.20-7483T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96971655 | |||||||
| chr5:96971908 | G | A | 189 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(186): Show |
197 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.20-7230G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96971908 | |||||||
| chr5:96971932 | A | G | 170 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(167): Show |
176 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.20-7206A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96971932 | |||||||
| chr5:96972042 | A | G | 1 | a0001c0003t0050g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.20-7096A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96972042 | |||||||
| chr5:96972256 | T | TA | 25 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(22): Show |
28 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.20-6881dupA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96972256 | ||||||
| chr5:96972261 | G | A | 1 | a0001c0001t0034g0054 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.20-6877G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96972261 | |||||||
| chr5:96972446 | G | T | 1 | a0002c0002t0002g0260 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.20-6692G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96972446 | |||||||
| chr5:96972675 | T | A | 21 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(18): Show |
21 | HG00597.hp1 HG00738.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.20-6463T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96972675 | |||||||
| chr5:96972676 | C | A | 21 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(18): Show |
21 | HG00597.hp1 HG00738.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.20-6462C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96972676 | |||||||
| chr5:96972731 | T | C | 1 | a0001c0001t0014g0163 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.20-6407T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96972731 | |||||||
| chr5:96972751 | G | C | 25 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(22): Show |
28 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.20-6387G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96972751 | |||||||
| chr5:96972820 | C | T | 3 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 |
3 | HG02451.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.20-6318C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96972820 | |||||||
| chr5:96973265 | A | G | 1 | a0001c0001t0018g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.20-5873A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96973265 | |||||||
| chr5:96973389 | T | G | 3 | a0001c0001t0018g0174 a0001c0001t0018g0175 a0001c0001t0018g0176 |
3 | HG01243.hp1 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.20-5749T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96973389 | |||||||
| chr5:96973396 | A | G | 19 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(16): Show |
21 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.20-5742A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96973396 | |||||||
| chr5:96973398 | A | G | 34 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(31): Show |
34 | HG00597.hp1 HG00642.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.20-5740A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96973398 | |||||||
| chr5:96973471 | G | A | 1 | a0002c0002t0004g0311 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.20-5667G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96973471 | |||||||
| chr5:96973476 | A | G | 25 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(22): Show |
28 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.20-5662A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96973476 | |||||||
| chr5:96973609 | G | A | 1 | a0001c0001t0003g0315 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.20-5529G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96973609 | |||||||
| chr5:96973641 | T | G | 1 | a0001c0001t0047g0334 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.20-5497T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96973641 | |||||||
| chr5:96973863 | T | C | 1 | a0002c0002t0002g0298 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.20-5275T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96973863 | |||||||
| chr5:96973981 | A | C | 1 | a0001c0001t0001g0090 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.20-5157A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96973981 | |||||||
| chr5:96974493 | G | C | 25 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(22): Show |
28 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.20-4645G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96974493 | |||||||
| chr5:96974923 | T | C | 2 | a0001c0001t0003g0331 a0001c0001t0003g0332 |
2 | HG00323.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.20-4215T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96974923 | |||||||
| chr5:96975055 | C | T | 8 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.20-4083C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96975055 | |||||||
| chr5:96975189 | A | G | 4 | a0003c0004t0003g0253 a0003c0004t0003g0254 a0003c0004t0003g0285 others(1): Show |
4 | HG01515.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-3949A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96975189 | |||||||
| chr5:96975338 | A | G | 3 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 |
3 | HG02451.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.20-3800A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96975338 | |||||||
| chr5:96975568 | G | A | 19 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(16): Show |
21 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.20-3570G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96975568 | |||||||
| chr5:96975638 | A | C | 21 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(18): Show |
21 | HG00597.hp1 HG00738.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.20-3500A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96975638 | |||||||
| chr5:96975655 | TA | T | 34 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(31): Show |
34 | HG00597.hp1 HG00642.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.20-3476delA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96975655 | ||||||
| chr5:96975796 | C | G | 21 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(18): Show |
21 | HG00597.hp1 HG00738.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.20-3342C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96975796 | |||||||
| chr5:96975900 | C | G | 1 | a0002c0002t0004g0243 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.20-3238C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96975900 | |||||||
| chr5:96976157 | G | A | 1 | a0001c0001t0003g0315 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.20-2981G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96976157 | |||||||
| chr5:96976487 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.20-2651A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96976487 | |||||||
| chr5:96976516 | G | A | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.20-2622G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96976516 | |||||||
| chr5:96976654 | G | A | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.20-2484G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96976654 | |||||||
| chr5:96976750 | T | TA | 16 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(13): Show |
18 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.20-2377dupA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96976750 | ||||||
| chr5:96976803 | C | T | 1 | a0001c0001t0016g0181 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.20-2335C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96976803 | |||||||
| chr5:96976826 | A | G | 2 | a0004c0005t0003g0284 a0004c0005t0003g0302 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.20-2312A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96976826 | |||||||
| chr5:96976926 | C | CT | 327 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(324): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.20-2201dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96976926 | ||||||
| chr5:96977404 | G | A | 186 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(183): Show |
193 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(190): Show |
intron_variant | MODIFIER | c.20-1734G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96977404 | |||||||
| chr5:96977404 | G | C | 3 | a0001c0001t0001g0070 a0001c0001t0001g0100 a0001c0001t0023g0005 |
4 | HG02027.hp1 HG03834.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-1734G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96977404 | |||||||
| chr5:96977502 | G | A | 1 | a0001c0001t0005g0008 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.20-1636G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96977502 | |||||||
| chr5:96977723 | G | A | 5 | a0001c0001t0011g0031 a0001c0001t0011g0032 a0001c0001t0011g0238 others(2): Show |
5 | HG00738.hp1 HG02818.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.20-1415G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96977723 | |||||||
| chr5:96977846 | G | A | 33 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(30): Show |
36 | HG00558.hp1 HG00609.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.20-1292G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96977846 | |||||||
| chr5:96977866 | T | G | 1 | a0002c0002t0002g0251 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.20-1272T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96977866 | |||||||
| chr5:96977898 | A | T | 15 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.20-1240A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96977898 | |||||||
| chr5:96977921 | A | T | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.20-1217A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96977921 | |||||||
| chr5:96977947 | G | A | 2 | a0001c0001t0022g0058 a0001c0001t0022g0089 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.20-1191G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96977947 | |||||||
| chr5:96978055 | G | T | 1 | a0001c0001t0001g0068 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.20-1083G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96978055 | |||||||
| chr5:96978119 | A | G | 1 | a0001c0001t0014g0168 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.20-1019A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96978119 | |||||||
| chr5:96978325 | T | C | 1 | a0001c0001t0003g0281 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.20-813T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96978325 | |||||||
| chr5:96978475 | C | T | 34 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(31): Show |
34 | HG00597.hp1 HG00642.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.20-663C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96978475 | |||||||
| chr5:96978526 | A | G | 102 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(99): Show |
105 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.20-612A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96978526 | |||||||
| chr5:96978699 | C | G | 1 | a0001c0001t0031g0098 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.20-439C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96978699 | |||||||
| chr5:96978723 | G | A | 4 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(1): Show |
4 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-415G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96978723 | |||||||
| chr5:96978798 | T | G | 189 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(186): Show |
197 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.20-340T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96978798 | |||||||
| chr5:96978852 | G | A | 11 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(8): Show |
13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.20-286G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96978852 | |||||||
| chr5:96979091 | T | G | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.20-47T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96979091 | |||||||
| chr5:96980061 | G | A | 1 | a0008c0011t0007g0021 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.860+83G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96980061 | |||||||
| chr5:96980069 | A | AT | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.860+102dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 96980069 | ||||||
| chr5:96980285 | A | G | 1 | a0001c0001t0040g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.860+307A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96980285 | |||||||
| chr5:96980342 | G | A | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.860+364G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96980342 | |||||||
| chr5:96980491 | G | A | 21 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(18): Show |
21 | HG00597.hp1 HG00738.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.860+513G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96980491 | |||||||
| chr5:96980545 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.860+567T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96980545 | |||||||
| chr5:96980714 | C | T | 2 | a0001c0001t0014g0162 a0001c0001t0014g0168 |
2 | NA19057.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.860+736C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96980714 | |||||||
| chr5:96980766 | A | G | 34 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(31): Show |
34 | HG00597.hp1 HG00642.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.860+788A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96980766 | |||||||
| chr5:96980943 | C | T | 1 | a0001c0012t0010g0188 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.860+965C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96980943 | |||||||
| chr5:96981054 | C | T | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.860+1076C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96981054 | |||||||
| chr5:96981259 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.860+1281T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96981259 | |||||||
| chr5:96981382 | G | A | 1 | a0002c0002t0002g0293 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.860+1404G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96981382 | |||||||
| chr5:96981760 | A | G | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.860+1782A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96981760 | |||||||
| chr5:96982141 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.860+2163G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96982141 | |||||||
| chr5:96982310 | G | T | 1 | a0001c0001t0038g0061 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.860+2332G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96982310 | |||||||
| chr5:96982341 | T | C | 1 | a0001c0001t0001g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.860+2363T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96982341 | |||||||
| chr5:96982424 | A | G | 4 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(1): Show |
4 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.860+2446A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96982424 | |||||||
| chr5:96982441 | G | A | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.860+2463G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96982441 | |||||||
| chr5:96982478 | T | C | 1 | a0001c0003t0050g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.860+2500T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96982478 | |||||||
| chr5:96982534 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.861-2546A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96982534 | |||||||
| chr5:96982681 | GA | G | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.861-2396delA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 96982681 | ||||||
| chr5:96982958 | G | A | 1 | a0001c0003t0007g0026 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.861-2122G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96982958 | |||||||
| chr5:96982972 | CAAGTCGT others(10): Show |
C | 11 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(8): Show |
13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.861-2105_861-2089d others(19): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 96982972 | ||||||
| chr5:96983276 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.861-1804A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96983276 | |||||||
| chr5:96983311 | CAT | C | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.861-1764_861-1763d others(4): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 96983311 | ||||||
| chr5:96983449 | CT | C | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.861-1622delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 96983449 | ||||||
| chr5:96983502 | G | C | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.861-1578G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96983502 | |||||||
| chr5:96983553 | C | T | 3 | a0001c0003t0020g0183 a0001c0003t0020g0184 a0001c0003t0020g0185 |
3 | HG02622.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.861-1527C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96983553 | |||||||
| chr5:96983726 | C | T | 5 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(2): Show |
5 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.861-1354C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96983726 | |||||||
| chr5:96983740 | C | A | 15 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.861-1340C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96983740 | |||||||
| chr5:96983787 | T | C | 170 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(167): Show |
176 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.861-1293T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96983787 | |||||||
| chr5:96983903 | T | G | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.861-1177T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96983903 | |||||||
| chr5:96983967 | TTCTTAAT others(2): Show |
T | 3 | a0001c0001t0018g0174 a0001c0001t0018g0175 a0001c0001t0018g0176 |
3 | HG01243.hp1 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.861-1108_861-1100d others(11): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 96983967 | ||||||
| chr5:96984101 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.861-979G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96984101 | |||||||
| chr5:96984226 | A | C | 189 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(186): Show |
197 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.861-854A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96984226 | |||||||
| chr5:96984252 | G | A | 1 | a0001c0003t0050g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.861-828G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96984252 | |||||||
| chr5:96984347 | C | T | 1 | a0001c0003t0050g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.861-733C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96984347 | |||||||
| chr5:96984358 | G | A | 1 | a0001c0001t0024g0093 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.861-722G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96984358 | |||||||
| chr5:96984703 | C | T | 2 | a0001c0001t0022g0058 a0001c0001t0022g0089 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.861-377C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96984703 | |||||||
| chr5:96984707 | G | A | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.861-373G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96984707 | |||||||
| chr5:96984764 | C | T | 25 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(22): Show |
28 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.861-316C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96984764 | |||||||
| chr5:96984791 | C | T | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.861-289C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96984791 | |||||||
| chr5:96984882 | T | C | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.861-198T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96984882 | |||||||
| chr5:96984938 | T | C | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.861-142T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96984938 | |||||||
| chr5:96985015 | C | T | 8 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.861-65C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 2/17 | chr5 | 96985015 | |||||||
| chr5:96985289 | T | C | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.999+71T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 3/17 | chr5 | 96985289 | |||||||
| chr5:96985394 | C | T | 1 | a0001c0016t0001g0097 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.999+176C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 3/17 | chr5 | 96985394 | |||||||
| chr5:96985435 | G | C | 19 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(16): Show |
21 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.999+217G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 3/17 | chr5 | 96985435 | |||||||
| chr5:96985690 | G | T | 5 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(2): Show |
5 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.999+472G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 3/17 | chr5 | 96985690 | |||||||
| chr5:96985750 | CT | C | 5 | a0002c0002t0002g0260 a0002c0002t0002g0267 a0002c0002t0002g0268 others(2): Show |
5 | HG00558.hp2 HG00621.hp1 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.999+539delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 96985750 | ||||||
| chr5:96985758 | G | GT | 31 | a0001c0001t0001g0057 a0001c0001t0001g0088 a0001c0001t0001g0103 others(28): Show |
33 | HG01109.hp1 HG01192.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.999+553dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 96985758 | ||||||
| chr5:96985758 | G | GTT | 15 | a0001c0003t0017g0186 a0001c0003t0045g0237 a0003c0004t0008g0141 others(12): Show |
15 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.999+552_999+553dup others(2): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 96985758 | ||||||
| chr5:96985769 | T | G | 15 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.999+551T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 3/17 | chr5 | 96985769 | |||||||
| chr5:96985773 | G | T | 21 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(18): Show |
21 | HG00597.hp1 HG00738.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.999+555G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 3/17 | chr5 | 96985773 | |||||||
| chr5:96985862 | G | T | 1 | a0001c0001t0005g0155 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.999+644G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 3/17 | chr5 | 96985862 | |||||||
| chr5:96986109 | A | G | 1 | a0001c0001t0011g0032 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1000-430A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 3/17 | chr5 | 96986109 | |||||||
| chr5:96986155 | G | A | 19 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(16): Show |
21 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1000-384G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 3/17 | chr5 | 96986155 | |||||||
| chr5:96986177 | A | T | 1 | a0001c0001t0002g0219 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1000-362A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 3/17 | chr5 | 96986177 | |||||||
| chr5:96986183 | T | C | 103 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(100): Show |
106 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.1000-356T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 3/17 | chr5 | 96986183 | |||||||
| chr5:96986305 | G | A | 33 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(30): Show |
36 | HG00558.hp1 HG00609.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.1000-234G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 3/17 | chr5 | 96986305 | |||||||
| chr5:96986401 | A | G | 2 | a0001c0001t0009g0291 a0001c0001t0009g0316 |
2 | HG01257.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1000-138A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 3/17 | chr5 | 96986401 | |||||||
| chr5:96986432 | A | G | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.1000-107A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 3/17 | chr5 | 96986432 | |||||||
| chr5:96986437 | C | A | 8 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1000-102C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 3/17 | chr5 | 96986437 | |||||||
| chr5:96986715 | C | T | 136 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.1131+45C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96986715 | |||||||
| chr5:96987246 | C | A | 33 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(30): Show |
36 | HG00558.hp1 HG00609.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.1131+576C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96987246 | |||||||
| chr5:96987277 | T | A | 19 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(16): Show |
21 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1131+607T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96987277 | |||||||
| chr5:96987307 | A | T | 3 | a0002c0002t0002g0266 a0002c0002t0002g0306 a0002c0002t0002g0319 |
3 | HG00140.hp1 HG00735.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1131+637A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96987307 | |||||||
| chr5:96987409 | A | T | 1 | a0001c0001t0010g0192 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1131+739A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96987409 | |||||||
| chr5:96987548 | A | G | 4 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 others(1): Show |
4 | HG02451.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1131+878A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96987548 | |||||||
| chr5:96987576 | C | T | 170 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(167): Show |
176 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.1131+906C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96987576 | |||||||
| chr5:96987649 | A | C | 1 | a0001c0001t0001g0042 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1131+979A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96987649 | |||||||
| chr5:96987799 | A | G | 189 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(186): Show |
197 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(194): Show |
intron_variant | MODIFIER | c.1131+1129A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96987799 | |||||||
| chr5:96987831 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1131+1161T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96987831 | |||||||
| chr5:96987845 | T | C | 17 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0225 others(14): Show |
17 | HG00738.hp1 HG01257.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.1131+1175T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96987845 | |||||||
| chr5:96988005 | C | T | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1131+1335C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96988005 | |||||||
| chr5:96988037 | C | G | 1 | a0001c0001t0001g0044 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1131+1367C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96988037 | |||||||
| chr5:96988112 | T | C | 3 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 |
3 | HG02451.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1131+1442T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96988112 | |||||||
| chr5:96988199 | C | G | 1 | a0002c0002t0002g0271 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1131+1529C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96988199 | |||||||
| chr5:96988282 | T | C | 4 | a0001c0001t0011g0031 a0001c0001t0011g0032 a0001c0001t0011g0238 others(1): Show |
4 | HG00738.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1131+1612T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96988282 | |||||||
| chr5:96988339 | C | CT | 11 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(8): Show |
11 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.1131+1685dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr5 | 96988339 | ||||||
| chr5:96988339 | C | CTT | 26 | a0001c0001t0001g0082 a0001c0001t0001g0107 a0001c0003t0006g0003 others(23): Show |
28 | HG00323.hp1 HG00642.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1131+1684_1131+168 others(6): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr5 | 96988339 | ||||||
| chr5:96988339 | C | CTTT | 108 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0037 others(105): Show |
112 | HG00140.hp2 HG00423.hp1 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1131+1683_1131+168 others(7): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr5 | 96988339 | ||||||
| chr5:96988339 | C | CTTTT | 25 | a0001c0001t0001g0117 a0001c0001t0005g0002 a0001c0001t0005g0152 others(22): Show |
27 | HG00558.hp1 HG00609.hp2 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.1131+1682_1131+168 others(8): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr5 | 96988339 | ||||||
| chr5:96988339 | C | T | 1 | a0001c0003t0017g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1131+1669C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96988339 | |||||||
| chr5:96988390 | T | C | 2 | a0001c0001t0009g0291 a0001c0001t0009g0316 |
2 | HG01257.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1131+1720T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96988390 | |||||||
| chr5:96988495 | C | T | 144 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(141): Show |
153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1131+1825C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96988495 | |||||||
| chr5:96988496 | G | A | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1131+1826G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96988496 | |||||||
| chr5:96988650 | A | G | 1 | a0001c0003t0043g0230 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1131+1980A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96988650 | |||||||
| chr5:96988803 | G | A | 3 | a0001c0001t0018g0174 a0001c0001t0018g0175 a0001c0001t0018g0176 |
3 | HG01243.hp1 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1131+2133G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96988803 | |||||||
| chr5:96988894 | T | A | 1 | a0001c0003t0048g0015 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1131+2224T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96988894 | |||||||
| chr5:96989013 | G | A | 1 | a0001c0001t0047g0334 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1131+2343G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96989013 | |||||||
| chr5:96989076 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1131+2406A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96989076 | |||||||
| chr5:96989239 | G | T | 3 | a0003c0004t0008g0143 a0003c0004t0008g0144 a0003c0004t0008g0150 |
3 | HG01934.hp2 HG03239.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1131+2569G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96989239 | |||||||
| chr5:96989247 | A | C | 1 | a0001c0012t0010g0188 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1131+2577A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96989247 | |||||||
| chr5:96989313 | TTATATAT others(92): Show |
T | 196 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(193): Show |
207 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1131+2650_1131+274 others(103): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr5 | 96989313 | ||||||
| chr5:96989314 | T | A | 26 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(23): Show |
29 | HG00558.hp1 HG00609.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.1131+2644T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96989314 | |||||||
| chr5:96989319 | ATAATATA others(75): Show |
A | 1 | a0009c0014t0003g0321 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1131+2650_1131+273 others(86): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96989319 | |||||||
| chr5:96989321 | A | T | 1 | a0001c0001t0001g0040 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1131+2651A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96989321 | |||||||
| chr5:96989321 | AATATATA others(31): Show |
A | 1 | a0001c0001t0005g0002 | 3 | NA18986.hp1 NA18992.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1131+2668_1131+270 others(42): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr5 | 96989321 | ||||||
| chr5:96989356 | TATTATAT others(3): Show |
T | 4 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(1): Show |
4 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1131+2696_1131+270 others(14): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr5 | 96989356 | ||||||
| chr5:96989413 | T | A | 196 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(193): Show |
207 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1131+2743T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96989413 | |||||||
| chr5:96989419 | A | T | 1 | a0009c0014t0003g0321 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1131+2749A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96989419 | |||||||
| chr5:96989783 | G | A | 2 | a0001c0001t0002g0195 a0001c0001t0002g0196 |
2 | HG00741.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1131+3113G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96989783 | |||||||
| chr5:96990061 | AG | A | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1132-2953delG | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96990061 | |||||||
| chr5:96990209 | C | T | 1 | a0002c0002t0002g0262 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1132-2806C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96990209 | |||||||
| chr5:96990220 | G | A | 6 | a0001c0001t0001g0042 a0001c0001t0001g0094 a0001c0001t0001g0129 others(3): Show |
6 | HG00621.hp2 HG02071.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1132-2795G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96990220 | |||||||
| chr5:96990235 | C | G | 3 | a0001c0003t0020g0183 a0001c0003t0020g0184 a0001c0003t0020g0185 |
3 | HG02622.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1132-2780C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96990235 | |||||||
| chr5:96990349 | G | C | 15 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.1132-2666G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96990349 | |||||||
| chr5:96990693 | T | G | 1 | a0001c0001t0052g0206 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1132-2322T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96990693 | |||||||
| chr5:96990831 | A | G | 4 | a0001c0001t0001g0050 a0001c0001t0001g0076 a0001c0001t0001g0079 others(1): Show |
4 | NA18984.hp1 NA18994.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.1132-2184A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96990831 | |||||||
| chr5:96990953 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1132-2062G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96990953 | |||||||
| chr5:96990985 | C | A | 3 | a0001c0001t0018g0174 a0001c0001t0018g0175 a0001c0001t0018g0176 |
3 | HG01243.hp1 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1132-2030C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96990985 | |||||||
| chr5:96991030 | C | A | 1 | a0001c0015t0010g0193 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1132-1985C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96991030 | |||||||
| chr5:96991061 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1132-1954C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96991061 | |||||||
| chr5:96991159 | G | A | 1 | a0001c0003t0017g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1132-1856G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96991159 | |||||||
| chr5:96991434 | G | A | 197 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(194): Show |
208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1132-1581G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96991434 | |||||||
| chr5:96991458 | G | A | 1 | a0002c0002t0002g0279 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1132-1557G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96991458 | |||||||
| chr5:96991464 | A | G | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1132-1551A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96991464 | |||||||
| chr5:96991551 | T | C | 2 | a0001c0012t0010g0188 a0001c0015t0010g0193 |
2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1132-1464T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96991551 | |||||||
| chr5:96991585 | C | T | 231 | a0001c0001t0001g0052 a0001c0001t0002g0009 a0001c0001t0002g0195 others(228): Show |
245 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1132-1430C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96991585 | |||||||
| chr5:96991605 | C | A | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1132-1410C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96991605 | |||||||
| chr5:96991616 | A | G | 5 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(2): Show |
5 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1132-1399A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96991616 | |||||||
| chr5:96991623 | T | C | 8 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1132-1392T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96991623 | |||||||
| chr5:96991637 | G | A | 1 | a0001c0003t0007g0027 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1132-1378G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96991637 | |||||||
| chr5:96991708 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1132-1307G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96991708 | |||||||
| chr5:96991778 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0122 a0001c0001t0001g0124 others(3): Show |
7 | HG00741.hp1 HG02965.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1132-1237G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96991778 | |||||||
| chr5:96991783 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG00609.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1132-1232A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96991783 | |||||||
| chr5:96991845 | A | ATT | 197 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(194): Show |
208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1132-1169_1132-116 others(6): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr5 | 96991845 | ||||||
| chr5:96991959 | A | G | 184 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(181): Show |
195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.1132-1056A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96991959 | |||||||
| chr5:96992035 | AT | A | 144 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(141): Show |
153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1132-979delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96992035 | |||||||
| chr5:96992127 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1132-888G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96992127 | |||||||
| chr5:96992252 | G | A | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1132-763G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96992252 | |||||||
| chr5:96992578 | C | T | 15 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.1132-437C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96992578 | |||||||
| chr5:96992779 | C | CGGGGCGG others(4): Show |
11 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(8): Show |
13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1132-226_1132-216d others(13): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr5 | 96992779 | ||||||
| chr5:96992792 | G | A | 1 | a0001c0012t0010g0188 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1132-223G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96992792 | |||||||
| chr5:96992894 | C | T | 3 | a0004c0005t0003g0284 a0004c0005t0003g0302 a0009c0014t0003g0321 |
3 | HG01070.hp1 HG01071.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1132-121C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96992894 | |||||||
| chr5:96993196 | A | T | 4 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(1): Show |
4 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1252+61A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 5/17 | chr5 | 96993196 | |||||||
| chr5:96993218 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1252+83C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 5/17 | chr5 | 96993218 | |||||||
| chr5:96993304 | ATAT | A | 163 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(160): Show |
174 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.1252+170_1252+172d others(5): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 5/17 | chr5 | 96993304 | |||||||
| chr5:96993361 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1252+226T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 5/17 | chr5 | 96993361 | |||||||
| chr5:96993394 | G | A | 1 | a0001c0001t0003g0281 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1252+259G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 5/17 | chr5 | 96993394 | |||||||
| chr5:96993425 | A | G | 1 | a0002c0002t0002g0329 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1252+290A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 5/17 | chr5 | 96993425 | |||||||
| chr5:96993455 | G | A | 1 | a0001c0001t0040g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1252+320G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 5/17 | chr5 | 96993455 | |||||||
| chr5:96994160 | G | A | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1407+189G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96994160 | |||||||
| chr5:96994164 | A | C | 1 | a0001c0001t0001g0126 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1407+193A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96994164 | |||||||
| chr5:96994182 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0035g0069 |
2 | HG01123.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1407+211C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96994182 | |||||||
| chr5:96994358 | G | A | 21 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(18): Show |
21 | HG00597.hp1 HG00738.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.1407+387G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96994358 | |||||||
| chr5:96994465 | AT | A | 194 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(191): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1407+509delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 96994465 | ||||||
| chr5:96994500 | G | C | 1 | a0001c0001t0002g0213 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1407+529G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96994500 | |||||||
| chr5:96994598 | A | G | 144 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(141): Show |
153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1407+627A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96994598 | |||||||
| chr5:96994641 | G | C | 1 | a0001c0001t0024g0093 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1407+670G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96994641 | |||||||
| chr5:96994884 | C | T | 9 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0066 others(6): Show |
9 | HG02083.hp2 NA18953.hp2 NA18971.hp1 others(6): Show |
intron_variant | MODIFIER | c.1407+913C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96994884 | |||||||
| chr5:96994972 | G | T | 11 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(8): Show |
13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1407+1001G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96994972 | |||||||
| chr5:96995078 | C | T | 15 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.1407+1107C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96995078 | |||||||
| chr5:96995162 | G | C | 1 | a0001c0001t0002g0223 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1407+1191G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96995162 | |||||||
| chr5:96995183 | C | T | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1408-1207C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96995183 | |||||||
| chr5:96995262 | T | C | 197 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(194): Show |
208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1408-1128T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96995262 | |||||||
| chr5:96995327 | C | T | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1408-1063C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96995327 | |||||||
| chr5:96995665 | C | A | 197 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(194): Show |
208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1408-725C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96995665 | |||||||
| chr5:96995667 | A | C | 197 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(194): Show |
208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1408-723A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96995667 | |||||||
| chr5:96995691 | G | T | 1 | a0001c0001t0001g0056 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1408-699G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96995691 | |||||||
| chr5:96995719 | C | G | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1408-671C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96995719 | |||||||
| chr5:96995761 | A | G | 2 | a0002c0002t0002g0298 a0002c0002t0002g0300 |
2 | NA18960.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1408-629A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96995761 | |||||||
| chr5:96995824 | T | G | 1 | a0001c0001t0001g0102 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1408-566T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96995824 | |||||||
| chr5:96996010 | C | T | 5 | a0001c0001t0011g0031 a0001c0001t0011g0032 a0001c0001t0011g0238 others(2): Show |
5 | HG00738.hp1 HG02818.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1408-380C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96996010 | |||||||
| chr5:96996063 | G | A | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1408-327G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96996063 | |||||||
| chr5:96996070 | G | A | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1408-320G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96996070 | |||||||
| chr5:96996076 | A | T | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1408-314A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96996076 | |||||||
| chr5:96996102 | A | G | 1 | a0001c0001t0025g0029 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1408-288A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96996102 | |||||||
| chr5:96996103 | T | C | 1 | a0002c0002t0002g0252 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1408-287T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96996103 | |||||||
| chr5:96996326 | A | C | 1 | a0001c0003t0017g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1408-64A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96996326 | |||||||
| chr5:96996381 | TC | T | 197 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(194): Show |
208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
splice_region_variant&intron_variant | LOW | c.1408-3delC | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 96996381 | ||||||
| chr5:96996647 | A | G | 2 | a0001c0012t0010g0188 a0001c0015t0010g0193 |
2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1521+144A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 7/17 | chr5 | 96996647 | |||||||
| chr5:96996749 | A | T | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1521+246A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 7/17 | chr5 | 96996749 | |||||||
| chr5:96996827 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1521+324A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 7/17 | chr5 | 96996827 | |||||||
| chr5:96997010 | C | T | 2 | a0001c0001t0003g0281 a0001c0001t0003g0287 |
2 | HG01884.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1521+507C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 7/17 | chr5 | 96997010 | |||||||
| chr5:96997045 | C | T | 15 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.1521+542C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 7/17 | chr5 | 96997045 | |||||||
| chr5:96997180 | G | T | 1 | a0001c0001t0036g0112 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1521+677G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 7/17 | chr5 | 96997180 | |||||||
| chr5:96997457 | T | A | 1 | a0001c0003t0050g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1522-557T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 7/17 | chr5 | 96997457 | |||||||
| chr5:96997630 | G | A | 144 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(141): Show |
153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1522-384G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 7/17 | chr5 | 96997630 | |||||||
| chr5:96997648 | C | T | 4 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(1): Show |
4 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1522-366C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 7/17 | chr5 | 96997648 | |||||||
| chr5:96997707 | A | G | 4 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(1): Show |
4 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1522-307A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 7/17 | chr5 | 96997707 | |||||||
| chr5:96997756 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0083 |
2 | HG00140.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1522-258A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 7/17 | chr5 | 96997756 | |||||||
| chr5:96997831 | G | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0129 a0001c0001t0001g0130 others(2): Show |
5 | HG00621.hp2 NA18970.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1522-183G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 7/17 | chr5 | 96997831 | |||||||
| chr5:96998195 | A | G | 1 | a0001c0001t0029g0161 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1653+50A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 96998195 | |||||||
| chr5:96998219 | T | C | 1 | a0004c0005t0003g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1653+74T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 96998219 | |||||||
| chr5:96998284 | T | C | 1 | a0001c0001t0037g0051 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1653+139T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 96998284 | |||||||
| chr5:96998343 | T | G | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1653+198T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 96998343 | |||||||
| chr5:96998393 | G | A | 21 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(18): Show |
21 | HG00597.hp1 HG00738.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.1653+248G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 96998393 | |||||||
| chr5:96998544 | T | C | 1 | a0001c0003t0006g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1653+399T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 96998544 | |||||||
| chr5:96998638 | G | T | 1 | a0001c0001t0002g0223 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1653+493G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 96998638 | |||||||
| chr5:96998673 | C | T | 1 | a0004c0008t0026g0007 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1653+528C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 96998673 | |||||||
| chr5:96998758 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1653+613T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 96998758 | |||||||
| chr5:96998854 | G | T | 230 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(227): Show |
244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1653+709G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 96998854 | |||||||
| chr5:96999271 | T | C | 1 | a0001c0003t0006g0226 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1653+1126T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 96999271 | |||||||
| chr5:96999346 | A | G | 28 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(25): Show |
31 | HG00558.hp1 HG00609.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1653+1201A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 96999346 | |||||||
| chr5:96999507 | A | G | 1 | a0002c0002t0002g0262 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1653+1362A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 96999507 | |||||||
| chr5:96999642 | A | C | 25 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(22): Show |
28 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.1653+1497A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 96999642 | |||||||
| chr5:96999646 | C | T | 144 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(141): Show |
153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1653+1501C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 96999646 | |||||||
| chr5:96999863 | G | A | 19 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(16): Show |
21 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1653+1718G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 96999863 | |||||||
| chr5:97000025 | G | A | 1 | a0001c0001t0003g0315 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1653+1880G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97000025 | |||||||
| chr5:97000150 | C | T | 1 | a0008c0011t0007g0021 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1653+2005C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97000150 | |||||||
| chr5:97000180 | A | G | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1653+2035A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97000180 | |||||||
| chr5:97000452 | C | CATG | 231 | a0001c0001t0001g0052 a0001c0001t0002g0009 a0001c0001t0002g0195 others(228): Show |
245 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1653+2309_1653+231 others(7): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr5 | 97000452 | ||||||
| chr5:97000556 | G | A | 21 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(18): Show |
21 | HG00597.hp1 HG00738.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.1653+2411G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97000556 | |||||||
| chr5:97000727 | T | A | 25 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(22): Show |
28 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.1653+2582T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97000727 | |||||||
| chr5:97001087 | A | G | 202 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(199): Show |
213 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.1654-2328A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97001087 | |||||||
| chr5:97001160 | G | T | 25 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(22): Show |
28 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.1654-2255G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97001160 | |||||||
| chr5:97001316 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1654-2099G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97001316 | |||||||
| chr5:97001320 | T | A | 18 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(15): Show |
18 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.1654-2095T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97001320 | |||||||
| chr5:97001389 | G | A | 15 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.1654-2026G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97001389 | |||||||
| chr5:97001450 | A | G | 15 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.1654-1965A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97001450 | |||||||
| chr5:97001570 | G | A | 1 | a0001c0001t0003g0288 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1654-1845G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97001570 | |||||||
| chr5:97001683 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1654-1732C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97001683 | |||||||
| chr5:97001719 | A | AGT | 19 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(16): Show |
21 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1654-1695_1654-169 others(6): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr5 | 97001719 | ||||||
| chr5:97001721 | T | C | 2 | a0001c0001t0009g0291 a0001c0001t0009g0316 |
2 | HG01257.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1654-1694T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97001721 | |||||||
| chr5:97001753 | G | A | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1654-1662G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97001753 | |||||||
| chr5:97001808 | A | G | 25 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(22): Show |
28 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.1654-1607A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97001808 | |||||||
| chr5:97001862 | G | A | 1 | a0001c0015t0010g0193 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1654-1553G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97001862 | |||||||
| chr5:97001862 | G | T | 2 | a0001c0001t0022g0058 a0001c0001t0022g0089 |
2 | HG02572.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1654-1553G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97001862 | |||||||
| chr5:97001873 | C | T | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1654-1542C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97001873 | |||||||
| chr5:97001945 | G | C | 184 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(181): Show |
195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.1654-1470G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97001945 | |||||||
| chr5:97002013 | C | T | 1 | a0001c0001t0002g0208 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1654-1402C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97002013 | |||||||
| chr5:97002028 | A | G | 1 | a0001c0001t0012g0160 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1654-1387A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97002028 | |||||||
| chr5:97002086 | T | C | 197 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(194): Show |
208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1654-1329T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97002086 | |||||||
| chr5:97002087 | G | A | 46 | a0002c0002t0002g0252 a0002c0002t0002g0259 a0002c0002t0002g0260 others(43): Show |
48 | HG00423.hp2 HG00558.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1654-1328G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97002087 | |||||||
| chr5:97002114 | G | A | 3 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 |
3 | HG02451.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1654-1301G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97002114 | |||||||
| chr5:97002406 | G | T | 1 | a0004c0005t0003g0283 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1654-1009G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97002406 | |||||||
| chr5:97002458 | A | C | 1 | a0001c0001t0025g0029 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1654-957A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97002458 | |||||||
| chr5:97002520 | G | T | 1 | a0004c0005t0003g0257 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1654-895G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97002520 | |||||||
| chr5:97002617 | G | A | 1 | a0001c0003t0043g0230 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1654-798G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97002617 | |||||||
| chr5:97002763 | A | G | 1 | a0001c0001t0005g0008 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1654-652A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97002763 | |||||||
| chr5:97002801 | C | G | 238 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0085 others(235): Show |
252 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.1654-614C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97002801 | |||||||
| chr5:97003026 | A | G | 5 | a0001c0001t0009g0235 a0001c0001t0009g0323 a0001c0001t0009g0324 others(2): Show |
5 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1654-389A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97003026 | |||||||
| chr5:97003131 | T | G | 15 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.1654-284T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97003131 | |||||||
| chr5:97003258 | A | G | 3 | a0001c0001t0018g0174 a0001c0001t0018g0175 a0001c0001t0018g0176 |
3 | HG01243.hp1 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1654-157A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97003258 | |||||||
| chr5:97003295 | A | G | 2 | a0002c0002t0002g0260 a0002c0002t0002g0268 |
2 | HG00558.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1654-120A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97003295 | |||||||
| chr5:97003358 | G | A | 1 | a0001c0001t0039g0115 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1654-57G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97003358 | |||||||
| chr5:97003398 | AC | A | 196 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(193): Show |
207 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1654-16delC | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97003398 | |||||||
| chr5:97003569 | T | G | 184 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(181): Show |
195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.1785+23T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97003569 | |||||||
| chr5:97003625 | G | A | 1 | a0002c0002t0004g0307 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1785+79G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97003625 | |||||||
| chr5:97003666 | G | T | 1 | a0001c0001t0005g0155 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1785+120G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97003666 | |||||||
| chr5:97003733 | G | C | 1 | a0001c0001t0005g0155 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1785+187G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97003733 | |||||||
| chr5:97003757 | G | C | 1 | a0002c0002t0002g0299 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1785+211G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97003757 | |||||||
| chr5:97003784 | G | T | 231 | a0001c0001t0001g0052 a0001c0001t0002g0009 a0001c0001t0002g0195 others(228): Show |
245 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1785+238G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97003784 | |||||||
| chr5:97003841 | T | C | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1785+295T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97003841 | |||||||
| chr5:97003844 | G | A | 2 | a0001c0001t0009g0291 a0001c0001t0009g0316 |
2 | HG01257.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1785+298G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97003844 | |||||||
| chr5:97004018 | G | T | 11 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(8): Show |
13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1785+472G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97004018 | |||||||
| chr5:97004121 | G | T | 1 | a0003c0004t0008g0150 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1785+575G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97004121 | |||||||
| chr5:97004127 | G | A | 3 | a0001c0001t0018g0174 a0001c0001t0018g0175 a0001c0001t0018g0176 |
3 | HG01243.hp1 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1785+581G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97004127 | |||||||
| chr5:97004263 | C | T | 15 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(12): Show |
15 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.1785+717C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97004263 | |||||||
| chr5:97004310 | C | T | 19 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(16): Show |
21 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1785+764C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97004310 | |||||||
| chr5:97004378 | G | A | 1 | a0001c0003t0007g0027 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1785+832G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97004378 | |||||||
| chr5:97004548 | T | C | 8 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1785+1002T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97004548 | |||||||
| chr5:97004771 | T | C | 2 | a0001c0003t0027g0016 a0001c0003t0027g0017 |
2 | NA18955.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1785+1225T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97004771 | |||||||
| chr5:97004912 | T | G | 144 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(141): Show |
153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1786-1161T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97004912 | |||||||
| chr5:97005007 | A | G | 1 | a0001c0003t0017g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1786-1066A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97005007 | |||||||
| chr5:97005274 | A | G | 1 | a0001c0003t0050g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1786-799A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97005274 | |||||||
| chr5:97005594 | T | C | 11 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(8): Show |
13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1786-479T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97005594 | |||||||
| chr5:97005624 | G | C | 25 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(22): Show |
28 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.1786-449G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97005624 | |||||||
| chr5:97005654 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0123 |
2 | HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1786-419G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97005654 | |||||||
| chr5:97005714 | A | G | 2 | a0001c0012t0010g0188 a0001c0015t0010g0193 |
2 | HG02738.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1786-359A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | chr5 | 97005714 | |||||||
| chr5:97006046 | T | TTA | 191 | a0001c0001t0001g0056 a0001c0001t0002g0009 a0001c0001t0002g0195 others(188): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
splice_region_variant&intron_variant | LOW | c.1786-9_1786-8dupAT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 97006046 | ||||||
| chr5:97006046 | T | TTATA | 5 | a0001c0001t0002g0216 a0001c0001t0005g0164 a0001c0003t0006g0236 others(2): Show |
5 | HG00597.hp2 HG02055.hp1 HG02451.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1786-11_1786-8dupA others(3): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 97006046 | ||||||
| chr5:97006046 | T | TTATATAT others(1): Show |
14 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(11): Show |
14 | HG00597.hp1 HG02083.hp1 NA18942.hp2 others(11): Show |
splice_region_variant&intron_variant | LOW | c.1786-15_1786-8dupA others(7): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 97006046 | ||||||
| chr5:97006046 | T | TTATATAT others(3): Show |
1 | a0001c0003t0027g0016 | 1 | NA18955.hp2 | splice_region_variant&intron_variant | LOW | c.1786-17_1786-8dupA others(9): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 97006046 | ||||||
| chr5:97006373 | T | TA | 24 | a0001c0001t0005g0002 a0001c0001t0005g0152 a0001c0001t0005g0153 others(21): Show |
26 | HG00558.hp1 HG00609.hp2 HG03688.hp2 others(23): Show |
intron_variant | MODIFIER | c.1947-39dupA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 97006373 | ||||||
| chr5:97006373 | TA | T | 181 | a0001c0001t0001g0052 a0001c0001t0001g0064 a0001c0001t0002g0009 others(178): Show |
192 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.1947-39delA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 97006373 | ||||||
| chr5:97006608 | A | G | 11 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(8): Show |
13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2035+93A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97006608 | |||||||
| chr5:97006833 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2035+318A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97006833 | |||||||
| chr5:97006940 | G | A | 1 | a0003c0004t0057g0146 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2035+425G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97006940 | |||||||
| chr5:97006986 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2035+471A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97006986 | |||||||
| chr5:97007123 | C | T | 1 | a0001c0003t0017g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2035+608C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97007123 | |||||||
| chr5:97007223 | T | A | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.2035+708T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97007223 | |||||||
| chr5:97007246 | G | T | 1 | a0001c0001t0055g0136 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2035+731G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97007246 | |||||||
| chr5:97007358 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0035g0069 |
2 | HG01123.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.2035+843T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97007358 | |||||||
| chr5:97007535 | T | C | 2 | a0001c0001t0009g0324 a0001c0001t0009g0325 |
2 | HG02145.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2035+1020T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97007535 | |||||||
| chr5:97007848 | A | G | 197 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(194): Show |
208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.2035+1333A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97007848 | |||||||
| chr5:97007945 | C | T | 1 | a0001c0001t0032g0046 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2035+1430C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97007945 | |||||||
| chr5:97008011 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2035+1496A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97008011 | |||||||
| chr5:97008062 | T | C | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2035+1547T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97008062 | |||||||
| chr5:97008143 | A | T | 1 | a0002c0002t0004g0278 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2035+1628A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97008143 | |||||||
| chr5:97008235 | A | T | 11 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(8): Show |
13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2035+1720A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97008235 | |||||||
| chr5:97008268 | G | A | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2035+1753G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97008268 | |||||||
| chr5:97008279 | T | C | 1 | a0001c0001t0002g0199 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2035+1764T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97008279 | |||||||
| chr5:97008337 | G | GT | 32 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(29): Show |
33 | HG00423.hp1 HG00621.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.2035+1853dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 97008337 | ||||||
| chr5:97008337 | GT | G | 23 | a0001c0001t0001g0057 a0001c0001t0001g0076 a0001c0001t0001g0090 others(20): Show |
24 | HG00558.hp1 HG00609.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.2035+1853delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 97008337 | ||||||
| chr5:97008337 | GTTTT | G | 8 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(5): Show |
8 | HG02055.hp1 HG02622.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.2035+1850_2035+185 others(8): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 97008337 | ||||||
| chr5:97008337 | GTTTTT | G | 16 | a0001c0001t0040g0030 a0001c0003t0006g0227 a0001c0003t0006g0228 others(13): Show |
16 | HG01243.hp2 HG02451.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.2035+1849_2035+185 others(9): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 97008337 | ||||||
| chr5:97008337 | GTTTTTT | G | 21 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0192 others(18): Show |
23 | HG00597.hp1 HG00738.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.2035+1848_2035+185 others(10): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 97008337 | ||||||
| chr5:97008337 | GTTTTTTT | G | 14 | a0001c0001t0010g0191 a0002c0002t0002g0293 a0003c0004t0008g0141 others(11): Show |
14 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2035+1847_2035+185 others(11): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 97008337 | ||||||
| chr5:97008337 | GTTTTTTT others(1): Show |
G | 26 | a0001c0001t0002g0195 a0001c0001t0002g0198 a0001c0001t0002g0205 others(23): Show |
28 | HG00323.hp2 HG00642.hp2 HG02071.hp1 others(25): Show |
intron_variant | MODIFIER | c.2035+1846_2035+185 others(12): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 97008337 | ||||||
| chr5:97008337 | GTTTTTTT others(2): Show |
G | 102 | a0001c0001t0002g0009 a0001c0001t0002g0196 a0001c0001t0002g0199 others(99): Show |
109 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.2035+1845_2035+185 others(13): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 97008337 | ||||||
| chr5:97008337 | GTTTTTTT others(3): Show |
G | 15 | a0001c0001t0001g0128 a0001c0001t0002g0201 a0001c0001t0002g0223 others(12): Show |
15 | HG01257.hp2 HG01433.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2035+1844_2035+185 others(14): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 97008337 | ||||||
| chr5:97008354 | T | G | 1 | a0002c0002t0002g0330 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2035+1839T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97008354 | |||||||
| chr5:97008426 | C | G | 1 | a0003c0004t0008g0151 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2035+1911C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97008426 | |||||||
| chr5:97008442 | C | T | 1 | a0001c0003t0050g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2035+1927C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97008442 | |||||||
| chr5:97008662 | C | CT | 18 | a0001c0001t0001g0056 a0001c0001t0005g0177 a0001c0001t0022g0089 others(15): Show |
18 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.2035+2167dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 97008662 | ||||||
| chr5:97008662 | C | CTT | 27 | a0001c0001t0002g0204 a0001c0001t0010g0189 a0001c0001t0010g0190 others(24): Show |
27 | HG00280.hp2 HG00597.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.2035+2166_2035+216 others(6): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 97008662 | ||||||
| chr5:97008662 | C | CTTT | 130 | a0001c0001t0001g0128 a0001c0001t0002g0009 a0001c0001t0002g0195 others(127): Show |
139 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.2035+2165_2035+216 others(7): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 97008662 | ||||||
| chr5:97008662 | C | CTTTT | 11 | a0001c0001t0002g0198 a0001c0001t0003g0292 a0001c0001t0003g0315 others(8): Show |
11 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2035+2164_2035+216 others(8): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 97008662 | ||||||
| chr5:97008662 | CT | C | 43 | a0001c0001t0001g0068 a0001c0001t0001g0134 a0001c0001t0003g0281 others(40): Show |
48 | HG00558.hp1 HG00609.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.2035+2167delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 97008662 | ||||||
| chr5:97008713 | A | G | 22 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(19): Show |
22 | HG00597.hp1 HG00738.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.2035+2198A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97008713 | |||||||
| chr5:97008813 | T | C | 3 | a0004c0005t0003g0284 a0004c0005t0003g0302 a0009c0014t0003g0321 |
3 | HG01070.hp1 HG01071.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.2035+2298T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97008813 | |||||||
| chr5:97008888 | G | A | 2 | a0004c0005t0003g0289 a0004c0005t0003g0335 |
2 | HG00280.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2035+2373G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97008888 | |||||||
| chr5:97008899 | A | G | 2 | a0002c0002t0002g0249 a0002c0002t0002g0251 |
2 | HG02698.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.2035+2384A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97008899 | |||||||
| chr5:97009186 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2035+2671C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97009186 | |||||||
| chr5:97009313 | CATAAT | C | 25 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(22): Show |
28 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.2035+2802_2035+280 others(9): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 97009313 | ||||||
| chr5:97009365 | T | TC | 230 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(227): Show |
244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.2035+2855dupC | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 97009365 | ||||||
| chr5:97009682 | T | TTGCTGC | 68 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(65): Show |
73 | HG00558.hp1 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.2035+3178_2035+318 others(10): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 97009682 | ||||||
| chr5:97009682 | T | TTGCTGCT others(2): Show |
19 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(16): Show |
19 | HG00642.hp1 HG00735.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.2035+3175_2035+318 others(13): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 97009682 | ||||||
| chr5:97009682 | TTGC | T | 143 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(140): Show |
152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.2035+3181_2035+318 others(7): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 97009682 | ||||||
| chr5:97010035 | A | G | 230 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(227): Show |
244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.2035+3520A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97010035 | |||||||
| chr5:97010079 | A | G | 1 | a0001c0001t0015g0096 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2035+3564A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97010079 | |||||||
| chr5:97010386 | T | A | 1 | a0002c0002t0002g0261 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2036-3262T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97010386 | |||||||
| chr5:97010574 | G | T | 197 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(194): Show |
208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.2036-3074G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97010574 | |||||||
| chr5:97011288 | T | C | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2036-2360T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97011288 | |||||||
| chr5:97011453 | C | T | 1 | a0001c0003t0045g0237 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2036-2195C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97011453 | |||||||
| chr5:97011467 | T | C | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.2036-2181T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97011467 | |||||||
| chr5:97011738 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2036-1910A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97011738 | |||||||
| chr5:97012018 | A | C | 1 | a0002c0002t0004g0243 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2036-1630A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97012018 | |||||||
| chr5:97012071 | C | G | 239 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0085 others(236): Show |
253 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.2036-1577C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97012071 | |||||||
| chr5:97012096 | G | A | 2 | a0002c0002t0002g0272 a0002c0002t0002g0279 |
2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2036-1552G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97012096 | |||||||
| chr5:97012657 | A | G | 1 | a0003c0004t0003g0254 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2036-991A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97012657 | |||||||
| chr5:97012661 | C | A | 2 | a0002c0002t0002g0252 a0002c0002t0002g0271 |
2 | NA18939.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.2036-987C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97012661 | |||||||
| chr5:97012702 | T | G | 1 | a0001c0003t0050g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2036-946T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97012702 | |||||||
| chr5:97012816 | T | C | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2036-832T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97012816 | |||||||
| chr5:97012865 | C | A | 1 | a0002c0002t0002g0312 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2036-783C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97012865 | |||||||
| chr5:97013426 | C | T | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2036-222C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97013426 | |||||||
| chr5:97013431 | A | G | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2036-217A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 11/17 | chr5 | 97013431 | |||||||
| chr5:97014008 | G | A | 4 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(1): Show |
4 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.2219+177G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 12/17 | chr5 | 97014008 | |||||||
| chr5:97014139 | A | AT | 3 | a0001c0001t0018g0174 a0001c0001t0018g0175 a0001c0001t0018g0176 |
3 | HG01243.hp1 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2219+312dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr5 | 97014139 | ||||||
| chr5:97014384 | G | A | 197 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(194): Show |
208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.2219+553G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 12/17 | chr5 | 97014384 | |||||||
| chr5:97014480 | G | A | 1 | a0001c0001t0021g0065 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2220-459G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 12/17 | chr5 | 97014480 | |||||||
| chr5:97014542 | A | C | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.2220-397A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 12/17 | chr5 | 97014542 | |||||||
| chr5:97014559 | A | T | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.2220-380A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 12/17 | chr5 | 97014559 | |||||||
| chr5:97014565 | AG | A | 54 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0225 others(51): Show |
56 | HG00597.hp1 HG00738.hp1 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.2220-373delG | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 12/17 | chr5 | 97014565 | |||||||
| chr5:97014566 | G | A | 143 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(140): Show |
152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.2220-373G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 12/17 | chr5 | 97014566 | |||||||
| chr5:97014870 | C | G | 4 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(1): Show |
4 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2220-69C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 12/17 | chr5 | 97014870 | |||||||
| chr5:97015142 | G | T | 25 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(22): Show |
28 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.2376+47G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97015142 | |||||||
| chr5:97015769 | C | G | 25 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(22): Show |
28 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.2376+674C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97015769 | |||||||
| chr5:97015835 | G | A | 25 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(22): Show |
28 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.2376+740G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97015835 | |||||||
| chr5:97015964 | T | C | 1 | a0001c0001t0005g0008 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2376+869T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97015964 | |||||||
| chr5:97015991 | C | T | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2376+896C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97015991 | |||||||
| chr5:97015999 | C | G | 1 | a0001c0001t0002g0223 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2376+904C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97015999 | |||||||
| chr5:97016364 | C | T | 187 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(184): Show |
198 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.2376+1269C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97016364 | |||||||
| chr5:97016584 | G | A | 1 | a0001c0001t0015g0096 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2376+1489G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97016584 | |||||||
| chr5:97016738 | T | A | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2376+1643T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97016738 | |||||||
| chr5:97016790 | C | T | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2376+1695C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97016790 | |||||||
| chr5:97016899 | G | A | 3 | a0001c0003t0020g0183 a0001c0003t0020g0184 a0001c0003t0020g0185 |
3 | HG02622.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2376+1804G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97016899 | |||||||
| chr5:97017049 | G | C | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2376+1954G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97017049 | |||||||
| chr5:97017106 | A | C | 4 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 others(1): Show |
4 | HG02451.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2376+2011A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97017106 | |||||||
| chr5:97017519 | C | G | 230 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(227): Show |
244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.2376+2424C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97017519 | |||||||
| chr5:97017528 | T | C | 1 | a0001c0015t0010g0193 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2376+2433T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97017528 | |||||||
| chr5:97017692 | T | C | 1 | a0001c0001t0003g0203 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2376+2597T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97017692 | |||||||
| chr5:97017742 | G | T | 1 | a0001c0001t0011g0238 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2376+2647G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97017742 | |||||||
| chr5:97017980 | C | T | 178 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(175): Show |
189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.2376+2885C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97017980 | |||||||
| chr5:97017998 | A | G | 1 | a0001c0001t0003g0292 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2376+2903A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97017998 | |||||||
| chr5:97018090 | G | A | 4 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(1): Show |
4 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2376+2995G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97018090 | |||||||
| chr5:97018154 | A | G | 3 | a0002c0002t0002g0266 a0002c0002t0002g0306 a0002c0002t0002g0319 |
3 | HG00140.hp1 HG00735.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2376+3059A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97018154 | |||||||
| chr5:97018225 | A | G | 11 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(8): Show |
13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2376+3130A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97018225 | |||||||
| chr5:97018449 | C | A | 3 | a0001c0001t0018g0174 a0001c0001t0018g0175 a0001c0001t0018g0176 |
3 | HG01243.hp1 HG02647.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2376+3354C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97018449 | |||||||
| chr5:97018474 | G | A | 1 | a0001c0003t0045g0237 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2376+3379G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97018474 | |||||||
| chr5:97018563 | T | C | 25 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(22): Show |
28 | HG00558.hp1 HG00609.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.2376+3468T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97018563 | |||||||
| chr5:97018600 | C | A | 4 | a0001c0001t0001g0057 a0001c0001t0001g0085 a0001c0001t0001g0088 others(1): Show |
4 | HG01109.hp2 HG01255.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2376+3505C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97018600 | |||||||
| chr5:97018721 | A | G | 3 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0225 |
3 | HG02970.hp1 HG03139.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2377-3579A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97018721 | |||||||
| chr5:97018810 | T | C | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2377-3490T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97018810 | |||||||
| chr5:97018937 | C | T | 3 | a0004c0005t0003g0284 a0004c0005t0003g0302 a0009c0014t0003g0321 |
3 | HG01070.hp1 HG01071.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.2377-3363C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97018937 | |||||||
| chr5:97019056 | C | T | 1 | a0001c0003t0017g0186 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2377-3244C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97019056 | |||||||
| chr5:97019164 | T | C | 1 | a0004c0005t0003g0289 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2377-3136T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97019164 | |||||||
| chr5:97019264 | C | T | 3 | a0001c0003t0020g0183 a0001c0003t0020g0184 a0001c0003t0020g0185 |
3 | HG02622.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2377-3036C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97019264 | |||||||
| chr5:97019448 | A | G | 3 | a0001c0003t0020g0183 a0001c0003t0020g0184 a0001c0003t0020g0185 |
3 | HG02622.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2377-2852A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97019448 | |||||||
| chr5:97019516 | A | T | 2 | a0007c0007t0005g0169 a0007c0007t0005g0171 |
2 | NA18973.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.2377-2784A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97019516 | |||||||
| chr5:97019648 | G | C | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.2377-2652G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97019648 | |||||||
| chr5:97019744 | A | G | 230 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(227): Show |
244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.2377-2556A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97019744 | |||||||
| chr5:97019899 | A | G | 230 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(227): Show |
244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.2377-2401A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97019899 | |||||||
| chr5:97019929 | C | G | 33 | a0001c0001t0005g0002 a0001c0001t0005g0008 a0001c0001t0005g0152 others(30): Show |
36 | HG00558.hp1 HG00609.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.2377-2371C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97019929 | |||||||
| chr5:97019946 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2377-2354G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97019946 | |||||||
| chr5:97019964 | G | A | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2377-2336G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97019964 | |||||||
| chr5:97020268 | C | T | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.2377-2032C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97020268 | |||||||
| chr5:97020310 | G | A | 1 | a0002c0002t0004g0241 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2377-1990G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97020310 | |||||||
| chr5:97020346 | A | G | 1 | a0001c0001t0040g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2377-1954A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97020346 | |||||||
| chr5:97020379 | C | T | 11 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(8): Show |
13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2377-1921C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97020379 | |||||||
| chr5:97020381 | C | T | 1 | a0001c0001t0016g0180 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2377-1919C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97020381 | |||||||
| chr5:97020413 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0074 |
2 | NA18949.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2377-1887G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97020413 | |||||||
| chr5:97020521 | G | T | 1 | a0001c0003t0007g0028 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2377-1779G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97020521 | |||||||
| chr5:97020540 | C | T | 1 | a0002c0002t0004g0245 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2377-1760C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97020540 | |||||||
| chr5:97020675 | G | A | 1 | a0001c0001t0003g0290 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2377-1625G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97020675 | |||||||
| chr5:97020721 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2377-1579G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97020721 | |||||||
| chr5:97020862 | T | C | 2 | a0002c0002t0002g0272 a0002c0002t0002g0279 |
2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2377-1438T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97020862 | |||||||
| chr5:97020942 | G | A | 1 | a0001c0001t0002g0215 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2377-1358G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97020942 | |||||||
| chr5:97020960 | G | A | 178 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(175): Show |
189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.2377-1340G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97020960 | |||||||
| chr5:97021169 | A | G | 34 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(31): Show |
36 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.2377-1131A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97021169 | |||||||
| chr5:97021242 | C | CAA | 230 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(227): Show |
244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.2377-1057_2377-105 others(6): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 97021242 | ||||||
| chr5:97021276 | A | G | 144 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(141): Show |
153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2377-1024A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97021276 | |||||||
| chr5:97021474 | A | G | 197 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(194): Show |
208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.2377-826A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97021474 | |||||||
| chr5:97021556 | T | G | 178 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(175): Show |
189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.2377-744T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97021556 | |||||||
| chr5:97021674 | G | A | 1 | a0001c0001t0052g0206 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2377-626G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97021674 | |||||||
| chr5:97021808 | CAT | C | 34 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(31): Show |
36 | HG00597.hp1 HG01109.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.2377-489_2377-488d others(4): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 97021808 | ||||||
| chr5:97021845 | C | CT | 69 | a0001c0001t0002g0247 a0001c0015t0010g0193 a0002c0002t0002g0011 others(66): Show |
73 | HG00140.hp1 HG00423.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.2377-446dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 97021845 | ||||||
| chr5:97021923 | G | GT | 51 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0042 others(48): Show |
53 | HG00597.hp1 HG00621.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.2377-351dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 97021923 | ||||||
| chr5:97021923 | G | T | 6 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(3): Show |
6 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.2377-377G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97021923 | |||||||
| chr5:97021923 | GT | G | 139 | a0001c0001t0001g0068 a0001c0001t0001g0079 a0001c0001t0002g0009 others(136): Show |
149 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.2377-351delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 97021923 | ||||||
| chr5:97021923 | GTT | G | 19 | a0001c0001t0003g0203 a0001c0001t0013g0157 a0001c0001t0014g0163 others(16): Show |
19 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.2377-352_2377-351d others(4): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 97021923 | ||||||
| chr5:97021933 | T | G | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2377-367T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97021933 | |||||||
| chr5:97021934 | T | G | 8 | a0001c0001t0001g0006 a0001c0001t0001g0122 a0001c0001t0001g0124 others(5): Show |
9 | HG00642.hp2 HG00741.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2377-366T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97021934 | |||||||
| chr5:97022152 | C | T | 4 | a0001c0003t0017g0033 a0001c0003t0017g0034 a0001c0003t0017g0035 others(1): Show |
4 | HG02451.hp1 HG03540.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2377-148C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97022152 | |||||||
| chr5:97022176 | G | A | 4 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(1): Show |
4 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.2377-124G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97022176 | |||||||
| chr5:97022490 | G | T | 4 | a0001c0001t0010g0189 a0001c0001t0010g0190 a0001c0001t0010g0191 others(1): Show |
4 | HG00738.hp2 HG01167.hp2 HG01975.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.2561+6G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97022490 | |||||||
| chr5:97022500 | A | G | 1 | a0001c0003t0050g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2561+16A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97022500 | |||||||
| chr5:97022616 | A | G | 10 | a0004c0005t0003g0240 a0004c0005t0003g0257 a0004c0005t0003g0282 others(7): Show |
10 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.2561+132A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97022616 | |||||||
| chr5:97022636 | CT | C | 14 | a0001c0003t0007g0028 a0003c0004t0008g0141 a0003c0004t0008g0142 others(11): Show |
14 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2561+165delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 97022636 | ||||||
| chr5:97022790 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2561+306C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97022790 | |||||||
| chr5:97022884 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2561+400G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97022884 | |||||||
| chr5:97022983 | C | T | 197 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(194): Show |
208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.2561+499C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97022983 | |||||||
| chr5:97023004 | TA | T | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2561+521delA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97023004 | |||||||
| chr5:97023052 | T | C | 5 | a0001c0001t0003g0001 a0001c0001t0003g0135 a0001c0001t0003g0137 others(2): Show |
7 | HG01069.hp1 HG01071.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.2561+568T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97023052 | |||||||
| chr5:97023203 | C | T | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2561+719C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97023203 | |||||||
| chr5:97023204 | G | T | 1 | a0001c0003t0043g0230 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2561+720G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97023204 | |||||||
| chr5:97023313 | G | T | 1 | a0001c0001t0047g0334 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2561+829G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97023313 | |||||||
| chr5:97023340 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2561+856A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97023340 | |||||||
| chr5:97023342 | T | C | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2561+858T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97023342 | |||||||
| chr5:97023384 | G | A | 6 | a0001c0001t0003g0001 a0001c0001t0003g0135 a0001c0001t0003g0137 others(3): Show |
8 | HG01069.hp1 HG01071.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.2561+900G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97023384 | |||||||
| chr5:97023545 | T | C | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2562-976T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97023545 | |||||||
| chr5:97023628 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2562-893C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97023628 | |||||||
| chr5:97023748 | A | AAGT | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2562-768_2562-766d others(5): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 97023748 | ||||||
| chr5:97023765 | C | T | 1 | a0001c0001t0040g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2562-756C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97023765 | |||||||
| chr5:97023782 | T | C | 1 | a0004c0005t0003g0289 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2562-739T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97023782 | |||||||
| chr5:97024037 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2562-484C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97024037 | |||||||
| chr5:97024168 | A | C | 1 | a0001c0001t0040g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2562-353A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97024168 | |||||||
| chr5:97024208 | A | G | 144 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(141): Show |
153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2562-313A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97024208 | |||||||
| chr5:97024239 | G | C | 10 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0080 others(7): Show |
10 | HG00140.hp2 HG00323.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.2562-282G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 14/17 | chr5 | 97024239 | |||||||
| chr5:97024739 | C | T | 23 | a0001c0003t0007g0018 a0001c0003t0007g0019 a0001c0003t0007g0023 others(20): Show |
23 | HG00597.hp1 HG02055.hp1 HG02083.hp1 others(20): Show |
intron_variant | MODIFIER | c.2723+57C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | chr5 | 97024739 | |||||||
| chr5:97025036 | A | G | 1 | a0001c0001t0038g0061 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2723+354A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | chr5 | 97025036 | |||||||
| chr5:97025076 | C | G | 2 | a0002c0002t0004g0244 a0002c0002t0004g0333 |
2 | NA18980.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.2723+394C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | chr5 | 97025076 | |||||||
| chr5:97025167 | G | A | 4 | a0001c0001t0016g0178 a0001c0001t0016g0179 a0001c0001t0016g0180 others(1): Show |
4 | HG02559.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2723+485G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | chr5 | 97025167 | |||||||
| chr5:97025206 | T | A | 1 | a0002c0002t0004g0255 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2723+524T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | chr5 | 97025206 | |||||||
| chr5:97025210 | G | A | 3 | a0001c0001t0001g0057 a0001c0001t0001g0088 a0001c0001t0001g0116 |
3 | HG01255.hp1 HG03195.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2723+528G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | chr5 | 97025210 | |||||||
| chr5:97025239 | G | T | 2 | a0001c0001t0005g0165 a0001c0001t0005g0177 |
2 | NA18984.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.2723+557G>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | chr5 | 97025239 | |||||||
| chr5:97025240 | A | T | 2 | a0001c0001t0005g0165 a0001c0001t0005g0177 |
2 | NA18984.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.2723+558A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | chr5 | 97025240 | |||||||
| chr5:97025629 | T | C | 179 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(176): Show |
191 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.2723+947T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | chr5 | 97025629 | |||||||
| chr5:97025686 | A | G | 1 | a0001c0001t0036g0112 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2724-931A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | chr5 | 97025686 | |||||||
| chr5:97025804 | C | G | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2724-813C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | chr5 | 97025804 | |||||||
| chr5:97025817 | TA | T | 198 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(195): Show |
210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.2724-791delA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr5 | 97025817 | ||||||
| chr5:97025828 | T | G | 2 | a0001c0001t0018g0174 a0001c0001t0018g0175 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2724-789T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | chr5 | 97025828 | |||||||
| chr5:97025829 | A | G | 4 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0204 others(1): Show |
4 | HG00280.hp2 HG00741.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2724-788A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | chr5 | 97025829 | |||||||
| chr5:97025838 | T | C | 1 | a0001c0003t0050g0187 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2724-779T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | chr5 | 97025838 | |||||||
| chr5:97025922 | C | T | 179 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(176): Show |
191 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.2724-695C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | chr5 | 97025922 | |||||||
| chr5:97025955 | G | A | 11 | a0001c0003t0006g0003 a0001c0003t0006g0226 a0001c0003t0006g0227 others(8): Show |
13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2724-662G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | chr5 | 97025955 | |||||||
| chr5:97026343 | C | T | 1 | a0002c0002t0002g0269 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2724-274C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | chr5 | 97026343 | |||||||
| chr5:97026431 | G | A | 4 | a0001c0001t0013g0157 a0001c0001t0013g0158 a0001c0001t0013g0166 others(1): Show |
4 | NA18962.hp1 NA18991.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.2724-186G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | chr5 | 97026431 | |||||||
| chr5:97026510 | T | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0067 |
2 | HG01069.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.2724-107T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | chr5 | 97026510 | |||||||
| chr5:97026539 | T | C | 1 | a0002c0002t0002g0310 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2724-78T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | chr5 | 97026539 | |||||||
| chr5:97026576 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2724-41T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 15/17 | chr5 | 97026576 | |||||||
| chr5:97026874 | A | G | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2864+117A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 16/17 | chr5 | 97026874 | |||||||
| chr5:97026897 | G | A | 3 | a0001c0001t0002g0199 a0001c0001t0002g0221 a0001c0001t0002g0222 |
3 | HG01175.hp2 HG01993.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.2864+140G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 16/17 | chr5 | 97026897 | |||||||
| chr5:97027096 | T | G | 198 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(195): Show |
210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.2864+339T>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 16/17 | chr5 | 97027096 | |||||||
| chr5:97027221 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0067 |
2 | HG01069.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.2864+464C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 16/17 | chr5 | 97027221 | |||||||
| chr5:97027347 | C | T | 179 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(176): Show |
191 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.2865-386C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 16/17 | chr5 | 97027347 | |||||||
| chr5:97027352 | C | CA | 42 | a0001c0001t0001g0059 a0001c0001t0005g0002 a0001c0001t0005g0008 others(39): Show |
47 | HG00558.hp1 HG00609.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.2865-369dupA | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 97027352 | ||||||
| chr5:97027436 | G | GT | 14 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(11): Show |
14 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.2865-291dupT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr5 | 97027436 | ||||||
| chr5:97027448 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2865-285T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 16/17 | chr5 | 97027448 | |||||||
| chr5:97027500 | G | A | 1 | a0001c0001t0024g0093 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2865-233G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 16/17 | chr5 | 97027500 | |||||||
| chr5:97027703 | C | T | 192 | a0001c0001t0002g0009 a0001c0001t0002g0195 a0001c0001t0002g0196 others(189): Show |
204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2865-30C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 16/17 | chr5 | 97027703 | |||||||
| chr5:97027727 | C | G | 1 | a0001c0001t0051g0229 | 1 | NA19030.hp2 | splice_region_variant&intron_variant | LOW | c.2865-6C>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 16/17 | chr5 | 97027727 | |||||||
| chr5:97027826 | A | G | 6 | a0001c0001t0005g0153 a0001c0001t0005g0154 a0001c0001t0013g0157 others(3): Show |
6 | NA18962.hp1 NA18985.hp1 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.2946+12A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 17/17 | chr5 | 97027826 | |||||||
| chr5:97027829 | A | G | 1 | a0002c0002t0002g0328 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2946+15A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 17/17 | chr5 | 97027829 | |||||||
| chr5:97028005 | A | T | 13 | a0003c0004t0008g0141 a0003c0004t0008g0142 a0003c0004t0008g0143 others(10): Show |
13 | HG00642.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2946+191A>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 17/17 | chr5 | 97028005 | |||||||
| chr5:97028299 | G | A | 6 | a0002c0002t0004g0255 a0002c0002t0004g0270 a0002c0002t0004g0273 others(3): Show |
6 | HG00423.hp2 HG02056.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.2947-103G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 17/17 | chr5 | 97028299 | |||||||
| chr5:97028359 | C | T | 240 | a0001c0001t0001g0052 a0001c0001t0001g0057 a0001c0001t0001g0085 others(237): Show |
254 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.2947-43C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 17/17 | chr5 | 97028359 |