Search by Gene
| 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 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1025 | 242 | 67 | 46 | 103 | 6 | 19 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0002 | 0/0 | 1025 | 71 | 11 | 6 | 44 | 1 | 9 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0003 | 0/0 | 1025 | 17 | 0 | 7 | 0 | 6 | 4 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0004 | 0/1 | 1025 | 12 | 3 | 3 | 0 | 1 | 4 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0005 | 0/0 | 1025 | 3 | 0 | 0 | 3 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0006 | 0/0 | 1025 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0007 | 0/0 | 1025 | 2 | 1 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0008 | 0/0 | 1025 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0009 | 0/0 | 1025 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0010 | 0/0 | 1025 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 3078 | 204 | 48 | 44 | 88 | 6 | 17 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| c0002 | 0/0 | 3078 | 71 | 11 | 6 | 44 | 1 | 9 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| c0003 | 0/0 | 3078 | 34 | 19 | 2 | 13 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| c0004 | 0/0 | 3078 | 17 | 0 | 7 | 0 | 6 | 4 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| c0005 | 0/1 | 3078 | 10 | 3 | 3 | 0 | 1 | 2 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| c0006 | 0/0 | 3078 | 3 | 0 | 0 | 3 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| c0007 | 0/0 | 3078 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| c0008 | 0/0 | 3078 | 2 | 0 | 0 | 0 | 0 | 2 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| c0009 | 0/0 | 3078 | 2 | 1 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| c0010 | 0/0 | 3078 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| c0011 | 0/0 | 3078 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| c0012 | 0/0 | 3078 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| c0013 | 0/0 | 3078 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| c0014 | 0/0 | 3078 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| c0015 | 0/0 | 3078 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| c0016 | 0/0 | 3078 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 9051 | 47 | 11 | 4 | 22 | 1 | 9 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0002 | 1/0 | 9057 | 44 | 10 | 4 | 23 | 3 | 3 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0003 | 0/0 | 9051 | 24 | 1 | 3 | 20 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0004 | 0/1 | 9050 | 18 | 4 | 5 | 0 | 5 | 3 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0005 | 0/0 | 9044 | 14 | 0 | 2 | 11 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0006 | 0/0 | 9059 | 13 | 2 | 1 | 9 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0007 | 0/0 | 9046 | 11 | 10 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0008 | 0/0 | 9055 | 10 | 0 | 2 | 8 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0009 | 0/0 | 9053 | 10 | 2 | 2 | 4 | 1 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0010 | 0/0 | 9051 | 9 | 0 | 0 | 9 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0011 | 0/0 | 9049 | 9 | 0 | 0 | 9 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0012 | 0/0 | 9042 | 8 | 0 | 4 | 0 | 2 | 2 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0013 | 0/0 | 9052 | 7 | 0 | 3 | 3 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0014 | 0/0 | 9051 | 6 | 4 | 2 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0015 | 0/0 | 9051 | 5 | 4 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0016 | 0/0 | 9044 | 4 | 0 | 4 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0017 | 0/0 | 9044 | 4 | 0 | 0 | 4 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0018 | 0/0 | 9044 | 4 | 0 | 0 | 4 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0019 | 0/0 | 9044 | 4 | 0 | 0 | 4 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0020 | 0/0 | 9048 | 4 | 4 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0021 | 0/0 | 9057 | 4 | 0 | 4 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0022 | 0/0 | 9050 | 4 | 4 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0023 | 0/0 | 9044 | 3 | 2 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0024 | 0/0 | 9057 | 3 | 2 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0025 | 0/0 | 9050 | 3 | 0 | 3 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0026 | 0/0 | 9052 | 3 | 3 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0027 | 0/0 | 9056 | 3 | 0 | 3 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0028 | 0/0 | 9044 | 2 | 0 | 0 | 0 | 0 | 2 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0029 | 0/0 | 9050 | 2 | 0 | 0 | 0 | 0 | 2 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0030 | 0/0 | 9041 | 2 | 0 | 0 | 0 | 0 | 2 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0031 | 0/0 | 9051 | 2 | 1 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0032 | 0/0 | 9057 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0033 | 0/0 | 9057 | 2 | 1 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0034 | 0/0 | 9061 | 2 | 1 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0035 | 0/0 | 9065 | 2 | 0 | 2 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0036 | 0/0 | 9050 | 2 | 1 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0037 | 0/0 | 9053 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0038 | 0/0 | 9055 | 2 | 0 | 1 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0039 | 0/0 | 9057 | 2 | 1 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0040 | 0/0 | 9051 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0041 | 0/0 | 9057 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0042 | 0/0 | 9050 | 2 | 1 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0043 | 0/0 | 9047 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0044 | 0/0 | 9042 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0045 | 0/0 | 9053 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0046 | 0/0 | 9057 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0047 | 0/0 | 9055 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0048 | 0/0 | 9057 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0049 | 0/0 | 9052 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0050 | 0/0 | 9053 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0051 | 0/0 | 9055 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0052 | 0/0 | 9055 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0053 | 0/0 | 9057 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0054 | 0/0 | 9057 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0055 | 0/0 | 9057 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0056 | 0/0 | 9057 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0057 | 0/0 | 9059 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0058 | 0/0 | 9059 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0059 | 0/0 | 9061 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0060 | 0/0 | 9065 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0061 | 0/0 | 9065 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0062 | 0/0 | 9042 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0063 | 0/0 | 9040 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0064 | 0/0 | 9044 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0065 | 0/0 | 9046 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0066 | 0/0 | 9037 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0067 | 0/0 | 9045 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0068 | 0/0 | 9046 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0069 | 0/0 | 9050 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0070 | 0/0 | 9051 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0071 | 0/0 | 9050 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0072 | 0/0 | 9048 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0073 | 0/0 | 9053 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0074 | 0/0 | 9051 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0075 | 0/0 | 9052 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0076 | 0/0 | 9053 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0077 | 0/0 | 9053 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0078 | 0/0 | 9053 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0079 | 0/0 | 9055 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0080 | 0/0 | 9054 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0081 | 0/0 | 9054 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0082 | 0/0 | 9051 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0083 | 0/0 | 9053 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0084 | 0/0 | 9042 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0085 | 0/0 | 9044 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| t0086 | 0/0 | 9055 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0002 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0198 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0321 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/0 | 204 | 48 | 44 | 88 | 6 | 17 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0003 | a0001 | c0003 | 0/0 | 34 | 19 | 2 | 13 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0012 | a0001 | c0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0013 | a0001 | c0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0015 | a0001 | c0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0016 | a0001 | c0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0002c0002 | a0002 | c0002 | 0/0 | 71 | 11 | 6 | 44 | 1 | 9 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0003c0004 | a0003 | c0004 | 0/0 | 17 | 0 | 7 | 0 | 6 | 4 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0004c0005 | a0004 | c0005 | 0/1 | 10 | 3 | 3 | 0 | 1 | 2 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0004c0008 | a0004 | c0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0005c0006 | a0005 | c0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0006c0007 | a0006 | c0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0007c0009 | a0007 | c0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0008c0011 | a0008 | c0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0009c0014 | a0009 | c0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0010c0010 | a0010 | c0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 0/0 | 15 | 3 | 3 | 5 | 1 | 3 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 1/0 | 39 | 10 | 4 | 18 | 3 | 3 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 12 | 0 | 2 | 9 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 13 | 2 | 1 | 9 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0011 | a0001 | c0001 | t0011 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 7 | 0 | 3 | 3 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0015 | a0001 | c0001 | t0015 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0016 | a0001 | c0001 | t0016 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0017 | a0001 | c0001 | t0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0018 | a0001 | c0001 | t0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0019 | a0001 | c0001 | t0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0020 | a0001 | c0001 | t0020 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0021 | a0001 | c0001 | t0021 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0023 | a0001 | c0001 | t0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0024 | a0001 | c0001 | t0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0025 | a0001 | c0001 | t0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0027 | a0001 | c0001 | t0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0030 | a0001 | c0001 | t0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0031 | a0001 | c0001 | t0031 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0032 | a0001 | c0001 | t0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0033 | a0001 | c0001 | t0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0034 | a0001 | c0001 | t0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0035 | a0001 | c0001 | t0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0036 | a0001 | c0001 | t0036 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0038 | a0001 | c0001 | t0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0039 | a0001 | c0001 | t0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0041 | a0001 | c0001 | t0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0043 | a0001 | c0001 | t0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0044 | a0001 | c0001 | t0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0045 | a0001 | c0001 | t0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0046 | a0001 | c0001 | t0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0047 | a0001 | c0001 | t0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0048 | a0001 | c0001 | t0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0049 | a0001 | c0001 | t0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0050 | a0001 | c0001 | t0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0051 | a0001 | c0001 | t0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0052 | a0001 | c0001 | t0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0053 | a0001 | c0001 | t0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0054 | a0001 | c0001 | t0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0055 | a0001 | c0001 | t0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0056 | a0001 | c0001 | t0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0057 | a0001 | c0001 | t0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0058 | a0001 | c0001 | t0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0059 | a0001 | c0001 | t0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0060 | a0001 | c0001 | t0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0061 | a0001 | c0001 | t0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0066 | a0001 | c0001 | t0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0072 | a0001 | c0001 | t0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0074 | a0001 | c0001 | t0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0075 | a0001 | c0001 | t0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0076 | a0001 | c0001 | t0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0077 | a0001 | c0001 | t0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0078 | a0001 | c0001 | t0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0079 | a0001 | c0001 | t0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0080 | a0001 | c0001 | t0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0081 | a0001 | c0001 | t0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0001t0086 | a0001 | c0001 | t0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0003t0007 | a0001 | c0003 | t0007 | 0/0 | 11 | 10 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0003t0010 | a0001 | c0003 | t0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0003t0022 | a0001 | c0003 | t0022 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0003t0026 | a0001 | c0003 | t0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0003t0040 | a0001 | c0003 | t0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0003t0065 | a0001 | c0003 | t0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0003t0067 | a0001 | c0003 | t0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0003t0068 | a0001 | c0003 | t0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0003t0069 | a0001 | c0003 | t0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0003t0070 | a0001 | c0003 | t0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0003t0071 | a0001 | c0003 | t0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0003t0073 | a0001 | c0003 | t0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0012t0028 | a0001 | c0012 | t0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0013t0002 | a0001 | c0013 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0015t0028 | a0001 | c0015 | t0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0001c0016t0002 | a0001 | c0016 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0002c0002t0001 | a0002 | c0002 | t0001 | 0/0 | 32 | 8 | 1 | 17 | 0 | 6 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0002c0002t0003 | a0002 | c0002 | t0003 | 0/0 | 24 | 1 | 3 | 20 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0002c0002t0009 | a0002 | c0002 | t0009 | 0/0 | 9 | 1 | 2 | 4 | 1 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0002c0002t0037 | a0002 | c0002 | t0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0002c0002t0038 | a0002 | c0002 | t0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0002c0002t0039 | a0002 | c0002 | t0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0002c0002t0082 | a0002 | c0002 | t0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0002c0002t0083 | a0002 | c0002 | t0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0003c0004t0004 | a0003 | c0004 | t0004 | 0/0 | 4 | 0 | 1 | 0 | 3 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0003c0004t0012 | a0003 | c0004 | t0012 | 0/0 | 8 | 0 | 4 | 0 | 2 | 2 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0003c0004t0062 | a0003 | c0004 | t0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0003c0004t0063 | a0003 | c0004 | t0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0003c0004t0064 | a0003 | c0004 | t0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0003c0004t0084 | a0003 | c0004 | t0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0003c0004t0085 | a0003 | c0004 | t0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0004c0005t0004 | a0004 | c0005 | t0004 | 0/1 | 9 | 3 | 2 | 0 | 1 | 2 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0004c0005t0027 | a0004 | c0005 | t0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0004c0008t0029 | a0004 | c0008 | t0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0005c0006t0002 | a0005 | c0006 | t0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0006c0007t0005 | a0006 | c0007 | t0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0007c0009t0042 | a0007 | c0009 | t0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0008c0011t0010 | a0008 | c0011 | t0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0009c0014t0004 | a0009 | c0014 | t0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| a0010c0010t0010 | a0010 | c0010 | t0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP | copy fasta |
| actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0196 | a0001 | c0001 | t0001 | g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0001g0197 | a0001 | c0001 | t0001 | g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0001g0200 | a0001 | c0001 | t0001 | g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0001g0204 | a0001 | c0001 | t0001 | g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0001g0206 | a0001 | c0001 | t0001 | g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0001g0209 | a0001 | c0001 | t0001 | g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0001g0210 | a0001 | c0001 | t0001 | g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0001g0211 | a0001 | c0001 | t0001 | g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0001g0217 | a0001 | c0001 | t0001 | g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0001g0218 | a0001 | c0001 | t0001 | g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0001g0219 | a0001 | c0001 | t0001 | g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0001g0221 | a0001 | c0001 | t0001 | g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0001g0224 | a0001 | c0001 | t0001 | g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0001g0225 | a0001 | c0001 | t0001 | g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0001g0226 | a0001 | c0001 | t0001 | g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0033 | a0001 | c0001 | t0002 | g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0038 | a0001 | c0001 | t0002 | g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0043 | a0001 | c0001 | t0002 | g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0045 | a0001 | c0001 | t0002 | g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0055 | a0001 | c0001 | t0002 | g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0058 | a0001 | c0001 | t0002 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0066 | a0001 | c0001 | t0002 | g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0069 | a0001 | c0001 | t0002 | g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0070 | a0001 | c0001 | t0002 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0073 | a0001 | c0001 | t0002 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0074 | a0001 | c0001 | t0002 | g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0076 | a0001 | c0001 | t0002 | g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0078 | a0001 | c0001 | t0002 | g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0079 | a0001 | c0001 | t0002 | g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0081 | a0001 | c0001 | t0002 | g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0086 | a0001 | c0001 | t0002 | g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0087 | a0001 | c0001 | t0002 | g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0088 | a0001 | c0001 | t0002 | g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0095 | a0001 | c0001 | t0002 | g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0099 | a0001 | c0001 | t0002 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0103 | a0001 | c0001 | t0002 | g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0109 | a0001 | c0001 | t0002 | g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0116 | a0001 | c0001 | t0002 | g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0118 | a0001 | c0001 | t0002 | g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0120 | a0001 | c0001 | t0002 | g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0121 | a0001 | c0001 | t0002 | g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0122 | a0001 | c0001 | t0002 | g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0123 | a0001 | c0001 | t0002 | g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0124 | a0001 | c0001 | t0002 | g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0125 | a0001 | c0001 | t0002 | g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0126 | a0001 | c0001 | t0002 | g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0127 | a0001 | c0001 | t0002 | g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0129 | a0001 | c0001 | t0002 | g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0130 | a0001 | c0001 | t0002 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0131 | a0001 | c0001 | t0002 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0132 | a0001 | c0001 | t0002 | g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0133 | a0001 | c0001 | t0002 | g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0134 | a0001 | c0001 | t0002 | g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0002g0198 | a0001 | c0001 | t0002 | g0198 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0004g0205 | a0001 | c0001 | t0004 | g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0004g0291 | a0001 | c0001 | t0004 | g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0004g0298 | a0001 | c0001 | t0004 | g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0004g0328 | a0001 | c0001 | t0004 | g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0005g0001 | a0001 | c0001 | t0005 | g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0005g0005 | a0001 | c0001 | t0005 | g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0005g0153 | a0001 | c0001 | t0005 | g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0005g0154 | a0001 | c0001 | t0005 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0005g0155 | a0001 | c0001 | t0005 | g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0005g0156 | a0001 | c0001 | t0005 | g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0005g0165 | a0001 | c0001 | t0005 | g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0005g0166 | a0001 | c0001 | t0005 | g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0005g0171 | a0001 | c0001 | t0005 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0005g0178 | a0001 | c0001 | t0005 | g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0006g0032 | a0001 | c0001 | t0006 | g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0006g0040 | a0001 | c0001 | t0006 | g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0006g0048 | a0001 | c0001 | t0006 | g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0006g0051 | a0001 | c0001 | t0006 | g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0006g0056 | a0001 | c0001 | t0006 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0006g0071 | a0001 | c0001 | t0006 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0006g0072 | a0001 | c0001 | t0006 | g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0006g0075 | a0001 | c0001 | t0006 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0006g0094 | a0001 | c0001 | t0006 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0006g0096 | a0001 | c0001 | t0006 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0006g0100 | a0001 | c0001 | t0006 | g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0006g0106 | a0001 | c0001 | t0006 | g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0006g0111 | a0001 | c0001 | t0006 | g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0008g0035 | a0001 | c0001 | t0008 | g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0008g0046 | a0001 | c0001 | t0008 | g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0008g0057 | a0001 | c0001 | t0008 | g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0008g0063 | a0001 | c0001 | t0008 | g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0008g0064 | a0001 | c0001 | t0008 | g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0008g0082 | a0001 | c0001 | t0008 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0008g0083 | a0001 | c0001 | t0008 | g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0008g0108 | a0001 | c0001 | t0008 | g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0008g0112 | a0001 | c0001 | t0008 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0008g0115 | a0001 | c0001 | t0008 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0009g0228 | a0001 | c0001 | t0009 | g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0011g0199 | a0001 | c0001 | t0011 | g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0011g0201 | a0001 | c0001 | t0011 | g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0011g0202 | a0001 | c0001 | t0011 | g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0011g0203 | a0001 | c0001 | t0011 | g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0011g0213 | a0001 | c0001 | t0011 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0011g0214 | a0001 | c0001 | t0011 | g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0011g0216 | a0001 | c0001 | t0011 | g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0011g0223 | a0001 | c0001 | t0011 | g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0011g0250 | a0001 | c0001 | t0011 | g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0013g0004 | a0001 | c0001 | t0013 | g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0013g0137 | a0001 | c0001 | t0013 | g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0013g0139 | a0001 | c0001 | t0013 | g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0013g0261 | a0001 | c0001 | t0013 | g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0013g0287 | a0001 | c0001 | t0013 | g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0013g0296 | a0001 | c0001 | t0013 | g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0013g0320 | a0001 | c0001 | t0013 | g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0014g0297 | a0001 | c0001 | t0014 | g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0014g0322 | a0001 | c0001 | t0014 | g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0014g0329 | a0001 | c0001 | t0014 | g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0014g0330 | a0001 | c0001 | t0014 | g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0014g0332 | a0001 | c0001 | t0014 | g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0014g0333 | a0001 | c0001 | t0014 | g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0015g0027 | a0001 | c0001 | t0015 | g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0015g0028 | a0001 | c0001 | t0015 | g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0015g0241 | a0001 | c0001 | t0015 | g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0015g0242 | a0001 | c0001 | t0015 | g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0015g0324 | a0001 | c0001 | t0015 | g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0016g0190 | a0001 | c0001 | t0016 | g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0016g0191 | a0001 | c0001 | t0016 | g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0016g0192 | a0001 | c0001 | t0016 | g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0016g0193 | a0001 | c0001 | t0016 | g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0017g0157 | a0001 | c0001 | t0017 | g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0017g0161 | a0001 | c0001 | t0017 | g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0017g0173 | a0001 | c0001 | t0017 | g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0017g0174 | a0001 | c0001 | t0017 | g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0018g0158 | a0001 | c0001 | t0018 | g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0018g0159 | a0001 | c0001 | t0018 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0018g0167 | a0001 | c0001 | t0018 | g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0018g0168 | a0001 | c0001 | t0018 | g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0019g0160 | a0001 | c0001 | t0019 | g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0019g0163 | a0001 | c0001 | t0019 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0019g0164 | a0001 | c0001 | t0019 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0019g0169 | a0001 | c0001 | t0019 | g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0020g0179 | a0001 | c0001 | t0020 | g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0020g0180 | a0001 | c0001 | t0020 | g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0020g0181 | a0001 | c0001 | t0020 | g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0020g0182 | a0001 | c0001 | t0020 | g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0021g0059 | a0001 | c0001 | t0021 | g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0021g0089 | a0001 | c0001 | t0021 | g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0021g0105 | a0001 | c0001 | t0021 | g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0021g0117 | a0001 | c0001 | t0021 | g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0023g0175 | a0001 | c0001 | t0023 | g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0023g0176 | a0001 | c0001 | t0023 | g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0023g0177 | a0001 | c0001 | t0023 | g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0024g0053 | a0001 | c0001 | t0024 | g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0024g0084 | a0001 | c0001 | t0024 | g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0024g0114 | a0001 | c0001 | t0024 | g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0025g0008 | a0001 | c0001 | t0025 | g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0025g0292 | a0001 | c0001 | t0025 | g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0027g0004 | a0001 | c0001 | t0027 | g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0027g0135 | a0001 | c0001 | t0027 | g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0030g0052 | a0001 | c0001 | t0030 | g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0030g0104 | a0001 | c0001 | t0030 | g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0031g0036 | a0001 | c0001 | t0031 | g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0031g0119 | a0001 | c0001 | t0031 | g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0032g0037 | a0001 | c0001 | t0032 | g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0032g0091 | a0001 | c0001 | t0032 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0033g0025 | a0001 | c0001 | t0033 | g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0033g0068 | a0001 | c0001 | t0033 | g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0034g0077 | a0001 | c0001 | t0034 | g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0034g0128 | a0001 | c0001 | t0034 | g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0035g0080 | a0001 | c0001 | t0035 | g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0035g0107 | a0001 | c0001 | t0035 | g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0036g0337 | a0001 | c0001 | t0036 | g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0036g0338 | a0001 | c0001 | t0036 | g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0038g0222 | a0001 | c0001 | t0038 | g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0039g0227 | a0001 | c0001 | t0039 | g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0041g0034 | a0001 | c0001 | t0041 | g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0041g0039 | a0001 | c0001 | t0041 | g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0043g0162 | a0001 | c0001 | t0043 | g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0044g0001 | a0001 | c0001 | t0044 | g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0045g0054 | a0001 | c0001 | t0045 | g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0046g0085 | a0001 | c0001 | t0046 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0047g0044 | a0001 | c0001 | t0047 | g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0048g0041 | a0001 | c0001 | t0048 | g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0049g0026 | a0001 | c0001 | t0049 | g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0050g0110 | a0001 | c0001 | t0050 | g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0051g0062 | a0001 | c0001 | t0051 | g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0052g0047 | a0001 | c0001 | t0052 | g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0053g0093 | a0001 | c0001 | t0053 | g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0054g0090 | a0001 | c0001 | t0054 | g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0055g0050 | a0001 | c0001 | t0055 | g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0056g0067 | a0001 | c0001 | t0056 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0057g0049 | a0001 | c0001 | t0057 | g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0058g0097 | a0001 | c0001 | t0058 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0059g0098 | a0001 | c0001 | t0059 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0060g0042 | a0001 | c0001 | t0060 | g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0061g0113 | a0001 | c0001 | t0061 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0066g0340 | a0001 | c0001 | t0066 | g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0072g0289 | a0001 | c0001 | t0072 | g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0074g0207 | a0001 | c0001 | t0074 | g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0075g0208 | a0001 | c0001 | t0075 | g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0076g0232 | a0001 | c0001 | t0076 | g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0077g0331 | a0001 | c0001 | t0077 | g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0078g0220 | a0001 | c0001 | t0078 | g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0079g0238 | a0001 | c0001 | t0079 | g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0080g0136 | a0001 | c0001 | t0080 | g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0081g0138 | a0001 | c0001 | t0081 | g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0001t0086g0065 | a0001 | c0001 | t0086 | g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0007g0002 | a0001 | c0003 | t0007 | g0002 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0007g0229 | a0001 | c0003 | t0007 | g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0007g0230 | a0001 | c0003 | t0007 | g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0007g0231 | a0001 | c0003 | t0007 | g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0007g0234 | a0001 | c0003 | t0007 | g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0007g0235 | a0001 | c0003 | t0007 | g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0007g0236 | a0001 | c0003 | t0007 | g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0007g0237 | a0001 | c0003 | t0007 | g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0007g0239 | a0001 | c0003 | t0007 | g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0010g0016 | a0001 | c0003 | t0010 | g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0010g0019 | a0001 | c0003 | t0010 | g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0010g0020 | a0001 | c0003 | t0010 | g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0010g0021 | a0001 | c0003 | t0010 | g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0010g0022 | a0001 | c0003 | t0010 | g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0010g0023 | a0001 | c0003 | t0010 | g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0010g0024 | a0001 | c0003 | t0010 | g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0022g0029 | a0001 | c0003 | t0022 | g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0022g0030 | a0001 | c0003 | t0022 | g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0022g0031 | a0001 | c0003 | t0022 | g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0022g0187 | a0001 | c0003 | t0022 | g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0026g0184 | a0001 | c0003 | t0026 | g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0026g0185 | a0001 | c0003 | t0026 | g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0026g0186 | a0001 | c0003 | t0026 | g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0040g0013 | a0001 | c0003 | t0040 | g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0040g0014 | a0001 | c0003 | t0040 | g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0065g0233 | a0001 | c0003 | t0065 | g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0067g0018 | a0001 | c0003 | t0067 | g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0068g0240 | a0001 | c0003 | t0068 | g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0069g0012 | a0001 | c0003 | t0069 | g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0070g0015 | a0001 | c0003 | t0070 | g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0071g0188 | a0001 | c0003 | t0071 | g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0003t0073g0011 | a0001 | c0003 | t0073 | g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0012t0028g0189 | a0001 | c0012 | t0028 | g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0013t0002g0102 | a0001 | c0013 | t0002 | g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0015t0028g0194 | a0001 | c0015 | t0028 | g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0001c0016t0002g0101 | a0001 | c0016 | t0002 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0007 | a0002 | c0002 | t0001 | g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0009 | a0002 | c0002 | t0001 | g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0195 | a0002 | c0002 | t0001 | g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0255 | a0002 | c0002 | t0001 | g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0259 | a0002 | c0002 | t0001 | g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0262 | a0002 | c0002 | t0001 | g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0263 | a0002 | c0002 | t0001 | g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0264 | a0002 | c0002 | t0001 | g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0265 | a0002 | c0002 | t0001 | g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0266 | a0002 | c0002 | t0001 | g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0267 | a0002 | c0002 | t0001 | g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0273 | a0002 | c0002 | t0001 | g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0274 | a0002 | c0002 | t0001 | g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0284 | a0002 | c0002 | t0001 | g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0299 | a0002 | c0002 | t0001 | g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0300 | a0002 | c0002 | t0001 | g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0301 | a0002 | c0002 | t0001 | g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0302 | a0002 | c0002 | t0001 | g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0303 | a0002 | c0002 | t0001 | g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0304 | a0002 | c0002 | t0001 | g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0305 | a0002 | c0002 | t0001 | g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0306 | a0002 | c0002 | t0001 | g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0307 | a0002 | c0002 | t0001 | g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0310 | a0002 | c0002 | t0001 | g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0311 | a0002 | c0002 | t0001 | g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0315 | a0002 | c0002 | t0001 | g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0316 | a0002 | c0002 | t0001 | g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0323 | a0002 | c0002 | t0001 | g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0334 | a0002 | c0002 | t0001 | g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0335 | a0002 | c0002 | t0001 | g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0001g0336 | a0002 | c0002 | t0001 | g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0006 | a0002 | c0002 | t0003 | g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0212 | a0002 | c0002 | t0003 | g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0215 | a0002 | c0002 | t0003 | g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0244 | a0002 | c0002 | t0003 | g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0245 | a0002 | c0002 | t0003 | g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0246 | a0002 | c0002 | t0003 | g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0247 | a0002 | c0002 | t0003 | g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0248 | a0002 | c0002 | t0003 | g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0249 | a0002 | c0002 | t0003 | g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0258 | a0002 | c0002 | t0003 | g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0272 | a0002 | c0002 | t0003 | g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0275 | a0002 | c0002 | t0003 | g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0276 | a0002 | c0002 | t0003 | g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0278 | a0002 | c0002 | t0003 | g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0279 | a0002 | c0002 | t0003 | g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0280 | a0002 | c0002 | t0003 | g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0281 | a0002 | c0002 | t0003 | g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0282 | a0002 | c0002 | t0003 | g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0285 | a0002 | c0002 | t0003 | g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0312 | a0002 | c0002 | t0003 | g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0313 | a0002 | c0002 | t0003 | g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0314 | a0002 | c0002 | t0003 | g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0003g0339 | a0002 | c0002 | t0003 | g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0009g0007 | a0002 | c0002 | t0009 | g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0009g0253 | a0002 | c0002 | t0009 | g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0009g0268 | a0002 | c0002 | t0009 | g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0009g0270 | a0002 | c0002 | t0009 | g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0009g0283 | a0002 | c0002 | t0009 | g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0009g0318 | a0002 | c0002 | t0009 | g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0009g0319 | a0002 | c0002 | t0009 | g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0009g0325 | a0002 | c0002 | t0009 | g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0009g0326 | a0002 | c0002 | t0009 | g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0037g0277 | a0002 | c0002 | t0037 | g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0037g0317 | a0002 | c0002 | t0037 | g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0038g0254 | a0002 | c0002 | t0038 | g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0039g0271 | a0002 | c0002 | t0039 | g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0082g0269 | a0002 | c0002 | t0082 | g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0002c0002t0083g0252 | a0002 | c0002 | t0083 | g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0003c0004t0004g0256 | a0003 | c0004 | t0004 | g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0003c0004t0004g0257 | a0003 | c0004 | t0004 | g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0003c0004t0004g0294 | a0003 | c0004 | t0004 | g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0003c0004t0004g0295 | a0003 | c0004 | t0004 | g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0003c0004t0012g0142 | a0003 | c0004 | t0012 | g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0003c0004t0012g0143 | a0003 | c0004 | t0012 | g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0003c0004t0012g0145 | a0003 | c0004 | t0012 | g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0003c0004t0012g0147 | a0003 | c0004 | t0012 | g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0003c0004t0012g0149 | a0003 | c0004 | t0012 | g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0003c0004t0012g0150 | a0003 | c0004 | t0012 | g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0003c0004t0012g0151 | a0003 | c0004 | t0012 | g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0003c0004t0012g0152 | a0003 | c0004 | t0012 | g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0003c0004t0062g0148 | a0003 | c0004 | t0062 | g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0003c0004t0063g0141 | a0003 | c0004 | t0063 | g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0003c0004t0064g0146 | a0003 | c0004 | t0064 | g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0003c0004t0084g0144 | a0003 | c0004 | t0084 | g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0003c0004t0085g0140 | a0003 | c0004 | t0085 | g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0004c0005t0004g0243 | a0004 | c0005 | t0004 | g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0004c0005t0004g0260 | a0004 | c0005 | t0004 | g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0004c0005t0004g0286 | a0004 | c0005 | t0004 | g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0004c0005t0004g0288 | a0004 | c0005 | t0004 | g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0004c0005t0004g0290 | a0004 | c0005 | t0004 | g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0004c0005t0004g0308 | a0004 | c0005 | t0004 | g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0004c0005t0004g0309 | a0004 | c0005 | t0004 | g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0004c0005t0004g0321 | a0004 | c0005 | t0004 | g0321 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0004c0005t0004g0341 | a0004 | c0005 | t0004 | g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0004c0005t0027g0293 | a0004 | c0005 | t0027 | g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0004c0008t0029g0003 | a0004 | c0008 | t0029 | g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0005c0006t0002g0060 | a0005 | c0006 | t0002 | g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0005c0006t0002g0061 | a0005 | c0006 | t0002 | g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0005c0006t0002g0092 | a0005 | c0006 | t0002 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0006c0007t0005g0170 | a0006 | c0007 | t0005 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0006c0007t0005g0172 | a0006 | c0007 | t0005 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0007c0009t0042g0183 | a0007 | c0009 | t0042 | g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0007c0009t0042g0251 | a0007 | c0009 | t0042 | g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0008c0011t0010g0017 | a0008 | c0011 | t0010 | g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0009c0014t0004g0327 | a0009 | c0014 | t0004 | g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| a0010c0010t0010g0010 | a0010 | c0010 | t0010 | g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNPEP_chr5_96931080_97042513 | LNPEP |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0009 | g0326 | EUR | GBR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0079 | EUR | GBR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00280 | hp1 | a0004 | c0005 | t0004 | g0341 | EUR | FIN | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | FIN | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0078 | EUR | FIN | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00323 | hp2 | a0001 | c0001 | t0036 | g0338 | EUR | FIN | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | CHS | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00423 | hp2 | a0002 | c0002 | t0003 | g0276 | EAS | CHS | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00558 | hp1 | a0001 | c0001 | t0019 | g0160 | EAS | CHS | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00558 | hp2 | a0002 | c0002 | t0009 | g0268 | EAS | CHS | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00597 | hp1 | a0008 | c0011 | t0010 | g0017 | EAS | CHS | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00609 | hp1 | a0001 | c0001 | t0031 | g0036 | EAS | CHS | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00609 | hp2 | a0001 | c0001 | t0017 | g0161 | EAS | CHS | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00621 | hp1 | a0002 | c0002 | t0009 | g0318 | EAS | CHS | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00621 | hp2 | a0001 | c0001 | t0006 | g0040 | EAS | CHS | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00642 | hp1 | a0003 | c0004 | t0012 | g0149 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0300 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00735 | hp1 | a0002 | c0002 | t0009 | g0319 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00735 | hp2 | a0003 | c0004 | t0085 | g0140 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00738 | hp1 | a0001 | c0001 | t0015 | g0242 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00738 | hp2 | a0001 | c0001 | t0016 | g0191 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01069 | hp1 | a0001 | c0001 | t0027 | g0004 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01070 | hp1 | a0004 | c0005 | t0004 | g0308 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01070 | hp2 | a0001 | c0001 | t0021 | g0059 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01071 | hp1 | a0001 | c0001 | t0027 | g0135 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01071 | hp2 | a0004 | c0005 | t0027 | g0293 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01074 | hp2 | a0007 | c0009 | t0042 | g0183 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01081 | hp1 | a0009 | c0014 | t0004 | g0327 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01081 | hp2 | a0001 | c0001 | t0021 | g0089 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01099 | hp1 | a0001 | c0001 | t0035 | g0080 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01099 | hp2 | a0004 | c0005 | t0004 | g0290 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01109 | hp1 | a0001 | c0003 | t0007 | g0002 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01167 | hp1 | a0001 | c0001 | t0025 | g0008 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01167 | hp2 | a0001 | c0001 | t0016 | g0192 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0205 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01168 | hp2 | a0003 | c0004 | t0012 | g0142 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01169 | hp1 | a0001 | c0001 | t0025 | g0292 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01169 | hp2 | a0003 | c0004 | t0012 | g0150 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01175 | hp1 | a0001 | c0001 | t0035 | g0107 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01192 | hp1 | a0001 | c0001 | t0033 | g0068 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01192 | hp2 | a0001 | c0001 | t0038 | g0222 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01243 | hp1 | a0001 | c0001 | t0023 | g0175 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01243 | hp2 | a0001 | c0003 | t0065 | g0233 | AMR | PUR | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01255 | hp1 | a0001 | c0001 | t0024 | g0114 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01255 | hp2 | a0002 | c0002 | t0003 | g0280 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01257 | hp2 | a0001 | c0001 | t0014 | g0297 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01258 | hp1 | a0002 | c0002 | t0009 | g0283 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01261 | hp1 | a0001 | c0001 | t0021 | g0105 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01261 | hp2 | a0001 | c0001 | t0025 | g0008 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01433 | hp1 | a0001 | c0001 | t0008 | g0064 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01433 | hp2 | a0001 | c0001 | t0014 | g0322 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0076 | EUR | IBS | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01515 | hp2 | a0003 | c0004 | t0004 | g0294 | EUR | IBS | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01516 | hp1 | a0003 | c0004 | t0012 | g0143 | EUR | IBS | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01516 | hp2 | a0003 | c0004 | t0004 | g0257 | EUR | IBS | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01517 | hp1 | a0003 | c0004 | t0004 | g0256 | EUR | IBS | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01517 | hp2 | a0003 | c0004 | t0012 | g0147 | EUR | IBS | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01884 | hp1 | a0001 | c0003 | t0007 | g0002 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01884 | hp2 | a0001 | c0001 | t0072 | g0289 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01934 | hp1 | a0001 | c0001 | t0034 | g0077 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01934 | hp2 | a0003 | c0004 | t0012 | g0151 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01943 | hp1 | a0001 | c0001 | t0060 | g0042 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01943 | hp2 | a0002 | c0002 | t0003 | g0281 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01975 | hp1 | a0001 | c0001 | t0080 | g0136 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01975 | hp2 | a0001 | c0001 | t0016 | g0190 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01978 | hp1 | a0002 | c0002 | t0003 | g0279 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01978 | hp2 | a0003 | c0004 | t0004 | g0295 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01981 | hp1 | a0001 | c0001 | t0013 | g0004 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01981 | hp2 | a0001 | c0001 | t0016 | g0193 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01993 | hp1 | a0001 | c0001 | t0008 | g0063 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02027 | hp1 | a0001 | c0001 | t0006 | g0096 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0307 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02055 | hp1 | a0001 | c0003 | t0071 | g0188 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02055 | hp2 | a0001 | c0001 | t0079 | g0238 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02056 | hp2 | a0002 | c0002 | t0003 | g0313 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02071 | hp1 | a0002 | c0002 | t0009 | g0270 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02071 | hp2 | a0001 | c0001 | t0006 | g0094 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02083 | hp1 | a0001 | c0003 | t0010 | g0022 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02083 | hp2 | a0001 | c0001 | t0008 | g0115 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02129 | hp1 | a0001 | c0001 | t0056 | g0067 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02129 | hp2 | a0002 | c0002 | t0003 | g0282 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02135 | hp2 | a0001 | c0016 | t0002 | g0101 | EAS | KHV | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02145 | hp1 | a0001 | c0001 | t0077 | g0331 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02145 | hp2 | a0001 | c0001 | t0036 | g0337 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02148 | hp1 | a0001 | c0001 | t0006 | g0100 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02148 | hp2 | a0001 | c0001 | t0013 | g0139 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02257 | hp1 | a0001 | c0001 | t0033 | g0025 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02293 | hp1 | a0001 | c0001 | t0021 | g0117 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02293 | hp2 | a0001 | c0001 | t0081 | g0138 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02300 | hp1 | a0001 | c0001 | t0057 | g0049 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02300 | hp2 | a0001 | c0001 | t0013 | g0137 | AMR | PEL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02451 | hp1 | a0001 | c0003 | t0022 | g0029 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02451 | hp2 | a0001 | c0003 | t0068 | g0240 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02572 | hp1 | a0004 | c0005 | t0004 | g0309 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02572 | hp2 | a0001 | c0001 | t0046 | g0085 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02615 | hp1 | a0001 | c0001 | t0014 | g0329 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02615 | hp2 | a0001 | c0001 | t0034 | g0128 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02622 | hp1 | a0001 | c0003 | t0007 | g0235 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02622 | hp2 | a0001 | c0003 | t0026 | g0184 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02630 | hp1 | a0002 | c0002 | t0009 | g0007 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02630 | hp2 | a0001 | c0003 | t0007 | g0239 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0311 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02647 | hp2 | a0001 | c0001 | t0023 | g0176 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02698 | hp1 | a0002 | c0002 | t0083 | g0252 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02698 | hp2 | a0001 | c0001 | t0030 | g0052 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0051 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02738 | hp1 | a0001 | c0012 | t0028 | g0189 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02809 | hp1 | a0001 | c0003 | t0026 | g0186 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0263 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02818 | hp1 | a0001 | c0001 | t0015 | g0241 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02886 | hp1 | a0001 | c0003 | t0026 | g0185 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0291 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02895 | hp1 | a0001 | c0003 | t0007 | g0230 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02895 | hp2 | a0001 | c0001 | t0050 | g0110 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02896 | hp1 | a0001 | c0001 | t0020 | g0181 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02897 | hp1 | a0001 | c0003 | t0007 | g0236 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0267 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02970 | hp1 | a0001 | c0001 | t0009 | g0228 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02976 | hp1 | a0001 | c0001 | t0020 | g0180 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03098 | hp1 | a0001 | c0003 | t0007 | g0229 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03098 | hp2 | a0001 | c0001 | t0045 | g0054 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03130 | hp1 | a0001 | c0001 | t0052 | g0047 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03130 | hp2 | a0001 | c0001 | t0023 | g0177 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03139 | hp2 | a0002 | c0002 | t0082 | g0269 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03195 | hp1 | a0001 | c0001 | t0024 | g0053 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0266 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03209 | hp1 | a0001 | c0001 | t0066 | g0340 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0259 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03225 | hp1 | a0001 | c0003 | t0007 | g0231 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03225 | hp2 | a0004 | c0005 | t0004 | g0260 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03239 | hp1 | a0003 | c0004 | t0064 | g0146 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03239 | hp2 | a0004 | c0005 | t0004 | g0286 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03453 | hp2 | a0004 | c0005 | t0004 | g0243 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03486 | hp1 | a0001 | c0001 | t0031 | g0119 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03486 | hp2 | a0001 | c0003 | t0007 | g0234 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03491 | hp1 | a0004 | c0008 | t0029 | g0003 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0195 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03492 | hp1 | a0004 | c0008 | t0029 | g0003 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03492 | hp2 | a0001 | c0001 | t0074 | g0207 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03516 | hp2 | a0001 | c0001 | t0015 | g0028 | AFR | ESN | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03540 | hp1 | a0001 | c0003 | t0007 | g0237 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03540 | hp2 | a0001 | c0003 | t0022 | g0187 | AFR | GWD | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03579 | hp1 | a0001 | c0001 | t0020 | g0179 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03579 | hp2 | a0001 | c0001 | t0014 | g0333 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0299 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03654 | hp2 | a0001 | c0001 | t0053 | g0093 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | STU | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0165 | SAS | STU | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0335 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0274 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03710 | hp1 | a0001 | c0001 | t0055 | g0050 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03710 | hp2 | a0003 | c0004 | t0012 | g0145 | SAS | PJL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0298 | SAS | BEB | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03831 | hp2 | a0001 | c0015 | t0028 | g0194 | SAS | BEB | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03834 | hp1 | a0001 | c0001 | t0078 | g0220 | SAS | BEB | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0072 | SAS | BEB | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03927 | hp1 | a0002 | c0002 | t0038 | g0254 | SAS | BEB | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03927 | hp2 | a0003 | c0004 | t0012 | g0152 | SAS | BEB | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG04184 | hp1 | a0001 | c0001 | t0048 | g0041 | SAS | BEB | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG04184 | hp2 | a0001 | c0001 | t0013 | g0287 | SAS | BEB | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | STU | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG04199 | hp2 | a0001 | c0001 | t0030 | g0104 | SAS | STU | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0334 | SAS | STU | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG04204 | hp2 | a0003 | c0004 | t0063 | g0141 | SAS | STU | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | STU | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG04228 | hp2 | a0002 | c0002 | t0009 | g0253 | SAS | STU | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18522 | hp1 | a0001 | c0003 | t0022 | g0030 | AFR | YRI | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHB | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0305 | EAS | CHB | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18747 | hp1 | a0002 | c0002 | t0009 | g0325 | EAS | CHB | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18747 | hp2 | a0001 | c0001 | t0006 | g0071 | EAS | CHB | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18942 | hp2 | a0001 | c0003 | t0010 | g0019 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18945 | hp2 | a0001 | c0001 | t0008 | g0057 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18946 | hp1 | a0001 | c0001 | t0006 | g0111 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18946 | hp2 | a0001 | c0001 | t0011 | g0202 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18947 | hp1 | a0001 | c0001 | t0061 | g0113 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18949 | hp1 | a0001 | c0001 | t0013 | g0320 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18949 | hp2 | a0001 | c0001 | t0006 | g0032 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18950 | hp1 | a0001 | c0001 | t0017 | g0157 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18950 | hp2 | a0002 | c0002 | t0003 | g0285 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18953 | hp1 | a0001 | c0001 | t0011 | g0216 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18953 | hp2 | a0001 | c0001 | t0008 | g0046 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18960 | hp1 | a0005 | c0006 | t0002 | g0092 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0304 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18961 | hp1 | a0001 | c0001 | t0011 | g0213 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18961 | hp2 | a0001 | c0003 | t0073 | g0011 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18962 | hp1 | a0001 | c0001 | t0018 | g0158 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18962 | hp2 | a0002 | c0002 | t0003 | g0248 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0153 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18967 | hp1 | a0001 | c0001 | t0032 | g0091 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18967 | hp2 | a0001 | c0001 | t0011 | g0203 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18968 | hp1 | a0001 | c0001 | t0041 | g0039 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18968 | hp2 | a0001 | c0001 | t0017 | g0174 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18971 | hp1 | a0001 | c0001 | t0008 | g0112 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18971 | hp2 | a0001 | c0001 | t0013 | g0261 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18972 | hp2 | a0002 | c0002 | t0001 | g0323 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18973 | hp1 | a0006 | c0007 | t0005 | g0172 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18973 | hp2 | a0002 | c0002 | t0003 | g0249 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18975 | hp1 | a0001 | c0001 | t0011 | g0199 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18977 | hp1 | a0001 | c0001 | t0008 | g0035 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18977 | hp2 | a0001 | c0003 | t0067 | g0018 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0315 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18978 | hp2 | a0001 | c0003 | t0010 | g0021 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18979 | hp1 | a0002 | c0002 | t0003 | g0272 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18980 | hp1 | a0001 | c0001 | t0008 | g0083 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18980 | hp2 | a0002 | c0002 | t0003 | g0339 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18981 | hp1 | a0002 | c0002 | t0003 | g0314 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18981 | hp2 | a0001 | c0001 | t0017 | g0173 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18982 | hp2 | a0001 | c0003 | t0040 | g0014 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18984 | hp2 | a0001 | c0001 | t0005 | g0166 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18985 | hp1 | a0001 | c0001 | t0005 | g0155 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18985 | hp2 | a0002 | c0002 | t0037 | g0317 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18986 | hp1 | a0001 | c0001 | t0044 | g0001 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18986 | hp2 | a0002 | c0002 | t0039 | g0271 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18987 | hp1 | a0001 | c0003 | t0010 | g0024 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18987 | hp2 | a0002 | c0002 | t0003 | g0245 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18988 | hp1 | a0002 | c0002 | t0003 | g0244 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18988 | hp2 | a0005 | c0006 | t0002 | g0060 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18990 | hp1 | a0001 | c0001 | t0043 | g0162 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18990 | hp2 | a0001 | c0001 | t0006 | g0075 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18991 | hp1 | a0001 | c0001 | t0018 | g0168 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18991 | hp2 | a0001 | c0003 | t0069 | g0012 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18992 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18992 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18993 | hp2 | a0001 | c0001 | t0011 | g0214 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18994 | hp1 | a0006 | c0007 | t0005 | g0170 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18994 | hp2 | a0001 | c0001 | t0006 | g0056 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18999 | hp1 | a0002 | c0002 | t0003 | g0215 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18999 | hp2 | a0001 | c0001 | t0011 | g0250 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19000 | hp2 | a0001 | c0001 | t0047 | g0044 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19002 | hp1 | a0001 | c0003 | t0010 | g0020 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19002 | hp2 | a0001 | c0001 | t0018 | g0159 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0178 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19005 | hp1 | a0005 | c0006 | t0002 | g0061 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19005 | hp2 | a0002 | c0002 | t0037 | g0277 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19006 | hp1 | a0001 | c0003 | t0010 | g0023 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19006 | hp2 | a0001 | c0001 | t0006 | g0106 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19007 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19009 | hp2 | a0002 | c0002 | t0003 | g0312 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19010 | hp1 | a0001 | c0001 | t0058 | g0097 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19010 | hp2 | a0001 | c0001 | t0005 | g0156 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | LWK | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19030 | hp2 | a0001 | c0001 | t0076 | g0232 | AFR | LWK | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | LWK | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19043 | hp2 | a0001 | c0001 | t0049 | g0026 | AFR | LWK | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19056 | hp1 | a0001 | c0001 | t0041 | g0034 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19057 | hp1 | a0001 | c0001 | t0019 | g0164 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19057 | hp2 | a0001 | c0001 | t0008 | g0108 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19058 | hp2 | a0001 | c0003 | t0070 | g0015 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19060 | hp1 | a0001 | c0003 | t0010 | g0016 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19060 | hp2 | a0002 | c0002 | t0003 | g0246 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19064 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19064 | hp2 | a0001 | c0001 | t0075 | g0208 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19066 | hp1 | a0001 | c0001 | t0032 | g0037 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19067 | hp1 | a0001 | c0001 | t0013 | g0296 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19068 | hp1 | a0002 | c0002 | t0003 | g0275 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19068 | hp2 | a0001 | c0001 | t0059 | g0098 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19074 | hp1 | a0001 | c0001 | t0018 | g0167 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19076 | hp1 | a0001 | c0001 | t0008 | g0082 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0316 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19077 | hp1 | a0001 | c0001 | t0011 | g0223 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19077 | hp2 | a0001 | c0001 | t0019 | g0163 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19080 | hp1 | a0002 | c0002 | t0003 | g0258 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19081 | hp1 | a0001 | c0013 | t0002 | g0102 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19081 | hp2 | a0001 | c0001 | t0011 | g0201 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19083 | hp1 | a0010 | c0010 | t0010 | g0010 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19083 | hp2 | a0001 | c0001 | t0086 | g0065 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19087 | hp1 | a0001 | c0001 | t0019 | g0169 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19087 | hp2 | a0002 | c0002 | t0003 | g0247 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0171 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19088 | hp2 | a0001 | c0001 | t0054 | g0090 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19090 | hp1 | a0002 | c0002 | t0003 | g0278 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19090 | hp2 | a0001 | c0001 | t0005 | g0154 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19240 | hp1 | a0001 | c0001 | t0039 | g0227 | AFR | YRI | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA19240 | hp2 | a0001 | c0003 | t0007 | g0002 | AFR | YRI | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA20129 | hp1 | a0001 | c0001 | t0015 | g0027 | AFR | ASW | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA20129 | hp2 | a0001 | c0001 | t0014 | g0330 | AFR | ASW | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA20752 | hp1 | a0003 | c0004 | t0084 | g0144 | EUR | TSI | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0328 | EUR | TSI | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0284 | SAS | GIH | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA20905 | hp2 | a0004 | c0005 | t0004 | g0288 | SAS | GIH | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01123 | hp1 | a0003 | c0004 | t0062 | g0148 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG01123 | hp2 | a0001 | c0001 | t0051 | g0062 | AMR | CLM | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02559 | hp1 | a0001 | c0001 | t0020 | g0182 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG02559 | hp2 | a0001 | c0001 | t0014 | g0332 | AFR | ACB | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03471 | hp1 | a0001 | c0001 | t0015 | g0324 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG03471 | hp2 | a0001 | c0001 | t0024 | g0084 | AFR | MSL | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | USA | LNPEP_chr5_96931080_97042513 | LNPEP |
| HG06807 | hp2 | a0007 | c0009 | t0042 | g0251 | AFR | USA | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0336 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA18955 | hp2 | a0001 | c0003 | t0040 | g0013 | EAS | JPT | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA20300 | hp1 | a0001 | c0003 | t0022 | g0031 | AFR | USA | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA20300 | hp2 | a0002 | c0002 | t0003 | g0212 | AFR | USA | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0116 | AFR | LWK | LNPEP_chr5_96931080_97042513 | LNPEP |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0048 | AFR | LWK | LNPEP_chr5_96931080_97042513 | LNPEP |
| homoSapiens_chm13v2 | hp1 | a0004 | c0005 | t0004 | g0321 | REF | REF | LNPEP_chr5_96931080_97042513 | LNPEP |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0198 | REF | REF | LNPEP_chr5_96931080_97042513 | LNPEP |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:96979374
|
T | C | 1 | a0006 | 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 | a0007 | 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 | a0004a0009 | 13 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(10): 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 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | 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 | a0001c0003a0008c0011a0010c0010 | 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 | a0001c0012a0001c0015 | 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 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:96936100
|
C | T | 1 | a0007c0009t0042 | 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 | 2 | a0001c0001t0041a0001c0001t0086 | 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 | a0003c0004t0084a0003c0004t0085 | 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 | 55 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(52): Show | 203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): 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 | a0001c0003t0040 | 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 | 6 | a0003c0004t0012a0003c0004t0062a0003c0004t0063others(3): 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 | a0001c0001t0016a0001c0012t0028a0001c0015t0028 | 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 | 7 | a0001c0001t0005a0001c0001t0017a0001c0001t0018others(4): 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 | a0001c0001t0043 | 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 | a0001c0001t0043 | 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 | a0001c0001t0043 | 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 | a0001c0001t0043 | 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 | a0001c0001t0043 | 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 | 6 | a0003c0004t0012a0003c0004t0062a0003c0004t0063others(3): 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 | a0001c0001t0043 | 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 | a0001c0001t0043 | 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 | a0001c0001t0043 | 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 | a0001c0001t0043 | 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 | a0001c0012t0028a0001c0015t0028 | 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 | 6 | a0001c0001t0005a0001c0001t0017a0001c0001t0018others(3): 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 | a0001c0001t0043 | 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 | a0001c0003t0065 | 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 | 2 | a0001c0001t0045a0001c0001t0046 | 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 | a0001c0001t0016a0001c0012t0028a0001c0015t0028 | 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 | a0001c0001t0023 | 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 | a0001c0001t0006a0001c0001t0057a0001c0001t0058 | 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 | a0001c0001t0034a0001c0001t0043a0001c0001t0059 | 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 | a0001c0001t0035a0001c0001t0060a0001c0001t0061 | 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 | a0001c0001t0024 | 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 | 10 | a0001c0001t0008a0001c0001t0038a0001c0001t0047others(7): 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 | 10 | a0001c0001t0009a0001c0001t0013a0001c0001t0045others(7): 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 | 20 | a0001c0001t0001a0001c0001t0004a0001c0001t0014others(17): Show | 119 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(116): 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 | a0001c0001t0011a0001c0001t0072a0001c0003t0010others(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 | a0001c0001t0020 | 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 | a0001c0003t0007a0001c0003t0065a0001c0003t0068others(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 | a0001c0001t0005a0001c0001t0017a0001c0001t0018others(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 | a0001c0001t0030a0001c0001t0044 | 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 | a0001c0001t0066 | 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 | a0001c0001t0027a0001c0001t0039a0001c0001t0048others(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 | a0001c0001t0038a0001c0001t0047a0001c0001t0079others(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 | a0001c0001t0009a0001c0001t0013a0001c0001t0076others(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 | 17 | a0001c0001t0001a0001c0001t0004a0001c0001t0014others(14): Show | 115 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(112): 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 | 12 | a0001c0001t0011a0001c0001t0036a0001c0001t0072others(9): 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 | a0001c0003t0007a0001c0003t0065a0001c0003t0068 | 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 | a0001c0003t0067 | 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 | a0001c0001t0066 | 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 | a0003c0004t0062 | 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 | a0001c0003t0026 | 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 | a0003c0004t0062 | 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 | 14 | a0001c0001t0004a0001c0001t0013a0001c0001t0025others(11): Show | 40 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(37): 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 | a0001c0001t0057 | 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 | a0001c0001t0020a0001c0001t0049 | 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 | 6 | a0003c0004t0012a0003c0004t0062a0003c0004t0063others(3): 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 | 6 | a0003c0004t0012a0003c0004t0062a0003c0004t0063others(3): 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 | a0001c0003t0007a0001c0003t0065a0001c0003t0068 | 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 | 60 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(57): Show | 212 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(209): 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 | 8 | a0001c0003t0010a0001c0003t0040a0001c0003t0067others(5): 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 | 5 | a0003c0004t0012a0003c0004t0062a0003c0004t0064others(2): 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 | a0001c0001t0021 | 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 | a0001c0001t0080 | 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 | a0001c0001t0020a0001c0001t0049 | 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 | 2 | a0001c0001t0058a0001c0001t0059 | 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 | 6 | a0003c0004t0012a0003c0004t0062a0003c0004t0063others(3): 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 | 6 | a0003c0004t0012a0003c0004t0062a0003c0004t0063others(3): 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 | 14 | a0001c0003t0007a0001c0003t0010a0001c0003t0022others(11): 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 | a0001c0001t0061 | 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 | 6 | a0003c0004t0012a0003c0004t0062a0003c0004t0063others(3): 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 | a0001c0001t0016a0001c0012t0028a0001c0015t0028 | 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 | a0001c0001t0023 | 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 | 2 | a0002c0002t0003a0002c0002t0037 | 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 | a0001c0001t0076 | 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 | a0007c0009t0042 | 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 | a0001c0003t0070 | 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 | a0001c0001t0025 | 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 | a0001c0001t0016a0001c0012t0028a0001c0015t0028 | 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 | a0001c0001t0056 | 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 | a0001c0001t0019 | 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 | 12 | a0001c0001t0005a0001c0001t0016a0001c0001t0017others(9): 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 | 14 | a0001c0001t0075a0001c0003t0007a0001c0003t0010others(11): 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 | a0001c0001t0032a0001c0001t0056 | 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 | a0001c0001t0033 | 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 | 6 | a0003c0004t0012a0003c0004t0062a0003c0004t0063others(3): 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 | a0001c0001t0060 | 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 | a0001c0001t0052 | 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 | a0001c0001t0066 | 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 | a0001c0001t0078 | 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 | 35 | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(32): Show | 155 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(152): 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 | a0001c0001t0016a0001c0012t0028a0001c0015t0028 | 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 | a0001c0001t0049 | 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 | 9 | a0001c0001t0005a0001c0001t0017a0001c0001t0018others(6): 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 | 6 | a0003c0004t0012a0003c0004t0062a0003c0004t0063others(3): 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 | a0001c0001t0054 | 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 | a0001c0001t0018 | 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 | a0001c0001t0015 | 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 | 9 | a0001c0001t0005a0001c0001t0017a0001c0001t0018others(6): 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 | a0001c0001t0017 | 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 | a0001c0001t0055 | 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 | 8 | a0001c0003t0010a0001c0003t0040a0001c0003t0067others(5): 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 | a0001c0001t0056 | 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 | a0001c0003t0071 | 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 | 6 | a0003c0004t0012a0003c0004t0062a0003c0004t0063others(3): 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 | 47 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(44): Show | 196 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(193): 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 | 9 | a0001c0001t0005a0001c0001t0017a0001c0001t0018others(6): 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 | a0001c0001t0050 | 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 | a0001c0001t0051 | 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 | 4 | a0001c0001t0014a0001c0001t0076a0001c0001t0077others(1): Show | 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 | a0003c0004t0084 | 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 | a0001c0001t0074 | 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 | a0001c0003t0068 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8856G>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 18/18 | 8856 | chr5 | 97037389 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:96936238
|
G | A | 15 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0001c0001t0033g0025 | 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 | a0001c0001t0049g0026 | 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 | a0001c0001t0015g0027a0001c0001t0015g0028 | 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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031 | 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 | 105 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(102): 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 | a0001c0001t0002g0134 | 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 | 7 | a0001c0001t0013g0004a0001c0001t0013g0137a0001c0001t0013g0139others(4): 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0006g0032 | 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0007c0009t0042g0183 | 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 | a0004c0005t0004g0341 | 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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031others(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 | a0001c0001t0002g0133 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | 105 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(102): 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | 140 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(137): 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 | a0001c0001t0066g0340 | 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0004c0008t0029g0003 | 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 | 152 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(149): 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 | a0001c0001t0034g0128a0001c0003t0010g0022a0001c0003t0010g0023others(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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031others(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 | a0001c0001t0002g0127 | 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 | a0003c0004t0085g0140 | 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 | a0002c0002t0001g0195 | 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 | 221 | a0001c0001t0002g0043a0001c0001t0002g0045a0001c0001t0002g0055others(218): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): 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 | 35 | a0001c0001t0002g0116a0001c0001t0002g0118a0001c0001t0002g0120others(32): 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0002c0002t0001g0334a0002c0002t0001g0335 | 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 | 135 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(132): 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 | a0001c0001t0005g0178a0001c0001t0023g0175a0001c0001t0023g0176others(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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031 | 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 | 105 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(102): 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | 105 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(102): 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | 194 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(191): 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 | 26 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(23): 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031others(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 | a0001c0001t0001g0226a0001c0001t0009g0228a0001c0001t0014g0329others(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 | 25 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0154others(22): 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 | a0001c0001t0049g0026 | 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 | a0001c0001t0024g0114 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0006g0032 | 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 | a0001c0001t0015g0027a0001c0001t0015g0028a0001c0001t0015g0241others(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 | a0001c0001t0001g0196a0001c0001t0001g0197 | 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0001c0012t0028g0189a0001c0015t0028g0194 | 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 | a0001c0003t0071g0188 | 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 | 105 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(102): 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 | a0001c0001t0014g0332a0001c0001t0014g0333 | 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | 26 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(23): 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 | a0001c0001t0061g0113 | 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 | a0001c0001t0049g0026 | 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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0002g0043a0001c0001t0002g0045a0001c0001t0008g0046others(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 | 190 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(187): Show | 195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): 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 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0004g0328others(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 | 26 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(23): 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 | a0001c0003t0071g0188 | 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 | a0002c0002t0009g0325a0002c0002t0009g0326a0003c0004t0012g0145others(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 | 31 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(28): 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 | 107 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(104): 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 | 105 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(102): 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0001c0001t0001g0225 | 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 | a0004c0005t0004g0243 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0003t0022g0187 | 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0001c0001t0011g0250a0002c0002t0003g0006a0002c0002t0003g0244others(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 | a0001c0001t0011g0223 | 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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | a0001c0001t0005g0153 | 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 | a0001c0001t0017g0173a0001c0001t0017g0174 | 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 | 138 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(135): 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | 104 | a0001c0001t0001g0211a0001c0001t0001g0217a0001c0001t0001g0218others(101): Show | 105 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(102): 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 | 52 | a0001c0001t0002g0038a0001c0001t0002g0045a0001c0001t0002g0086others(49): 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 | 17 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(14): 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 | a0001c0001t0005g0171a0001c0001t0018g0167a0001c0001t0018g0168others(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 | a0001c0001t0011g0199a0001c0001t0014g0330a0001c0001t0016g0190others(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 | a0001c0001t0014g0329a0001c0001t0079g0238a0001c0003t0007g0236others(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 | a0001c0001t0076g0232a0001c0003t0007g0002a0001c0003t0007g0229others(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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | a0001c0001t0052g0047 | 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 | a0001c0001t0057g0049 | 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 | a0001c0001t0057g0049 | 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 | a0001c0001t0002g0132 | 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 | a0002c0002t0003g0244 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | ||||||
| chr5:96944791
|
T | C | 343 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(340): Show | 351 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.19+8617T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96944791 | ||||||
| chr5:96944792
|
G | A | 1 | a0001c0001t0002g0133 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0001c0001t0014g0329a0001c0001t0014g0330a0001c0001t0077g0331 | 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 | a0001c0001t0076g0232a0001c0001t0079g0238a0001c0003t0007g0002others(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 | 152 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(149): 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0001c0001t0002g0109a0001c0001t0008g0046a0001c0001t0008g0082others(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 | a0001c0001t0001g0211a0001c0001t0008g0115a0001c0001t0016g0190others(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 | a0001c0001t0001g0210a0001c0001t0001g0221a0001c0001t0050g0110others(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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0004c0008t0029g0003 | 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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | 152 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(149): 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0006g0051 | 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 | a0001c0003t0007g0002a0001c0003t0007g0234a0001c0003t0007g0235 | 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 | a0002c0002t0001g0335 | 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 | a0002c0002t0001g0335 | 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 | a0004c0005t0004g0260a0004c0005t0004g0309 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0002c0002t0001g0307 | 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 | a0001c0001t0023g0175a0001c0001t0023g0176a0001c0001t0023g0177 | 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 | 152 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(149): 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 | a0001c0001t0005g0156a0001c0001t0005g0166a0001c0001t0005g0171others(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 | a0001c0001t0076g0232a0001c0001t0079g0238a0001c0003t0007g0002others(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 | a0001c0001t0002g0081 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0017g0157 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0010c0010t0010g0010 | 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 | a0001c0001t0030g0052 | 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 | a0001c0001t0001g0200 | 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 | 152 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(149): 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 | 96 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(93): 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 | a0001c0001t0030g0052 | 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 | 34 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(31): 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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031others(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 | a0001c0001t0045g0054a0001c0001t0046g0085 | 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 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0018g0158others(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 | a0001c0001t0076g0232a0001c0001t0079g0238a0001c0003t0007g0002others(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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031 | 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 | 105 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(102): 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 | a0001c0001t0034g0128 | 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 | a0001c0001t0076g0232a0001c0001t0079g0238a0001c0003t0007g0002others(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 | a0001c0001t0004g0328 | 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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031 | 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 | 105 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(102): 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 | a0001c0001t0005g0165 | 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 | a0001c0001t0008g0115 | 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 | a0001c0001t0076g0232a0001c0001t0079g0238a0001c0003t0007g0002others(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 | a0002c0002t0001g0304a0002c0002t0001g0305a0002c0002t0001g0306others(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 | a0001c0001t0017g0173a0001c0001t0017g0174 | 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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031others(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 | a0001c0001t0002g0033a0001c0001t0002g0043a0001c0001t0002g0076others(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 | a0001c0001t0035g0107a0001c0012t0028g0189a0001c0015t0028g0194others(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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | 194 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(191): 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 | a0001c0003t0007g0229a0001c0003t0007g0230a0001c0003t0007g0231others(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 | a0002c0002t0001g0009 | 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 | 26 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(23): 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | 8 | a0001c0001t0013g0004a0001c0001t0013g0137a0001c0001t0013g0139others(5): 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 | a0001c0001t0006g0111 | 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 | 152 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(149): 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 | a0001c0001t0076g0232a0001c0001t0079g0238a0001c0003t0007g0002others(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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | 192 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(189): 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 | a0001c0001t0001g0210 | 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 | a0002c0002t0001g0301a0002c0002t0001g0302a0002c0002t0001g0303others(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 | 105 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(102): 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0049g0026 | 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 | a0001c0001t0002g0103 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | 173 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(170): 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0002c0002t0001g0299a0002c0002t0001g0300 | 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0001c0001t0011g0250 | 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 | a0001c0001t0002g0043 | 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 | a0001c0013t0002g0102 | 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 | 192 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(189): 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 | 69 | a0001c0001t0011g0250a0002c0002t0001g0007a0002c0002t0001g0009others(66): 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | 9 | a0001c0001t0011g0199a0001c0001t0011g0201a0001c0001t0011g0202others(6): 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 | a0001c0001t0004g0298a0001c0001t0036g0337a0001c0001t0036g0338 | 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 | a0002c0002t0001g0307 | 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 | a0001c0001t0013g0261 | 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 | a0001c0001t0009g0228 | 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0001c0001t0002g0055a0001c0001t0030g0104a0001c0001t0034g0128 | 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 | a0001c0001t0008g0112a0001c0001t0024g0053a0001c0001t0024g0084others(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 | 60 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(57): 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 | a0001c0003t0007g0239a0002c0002t0001g0304a0003c0004t0012g0151others(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 | a0003c0004t0012g0149a0003c0004t0085g0140 | 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 | a0003c0004t0012g0142a0003c0004t0012g0150 | 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 | 146 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0206others(143): Show | 152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.19+18446A>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96954620 | ||||||
| chr5:96954622
|
A | C | 13 | a0001c0001t0006g0048a0001c0001t0011g0223a0001c0001t0014g0297others(10): Show | 13 | HG01243.hp1 HG01257.hp2 HG01433.hp2 others(10): 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 | 24 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(21): 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 | a0001c0001t0001g0226a0001c0001t0009g0228a0003c0004t0012g0142others(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 | a0003c0004t0012g0143a0003c0004t0012g0145a0003c0004t0012g0147others(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 | 40 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0073others(37): 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 | a0001c0001t0023g0175a0001c0001t0023g0177 | 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 | a0001c0001t0005g0166a0001c0001t0005g0178 | 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 | 67 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(64): 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 | a0001c0001t0014g0333 | 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0004c0008t0029g0003 | 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 | a0002c0002t0009g0283a0002c0002t0009g0319a0002c0002t0009g0326 | 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 | a0004c0008t0029g0003 | 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 | a0001c0001t0023g0176 | 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 | a0001c0001t0023g0176 | 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 | 108 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(105): 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 | a0004c0008t0029g0003 | 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 | 24 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(21): 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 | a0001c0001t0002g0103 | 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 | a0001c0001t0002g0103 | 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 | a0001c0001t0002g0103 | 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 | a0001c0001t0049g0026 | 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 | a0001c0001t0002g0081a0001c0001t0002g0103a0001c0001t0006g0048 | 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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031 | 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 | 111 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(108): 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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | a0001c0001t0002g0103 | 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 | a0001c0001t0002g0081a0001c0001t0006g0048 | 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 | a0001c0001t0002g0103a0001c0001t0033g0068a0001c0001t0056g0067 | 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 | a0001c0001t0033g0068 | 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 | a0001c0001t0002g0081a0001c0001t0002g0095a0001c0001t0006g0048others(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 | 114 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(111): 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 | 109 | a0001c0001t0004g0205a0001c0001t0004g0291a0001c0001t0004g0298others(106): Show | 112 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(109): 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 | a0001c0001t0033g0068 | 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 | a0001c0001t0002g0095a0001c0001t0033g0068 | 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 | a0001c0001t0002g0095 | 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 | a0001c0001t0033g0068 | 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 | a0002c0002t0001g0195 | 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 | a0001c0001t0013g0320 | 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 | a0001c0001t0002g0095a0001c0001t0013g0320a0001c0001t0033g0068 | 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 | a0001c0003t0073g0011 | 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 | a0001c0001t0023g0175a0001c0001t0023g0176a0001c0001t0023g0177others(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 | a0001c0001t0002g0095a0001c0001t0023g0175a0001c0001t0023g0176others(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 | a0001c0001t0016g0191a0001c0001t0016g0192a0001c0001t0016g0193 | 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 | a0001c0001t0002g0095a0001c0001t0002g0103a0001c0001t0023g0175others(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 | a0001c0001t0002g0095a0001c0001t0002g0103a0001c0001t0023g0175others(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 | a0001c0003t0010g0024a0001c0003t0069g0012a0001c0012t0028g0189others(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 | a0001c0001t0002g0095a0001c0001t0002g0103a0001c0001t0033g0068 | 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 | a0001c0001t0005g0165a0001c0001t0017g0173a0001c0001t0019g0160 | 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 | 29 | a0001c0001t0002g0069a0001c0001t0002g0081a0001c0001t0002g0086others(26): 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 | a0001c0001t0049g0026 | 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 |
89 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(86): 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 | a0001c0001t0023g0175a0001c0001t0023g0176a0001c0001t0023g0177others(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 | a0001c0001t0034g0128 | 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 | a0001c0001t0024g0114 | 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 | a0001c0001t0002g0095a0001c0001t0016g0190a0001c0001t0023g0175others(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 | a0001c0001t0039g0227a0001c0003t0010g0019a0001c0003t0010g0021others(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 | a0001c0003t0007g0230a0001c0003t0007g0231a0001c0003t0007g0236others(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 | a0001c0001t0013g0287a0001c0003t0007g0239a0003c0004t0012g0142others(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 | a0001c0012t0028g0189a0001c0015t0028g0194 | 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 | a0001c0001t0005g0165a0001c0001t0017g0173a0001c0001t0019g0160others(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 | a0001c0001t0039g0227a0001c0001t0050g0110 | 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 | a0001c0001t0016g0191a0001c0001t0016g0192a0001c0001t0016g0193 | 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 | a0001c0001t0050g0110 | 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 | a0003c0004t0012g0143a0003c0004t0012g0145a0003c0004t0012g0147others(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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | a0002c0002t0003g0282 | 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 | a0003c0004t0012g0142a0003c0004t0012g0149a0003c0004t0012g0150others(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 | a0003c0004t0012g0151 | 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 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0122others(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 | a0001c0003t0026g0185a0001c0003t0026g0186a0001c0003t0071g0188others(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 | a0001c0001t0023g0175a0001c0001t0023g0176a0001c0001t0023g0177others(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 | a0001c0001t0002g0033a0001c0001t0002g0120a0001c0001t0002g0126others(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 | a0001c0001t0002g0132a0001c0001t0008g0063a0001c0001t0048g0041others(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 | a0001c0001t0002g0043a0001c0001t0002g0066a0001c0001t0002g0099others(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 | a0001c0001t0008g0112 | 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 | a0001c0001t0031g0036 | 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 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0116others(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 | a0001c0001t0004g0298a0001c0001t0011g0250a0001c0001t0013g0137others(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 | 29 | a0001c0001t0013g0004a0001c0001t0013g0139a0001c0001t0013g0261others(26): Show | 30 | HG00738.hp1 HG01069.hp1 HG01070.hp1 others(27): 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 | a0001c0001t0004g0205a0001c0001t0014g0297a0001c0003t0007g0002others(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 | 8 | a0001c0001t0005g0001a0001c0001t0005g0153a0001c0001t0019g0163others(5): 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 | a0001c0001t0002g0087a0001c0001t0006g0056 | 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 | a0001c0001t0002g0070 | 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 | a0001c0001t0008g0057 | 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 | a0001c0001t0002g0088 | 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 | a0001c0001t0002g0058a0001c0001t0002g0123a0001c0001t0021g0089others(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 | a0001c0001t0002g0045a0001c0001t0008g0082 | 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 | a0001c0001t0002g0038a0001c0001t0002g0055a0001c0001t0047g0044 | 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 | a0001c0001t0008g0035a0001c0001t0054g0090 | 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 | a0001c0001t0002g0076a0001c0001t0002g0129a0001c0001t0006g0071others(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 | a0001c0001t0002g0073a0001c0001t0002g0103a0001c0001t0002g0118others(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 | a0001c0001t0006g0040a0001c0001t0008g0046a0001c0001t0008g0083others(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 | a0001c0001t0002g0109 | 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 | 61 | a0001c0001t0002g0033a0001c0001t0002g0043a0001c0001t0002g0066others(58): 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 | 26 | a0001c0001t0005g0005a0001c0001t0005g0166a0001c0001t0005g0178others(23): 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 | a0001c0001t0004g0328a0001c0001t0014g0329a0001c0001t0014g0332others(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 | a0001c0001t0014g0330a0001c0001t0015g0027a0002c0002t0001g0255others(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 | 11 | a0001c0001t0001g0197a0001c0001t0006g0048a0001c0001t0011g0201others(8): 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 | a0001c0001t0001g0196a0001c0001t0001g0206a0001c0001t0001g0217others(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 | 9 | a0002c0002t0001g0007a0002c0002t0001g0009a0002c0002t0001g0259others(6): 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 | a0001c0001t0014g0332a0001c0001t0014g0333a0001c0001t0038g0222others(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 | a0002c0002t0001g0266a0002c0002t0001g0284a0002c0002t0009g0326others(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 | a0001c0001t0050g0110 | 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 | a0001c0003t0022g0029a0002c0002t0009g0326 | 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 | a0001c0001t0050g0110 | 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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031 | 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 | a0001c0003t0022g0029a0001c0003t0022g0030 | 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 | a0001c0003t0026g0184a0001c0003t0026g0185a0001c0003t0026g0186 | 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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | 140 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(137): 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 | a0001c0001t0023g0175a0001c0001t0023g0176a0001c0001t0023g0177 | 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 | a0002c0002t0003g0212 | 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 | a0001c0001t0056g0067 | 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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0001c0001t0024g0084 | 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 | a0001c0001t0002g0070 | 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 | 173 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(170): 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 | 39 | a0001c0001t0004g0205a0001c0001t0004g0291a0001c0001t0004g0298others(36): Show | 40 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(37): 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 | a0001c0001t0011g0250a0002c0002t0003g0244a0002c0002t0003g0248others(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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0076g0232a0001c0001t0079g0238 | 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 | a0001c0001t0050g0110 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0049g0026 | 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 | a0002c0002t0009g0253 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0003t0022g0187 | 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | 39 | a0001c0001t0004g0205a0001c0001t0004g0291a0001c0001t0004g0298others(36): Show | 40 | HG00280.hp1 HG00323.hp2 HG01069.hp1 others(37): 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 | a0001c0001t0001g0210 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0002c0002t0009g0253a0002c0002t0038g0254a0002c0002t0083g0252 | 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0001c0001t0006g0051 | 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 | a0002c0002t0001g0316 | 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0001c0001t0023g0175a0001c0001t0023g0176a0001c0001t0023g0177 | 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 | a0001c0001t0006g0048 | 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | 26 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(23): 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 | a0001c0001t0013g0296 | 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0001c0003t0071g0188 | 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0002c0002t0003g0276 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | 58 | a0001c0001t0002g0043a0001c0001t0002g0058a0001c0001t0002g0122others(55): 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 | a0001c0001t0002g0116a0001c0001t0008g0082a0001c0001t0016g0190others(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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031others(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 | a0001c0001t0078g0220 | 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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031 | 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 | a0001c0003t0010g0016 | 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 | a0001c0001t0002g0076 | 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0004g0298 | 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 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0002g0095others(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 | a0001c0001t0001g0211a0001c0001t0002g0118a0001c0001t0002g0125others(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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0001c0001t0021g0059 | 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 | a0001c0001t0001g0221 | 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 | a0003c0004t0085g0140 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.20-18902C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96960236 | ||||||
| chr5:96960819
|
G | GTAGA | 343 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(340): Show | 351 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.20-18316_20-18315i others(6): Show |
LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 96960819 | |||||
| chr5:96960880
|
GT | G | 150 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(147): 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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031 | 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 | a0001c0001t0002g0086 | 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 | a0002c0002t0009g0283a0002c0002t0009g0319a0002c0002t0009g0326 | 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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | a0001c0001t0066g0340 | 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 | a0001c0001t0020g0182 | 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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0030g0104 | 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 | a0001c0001t0031g0119 | 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 | a0003c0004t0064g0146 | 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 | 105 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(102): 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 | a0001c0001t0034g0128 | 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 | a0001c0001t0023g0175a0001c0001t0023g0176a0001c0001t0023g0177 | 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 | a0001c0003t0022g0187 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | 101 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(98): 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 | a0001c0003t0071g0188 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0002g0081 | 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 | a0001c0003t0010g0016 | 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0001c0001t0001g0218a0003c0004t0012g0142a0003c0004t0012g0143others(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 | a0002c0002t0001g0299a0002c0002t0001g0300a0002c0002t0009g0283others(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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0002g0130a0001c0001t0011g0201a0001c0001t0016g0190others(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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0066g0340 | 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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0001c0001t0048g0041 | 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 | a0001c0003t0010g0019a0001c0003t0010g0020a0001c0003t0010g0021 | 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 | 192 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(189): 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0014g0332 | 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 | a0001c0001t0002g0133 | 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 | a0001c0001t0023g0175a0001c0001t0023g0176a0001c0001t0023g0177 | 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 | a0001c0001t0002g0043a0001c0001t0002g0058a0001c0001t0002g0073others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0002c0002t0009g0283a0002c0002t0009g0319a0002c0002t0009g0326 | 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 | a0001c0001t0006g0111 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0014g0329a0001c0001t0014g0330a0001c0001t0076g0232others(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 | a0001c0003t0022g0187a0001c0003t0065g0233a0001c0003t0068g0240 | 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 | a0001c0001t0008g0064a0001c0001t0027g0135a0003c0004t0012g0142 | 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 | a0002c0002t0003g0215 | 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 | 21 | a0001c0001t0001g0197a0001c0001t0001g0204a0001c0001t0001g0209others(18): 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 | 21 | a0001c0001t0001g0196a0001c0001t0001g0206a0001c0001t0001g0211others(18): 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0231others(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 | 176 | a0001c0001t0001g0226a0001c0001t0002g0033a0001c0001t0002g0043others(173): Show | 180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): 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 | a0001c0001t0002g0066a0001c0001t0005g0155a0001c0001t0014g0333others(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 | 41 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(38): 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 | a0001c0001t0049g0026 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0012t0028g0189a0001c0015t0028g0194 | 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 | a0001c0003t0071g0188 | 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 | a0001c0001t0023g0175 | 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 | a0001c0003t0071g0188 | 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 | a0001c0001t0002g0043 | 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 | a0001c0001t0033g0025a0001c0001t0033g0068 | 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0004c0005t0004g0288a0004c0005t0004g0341 | 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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | 304 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0204others(301): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.20-11823T>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 1/17 | chr5 | 96967315 | ||||||
| chr5:96967444
|
G | C | 192 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(189): 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 | a0001c0001t0006g0048 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0006g0048 | 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 | a0001c0001t0002g0118 | 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 | 192 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(189): 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 | a0003c0004t0012g0149 | 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 | a0001c0001t0001g0226a0001c0001t0009g0228 | 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 | a0002c0002t0009g0319 | 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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031 | 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 | a0001c0001t0033g0068 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0079g0238 | 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 | a0001c0001t0002g0087 | 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 | 5 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0122others(2): 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 | 46 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(43): 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0002g0130 | 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 | a0001c0001t0002g0130 | 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 | a0001c0001t0020g0181 | 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 | a0001c0001t0015g0027a0001c0001t0015g0028 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0024g0053a0001c0001t0024g0084a0001c0001t0024g0114 | 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0003t0026g0184a0001c0003t0026g0185a0001c0003t0026g0186 | 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 | a0001c0001t0036g0337a0001c0001t0036g0338 | 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 | a0001c0003t0065g0233 | 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 | a0001c0003t0022g0029 | 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 | 105 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(102): 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 | a0007c0009t0042g0183 | 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 | a0001c0001t0043g0162 | 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 | a0001c0003t0026g0186 | 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 | a0002c0002t0001g0274 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0002c0002t0038g0254 | 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 | 109 | a0001c0001t0001g0211a0001c0001t0002g0033a0001c0001t0002g0038others(106): 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 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0088others(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 | a0001c0001t0001g0226a0001c0001t0002g0055a0001c0001t0005g0154others(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 |
2 | a0001c0001t0005g0001a0001c0001t0044g0001 | 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 | a0001c0015t0028g0194 | 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 | a0001c0012t0028g0189 | 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 | a0001c0001t0020g0180a0001c0001t0020g0181a0001c0001t0020g0182others(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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | 173 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(170): 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0017g0157a0001c0001t0017g0173a0001c0001t0017g0174others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | 192 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(189): 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 | 173 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(170): 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 | a0001c0003t0071g0188 | 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 | 26 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(23): 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 | a0001c0001t0055g0050 | 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 | a0002c0002t0009g0268 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0019g0160 | 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 | 26 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(23): 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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031 | 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 | a0001c0001t0023g0177 | 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 | a0001c0001t0023g0175a0001c0001t0023g0176a0001c0001t0023g0177 | 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0002c0002t0003g0314 | 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 | 26 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(23): 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 | a0001c0001t0013g0320 | 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 | a0001c0001t0066g0340 | 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 | a0002c0002t0001g0304 | 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 | a0001c0001t0002g0095 | 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 | 26 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(23): 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 | a0001c0001t0036g0337a0001c0001t0036g0338 | 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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031others(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 | a0003c0004t0004g0256a0003c0004t0004g0257a0003c0004t0004g0294others(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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031 | 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0002c0002t0003g0246 | 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 | a0001c0001t0013g0320 | 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 | a0001c0001t0030g0052 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0001c0001t0020g0182 | 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 | a0004c0005t0004g0308a0004c0005t0027g0293 | 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 | 337 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0204others(334): Show | 345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): 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 | 188 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(185): 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 | 4 | a0001c0001t0006g0072a0001c0001t0006g0096a0001c0001t0058g0097others(1): Show | 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 | a0001c0001t0005g0005 | 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 | a0001c0001t0015g0027a0001c0001t0015g0028a0001c0001t0015g0241others(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 | 34 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(31): 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 | a0002c0002t0038g0254 | 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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0045g0054a0001c0001t0046g0085 | 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 | a0001c0001t0006g0071 | 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 | a0001c0001t0019g0169 | 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 | a0001c0001t0072g0289 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | 104 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(101): 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 | a0001c0001t0053g0093 | 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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | 192 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(189): 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0008c0011t0010g0017 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0049g0026 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0002g0095 | 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 | a0001c0001t0019g0164a0001c0001t0019g0169 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0012t0028g0189 | 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0001c0001t0002g0086 | 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 | a0002c0002t0001g0299 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0002g0129 | 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 | a0001c0001t0056g0067 | 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 | a0001c0001t0002g0033 | 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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0001c0003t0071g0188 | 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 | a0001c0001t0002g0123 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0003t0010g0022 | 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0001c0001t0035g0080 | 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0003t0026g0184a0001c0003t0026g0185a0001c0003t0026g0186 | 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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | 173 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(170): 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0001c0001t0023g0175a0001c0001t0023g0176a0001c0001t0023g0177 | 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 | a0001c0001t0006g0111 | 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 | 192 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(189): 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 | a0001c0003t0071g0188 | 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 | a0001c0003t0071g0188 | 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 | a0001c0001t0032g0091 | 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 | a0001c0001t0045g0054a0001c0001t0046g0085 | 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | 26 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(23): 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031others(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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0016t0002g0101 | 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | a0002c0002t0009g0268a0002c0002t0009g0270a0002c0002t0009g0318others(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 | a0001c0001t0002g0099a0001c0001t0005g0165a0001c0001t0013g0320others(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 | a0001c0003t0022g0187a0001c0003t0068g0240a0003c0004t0012g0142others(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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0005g0156 | 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 | a0001c0001t0015g0028 | 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0001c0001t0038g0222 | 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 | 105 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(102): 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 | 34 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(31): 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 | a0001c0001t0014g0297a0001c0001t0014g0322 | 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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031others(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 | 139 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(136): 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 | 34 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(31): 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0002c0002t0009g0283a0002c0002t0009g0319a0002c0002t0009g0326 | 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 | a0001c0001t0016g0193 | 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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031others(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 | 173 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(170): 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 | a0001c0001t0006g0040 | 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 | 192 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(189): 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 | a0001c0001t0002g0103 | 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 | a0001c0001t0001g0226a0001c0001t0009g0228a0001c0001t0014g0297others(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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0002g0038 | 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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031 | 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 | a0002c0002t0001g0273 | 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 | a0001c0001t0015g0027a0001c0001t0015g0028a0001c0001t0015g0241others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0002g0078a0001c0001t0006g0106a0001c0003t0007g0002others(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 | 110 | a0001c0001t0002g0033a0001c0001t0002g0038a0001c0001t0002g0043others(107): 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 | 26 | a0001c0001t0005g0001a0001c0001t0005g0153a0001c0001t0005g0154others(23): 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 | a0001c0003t0022g0187 | 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 | a0001c0001t0014g0297a0001c0001t0014g0322 | 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 | 151 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(148): Show | 154 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(151): 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0003t0065g0233 | 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 | a0001c0001t0023g0175a0001c0001t0023g0176a0001c0001t0023g0177 | 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 | a0001c0003t0069g0012 | 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 | a0001c0001t0066g0340 | 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 | a0001c0001t0002g0095 | 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 | a0003c0004t0012g0145a0003c0004t0012g0151a0003c0004t0064g0146 | 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 | a0001c0012t0028g0189 | 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 | 203 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(200): Show | 208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): 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 | 27 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(24): 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 | a0009c0014t0004g0327 | 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 | a0001c0001t0008g0035 | 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 | 2 | a0001c0001t0005g0001a0001c0001t0044g0001 | 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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | 203 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(200): Show | 208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): 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 | a0009c0014t0004g0327 | 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 | a0001c0001t0001g0196a0001c0001t0001g0197 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0002c0002t0082g0269 | 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 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0003t0026g0184a0001c0003t0026g0185a0001c0003t0026g0186 | 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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0001c0001t0074g0207 | 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 | a0001c0001t0002g0045a0001c0001t0002g0070a0001c0001t0002g0087others(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 | a0001c0001t0006g0048 | 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 | a0001c0001t0023g0175a0001c0001t0023g0176a0001c0001t0023g0177 | 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 | a0001c0015t0028g0194 | 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 | a0001c0001t0002g0045 | 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 | a0001c0003t0022g0187 | 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 | 204 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(201): Show | 209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): 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 | a0002c0002t0001g0284 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0012t0028g0189a0001c0015t0028g0194 | 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 | 239 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(236): Show | 246 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(243): 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031others(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 | a0001c0003t0010g0023 | 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 | a0001c0001t0002g0086 | 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 | 7 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0122others(4): 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 | a0001c0001t0008g0035a0001c0001t0031g0036 | 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 | 204 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(201): Show | 209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): 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 | 191 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(188): Show | 196 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1132-1056A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96991959 | ||||||
| chr5:96992035
|
AT | A | 151 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(148): Show | 154 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.1132-979delT | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 4/17 | chr5 | 96992035 | ||||||
| chr5:96992127
|
G | A | 1 | a0001c0001t0024g0114 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0001c0012t0028g0189 | 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 | a0004c0005t0004g0308a0004c0005t0027g0293a0009c0014t0004g0327 | 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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | a0001c0001t0008g0063 | 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 | 170 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(167): Show | 175 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(172): 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 | a0001c0001t0006g0048 | 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 | a0001c0001t0072g0289 | 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 | a0002c0002t0001g0335 | 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 | a0001c0001t0049g0026 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0002g0126 | 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 | a0001c0001t0008g0064a0001c0001t0051g0062 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | 201 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(198): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): 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 | a0001c0001t0011g0216 | 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 | 151 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(148): Show | 154 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(151): 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 | a0001c0001t0032g0091 | 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 | a0001c0001t0002g0066a0001c0001t0002g0109a0001c0001t0008g0046others(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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0001c0001t0039g0227 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | 204 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(201): Show | 209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | 204 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(201): Show | 209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1408-725C>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 6/17 | chr5 | 96995665 | ||||||
| chr5:96995667
|
A | C | 204 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(201): Show | 209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): 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 | a0001c0001t0030g0052 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0002c0002t0001g0304a0002c0002t0001g0306 | 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 | a0001c0001t0002g0088 | 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 | a0001c0001t0015g0027a0001c0001t0015g0028a0001c0001t0015g0241others(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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0033g0025 | 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 | a0002c0002t0001g0255 | 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 | a0001c0003t0022g0187 | 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 | 204 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(201): Show | 209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): 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 | a0001c0012t0028g0189a0001c0015t0028g0194 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0002g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1521+324A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 7/17 | chr5 | 96996827 | ||||||
| chr5:96996915
|
G | A | 1 | a0004c0005t0004g0321 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1521+412G>A | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 7/17 | chr5 | 96996915 | ||||||
| chr5:96997010
|
C | T | 2 | a0001c0001t0004g0291a0001c0001t0072g0289 | 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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0001c0001t0050g0110 | 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 | a0001c0003t0071g0188 | 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 | 151 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(148): Show | 154 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(151): 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | a0001c0001t0002g0079a0001c0001t0035g0080 | 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 | a0001c0001t0002g0129a0001c0001t0002g0130a0001c0001t0002g0131others(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 | a0001c0001t0043g0162 | 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 | a0004c0005t0004g0290 | 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 | a0001c0001t0052g0047 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0003t0007g0234 | 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 | a0001c0001t0039g0227 | 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 | a0004c0008t0029g0003 | 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 | a0001c0001t0006g0048 | 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 | 238 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(235): Show | 245 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(242): 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 | a0001c0003t0007g0229 | 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 | 29 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(26): 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 | a0002c0002t0082g0269 | 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 | 26 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(23): 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 | 151 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(148): Show | 154 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(151): 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0001c0001t0013g0320 | 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 | a0008c0011t0010g0017 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | 239 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(236): Show | 246 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(243): 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | 26 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(23): 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 | 209 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(206): Show | 214 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1654-2328A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97001087 | ||||||
| chr5:97001160
|
G | T | 26 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(23): 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 | a0001c0001t0002g0133 | 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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0001c0001t0013g0296 | 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 | a0001c0001t0001g0217 | 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0001c0001t0014g0297a0001c0001t0014g0322 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | 26 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(23): 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 | a0001c0015t0028g0194 | 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 | a0001c0001t0045g0054a0001c0001t0046g0085 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | 191 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(188): Show | 196 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(193): 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0017g0161 | 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 | 204 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(201): Show | 209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1654-1329T>C | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97002086 | ||||||
| chr5:97002087
|
G | A | 47 | a0002c0002t0001g0255a0002c0002t0001g0262a0002c0002t0001g0264others(44): 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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031 | 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 | a0004c0005t0004g0286 | 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 | a0001c0001t0033g0025 | 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 | a0004c0005t0004g0260 | 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 | a0001c0003t0065g0233 | 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 | a0001c0001t0005g0005 | 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 | 246 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(243): Show | 253 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(250): 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 | a0001c0001t0014g0329a0001c0001t0014g0330a0001c0001t0076g0232others(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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0001c0001t0023g0175a0001c0001t0023g0176a0001c0001t0023g0177 | 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 | a0002c0002t0009g0268a0002c0002t0039g0271 | 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 | a0001c0001t0061g0113 | 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 | 203 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(200): Show | 208 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1654-16delC | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 8/17 | chr5 | 97003398 | ||||||
| chr5:97003569
|
T | G | 191 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(188): Show | 196 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(193): 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 | a0002c0002t0037g0317 | 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 | a0001c0001t0005g0156 | 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 | a0001c0001t0005g0156 | 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 | a0002c0002t0001g0305 | 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 | 239 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(236): Show | 246 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(243): 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0014g0297a0001c0001t0014g0322 | 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0003c0004t0012g0151 | 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 | a0001c0001t0023g0175a0001c0001t0023g0176a0001c0001t0023g0177 | 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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0001c0003t0010g0023 | 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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031others(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 | a0001c0003t0040g0013a0001c0003t0040g0014 | 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 | 151 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(148): Show | 154 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(151): 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 | a0001c0003t0022g0187 | 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 | a0001c0003t0071g0188 | 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | 26 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(23): 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 | a0001c0001t0002g0125a0001c0001t0031g0119 | 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 | a0001c0012t0028g0189a0001c0015t0028g0194 | 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 | 199 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(196): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): 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 | a0001c0001t0001g0219a0001c0001t0005g0165a0001c0003t0007g0239others(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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0001c0003t0040g0013 | 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 | 25 | a0001c0001t0005g0001a0001c0001t0005g0153a0001c0001t0005g0154others(22): 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 | 188 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(185): Show | 193 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(190): 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0001c0001t0006g0071 | 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 | a0003c0004t0084g0144 | 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 | a0001c0001t0006g0040 | 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 | a0001c0003t0022g0187 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0080g0136 | 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 | a0001c0001t0008g0064a0001c0001t0051g0062 | 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 | a0001c0001t0014g0330a0001c0001t0077g0331 | 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 | 204 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(201): Show | 209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): 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 | a0001c0001t0060g0042 | 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 | a0001c0001t0002g0038 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0002c0002t0003g0282 | 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0001g0200 | 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 | 33 | a0001c0001t0002g0038a0001c0001t0002g0043a0001c0001t0002g0045others(30): 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 | a0001c0001t0002g0095a0001c0001t0005g0005a0001c0001t0005g0156others(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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | a0001c0001t0049g0026a0001c0003t0007g0230a0001c0003t0007g0231others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0193others(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 | a0001c0001t0016g0192a0002c0002t0001g0299a0003c0004t0012g0142others(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 | 27 | a0001c0001t0001g0196a0001c0001t0001g0204a0001c0001t0001g0218others(24): 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 | 108 | a0001c0001t0001g0197a0001c0001t0001g0200a0001c0001t0001g0206others(105): Show | 110 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(107): 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 | a0001c0001t0001g0226a0001c0001t0009g0228a0001c0001t0011g0202others(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 | a0002c0002t0001g0336 | 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 | a0003c0004t0012g0152 | 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 | a0001c0003t0071g0188 | 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 | a0001c0001t0005g0178a0001c0001t0030g0052a0001c0001t0046g0085others(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 | a0001c0001t0001g0206a0001c0001t0016g0190a0001c0001t0016g0191others(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 | 137 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(134): Show | 140 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(137): 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 | a0001c0001t0004g0298a0001c0001t0011g0199a0001c0001t0013g0320others(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 | 44 | a0001c0001t0002g0134a0001c0001t0005g0001a0001c0001t0005g0005others(41): 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0004c0005t0004g0308a0004c0005t0027g0293a0009c0014t0004g0327 | 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 | a0004c0005t0004g0288a0004c0005t0004g0341 | 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 | a0002c0002t0038g0254a0002c0002t0083g0252 | 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 | a0001c0001t0002g0088 | 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 | 26 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(23): 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 | 238 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(235): Show | 245 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(242): 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 | 69 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(66): 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | 150 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(147): Show | 153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): 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 | 238 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(235): Show | 245 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(242): 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 | a0001c0001t0021g0089 | 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 | a0002c0002t0001g0262 | 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 | 204 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(201): Show | 209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0003t0068g0240 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0008g0057 | 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 | a0002c0002t0003g0246 | 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 | 247 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(244): Show | 254 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(251): 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 | a0002c0002t0001g0274a0002c0002t0001g0284 | 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 | a0003c0004t0004g0257 | 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 | a0002c0002t0001g0255a0002c0002t0001g0273 | 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 | a0001c0003t0071g0188 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0002c0002t0009g0318 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0023g0175a0001c0001t0023g0176a0001c0001t0023g0177 | 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 | 204 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(201): Show | 209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): 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 | a0001c0001t0086g0065 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0001g0226a0001c0001t0009g0228a0001c0001t0014g0297others(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 | 150 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(147): Show | 153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): 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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | 26 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(23): 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 | 26 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(23): 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 | 26 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(23): 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 | a0001c0001t0005g0005 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0039g0227 | 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 | 193 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(190): 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 | a0001c0001t0021g0089 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0003t0026g0184a0001c0003t0026g0185a0001c0003t0026g0186 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031others(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 | 238 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(235): Show | 245 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(242): 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 | a0001c0015t0028g0194 | 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 | a0001c0001t0004g0205 | 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 | a0001c0001t0015g0241 | 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 | 185 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(182): Show | 190 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(187): 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 | a0001c0001t0004g0298 | 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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | a0002c0002t0009g0283a0002c0002t0009g0319a0002c0002t0009g0326 | 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0001c0001t0023g0175a0001c0001t0023g0176a0001c0001t0023g0177 | 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 | a0001c0003t0068g0240 | 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 | 26 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(23): 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 | a0001c0001t0002g0081a0001c0001t0024g0053a0001c0001t0024g0084others(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 | a0001c0001t0001g0226a0001c0001t0009g0228a0001c0001t0039g0227 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0004c0005t0004g0308a0004c0005t0027g0293a0009c0014t0004g0327 | 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 | a0001c0003t0022g0187 | 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 | a0004c0005t0004g0288 | 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 | a0001c0003t0026g0184a0001c0003t0026g0185a0001c0003t0026g0186 | 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 | a0001c0003t0026g0184a0001c0003t0026g0185a0001c0003t0026g0186 | 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 | a0006c0007t0005g0170a0006c0007t0005g0172 | 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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | 238 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(235): Show | 245 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.2377-2556A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97019744 | ||||||
| chr5:97019899
|
A | G | 238 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(235): Show | 245 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.2377-2401A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97019899 | ||||||
| chr5:97019929
|
C | G | 34 | a0001c0001t0005g0001a0001c0001t0005g0005a0001c0001t0005g0153others(31): 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 | a0001c0001t0002g0055 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0002c0002t0003g0244 | 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 | a0001c0001t0049g0026 | 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0001c0001t0020g0181 | 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 | a0001c0001t0002g0073a0001c0001t0006g0032 | 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 | a0001c0003t0010g0024 | 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 | a0002c0002t0003g0248 | 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 | a0001c0001t0013g0287 | 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 | a0001c0001t0006g0048 | 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 | a0002c0002t0001g0274a0002c0002t0001g0284 | 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 | a0001c0001t0001g0218 | 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 | 185 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(182): Show | 190 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(187): 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | 238 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(235): Show | 245 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(242): 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 | 151 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(148): Show | 154 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.2377-1024A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97021276 | ||||||
| chr5:97021474
|
A | G | 204 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(201): Show | 209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.2377-826A>G | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 13/17 | chr5 | 97021474 | ||||||
| chr5:97021556
|
T | G | 185 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(182): Show | 190 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(187): 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 | a0001c0001t0074g0207 | 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | 71 | a0001c0001t0011g0250a0001c0015t0028g0194a0002c0002t0001g0007others(68): 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 | a0001c0001t0002g0055a0001c0001t0002g0131a0001c0001t0006g0032others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | 145 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0204others(142): Show | 150 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(147): 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 | a0001c0001t0004g0205a0001c0001t0018g0158a0001c0001t0019g0160others(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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | 9 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0122others(6): 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 | a0001c0003t0022g0029a0001c0003t0022g0030a0001c0003t0022g0031others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0001t0016g0190a0001c0001t0016g0191a0001c0001t0016g0192others(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 | a0001c0003t0071g0188 | 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 | 11 | a0004c0005t0004g0243a0004c0005t0004g0260a0004c0005t0004g0286others(8): Show | 11 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(8): 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 | a0001c0003t0010g0024a0003c0004t0012g0142a0003c0004t0012g0143others(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 | a0001c0001t0048g0041 | 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 | a0001c0001t0002g0076 | 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 | 204 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(201): Show | 209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | 7 | a0001c0001t0013g0004a0001c0001t0013g0137a0001c0001t0013g0139others(4): 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0003t0065g0233 | 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 | a0001c0001t0066g0340 | 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 | a0001c0001t0006g0071 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | 8 | a0001c0001t0013g0004a0001c0001t0013g0137a0001c0001t0013g0139others(5): 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0002g0133 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0049g0026 | 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 | a0004c0005t0004g0288 | 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 | a0001c0001t0002g0099 | 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 | a0001c0001t0049g0026 | 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 | 151 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(148): Show | 154 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(151): 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 | a0001c0001t0002g0033a0001c0001t0002g0076a0001c0001t0002g0078others(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 | a0001c0003t0010g0016a0001c0003t0010g0019a0001c0003t0010g0020others(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 | a0001c0001t0056g0067 | 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 | a0002c0002t0003g0247a0002c0002t0003g0339 | 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 | a0001c0001t0020g0179a0001c0001t0020g0180a0001c0001t0020g0181others(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 | a0002c0002t0003g0258 | 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 | a0001c0001t0024g0053a0001c0001t0024g0084a0001c0001t0024g0114 | 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 | a0001c0001t0005g0166a0001c0001t0005g0178 | 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 | a0001c0001t0005g0166a0001c0001t0005g0178 | 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 | 186 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(183): Show | 192 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(189): 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 | a0001c0001t0050g0110 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | 205 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(202): Show | 211 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(208): 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 | a0001c0001t0023g0175a0001c0001t0023g0177 | 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 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0206others(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 | a0001c0003t0071g0188 | 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 | 186 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(183): Show | 192 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(189): 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 | a0001c0003t0007g0002a0001c0003t0007g0229a0001c0003t0007g0230others(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 | a0002c0002t0001g0264 | 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 | a0001c0001t0018g0158a0001c0001t0018g0159a0001c0001t0018g0167others(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 | a0001c0001t0002g0069a0001c0001t0002g0074 | 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 | a0002c0002t0001g0310 | 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 | a0001c0001t0002g0103 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0001g0200a0001c0001t0001g0224a0001c0001t0001g0225 | 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 | 205 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(202): Show | 211 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(208): 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 | a0001c0001t0002g0069a0001c0001t0002g0074 | 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 | 186 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(183): Show | 192 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.2865-386C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 16/17 | chr5 | 97027347 | ||||||
| chr5:97027352
|
C | CA | 43 | a0001c0001t0002g0055a0001c0001t0005g0001a0001c0001t0005g0005others(40): 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0001c0001t0002g0086 | 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 | a0001c0001t0032g0091 | 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 | 199 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(196): Show | 205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): 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 | a0001c0001t0076g0232 | 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 | a0001c0001t0005g0154a0001c0001t0005g0155a0001c0001t0018g0158others(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 | a0002c0002t0001g0334 | 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 | a0003c0004t0012g0142a0003c0004t0012g0143a0003c0004t0012g0145others(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 | a0002c0002t0003g0258a0002c0002t0003g0272a0002c0002t0003g0276others(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 | 248 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0200others(245): Show | 255 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.2947-43C>T | LNPEP | ENSG00000113441.16 | transcript | ENST00000231368.10 | protein_coding | 17/17 | chr5 | 97028359 |