Search by Gene
| geneid | 91750 |
|---|---|
| ensemblid | ENSG00000205659.12 |
| hgncid | 19856 |
| symbol | LIN52 |
| name | lin-52 DREAM MuvB core complex component |
| refseq_nuc | NM_001024674.3 |
| refseq_prot | NP_001019845.2 |
| ensembl_nuc | ENST00000555028.7 |
| ensembl_prot | ENSP00000451812.2 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 74084956 |
| end | 74201493 |
| strand | + |
| ver | v1.2 |
| region | chr14:74084956-74201493 |
| region5000 | chr14:74079956-74206493 |
| regionname0 | LIN52_chr14_74084956_74201493 |
| regionname5000 | LIN52_chr14_74079956_74206493 |
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 | 1/1 | 112 | 352 | 82 | 68 | 146 | 12 | 42 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0002 | 0/0 | 112 | 2 | 2 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | 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 | 1/1 | 339 | 341 | 71 | 68 | 146 | 12 | 42 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| c0002 | 0/0 | 339 | 11 | 11 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| c0003 | 0/0 | 339 | 2 | 2 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | 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 | 2835 | 72 | 24 | 22 | 15 | 5 | 6 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0002 | 0/0 | 2537 | 53 | 9 | 7 | 31 | 2 | 4 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0003 | 0/1 | 2535 | 43 | 1 | 5 | 32 | 1 | 3 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0004 | 0/0 | 2536 | 33 | 10 | 5 | 17 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0005 | 0/0 | 2839 | 21 | 0 | 4 | 11 | 0 | 6 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0006 | 0/0 | 2538 | 19 | 3 | 1 | 12 | 0 | 3 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0007 | 0/0 | 2537 | 15 | 0 | 0 | 9 | 0 | 6 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0008 | 0/0 | 2841 | 15 | 0 | 12 | 1 | 1 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0009 | 0/0 | 2534 | 10 | 10 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0010 | 0/0 | 2538 | 7 | 0 | 1 | 2 | 1 | 3 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0011 | 0/0 | 2534 | 6 | 6 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0012 | 0/0 | 2537 | 5 | 3 | 2 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0013 | 0/0 | 2537 | 4 | 0 | 1 | 0 | 0 | 3 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0014 | 0/0 | 2535 | 4 | 4 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0015 | 0/0 | 2537 | 4 | 2 | 0 | 2 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0016 | 0/0 | 2534 | 4 | 0 | 0 | 4 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0017 | 0/0 | 2835 | 3 | 0 | 2 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0018 | 0/0 | 2837 | 3 | 2 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0019 | 0/0 | 2536 | 2 | 0 | 0 | 2 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0020 | 0/0 | 2524 | 2 | 0 | 2 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0021 | 0/0 | 2537 | 2 | 2 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0022 | 0/0 | 2535 | 2 | 0 | 0 | 2 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0023 | 0/0 | 2833 | 2 | 0 | 1 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0024 | 0/0 | 2835 | 2 | 0 | 0 | 0 | 0 | 2 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0025 | 0/0 | 2536 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0026 | 0/0 | 2537 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0027 | 0/0 | 2534 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0028 | 0/0 | 2538 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0029 | 0/0 | 2534 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0030 | 0/0 | 2539 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0031 | 1/0 | 2536 | 1 | 0 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0032 | 0/0 | 2535 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0033 | 0/0 | 2535 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0034 | 0/0 | 2539 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0035 | 0/0 | 2522 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0036 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0037 | 0/0 | 2538 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0038 | 0/0 | 2536 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0039 | 0/0 | 2536 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0040 | 0/0 | 2536 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0041 | 0/0 | 2840 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0042 | 0/0 | 2839 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0043 | 0/0 | 2835 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0044 | 0/0 | 2837 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| t0045 | 0/0 | 2537 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | 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 | 2 | 0 | 0 | 2 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0061 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0336 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| 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 | 1/1 | 341 | 71 | 68 | 146 | 12 | 42 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/0 | 11 | 11 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0002c0003 | a0002 | c0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | 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 | 72 | 24 | 22 | 15 | 5 | 6 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 53 | 9 | 7 | 31 | 2 | 4 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/1 | 43 | 1 | 5 | 32 | 1 | 3 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 33 | 10 | 5 | 17 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 21 | 0 | 4 | 11 | 0 | 6 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 19 | 3 | 1 | 12 | 0 | 3 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 15 | 0 | 0 | 9 | 0 | 6 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 15 | 0 | 12 | 1 | 1 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 7 | 0 | 1 | 2 | 1 | 3 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0011 | a0001 | c0001 | t0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0015 | a0001 | c0001 | t0015 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0016 | a0001 | c0001 | t0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0017 | a0001 | c0001 | t0017 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0018 | a0001 | c0001 | t0018 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0019 | a0001 | c0001 | t0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0020 | a0001 | c0001 | t0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0021 | a0001 | c0001 | t0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0022 | a0001 | c0001 | t0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0023 | a0001 | c0001 | t0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0024 | a0001 | c0001 | t0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0025 | a0001 | c0001 | t0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0026 | a0001 | c0001 | t0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0027 | a0001 | c0001 | t0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0028 | a0001 | c0001 | t0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0029 | a0001 | c0001 | t0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0030 | a0001 | c0001 | t0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0031 | a0001 | c0001 | t0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0033 | a0001 | c0001 | t0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0034 | a0001 | c0001 | t0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0035 | a0001 | c0001 | t0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0036 | a0001 | c0001 | t0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0037 | a0001 | c0001 | t0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0038 | a0001 | c0001 | t0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0039 | a0001 | c0001 | t0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0040 | a0001 | c0001 | t0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0041 | a0001 | c0001 | t0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0042 | a0001 | c0001 | t0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0043 | a0001 | c0001 | t0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0001t0045 | a0001 | c0001 | t0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0002t0009 | a0001 | c0002 | t0009 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0001c0002t0032 | a0001 | c0002 | t0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0002c0003t0018 | a0002 | c0003 | t0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | copy fasta |
| a0002c0003t0044 | a0002 | c0003 | t0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0191 | a0001 | c0001 | t0001 | g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0205 | a0001 | c0001 | t0001 | g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0213 | a0001 | c0001 | t0001 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0214 | a0001 | c0001 | t0001 | g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0215 | a0001 | c0001 | t0001 | g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0216 | a0001 | c0001 | t0001 | g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0217 | a0001 | c0001 | t0001 | g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0218 | a0001 | c0001 | t0001 | g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0219 | a0001 | c0001 | t0001 | g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0220 | a0001 | c0001 | t0001 | g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0226 | a0001 | c0001 | t0001 | g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0227 | a0001 | c0001 | t0001 | g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0228 | a0001 | c0001 | t0001 | g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0231 | a0001 | c0001 | t0001 | g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0232 | a0001 | c0001 | t0001 | g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0233 | a0001 | c0001 | t0001 | g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0234 | a0001 | c0001 | t0001 | g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0235 | a0001 | c0001 | t0001 | g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0236 | a0001 | c0001 | t0001 | g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0237 | a0001 | c0001 | t0001 | g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0238 | a0001 | c0001 | t0001 | g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0239 | a0001 | c0001 | t0001 | g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0240 | a0001 | c0001 | t0001 | g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0241 | a0001 | c0001 | t0001 | g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0242 | a0001 | c0001 | t0001 | g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0243 | a0001 | c0001 | t0001 | g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0244 | a0001 | c0001 | t0001 | g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0245 | a0001 | c0001 | t0001 | g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0246 | a0001 | c0001 | t0001 | g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0248 | a0001 | c0001 | t0001 | g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0250 | a0001 | c0001 | t0001 | g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0251 | a0001 | c0001 | t0001 | g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0252 | a0001 | c0001 | t0001 | g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0253 | a0001 | c0001 | t0001 | g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0254 | a0001 | c0001 | t0001 | g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0255 | a0001 | c0001 | t0001 | g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0256 | a0001 | c0001 | t0001 | g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0257 | a0001 | c0001 | t0001 | g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0258 | a0001 | c0001 | t0001 | g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0259 | a0001 | c0001 | t0001 | g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0263 | a0001 | c0001 | t0001 | g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0264 | a0001 | c0001 | t0001 | g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0265 | a0001 | c0001 | t0001 | g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0266 | a0001 | c0001 | t0001 | g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0267 | a0001 | c0001 | t0001 | g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0268 | a0001 | c0001 | t0001 | g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0269 | a0001 | c0001 | t0001 | g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0270 | a0001 | c0001 | t0001 | g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0272 | a0001 | c0001 | t0001 | g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0273 | a0001 | c0001 | t0001 | g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0274 | a0001 | c0001 | t0001 | g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0286 | a0001 | c0001 | t0001 | g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0287 | a0001 | c0001 | t0001 | g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0288 | a0001 | c0001 | t0001 | g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0289 | a0001 | c0001 | t0001 | g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0290 | a0001 | c0001 | t0001 | g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0291 | a0001 | c0001 | t0001 | g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0292 | a0001 | c0001 | t0001 | g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0293 | a0001 | c0001 | t0001 | g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0294 | a0001 | c0001 | t0001 | g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0335 | a0001 | c0001 | t0001 | g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0338 | a0001 | c0001 | t0001 | g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0339 | a0001 | c0001 | t0001 | g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0340 | a0001 | c0001 | t0001 | g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0341 | a0001 | c0001 | t0001 | g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0342 | a0001 | c0001 | t0001 | g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0346 | a0001 | c0001 | t0001 | g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0001g0347 | a0001 | c0001 | t0001 | g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0001 | a0001 | c0001 | t0002 | g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0027 | a0001 | c0001 | t0002 | g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0073 | a0001 | c0001 | t0002 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0092 | a0001 | c0001 | t0002 | g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0093 | a0001 | c0001 | t0002 | g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0117 | a0001 | c0001 | t0002 | g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0118 | a0001 | c0001 | t0002 | g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0127 | a0001 | c0001 | t0002 | g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0128 | a0001 | c0001 | t0002 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0129 | a0001 | c0001 | t0002 | g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0130 | a0001 | c0001 | t0002 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0131 | a0001 | c0001 | t0002 | g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0133 | a0001 | c0001 | t0002 | g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0134 | a0001 | c0001 | t0002 | g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0136 | a0001 | c0001 | t0002 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0137 | a0001 | c0001 | t0002 | g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0138 | a0001 | c0001 | t0002 | g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0140 | a0001 | c0001 | t0002 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0142 | a0001 | c0001 | t0002 | g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0143 | a0001 | c0001 | t0002 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0144 | a0001 | c0001 | t0002 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0145 | a0001 | c0001 | t0002 | g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0146 | a0001 | c0001 | t0002 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0147 | a0001 | c0001 | t0002 | g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0148 | a0001 | c0001 | t0002 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0150 | a0001 | c0001 | t0002 | g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0151 | a0001 | c0001 | t0002 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0153 | a0001 | c0001 | t0002 | g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0157 | a0001 | c0001 | t0002 | g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0158 | a0001 | c0001 | t0002 | g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0159 | a0001 | c0001 | t0002 | g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0160 | a0001 | c0001 | t0002 | g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0163 | a0001 | c0001 | t0002 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0164 | a0001 | c0001 | t0002 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0166 | a0001 | c0001 | t0002 | g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0170 | a0001 | c0001 | t0002 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0172 | a0001 | c0001 | t0002 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0173 | a0001 | c0001 | t0002 | g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0175 | a0001 | c0001 | t0002 | g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0177 | a0001 | c0001 | t0002 | g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0179 | a0001 | c0001 | t0002 | g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0181 | a0001 | c0001 | t0002 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0189 | a0001 | c0001 | t0002 | g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0190 | a0001 | c0001 | t0002 | g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0192 | a0001 | c0001 | t0002 | g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0195 | a0001 | c0001 | t0002 | g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0196 | a0001 | c0001 | t0002 | g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0197 | a0001 | c0001 | t0002 | g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0260 | a0001 | c0001 | t0002 | g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0261 | a0001 | c0001 | t0002 | g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0276 | a0001 | c0001 | t0002 | g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0002g0277 | a0001 | c0001 | t0002 | g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0005 | a0001 | c0001 | t0003 | g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0007 | a0001 | c0001 | t0003 | g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0008 | a0001 | c0001 | t0003 | g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0012 | a0001 | c0001 | t0003 | g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0013 | a0001 | c0001 | t0003 | g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0015 | a0001 | c0001 | t0003 | g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0016 | a0001 | c0001 | t0003 | g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0017 | a0001 | c0001 | t0003 | g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0018 | a0001 | c0001 | t0003 | g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0019 | a0001 | c0001 | t0003 | g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0022 | a0001 | c0001 | t0003 | g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0023 | a0001 | c0001 | t0003 | g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0024 | a0001 | c0001 | t0003 | g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0025 | a0001 | c0001 | t0003 | g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0032 | a0001 | c0001 | t0003 | g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0033 | a0001 | c0001 | t0003 | g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0034 | a0001 | c0001 | t0003 | g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0035 | a0001 | c0001 | t0003 | g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0038 | a0001 | c0001 | t0003 | g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0040 | a0001 | c0001 | t0003 | g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0042 | a0001 | c0001 | t0003 | g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0045 | a0001 | c0001 | t0003 | g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0046 | a0001 | c0001 | t0003 | g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0050 | a0001 | c0001 | t0003 | g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0052 | a0001 | c0001 | t0003 | g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0053 | a0001 | c0001 | t0003 | g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0054 | a0001 | c0001 | t0003 | g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0055 | a0001 | c0001 | t0003 | g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0058 | a0001 | c0001 | t0003 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0059 | a0001 | c0001 | t0003 | g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0060 | a0001 | c0001 | t0003 | g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0061 | a0001 | c0001 | t0003 | g0061 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0062 | a0001 | c0001 | t0003 | g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0064 | a0001 | c0001 | t0003 | g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0065 | a0001 | c0001 | t0003 | g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0068 | a0001 | c0001 | t0003 | g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0069 | a0001 | c0001 | t0003 | g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0071 | a0001 | c0001 | t0003 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0072 | a0001 | c0001 | t0003 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0074 | a0001 | c0001 | t0003 | g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0076 | a0001 | c0001 | t0003 | g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0088 | a0001 | c0001 | t0003 | g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0003g0323 | a0001 | c0001 | t0003 | g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0006 | a0001 | c0001 | t0004 | g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0009 | a0001 | c0001 | t0004 | g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0011 | a0001 | c0001 | t0004 | g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0014 | a0001 | c0001 | t0004 | g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0020 | a0001 | c0001 | t0004 | g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0021 | a0001 | c0001 | t0004 | g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0026 | a0001 | c0001 | t0004 | g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0028 | a0001 | c0001 | t0004 | g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0029 | a0001 | c0001 | t0004 | g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0030 | a0001 | c0001 | t0004 | g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0036 | a0001 | c0001 | t0004 | g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0037 | a0001 | c0001 | t0004 | g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0043 | a0001 | c0001 | t0004 | g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0044 | a0001 | c0001 | t0004 | g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0047 | a0001 | c0001 | t0004 | g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0049 | a0001 | c0001 | t0004 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0057 | a0001 | c0001 | t0004 | g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0063 | a0001 | c0001 | t0004 | g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0066 | a0001 | c0001 | t0004 | g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0067 | a0001 | c0001 | t0004 | g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0070 | a0001 | c0001 | t0004 | g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0077 | a0001 | c0001 | t0004 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0206 | a0001 | c0001 | t0004 | g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0207 | a0001 | c0001 | t0004 | g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0208 | a0001 | c0001 | t0004 | g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0210 | a0001 | c0001 | t0004 | g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0212 | a0001 | c0001 | t0004 | g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0344 | a0001 | c0001 | t0004 | g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0345 | a0001 | c0001 | t0004 | g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0348 | a0001 | c0001 | t0004 | g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0349 | a0001 | c0001 | t0004 | g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0350 | a0001 | c0001 | t0004 | g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0004g0351 | a0001 | c0001 | t0004 | g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0005g0295 | a0001 | c0001 | t0005 | g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0005g0297 | a0001 | c0001 | t0005 | g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0005g0299 | a0001 | c0001 | t0005 | g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0005g0300 | a0001 | c0001 | t0005 | g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0005g0301 | a0001 | c0001 | t0005 | g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0005g0303 | a0001 | c0001 | t0005 | g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0005g0304 | a0001 | c0001 | t0005 | g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0005g0305 | a0001 | c0001 | t0005 | g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0005g0306 | a0001 | c0001 | t0005 | g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0005g0310 | a0001 | c0001 | t0005 | g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0005g0315 | a0001 | c0001 | t0005 | g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0005g0316 | a0001 | c0001 | t0005 | g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0005g0317 | a0001 | c0001 | t0005 | g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0005g0318 | a0001 | c0001 | t0005 | g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0005g0319 | a0001 | c0001 | t0005 | g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0005g0320 | a0001 | c0001 | t0005 | g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0005g0324 | a0001 | c0001 | t0005 | g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0005g0325 | a0001 | c0001 | t0005 | g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0005g0326 | a0001 | c0001 | t0005 | g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0005g0328 | a0001 | c0001 | t0005 | g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0005g0330 | a0001 | c0001 | t0005 | g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0006g0100 | a0001 | c0001 | t0006 | g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0006g0102 | a0001 | c0001 | t0006 | g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0006g0135 | a0001 | c0001 | t0006 | g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0006g0139 | a0001 | c0001 | t0006 | g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0006g0154 | a0001 | c0001 | t0006 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0006g0156 | a0001 | c0001 | t0006 | g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0006g0162 | a0001 | c0001 | t0006 | g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0006g0165 | a0001 | c0001 | t0006 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0006g0167 | a0001 | c0001 | t0006 | g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0006g0168 | a0001 | c0001 | t0006 | g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0006g0169 | a0001 | c0001 | t0006 | g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0006g0171 | a0001 | c0001 | t0006 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0006g0174 | a0001 | c0001 | t0006 | g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0006g0176 | a0001 | c0001 | t0006 | g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0006g0178 | a0001 | c0001 | t0006 | g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0006g0183 | a0001 | c0001 | t0006 | g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0006g0194 | a0001 | c0001 | t0006 | g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0006g0211 | a0001 | c0001 | t0006 | g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0006g0275 | a0001 | c0001 | t0006 | g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0007g0004 | a0001 | c0001 | t0007 | g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0007g0095 | a0001 | c0001 | t0007 | g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0007g0098 | a0001 | c0001 | t0007 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0007g0099 | a0001 | c0001 | t0007 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0007g0103 | a0001 | c0001 | t0007 | g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0007g0105 | a0001 | c0001 | t0007 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0007g0107 | a0001 | c0001 | t0007 | g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0007g0108 | a0001 | c0001 | t0007 | g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0007g0109 | a0001 | c0001 | t0007 | g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0007g0114 | a0001 | c0001 | t0007 | g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0007g0115 | a0001 | c0001 | t0007 | g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0007g0116 | a0001 | c0001 | t0007 | g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0007g0121 | a0001 | c0001 | t0007 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0007g0122 | a0001 | c0001 | t0007 | g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0007g0247 | a0001 | c0001 | t0007 | g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0008g0003 | a0001 | c0001 | t0008 | g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0008g0296 | a0001 | c0001 | t0008 | g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0008g0307 | a0001 | c0001 | t0008 | g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0008g0308 | a0001 | c0001 | t0008 | g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0008g0309 | a0001 | c0001 | t0008 | g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0008g0311 | a0001 | c0001 | t0008 | g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0008g0312 | a0001 | c0001 | t0008 | g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0008g0313 | a0001 | c0001 | t0008 | g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0008g0327 | a0001 | c0001 | t0008 | g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0008g0329 | a0001 | c0001 | t0008 | g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0008g0331 | a0001 | c0001 | t0008 | g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0008g0332 | a0001 | c0001 | t0008 | g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0008g0333 | a0001 | c0001 | t0008 | g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0008g0334 | a0001 | c0001 | t0008 | g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0010g0096 | a0001 | c0001 | t0010 | g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0010g0104 | a0001 | c0001 | t0010 | g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0010g0106 | a0001 | c0001 | t0010 | g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0010g0112 | a0001 | c0001 | t0010 | g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0010g0113 | a0001 | c0001 | t0010 | g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0010g0123 | a0001 | c0001 | t0010 | g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0010g0126 | a0001 | c0001 | t0010 | g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0011g0204 | a0001 | c0001 | t0011 | g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0011g0221 | a0001 | c0001 | t0011 | g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0011g0222 | a0001 | c0001 | t0011 | g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0011g0223 | a0001 | c0001 | t0011 | g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0011g0224 | a0001 | c0001 | t0011 | g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0011g0225 | a0001 | c0001 | t0011 | g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0012g0078 | a0001 | c0001 | t0012 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0012g0081 | a0001 | c0001 | t0012 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0012g0083 | a0001 | c0001 | t0012 | g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0012g0086 | a0001 | c0001 | t0012 | g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0012g0209 | a0001 | c0001 | t0012 | g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0013g0094 | a0001 | c0001 | t0013 | g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0013g0111 | a0001 | c0001 | t0013 | g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0013g0120 | a0001 | c0001 | t0013 | g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0013g0125 | a0001 | c0001 | t0013 | g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0014g0198 | a0001 | c0001 | t0014 | g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0014g0199 | a0001 | c0001 | t0014 | g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0014g0200 | a0001 | c0001 | t0014 | g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0014g0203 | a0001 | c0001 | t0014 | g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0015g0039 | a0001 | c0001 | t0015 | g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0015g0041 | a0001 | c0001 | t0015 | g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0015g0090 | a0001 | c0001 | t0015 | g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0015g0185 | a0001 | c0001 | t0015 | g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0016g0010 | a0001 | c0001 | t0016 | g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0016g0048 | a0001 | c0001 | t0016 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0016g0051 | a0001 | c0001 | t0016 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0016g0089 | a0001 | c0001 | t0016 | g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0017g0314 | a0001 | c0001 | t0017 | g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0017g0321 | a0001 | c0001 | t0017 | g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0017g0322 | a0001 | c0001 | t0017 | g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0018g0085 | a0001 | c0001 | t0018 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0018g0271 | a0001 | c0001 | t0018 | g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0019g0141 | a0001 | c0001 | t0019 | g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0019g0149 | a0001 | c0001 | t0019 | g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0020g0132 | a0001 | c0001 | t0020 | g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0020g0155 | a0001 | c0001 | t0020 | g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0021g0079 | a0001 | c0001 | t0021 | g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0021g0084 | a0001 | c0001 | t0021 | g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0022g0056 | a0001 | c0001 | t0022 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0022g0075 | a0001 | c0001 | t0022 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0023g0337 | a0001 | c0001 | t0023 | g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0023g0343 | a0001 | c0001 | t0023 | g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0024g0229 | a0001 | c0001 | t0024 | g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0024g0230 | a0001 | c0001 | t0024 | g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0025g0087 | a0001 | c0001 | t0025 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0026g0186 | a0001 | c0001 | t0026 | g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0027g0124 | a0001 | c0001 | t0027 | g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0028g0101 | a0001 | c0001 | t0028 | g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0029g0202 | a0001 | c0001 | t0029 | g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0030g0262 | a0001 | c0001 | t0030 | g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0031g0336 | a0001 | c0001 | t0031 | g0336 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0033g0182 | a0001 | c0001 | t0033 | g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0034g0119 | a0001 | c0001 | t0034 | g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0035g0180 | a0001 | c0001 | t0035 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0036g0082 | a0001 | c0001 | t0036 | g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0037g0091 | a0001 | c0001 | t0037 | g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0038g0080 | a0001 | c0001 | t0038 | g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0039g0031 | a0001 | c0001 | t0039 | g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0040g0184 | a0001 | c0001 | t0040 | g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0041g0298 | a0001 | c0001 | t0041 | g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0042g0302 | a0001 | c0001 | t0042 | g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0043g0249 | a0001 | c0001 | t0043 | g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0001t0045g0188 | a0001 | c0001 | t0045 | g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0002t0009g0002 | a0001 | c0002 | t0009 | g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0002t0009g0193 | a0001 | c0002 | t0009 | g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0002t0009g0278 | a0001 | c0002 | t0009 | g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0002t0009g0279 | a0001 | c0002 | t0009 | g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0002t0009g0280 | a0001 | c0002 | t0009 | g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0002t0009g0281 | a0001 | c0002 | t0009 | g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0002t0009g0282 | a0001 | c0002 | t0009 | g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0002t0009g0283 | a0001 | c0002 | t0009 | g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0002t0009g0284 | a0001 | c0002 | t0009 | g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0001c0002t0032g0285 | a0001 | c0002 | t0032 | g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0002c0003t0018g0201 | a0002 | c0003 | t0018 | g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| a0002c0003t0044g0187 | a0002 | c0003 | t0044 | g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN52_chr14_74079956_74206493 | LIN52 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0263 | EUR | GBR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00099 | hp2 | a0001 | c0001 | t0010 | g0113 | EUR | GBR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00280 | hp1 | a0001 | c0001 | t0017 | g0321 | EUR | FIN | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0266 | EUR | FIN | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00323 | hp1 | a0001 | c0001 | t0008 | g0333 | EUR | FIN | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0069 | EUR | FIN | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00423 | hp1 | a0001 | c0001 | t0035 | g0180 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00438 | hp1 | a0001 | c0001 | t0010 | g0104 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0057 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00544 | hp1 | a0001 | c0001 | t0007 | g0099 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00558 | hp1 | a0001 | c0001 | t0043 | g0249 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00639 | hp2 | a0001 | c0001 | t0008 | g0003 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0176 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00673 | hp1 | a0001 | c0001 | t0006 | g0165 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | CHS | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0212 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00738 | hp1 | a0001 | c0001 | t0010 | g0112 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00741 | hp1 | a0001 | c0001 | t0008 | g0334 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0066 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01071 | hp2 | a0001 | c0001 | t0008 | g0003 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01074 | hp2 | a0001 | c0001 | t0034 | g0119 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01081 | hp1 | a0001 | c0001 | t0013 | g0111 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01099 | hp2 | a0001 | c0001 | t0008 | g0313 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01106 | hp2 | a0001 | c0001 | t0008 | g0332 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0348 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01167 | hp1 | a0001 | c0001 | t0020 | g0155 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01167 | hp2 | a0001 | c0001 | t0042 | g0302 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01168 | hp1 | a0001 | c0001 | t0008 | g0309 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01169 | hp1 | a0001 | c0001 | t0020 | g0132 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01169 | hp2 | a0001 | c0001 | t0008 | g0329 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0067 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01243 | hp1 | a0001 | c0001 | t0012 | g0086 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01243 | hp2 | a0001 | c0001 | t0012 | g0083 | AMR | PUR | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01255 | hp1 | a0001 | c0001 | t0023 | g0337 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01256 | hp1 | a0001 | c0001 | t0008 | g0331 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0310 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0059 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0326 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01346 | hp2 | a0001 | c0001 | t0041 | g0298 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01433 | hp2 | a0001 | c0001 | t0017 | g0322 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0062 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | IBS | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01515 | hp2 | a0001 | c0001 | t0023 | g0343 | EUR | IBS | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0157 | EUR | IBS | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | IBS | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01891 | hp1 | a0001 | c0001 | t0011 | g0223 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0063 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01928 | hp2 | a0001 | c0001 | t0017 | g0314 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01934 | hp1 | a0001 | c0001 | t0008 | g0307 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01943 | hp1 | a0001 | c0001 | t0008 | g0311 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0076 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0325 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01981 | hp1 | a0001 | c0001 | t0008 | g0312 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02040 | hp1 | a0001 | c0001 | t0008 | g0308 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02055 | hp2 | a0001 | c0001 | t0012 | g0209 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02071 | hp1 | a0001 | c0001 | t0006 | g0156 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0297 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0305 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02132 | hp1 | a0001 | c0001 | t0007 | g0105 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02135 | hp2 | a0001 | c0001 | t0006 | g0174 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0194 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02145 | hp2 | a0001 | c0001 | t0037 | g0091 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02148 | hp2 | a0001 | c0001 | t0008 | g0327 | AMR | PEL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | CDX | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02155 | hp2 | a0001 | c0001 | t0007 | g0109 | EAS | CDX | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | CDX | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02165 | hp2 | a0001 | c0001 | t0005 | g0319 | EAS | CDX | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0210 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02258 | hp2 | a0001 | c0002 | t0009 | g0280 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02280 | hp2 | a0001 | c0002 | t0009 | g0278 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02451 | hp2 | a0001 | c0002 | t0009 | g0002 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02572 | hp1 | a0001 | c0001 | t0014 | g0203 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0315 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02602 | hp2 | a0001 | c0001 | t0028 | g0101 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02622 | hp1 | a0001 | c0002 | t0009 | g0283 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02622 | hp2 | a0001 | c0002 | t0009 | g0282 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02647 | hp2 | a0001 | c0001 | t0011 | g0204 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0045 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02698 | hp1 | a0001 | c0001 | t0007 | g0122 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02717 | hp1 | a0001 | c0002 | t0009 | g0284 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02717 | hp2 | a0001 | c0001 | t0011 | g0221 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02723 | hp1 | a0001 | c0001 | t0025 | g0087 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0207 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0304 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02735 | hp2 | a0001 | c0001 | t0007 | g0247 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0299 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02809 | hp1 | a0002 | c0003 | t0018 | g0201 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02809 | hp2 | a0001 | c0001 | t0014 | g0200 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0208 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0102 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02895 | hp1 | a0001 | c0001 | t0021 | g0084 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02897 | hp1 | a0001 | c0001 | t0012 | g0081 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02922 | hp2 | a0001 | c0002 | t0009 | g0279 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02965 | hp1 | a0001 | c0002 | t0032 | g0285 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02965 | hp2 | a0001 | c0001 | t0018 | g0085 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0344 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02970 | hp2 | a0001 | c0002 | t0009 | g0193 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02976 | hp1 | a0001 | c0001 | t0045 | g0188 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03017 | hp1 | a0001 | c0001 | t0027 | g0124 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0068 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03041 | hp1 | a0001 | c0001 | t0014 | g0199 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03130 | hp2 | a0001 | c0001 | t0014 | g0198 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0277 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03139 | hp2 | a0001 | c0001 | t0011 | g0224 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0100 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0349 | AFR | ESN | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | MSL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03209 | hp2 | a0001 | c0002 | t0009 | g0002 | AFR | MSL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03453 | hp1 | a0001 | c0002 | t0009 | g0281 | AFR | MSL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0351 | AFR | MSL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03486 | hp1 | a0001 | c0001 | t0036 | g0082 | AFR | MSL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0303 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03491 | hp2 | a0001 | c0001 | t0026 | g0186 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03492 | hp1 | a0001 | c0001 | t0024 | g0229 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0306 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03540 | hp1 | a0001 | c0001 | t0021 | g0079 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03579 | hp1 | a0002 | c0003 | t0044 | g0187 | AFR | MSL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03579 | hp2 | a0001 | c0001 | t0011 | g0225 | AFR | MSL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03669 | hp1 | a0001 | c0001 | t0007 | g0114 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03669 | hp2 | a0001 | c0001 | t0024 | g0230 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0162 | SAS | STU | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03688 | hp2 | a0001 | c0001 | t0013 | g0094 | SAS | STU | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03704 | hp1 | a0001 | c0001 | t0007 | g0115 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0070 | SAS | BEB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03831 | hp2 | a0001 | c0001 | t0013 | g0125 | SAS | BEB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03834 | hp1 | a0001 | c0001 | t0010 | g0126 | SAS | BEB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0183 | SAS | BEB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03927 | hp1 | a0001 | c0001 | t0006 | g0168 | SAS | BEB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03927 | hp2 | a0001 | c0001 | t0008 | g0296 | SAS | BEB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03942 | hp1 | a0001 | c0001 | t0005 | g0330 | SAS | BEB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03942 | hp2 | a0001 | c0001 | t0013 | g0120 | SAS | BEB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | STU | LIN52_chr14_74079956_74206493 | LIN52 |
| HG04115 | hp2 | a0001 | c0001 | t0010 | g0096 | SAS | STU | LIN52_chr14_74079956_74206493 | LIN52 |
| HG04184 | hp1 | a0001 | c0001 | t0029 | g0202 | SAS | BEB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0341 | SAS | BEB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0153 | SAS | STU | LIN52_chr14_74079956_74206493 | LIN52 |
| HG04199 | hp2 | a0001 | c0001 | t0010 | g0106 | SAS | STU | LIN52_chr14_74079956_74206493 | LIN52 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | STU | LIN52_chr14_74079956_74206493 | LIN52 |
| HG04204 | hp2 | a0001 | c0001 | t0007 | g0004 | SAS | STU | LIN52_chr14_74079956_74206493 | LIN52 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0340 | SAS | STU | LIN52_chr14_74079956_74206493 | LIN52 |
| HG04228 | hp2 | a0001 | c0001 | t0007 | g0107 | SAS | STU | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | YRI | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | YRI | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | CHB | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18612 | hp2 | a0001 | c0001 | t0016 | g0089 | EAS | CHB | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0350 | AFR | YRI | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18906 | hp2 | a0001 | c0001 | t0038 | g0080 | AFR | YRI | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18940 | hp2 | a0001 | c0001 | t0006 | g0135 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18941 | hp2 | a0001 | c0001 | t0006 | g0171 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0320 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18946 | hp1 | a0001 | c0001 | t0019 | g0141 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18953 | hp1 | a0001 | c0001 | t0006 | g0154 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18956 | hp1 | a0001 | c0001 | t0006 | g0167 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18956 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18959 | hp2 | a0001 | c0001 | t0015 | g0039 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18963 | hp2 | a0001 | c0001 | t0006 | g0178 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0328 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18967 | hp2 | a0001 | c0001 | t0033 | g0182 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18971 | hp1 | a0001 | c0001 | t0007 | g0103 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18984 | hp2 | a0001 | c0001 | t0016 | g0048 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18988 | hp2 | a0001 | c0001 | t0016 | g0010 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18991 | hp1 | a0001 | c0001 | t0006 | g0169 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18991 | hp2 | a0001 | c0001 | t0022 | g0075 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18999 | hp1 | a0001 | c0001 | t0007 | g0121 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19002 | hp1 | a0001 | c0001 | t0006 | g0139 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19003 | hp1 | a0001 | c0001 | t0005 | g0300 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19009 | hp1 | a0001 | c0001 | t0022 | g0056 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19009 | hp2 | a0001 | c0001 | t0010 | g0123 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19010 | hp1 | a0001 | c0001 | t0006 | g0275 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19010 | hp2 | a0001 | c0001 | t0005 | g0318 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19030 | hp1 | a0001 | c0001 | t0040 | g0184 | AFR | LWK | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0345 | AFR | LWK | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19043 | hp1 | a0001 | c0001 | t0015 | g0090 | AFR | LWK | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | LWK | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19055 | hp1 | a0001 | c0001 | t0016 | g0051 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19055 | hp2 | a0001 | c0001 | t0019 | g0149 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19057 | hp2 | a0001 | c0001 | t0030 | g0262 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19062 | hp2 | a0001 | c0001 | t0005 | g0301 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19063 | hp1 | a0001 | c0001 | t0007 | g0116 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19067 | hp1 | a0001 | c0001 | t0007 | g0095 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19067 | hp2 | a0001 | c0001 | t0006 | g0211 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19070 | hp1 | a0001 | c0001 | t0005 | g0317 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19072 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19075 | hp1 | a0001 | c0001 | t0015 | g0041 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19077 | hp1 | a0001 | c0001 | t0018 | g0271 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19077 | hp2 | a0001 | c0001 | t0007 | g0108 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19079 | hp1 | a0001 | c0001 | t0007 | g0098 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19082 | hp1 | a0001 | c0001 | t0039 | g0031 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19082 | hp2 | a0001 | c0001 | t0005 | g0316 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19086 | hp1 | a0001 | c0001 | t0005 | g0295 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0020 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | YRI | LIN52_chr14_74079956_74206493 | LIN52 |
| NA19240 | hp2 | a0001 | c0001 | t0015 | g0185 | AFR | YRI | LIN52_chr14_74079956_74206493 | LIN52 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ASW | LIN52_chr14_74079956_74206493 | LIN52 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0206 | AFR | ASW | LIN52_chr14_74079956_74206493 | LIN52 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0269 | EUR | TSI | LIN52_chr14_74079956_74206493 | LIN52 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0150 | EUR | TSI | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0324 | AMR | CLM | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02486 | hp2 | a0001 | c0001 | t0012 | g0078 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | MSL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | LIN52_chr14_74079956_74206493 | LIN52 |
| HG06807 | hp1 | a0001 | c0001 | t0011 | g0222 | AFR | USA | LIN52_chr14_74079956_74206493 | LIN52 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | USA | LIN52_chr14_74079956_74206493 | LIN52 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | LWK | LIN52_chr14_74079956_74206493 | LIN52 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | LWK | LIN52_chr14_74079956_74206493 | LIN52 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0061 | REF | REF | LIN52_chr14_74079956_74206493 | LIN52 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0031 | g0336 | REF | REF | LIN52_chr14_74079956_74206493 | LIN52 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74198970
|
A | G | 1 | a0002 | 2 | HG02809.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.332A>G | p.Lys111Arg | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 351/2874 | 332/339 | 111/112 | chr14 | 74198970 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74198929
|
G | A | 1 | a0001c0002 | 11 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(8): Show |
synonymous_variant | LOW | c.291G>A | p.Glu97Glu | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 310/2874 | 291/339 | 97/112 | chr14 | 74198929 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74199022
|
C | T | 1 | a0001c0001t0024 | 2 | HG03492.hp1 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*45C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 45 | chr14 | 74199022 | |||||
| chr14:74199028
|
C | T | 1 | a0001c0001t0045 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*51C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 51 | chr14 | 74199028 | |||||
| chr14:74199173
|
A | T | 1 | a0002c0003t0044 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*196A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 196 | chr14 | 74199173 | |||||
| chr14:74199504
|
G | A | 1 | a0001c0001t0025 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*527G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 527 | chr14 | 74199504 | |||||
| chr14:74199522
|
T | C | 6 | a0001c0001t0007a0001c0001t0010a0001c0001t0013others(3): Show | 29 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*545T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 545 | chr14 | 74199522 | |||||
| chr14:74199862
|
G | A | 3 | a0001c0001t0011a0001c0001t0014a0001c0001t0029 | 11 | HG01891.hp1 HG02572.hp1 HG02647.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*885G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 885 | chr14 | 74199862 | |||||
| chr14:74199938
|
A | G | 25 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(22): Show | 221 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*961A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 961 | chr14 | 74199938 | |||||
| chr14:74200076
|
A | G | 1 | a0001c0001t0029 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1099A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1099 | chr14 | 74200076 | |||||
| chr14:74200097
|
A | G | 2 | a0001c0001t0013a0001c0001t0028 | 5 | HG01081.hp1 HG02602.hp2 HG03688.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1120A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1120 | chr14 | 74200097 | |||||
| chr14:74200121
|
A | G | 25 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(22): Show | 221 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*1144A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1144 | chr14 | 74200121 | |||||
| chr14:74200229
|
T | TATGGTGA others(302): Show |
11 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(8): Show | 120 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*1263_*1264insTCGT others(305): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1264 | INFO_REALIGN_3_PRIME | chr14 | 74200229 | ||||
| chr14:74200229
|
T | TATGGTGA others(302): Show |
1 | a0001c0001t0024 | 2 | HG03492.hp1 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1263_*1264insTCGT others(305): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1264 | INFO_REALIGN_3_PRIME | chr14 | 74200229 | ||||
| chr14:74200251
|
T | TA | 12 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(9): Show | 122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*1278dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1279 | INFO_REALIGN_3_PRIME | chr14 | 74200251 | ||||
| chr14:74200274
|
A | G | 12 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(9): Show | 122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*1297A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1297 | chr14 | 74200274 | |||||
| chr14:74200320
|
C | T | 1 | a0001c0001t0040 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1343C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1343 | chr14 | 74200320 | |||||
| chr14:74200414
|
G | GA | 4 | a0001c0001t0012a0001c0001t0021a0001c0001t0030others(1): Show | 9 | HG01243.hp1 HG01243.hp2 HG02055.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1466dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1467 | INFO_REALIGN_3_PRIME | chr14 | 74200414 | ||||
| chr14:74200414
|
GA | G | 12 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(9): Show | 130 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*1466delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1466 | INFO_REALIGN_3_PRIME | chr14 | 74200414 | ||||
| chr14:74200414
|
GAA | G | 6 | a0001c0001t0011a0001c0001t0016a0001c0001t0019others(3): Show | 24 | HG01891.hp1 HG02258.hp2 HG02280.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1465_*1466delAA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1465 | INFO_REALIGN_3_PRIME | chr14 | 74200414 | ||||
| chr14:74200414
|
GAAAAAAA others(3): Show |
G | 1 | a0001c0001t0041 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1457_*1466delAAAA others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1457 | INFO_REALIGN_3_PRIME | chr14 | 74200414 | ||||
| chr14:74200414
|
GAAAAAAA others(4): Show |
G | 4 | a0001c0001t0005a0001c0001t0008a0001c0001t0017others(1): Show | 40 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1456_*1466delAAAA others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1456 | INFO_REALIGN_3_PRIME | chr14 | 74200414 | ||||
| chr14:74200414
|
GAAAAAAA others(6): Show |
G | 7 | a0001c0001t0001a0001c0001t0018a0001c0001t0023others(4): Show | 81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1454_*1466delAAAA others(9): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1454 | INFO_REALIGN_3_PRIME | chr14 | 74200414 | ||||
| chr14:74200414
|
GAAAAAAA others(7): Show |
G | 2 | a0001c0001t0020a0001c0001t0035 | 3 | HG00423.hp1 HG01167.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1453_*1466delAAAA others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1453 | INFO_REALIGN_3_PRIME | chr14 | 74200414 | ||||
| chr14:74200494
|
T | C | 1 | a0001c0001t0026 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1517T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1517 | chr14 | 74200494 | |||||
| chr14:74200640
|
C | T | 2 | a0001c0001t0022a0001c0001t0039 | 3 | NA18991.hp2 NA19009.hp1 NA19082.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1663C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1663 | chr14 | 74200640 | |||||
| chr14:74200778
|
C | T | 1 | a0001c0001t0042 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1801C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1801 | chr14 | 74200778 | |||||
| chr14:74200817
|
G | T | 2 | a0001c0001t0036a0001c0001t0038 | 2 | HG03486.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1840G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1840 | chr14 | 74200817 | |||||
| chr14:74200820
|
T | C | 15 | a0001c0001t0003a0001c0001t0004a0001c0001t0011others(12): Show | 115 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*1843T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1843 | chr14 | 74200820 | |||||
| chr14:74200820
|
T | TGC | 16 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(13): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*1852_*1853dupGC | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1854 | INFO_REALIGN_3_PRIME | chr14 | 74200820 | ||||
| chr14:74200820
|
T | TGTGC | 7 | a0001c0001t0005a0001c0001t0018a0001c0001t0034others(4): Show | 28 | HG01074.hp2 HG01123.hp2 HG01167.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1844_*1845insTGCG | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1845 | INFO_REALIGN_3_PRIME | chr14 | 74200820 | ||||
| chr14:74200820
|
T | TGTGTGC | 1 | a0001c0001t0008 | 15 | HG00323.hp1 HG00639.hp2 HG00741.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1844_*1845insTGTG others(2): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1845 | INFO_REALIGN_3_PRIME | chr14 | 74200820 | ||||
| chr14:74200880
|
T | A | 3 | a0001c0001t0021a0001c0001t0036a0001c0001t0038 | 4 | HG02895.hp1 HG03486.hp1 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1903T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 1903 | chr14 | 74200880 | |||||
| chr14:74201138
|
A | G | 5 | a0001c0001t0005a0001c0001t0008a0001c0001t0017others(2): Show | 41 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2161A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 2161 | chr14 | 74201138 | |||||
| chr14:74201490
|
G | A | 1 | a0001c0001t0043 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2513G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 6/6 | 2513 | chr14 | 74201490 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:74085018
|
G | T | 4 | a0001c0001t0004g0348a0001c0001t0004g0349a0001c0001t0004g0350others(1): Show | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+25G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085018 | ||||||
| chr14:74085082
|
T | C | 1 | a0001c0001t0007g0004 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.19+89T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085082 | ||||||
| chr14:74085267
|
G | C | 207 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(204): Show | 209 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.19+274G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085267 | ||||||
| chr14:74085273
|
C | T | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.19+280C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085273 | ||||||
| chr14:74085345
|
T | C | 339 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(336): Show | 342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.19+352T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085345 | ||||||
| chr14:74085444
|
C | G | 1 | a0001c0001t0016g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.19+451C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085444 | ||||||
| chr14:74085502
|
A | G | 7 | a0001c0001t0011g0204a0001c0001t0014g0198a0001c0001t0014g0199others(4): Show | 7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+509A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085502 | ||||||
| chr14:74085705
|
CAATT | C | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.19+715_19+718delTT others(2): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74085705 | |||||
| chr14:74085710
|
A | C | 1 | a0001c0001t0002g0197 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.19+717A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085710 | ||||||
| chr14:74085739
|
C | G | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.19+746C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085739 | ||||||
| chr14:74085807
|
C | T | 1 | a0001c0001t0001g0335 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.19+814C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085807 | ||||||
| chr14:74085840
|
T | C | 1 | a0001c0001t0001g0205 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.19+847T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085840 | ||||||
| chr14:74085886
|
A | G | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.19+893A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085886 | ||||||
| chr14:74085967
|
G | T | 3 | a0001c0001t0008g0332a0001c0001t0008g0333a0001c0001t0008g0334 | 3 | HG00323.hp1 HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.19+974G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74085967 | ||||||
| chr14:74086011
|
AT | A | 9 | a0001c0001t0001g0335a0001c0001t0002g0092a0001c0001t0004g0206others(6): Show | 9 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+1029delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74086011 | |||||
| chr14:74086041
|
T | C | 1 | a0001c0001t0003g0005 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.19+1048T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74086041 | ||||||
| chr14:74086092
|
C | A | 1 | a0001c0001t0002g0093 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.19+1099C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74086092 | ||||||
| chr14:74086186
|
G | C | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.19+1193G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74086186 | ||||||
| chr14:74086344
|
G | A | 73 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(70): Show | 73 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.19+1351G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74086344 | ||||||
| chr14:74086549
|
G | C | 2 | a0001c0001t0004g0077a0001c0001t0012g0078 | 2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.19+1556G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74086549 | ||||||
| chr14:74086656
|
G | A | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.19+1663G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74086656 | ||||||
| chr14:74086669
|
GA | G | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.19+1685delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74086669 | |||||
| chr14:74086898
|
T | C | 34 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0002g0117others(31): Show | 34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.19+1905T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74086898 | ||||||
| chr14:74086948
|
G | GA | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.19+1964dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74086948 | |||||
| chr14:74086999
|
A | G | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0006g0194 | 3 | HG01496.hp1 HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.19+2006A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74086999 | ||||||
| chr14:74087011
|
A | C | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.19+2018A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74087011 | ||||||
| chr14:74087109
|
G | A | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.19+2116G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74087109 | ||||||
| chr14:74087140
|
G | A | 106 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(103): Show | 107 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.19+2147G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74087140 | ||||||
| chr14:74087371
|
A | G | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.19+2378A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74087371 | ||||||
| chr14:74087384
|
C | T | 1 | a0001c0001t0012g0078 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.19+2391C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74087384 | ||||||
| chr14:74087413
|
C | CA | 13 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(10): Show | 13 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.19+2443dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74087413 | |||||
| chr14:74087413
|
CA | C | 115 | a0001c0001t0001g0097a0001c0001t0001g0152a0001c0001t0001g0161others(112): Show | 117 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.19+2443delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74087413 | |||||
| chr14:74087413
|
CAA | C | 39 | a0001c0001t0001g0110a0001c0001t0001g0191a0001c0001t0002g0117others(36): Show | 39 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.19+2442_19+2443del others(2): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74087413 | |||||
| chr14:74087413
|
CAAAAAAA others(1): Show |
C | 73 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(70): Show | 73 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.19+2436_19+2443del others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74087413 | |||||
| chr14:74087413
|
CAAAAAAA others(3): Show |
C | 9 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(6): Show | 9 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+2434_19+2443del others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74087413 | |||||
| chr14:74087469
|
G | C | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.19+2476G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74087469 | ||||||
| chr14:74087762
|
C | T | 3 | a0001c0001t0011g0204a0001c0001t0014g0203a0001c0001t0029g0202 | 3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.19+2769C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74087762 | ||||||
| chr14:74087974
|
A | C | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.19+2981A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74087974 | ||||||
| chr14:74088022
|
C | T | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+3029C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088022 | ||||||
| chr14:74088024
|
C | T | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.19+3031C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088024 | ||||||
| chr14:74088029
|
C | T | 3 | a0001c0001t0005g0299a0001c0001t0005g0330a0001c0001t0041g0298 | 3 | HG01346.hp2 HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.19+3036C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088029 | ||||||
| chr14:74088070
|
G | A | 8 | a0001c0001t0004g0077a0001c0001t0012g0078a0001c0001t0012g0081others(5): Show | 8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.19+3077G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088070 | ||||||
| chr14:74088167
|
T | A | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.20-3065T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088167 | ||||||
| chr14:74088204
|
C | T | 2 | a0001c0001t0012g0086a0001c0001t0025g0087 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.20-3028C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088204 | ||||||
| chr14:74088256
|
A | G | 12 | a0001c0001t0004g0077a0001c0001t0004g0348a0001c0001t0004g0349others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.20-2976A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088256 | ||||||
| chr14:74088333
|
C | A | 1 | a0001c0001t0007g0099 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.20-2899C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088333 | ||||||
| chr14:74088474
|
C | T | 5 | a0001c0001t0004g0206a0001c0001t0004g0207a0001c0001t0004g0208others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-2758C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088474 | ||||||
| chr14:74088565
|
C | T | 9 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(6): Show | 9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-2667C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088565 | ||||||
| chr14:74088566
|
G | A | 61 | a0001c0001t0001g0152a0001c0001t0001g0161a0001c0001t0002g0001others(58): Show | 62 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.20-2666G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088566 | ||||||
| chr14:74088706
|
C | T | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.20-2526C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088706 | ||||||
| chr14:74088721
|
T | G | 4 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200others(1): Show | 4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.20-2511T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088721 | ||||||
| chr14:74088753
|
C | T | 1 | a0001c0001t0003g0076 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.20-2479C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088753 | ||||||
| chr14:74088911
|
T | G | 4 | a0001c0001t0004g0348a0001c0001t0004g0349a0001c0001t0004g0350others(1): Show | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-2321T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088911 | ||||||
| chr14:74088912
|
G | T | 4 | a0001c0001t0004g0348a0001c0001t0004g0349a0001c0001t0004g0350others(1): Show | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-2320G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74088912 | ||||||
| chr14:74089022
|
C | T | 2 | a0001c0001t0012g0086a0001c0001t0025g0087 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.20-2210C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74089022 | ||||||
| chr14:74089066
|
C | T | 2 | a0001c0001t0012g0086a0001c0001t0025g0087 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.20-2166C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74089066 | ||||||
| chr14:74089087
|
GT | G | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.20-2144delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74089087 | ||||||
| chr14:74089370
|
A | AT | 123 | a0001c0001t0001g0152a0001c0001t0001g0161a0001c0001t0001g0191others(120): Show | 126 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.20-1846dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74089370 | |||||
| chr14:74089370
|
A | ATT | 37 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0002g0092others(34): Show | 37 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.20-1847_20-1846dup others(2): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74089370 | |||||
| chr14:74089560
|
T | G | 207 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(204): Show | 209 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.20-1672T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74089560 | ||||||
| chr14:74089796
|
TA | T | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.20-1432delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74089796 | |||||
| chr14:74089868
|
T | C | 1 | a0001c0001t0007g0103 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.20-1364T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74089868 | ||||||
| chr14:74089897
|
C | A | 8 | a0001c0001t0004g0077a0001c0001t0012g0078a0001c0001t0012g0081others(5): Show | 8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.20-1335C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74089897 | ||||||
| chr14:74089952
|
C | T | 1 | a0001c0001t0012g0078 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.20-1280C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74089952 | ||||||
| chr14:74090018
|
C | CT | 148 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(145): Show | 151 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.20-1196dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74090018 | |||||
| chr14:74090018
|
C | CTT | 9 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0005g0297others(6): Show | 9 | HG02071.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-1197_20-1196dup others(2): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74090018 | |||||
| chr14:74090018
|
C | CTTT | 9 | a0001c0001t0001g0191a0001c0001t0002g0092a0001c0001t0011g0204others(6): Show | 9 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.20-1198_20-1196dup others(3): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74090018 | |||||
| chr14:74090181
|
A | G | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.20-1051A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090181 | ||||||
| chr14:74090219
|
A | G | 1 | a0001c0001t0040g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.20-1013A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090219 | ||||||
| chr14:74090246
|
G | T | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.20-986G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090246 | ||||||
| chr14:74090317
|
C | T | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-915C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090317 | ||||||
| chr14:74090399
|
A | G | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.20-833A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090399 | ||||||
| chr14:74090428
|
C | T | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.20-804C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090428 | ||||||
| chr14:74090494
|
C | T | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.20-738C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090494 | ||||||
| chr14:74090563
|
C | T | 1 | a0001c0001t0002g0181 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.20-669C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090563 | ||||||
| chr14:74090689
|
CTTTTTAA others(5): Show |
C | 1 | a0001c0001t0002g0073 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.20-531_20-520delAT others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr14 | 74090689 | |||||
| chr14:74090769
|
G | T | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.20-463G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090769 | ||||||
| chr14:74090815
|
A | G | 1 | a0001c0001t0003g0072 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.20-417A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090815 | ||||||
| chr14:74090866
|
A | G | 5 | a0001c0001t0004g0206a0001c0001t0004g0207a0001c0001t0004g0208others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-366A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090866 | ||||||
| chr14:74090889
|
G | T | 1 | a0001c0001t0010g0126 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.20-343G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090889 | ||||||
| chr14:74090905
|
C | T | 4 | a0001c0001t0004g0348a0001c0001t0004g0349a0001c0001t0004g0350others(1): Show | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-327C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74090905 | ||||||
| chr14:74091144
|
T | C | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.20-88T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74091144 | ||||||
| chr14:74091196
|
C | A | 5 | a0001c0001t0011g0221a0001c0001t0011g0222a0001c0001t0011g0223others(2): Show | 5 | HG01891.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-36C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 1/5 | chr14 | 74091196 | ||||||
| chr14:74091758
|
G | A | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.94+452G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74091758 | ||||||
| chr14:74091761
|
G | A | 2 | a0001c0001t0012g0086a0001c0001t0025g0087 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.94+455G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74091761 | ||||||
| chr14:74091764
|
ACT | A | 88 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(85): Show | 88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.94+461_94+462delCT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74091764 | |||||
| chr14:74091767
|
C | G | 1 | a0001c0001t0003g0007 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.94+461C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74091767 | ||||||
| chr14:74091768
|
T | C | 4 | a0001c0001t0002g0133a0001c0001t0002g0134a0001c0001t0002g0136others(1): Show | 4 | NA18940.hp2 NA18947.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+462T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74091768 | ||||||
| chr14:74091769
|
G | C | 1 | a0001c0001t0003g0007 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.94+463G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74091769 | ||||||
| chr14:74091772
|
T | A | 1 | a0001c0001t0003g0007 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.94+466T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74091772 | ||||||
| chr14:74091773
|
C | A | 1 | a0001c0001t0003g0007 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.94+467C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74091773 | ||||||
| chr14:74091773
|
C | CA | 13 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0003g0008others(10): Show | 13 | HG00597.hp1 HG00735.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+491dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74091773 | |||||
| chr14:74091773
|
CA | C | 134 | a0001c0001t0001g0152a0001c0001t0001g0161a0001c0001t0001g0191others(131): Show | 136 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.94+491delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74091773 | |||||
| chr14:74091773
|
CAA | C | 41 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0002g0093others(38): Show | 41 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.94+490_94+491delAA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74091773 | |||||
| chr14:74091966
|
A | T | 207 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(204): Show | 209 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.94+660A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74091966 | ||||||
| chr14:74092101
|
G | C | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.94+795G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092101 | ||||||
| chr14:74092189
|
C | A | 2 | a0001c0001t0003g0013a0001c0001t0004g0014 | 2 | HG00597.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.94+883C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092189 | ||||||
| chr14:74092189
|
C | G | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.94+883C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092189 | ||||||
| chr14:74092195
|
C | T | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.94+889C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092195 | ||||||
| chr14:74092235
|
G | A | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.94+929G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092235 | ||||||
| chr14:74092281
|
T | A | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.94+975T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092281 | ||||||
| chr14:74092299
|
G | A | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.94+993G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092299 | ||||||
| chr14:74092299
|
GTA | G | 221 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(218): Show | 223 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.94+1007_94+1008del others(2): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74092299 | |||||
| chr14:74092301
|
A | G | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.94+995A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092301 | ||||||
| chr14:74092312
|
TATG | T | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.94+1007_94+1009del others(3): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092312 | ||||||
| chr14:74092316
|
T | G | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.94+1010T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092316 | ||||||
| chr14:74092328
|
G | A | 12 | a0001c0001t0002g0128a0001c0001t0002g0140a0001c0001t0002g0142others(9): Show | 12 | HG00408.hp1 HG02083.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+1022G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092328 | ||||||
| chr14:74092335
|
C | T | 1 | a0001c0001t0014g0198 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.94+1029C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092335 | ||||||
| chr14:74092362
|
A | G | 1 | a0001c0001t0003g0012 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.94+1056A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092362 | ||||||
| chr14:74092484
|
T | G | 2 | a0001c0001t0024g0229a0001c0001t0024g0230 | 2 | HG03492.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.94+1178T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092484 | ||||||
| chr14:74092586
|
G | A | 1 | a0001c0001t0045g0188 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.94+1280G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092586 | ||||||
| chr14:74092586
|
G | T | 76 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(73): Show | 76 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.94+1280G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092586 | ||||||
| chr14:74092645
|
G | T | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.94+1339G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092645 | ||||||
| chr14:74092862
|
A | G | 1 | a0002c0003t0018g0201 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.94+1556A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092862 | ||||||
| chr14:74092868
|
G | C | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.94+1562G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092868 | ||||||
| chr14:74092885
|
C | T | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.94+1579C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092885 | ||||||
| chr14:74092981
|
T | C | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.94+1675T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74092981 | ||||||
| chr14:74093217
|
A | G | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.94+1911A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74093217 | ||||||
| chr14:74093321
|
C | CT | 29 | a0001c0001t0001g0220a0001c0001t0001g0265a0001c0001t0001g0266others(26): Show | 29 | HG00280.hp2 HG00735.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.94+2035dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74093321 | |||||
| chr14:74093321
|
CT | C | 19 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0335others(16): Show | 19 | HG01069.hp1 HG02055.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.94+2035delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74093321 | |||||
| chr14:74093504
|
A | G | 348 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(345): Show | 351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.94+2198A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74093504 | ||||||
| chr14:74093553
|
A | T | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.94+2247A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74093553 | ||||||
| chr14:74093623
|
G | T | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.94+2317G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74093623 | ||||||
| chr14:74093633
|
A | G | 1 | a0001c0001t0027g0124 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.95-2315A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74093633 | ||||||
| chr14:74093634
|
T | C | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.95-2314T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74093634 | ||||||
| chr14:74093822
|
CT | C | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.95-2125delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74093822 | ||||||
| chr14:74094003
|
C | T | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.95-1945C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094003 | ||||||
| chr14:74094039
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.95-1909T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094039 | ||||||
| chr14:74094125
|
C | T | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.95-1823C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094125 | ||||||
| chr14:74094182
|
A | C | 2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG00642.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.95-1766A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094182 | ||||||
| chr14:74094258
|
G | GT | 116 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(113): Show | 118 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.95-1675dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74094258 | |||||
| chr14:74094263
|
T | G | 88 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(85): Show | 88 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.95-1685T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094263 | ||||||
| chr14:74094337
|
G | A | 264 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(261): Show | 267 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.95-1611G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094337 | ||||||
| chr14:74094441
|
G | C | 1 | a0001c0001t0001g0338 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.95-1507G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094441 | ||||||
| chr14:74094466
|
C | G | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.95-1482C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094466 | ||||||
| chr14:74094575
|
C | T | 1 | a0001c0001t0002g0190 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.95-1373C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094575 | ||||||
| chr14:74094733
|
C | CT | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.95-1203dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74094733 | |||||
| chr14:74094776
|
G | T | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.95-1172G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094776 | ||||||
| chr14:74094880
|
G | A | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.95-1068G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094880 | ||||||
| chr14:74094935
|
C | G | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.95-1013C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094935 | ||||||
| chr14:74094985
|
T | C | 7 | a0001c0001t0001g0205a0001c0001t0001g0231a0001c0001t0001g0234others(4): Show | 7 | HG01081.hp2 HG01884.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-963T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094985 | ||||||
| chr14:74094986
|
A | G | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-962A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74094986 | ||||||
| chr14:74095058
|
C | T | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG00099.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.95-890C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74095058 | ||||||
| chr14:74095149
|
G | GT | 23 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(20): Show | 23 | HG01099.hp1 HG01175.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.95-779dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74095149 | |||||
| chr14:74095149
|
G | GTT | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.95-780_95-779dupTT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74095149 | |||||
| chr14:74095149
|
G | GTTTTT | 98 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(95): Show | 100 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.95-783_95-779dupTT others(3): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74095149 | |||||
| chr14:74095149
|
G | GTTTTTT | 18 | a0001c0001t0002g0127a0001c0001t0002g0138a0001c0001t0002g0175others(15): Show | 18 | HG00423.hp1 HG00642.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.95-784_95-779dupTT others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr14 | 74095149 | |||||
| chr14:74095186
|
C | T | 2 | a0001c0002t0009g0283a0001c0002t0009g0284 | 2 | HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.95-762C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74095186 | ||||||
| chr14:74095324
|
G | A | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.95-624G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74095324 | ||||||
| chr14:74095678
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.95-270A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74095678 | ||||||
| chr14:74095736
|
C | G | 12 | a0001c0001t0004g0077a0001c0001t0004g0348a0001c0001t0004g0349others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.95-212C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74095736 | ||||||
| chr14:74095777
|
T | C | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.95-171T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74095777 | ||||||
| chr14:74095808
|
C | T | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.95-140C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74095808 | ||||||
| chr14:74095838
|
CTT | C | 18 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0272others(15): Show | 18 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.95-109_95-108delTT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 2/5 | chr14 | 74095838 | ||||||
| chr14:74096217
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.132+232C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74096217 | ||||||
| chr14:74096259
|
C | G | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.132+274C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74096259 | ||||||
| chr14:74096342
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.132+357G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74096342 | ||||||
| chr14:74096351
|
C | T | 10 | a0001c0001t0002g0092a0001c0001t0011g0204a0001c0001t0014g0198others(7): Show | 10 | HG02145.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.132+366C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74096351 | ||||||
| chr14:74096467
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.132+482A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74096467 | ||||||
| chr14:74096561
|
T | G | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.132+576T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74096561 | ||||||
| chr14:74096586
|
G | A | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.132+601G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74096586 | ||||||
| chr14:74096664
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.132+679C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74096664 | ||||||
| chr14:74096874
|
T | A | 1 | a0001c0001t0003g0007 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.132+889T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74096874 | ||||||
| chr14:74097079
|
T | G | 248 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(245): Show | 251 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.133-715T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74097079 | ||||||
| chr14:74097115
|
G | A | 106 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(103): Show | 107 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.133-679G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74097115 | ||||||
| chr14:74097327
|
A | T | 1 | a0001c0001t0003g0069 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.133-467A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74097327 | ||||||
| chr14:74097425
|
C | CT | 82 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(79): Show | 82 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.133-351dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr14 | 74097425 | |||||
| chr14:74097425
|
CT | C | 59 | a0001c0001t0001g0239a0001c0001t0001g0335a0001c0001t0002g0092others(56): Show | 61 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.133-351delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr14 | 74097425 | |||||
| chr14:74097425
|
CTT | C | 12 | a0001c0001t0004g0206a0001c0001t0005g0301a0001c0001t0011g0204others(9): Show | 12 | HG01167.hp2 HG02572.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.133-352_133-351del others(2): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr14 | 74097425 | |||||
| chr14:74097425
|
CTTT | C | 104 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(101): Show | 105 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.133-353_133-351del others(3): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr14 | 74097425 | |||||
| chr14:74097461
|
T | C | 61 | a0001c0001t0001g0152a0001c0001t0001g0161a0001c0001t0002g0001others(58): Show | 62 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.133-333T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74097461 | ||||||
| chr14:74097504
|
A | G | 9 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0272others(6): Show | 9 | HG01192.hp1 HG02027.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.133-290A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74097504 | ||||||
| chr14:74097582
|
G | A | 1 | a0002c0003t0044g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.133-212G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74097582 | ||||||
| chr14:74097655
|
C | T | 11 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(8): Show | 11 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.133-139C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74097655 | ||||||
| chr14:74097688
|
C | T | 1 | a0001c0001t0003g0012 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.133-106C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74097688 | ||||||
| chr14:74097765
|
G | T | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.133-29G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 3/5 | chr14 | 74097765 | ||||||
| chr14:74097867
|
G | A | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
splice_region_variant&intron_variant | LOW | c.199+7G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74097867 | ||||||
| chr14:74097902
|
T | C | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.199+42T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74097902 | ||||||
| chr14:74097906
|
C | A | 61 | a0001c0001t0001g0152a0001c0001t0001g0161a0001c0001t0002g0001others(58): Show | 62 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.199+46C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74097906 | ||||||
| chr14:74098315
|
T | C | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.199+455T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74098315 | ||||||
| chr14:74098463
|
G | A | 1 | a0001c0001t0003g0074 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.199+603G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74098463 | ||||||
| chr14:74098550
|
G | GT | 118 | a0001c0001t0001g0110a0001c0001t0001g0152a0001c0001t0001g0161others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.199+704dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 74098550 | |||||
| chr14:74098550
|
G | GTT | 6 | a0001c0001t0001g0097a0001c0001t0002g0131a0001c0001t0002g0179others(3): Show | 6 | HG01175.hp2 HG01981.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.199+703_199+704dup others(2): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 74098550 | |||||
| chr14:74098550
|
G | T | 1 | a0001c0001t0007g0099 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.199+690G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74098550 | ||||||
| chr14:74098672
|
C | T | 2 | a0001c0001t0007g0098a0002c0003t0018g0201 | 2 | HG02809.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.199+812C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74098672 | ||||||
| chr14:74098799
|
C | T | 4 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200others(1): Show | 4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.199+939C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74098799 | ||||||
| chr14:74098845
|
G | A | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.199+985G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74098845 | ||||||
| chr14:74098884
|
A | G | 7 | a0001c0001t0011g0204a0001c0001t0014g0198a0001c0001t0014g0199others(4): Show | 7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.199+1024A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74098884 | ||||||
| chr14:74098896
|
C | G | 7 | a0001c0001t0011g0204a0001c0001t0014g0198a0001c0001t0014g0199others(4): Show | 7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.199+1036C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74098896 | ||||||
| chr14:74099125
|
A | G | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.199+1265A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74099125 | ||||||
| chr14:74099234
|
A | T | 74 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(71): Show | 74 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.199+1374A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74099234 | ||||||
| chr14:74099280
|
A | T | 1 | a0001c0001t0007g0099 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.199+1420A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74099280 | ||||||
| chr14:74099288
|
AC | A | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.199+1429delC | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74099288 | ||||||
| chr14:74099294
|
T | G | 1 | a0001c0001t0001g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.199+1434T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74099294 | ||||||
| chr14:74099586
|
T | G | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.200-1569T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74099586 | ||||||
| chr14:74099586
|
T | TTGTGTG | 9 | a0001c0001t0002g0192a0001c0001t0011g0204a0001c0001t0014g0198others(6): Show | 9 | HG01109.hp1 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.200-1551_200-1546d others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 74099586 | |||||
| chr14:74099586
|
T | TTGTGTGT others(1): Show |
93 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(90): Show | 93 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.200-1553_200-1546d others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 74099586 | |||||
| chr14:74099586
|
T | TTGTGTGT others(3): Show |
13 | a0001c0001t0002g0001a0001c0001t0002g0093a0001c0001t0002g0170others(10): Show | 15 | HG02451.hp2 HG02698.hp1 HG02970.hp2 others(12): Show |
intron_variant | MODIFIER | c.200-1555_200-1546d others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 74099586 | |||||
| chr14:74099586
|
T | TTGTGTGT others(5): Show |
1 | a0001c0001t0002g0173 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.200-1557_200-1546d others(14): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 74099586 | |||||
| chr14:74099586
|
TTG | T | 14 | a0001c0001t0001g0214a0001c0001t0001g0240a0001c0001t0004g0077others(11): Show | 14 | HG01109.hp2 HG01192.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.200-1547_200-1546d others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr14 | 74099586 | |||||
| chr14:74099691
|
G | A | 29 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0007g0004others(26): Show | 29 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.200-1464G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74099691 | ||||||
| chr14:74099719
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.200-1436G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74099719 | ||||||
| chr14:74099994
|
T | C | 1 | a0001c0001t0011g0221 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.200-1161T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74099994 | ||||||
| chr14:74100241
|
G | A | 1 | a0001c0001t0002g0133 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.200-914G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74100241 | ||||||
| chr14:74100574
|
C | A | 3 | a0001c0001t0004g0020a0001c0001t0004g0021a0001c0001t0016g0010 | 3 | NA18975.hp2 NA18988.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.200-581C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74100574 | ||||||
| chr14:74100624
|
T | C | 248 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(245): Show | 251 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.200-531T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74100624 | ||||||
| chr14:74100664
|
C | T | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.200-491C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74100664 | ||||||
| chr14:74100712
|
G | C | 1 | a0001c0001t0001g0335 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.200-443G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74100712 | ||||||
| chr14:74100785
|
C | T | 264 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(261): Show | 267 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.200-370C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74100785 | ||||||
| chr14:74101033
|
T | C | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.200-122T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74101033 | ||||||
| chr14:74101148
|
G | A | 6 | a0001c0001t0012g0081a0001c0001t0012g0083a0001c0001t0021g0079others(3): Show | 6 | HG01243.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.200-7G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 4/5 | chr14 | 74101148 | ||||||
| chr14:74101249
|
C | T | 61 | a0001c0001t0001g0152a0001c0001t0001g0161a0001c0001t0002g0001others(58): Show | 62 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.283+11C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101249 | ||||||
| chr14:74101386
|
A | G | 3 | a0001c0001t0003g0015a0001c0001t0004g0066a0001c0001t0004g0067 | 3 | HG01069.hp1 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.283+148A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101386 | ||||||
| chr14:74101460
|
C | CT | 15 | a0001c0001t0001g0292a0001c0001t0003g0064a0001c0001t0003g0065others(12): Show | 15 | HG00673.hp2 HG01109.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+238dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74101460 | |||||
| chr14:74101460
|
CT | C | 115 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(112): Show | 117 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.283+238delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74101460 | |||||
| chr14:74101520
|
G | A | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+282G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101520 | ||||||
| chr14:74101602
|
G | A | 3 | a0001c0001t0001g0220a0001c0001t0001g0266a0001c0001t0001g0267 | 3 | HG00280.hp2 HG01255.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.283+364G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101602 | ||||||
| chr14:74101607
|
C | T | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283+369C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101607 | ||||||
| chr14:74101650
|
C | T | 1 | a0001c0001t0008g0331 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.283+412C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101650 | ||||||
| chr14:74101661
|
C | T | 3 | a0001c0001t0005g0324a0001c0001t0005g0325a0001c0001t0005g0326 | 3 | HG01123.hp2 HG01261.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.283+423C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101661 | ||||||
| chr14:74101672
|
G | T | 1 | a0001c0001t0002g0177 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.283+434G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101672 | ||||||
| chr14:74101679
|
C | T | 1 | a0001c0001t0003g0019 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.283+441C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101679 | ||||||
| chr14:74101708
|
C | T | 1 | a0001c0002t0032g0285 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.283+470C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101708 | ||||||
| chr14:74101824
|
G | A | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283+586G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74101824 | ||||||
| chr14:74102045
|
G | A | 106 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(103): Show | 107 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.283+807G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74102045 | ||||||
| chr14:74102289
|
C | T | 1 | a0001c0001t0002g0179 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.283+1051C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74102289 | ||||||
| chr14:74102384
|
A | G | 1 | a0001c0001t0011g0225 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.283+1146A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74102384 | ||||||
| chr14:74102858
|
T | C | 2 | a0001c0002t0009g0283a0001c0002t0009g0284 | 2 | HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.283+1620T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74102858 | ||||||
| chr14:74102870
|
T | C | 61 | a0001c0001t0001g0152a0001c0001t0001g0161a0001c0001t0002g0001others(58): Show | 62 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.283+1632T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74102870 | ||||||
| chr14:74102890
|
A | G | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+1652A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74102890 | ||||||
| chr14:74102942
|
C | T | 10 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(7): Show | 10 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.283+1704C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74102942 | ||||||
| chr14:74102942
|
CAT | C | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+1708_283+1709d others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74102942 | |||||
| chr14:74103024
|
C | T | 1 | a0002c0003t0044g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.283+1786C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103024 | ||||||
| chr14:74103166
|
T | C | 12 | a0001c0001t0004g0077a0001c0001t0004g0348a0001c0001t0004g0349others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.283+1928T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103166 | ||||||
| chr14:74103178
|
A | G | 3 | a0001c0001t0011g0204a0001c0001t0014g0203a0001c0001t0029g0202 | 3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.283+1940A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103178 | ||||||
| chr14:74103427
|
A | AT | 6 | a0001c0001t0002g0073a0001c0001t0004g0014a0001c0001t0004g0021others(3): Show | 6 | HG00597.hp2 HG01928.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+2211dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103427 | |||||
| chr14:74103427
|
AT | A | 193 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0161others(190): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.283+2211delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103427 | |||||
| chr14:74103427
|
ATT | A | 20 | a0001c0001t0001g0152a0001c0001t0001g0265a0001c0001t0001g0273others(17): Show | 21 | HG01069.hp2 HG01074.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.283+2210_283+2211d others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103427 | |||||
| chr14:74103427
|
ATTTTTTT others(6): Show |
A | 24 | a0001c0001t0005g0303a0001c0001t0005g0304a0001c0001t0005g0305others(21): Show | 25 | HG00323.hp1 HG00639.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.283+2199_283+2211d others(15): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103427 | |||||
| chr14:74103487
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.283+2249C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103487 | ||||||
| chr14:74103506
|
T | C | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+2268T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103506 | ||||||
| chr14:74103558
|
G | A | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+2320G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103558 | ||||||
| chr14:74103564
|
C | G | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+2326C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103564 | ||||||
| chr14:74103589
|
G | A | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+2351G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103589 | ||||||
| chr14:74103651
|
T | C | 196 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(193): Show | 199 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.283+2413T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103651 | ||||||
| chr14:74103684
|
C | T | 2 | a0001c0001t0002g0166a0001c0001t0006g0167 | 2 | NA18956.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.283+2446C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103684 | ||||||
| chr14:74103733
|
G | GT | 17 | a0001c0001t0001g0228a0001c0001t0001g0256a0001c0001t0001g0257others(14): Show | 17 | HG01099.hp1 HG01123.hp1 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.283+2531dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | |||||
| chr14:74103733
|
G | GTT | 10 | a0001c0001t0001g0214a0001c0001t0001g0218a0001c0001t0001g0258others(7): Show | 10 | HG01175.hp1 HG01192.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.283+2530_283+2531d others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | |||||
| chr14:74103733
|
GT | G | 22 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0220others(19): Show | 22 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+2531delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | |||||
| chr14:74103733
|
GTT | G | 6 | a0001c0001t0001g0205a0001c0001t0001g0232a0001c0001t0001g0234others(3): Show | 6 | HG01081.hp2 HG01884.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+2530_283+2531d others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | |||||
| chr14:74103733
|
GTTT | G | 7 | a0001c0001t0002g0277a0001c0001t0003g0013a0001c0001t0003g0059others(4): Show | 7 | HG00323.hp2 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+2529_283+2531d others(5): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | |||||
| chr14:74103733
|
GTTTTT | G | 20 | a0001c0001t0002g0276a0001c0001t0003g0012a0001c0001t0003g0053others(17): Show | 20 | HG00438.hp2 HG00597.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.283+2527_283+2531d others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | |||||
| chr14:74103733
|
GTTTTTT | G | 85 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(82): Show | 86 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.283+2526_283+2531d others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | |||||
| chr14:74103733
|
GTTTTTTT | G | 19 | a0001c0001t0003g0007a0001c0001t0003g0015a0001c0001t0003g0019others(16): Show | 19 | HG01069.hp1 HG01123.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.283+2525_283+2531d others(9): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | |||||
| chr14:74103733
|
GTTTTTTT others(1): Show |
G | 6 | a0001c0001t0004g0348a0001c0001t0004g0349a0001c0001t0004g0350others(3): Show | 6 | HG01109.hp2 HG02809.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+2524_283+2531d others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | |||||
| chr14:74103733
|
GTTTTTTT others(3): Show |
G | 16 | a0001c0001t0002g0092a0001c0001t0002g0127a0001c0001t0002g0129others(13): Show | 16 | HG01981.hp2 HG02145.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.283+2522_283+2531d others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | |||||
| chr14:74103733
|
GTTTTTTT others(4): Show |
G | 62 | a0001c0001t0001g0152a0001c0001t0001g0161a0001c0001t0001g0191others(59): Show | 63 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.283+2521_283+2531d others(13): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | |||||
| chr14:74103733
|
GTTTTTTT others(5): Show |
G | 35 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0002g0117others(32): Show | 36 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.283+2520_283+2531d others(14): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | |||||
| chr14:74103733
|
GTTTTTTT others(6): Show |
G | 3 | a0001c0001t0001g0213a0001c0001t0007g0105a0001c0001t0007g0121 | 3 | HG02027.hp2 HG02132.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.283+2519_283+2531d others(15): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | |||||
| chr14:74103733
|
GTTTTTTT others(7): Show |
G | 8 | a0001c0001t0001g0217a0001c0001t0001g0226a0001c0001t0001g0241others(5): Show | 8 | NA18947.hp2 NA18962.hp2 NA18984.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+2518_283+2531d others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103733 | |||||
| chr14:74103748
|
T | G | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+2510T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74103748 | ||||||
| chr14:74103896
|
C | CT | 13 | a0001c0001t0004g0077a0001c0001t0004g0348a0001c0001t0004g0349others(10): Show | 13 | HG01109.hp2 HG01169.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.283+2672dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74103896 | |||||
| chr14:74104017
|
G | T | 3 | a0001c0001t0011g0222a0001c0001t0011g0223a0001c0001t0011g0224 | 3 | HG01891.hp1 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.283+2779G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104017 | ||||||
| chr14:74104173
|
A | G | 1 | a0001c0001t0004g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.283+2935A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104173 | ||||||
| chr14:74104220
|
A | G | 1 | a0001c0001t0001g0335 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.283+2982A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104220 | ||||||
| chr14:74104247
|
C | A | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+3009C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104247 | ||||||
| chr14:74104319
|
A | G | 2 | a0001c0001t0012g0086a0001c0001t0025g0087 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.283+3081A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104319 | ||||||
| chr14:74104355
|
C | G | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.283+3117C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104355 | ||||||
| chr14:74104576
|
A | G | 1 | a0001c0001t0004g0020 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.283+3338A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104576 | ||||||
| chr14:74104588
|
T | G | 2 | a0001c0001t0006g0156a0001c0001t0033g0182 | 2 | HG02071.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.283+3350T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104588 | ||||||
| chr14:74104591
|
A | AT | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+3365dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74104591 | |||||
| chr14:74104670
|
A | T | 4 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200others(1): Show | 4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+3432A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104670 | ||||||
| chr14:74104699
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.283+3461G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104699 | ||||||
| chr14:74104813
|
C | T | 348 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(345): Show | 351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.283+3575C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104813 | ||||||
| chr14:74104823
|
G | A | 1 | a0001c0001t0001g0335 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.283+3585G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74104823 | ||||||
| chr14:74105085
|
TATTA | T | 9 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(6): Show | 9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+3848_283+3851d others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74105085 | ||||||
| chr14:74105104
|
G | C | 76 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(73): Show | 76 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.283+3866G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74105104 | ||||||
| chr14:74105161
|
A | G | 2 | a0001c0001t0003g0013a0001c0001t0004g0014 | 2 | HG00597.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.283+3923A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74105161 | ||||||
| chr14:74105171
|
G | A | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+3933G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74105171 | ||||||
| chr14:74105395
|
C | A | 248 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(245): Show | 251 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.283+4157C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74105395 | ||||||
| chr14:74105578
|
AT | A | 205 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(202): Show | 207 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.283+4353delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74105578 | |||||
| chr14:74105578
|
ATT | A | 43 | a0001c0001t0003g0007a0001c0001t0003g0323a0001c0001t0005g0295others(40): Show | 44 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.283+4352_283+4353d others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74105578 | |||||
| chr14:74105657
|
A | G | 264 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(261): Show | 267 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.283+4419A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74105657 | ||||||
| chr14:74105719
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.283+4481G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74105719 | ||||||
| chr14:74105801
|
T | C | 1 | a0001c0001t0002g0158 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.283+4563T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74105801 | ||||||
| chr14:74105984
|
A | C | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+4746A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74105984 | ||||||
| chr14:74106080
|
T | C | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+4842T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74106080 | ||||||
| chr14:74106312
|
C | G | 1 | a0001c0001t0005g0315 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.283+5074C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74106312 | ||||||
| chr14:74106356
|
A | G | 1 | a0001c0001t0003g0017 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.283+5118A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74106356 | ||||||
| chr14:74106725
|
A | C | 1 | a0001c0001t0003g0052 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.283+5487A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74106725 | ||||||
| chr14:74106887
|
G | A | 9 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(6): Show | 9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+5649G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74106887 | ||||||
| chr14:74106981
|
G | A | 2 | a0001c0001t0002g0192a0001c0001t0015g0185 | 2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.283+5743G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74106981 | ||||||
| chr14:74107019
|
A | G | 248 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(245): Show | 251 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.283+5781A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107019 | ||||||
| chr14:74107076
|
T | C | 3 | a0001c0001t0011g0204a0001c0001t0014g0203a0001c0001t0029g0202 | 3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.283+5838T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107076 | ||||||
| chr14:74107267
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.283+6029A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107267 | ||||||
| chr14:74107442
|
C | G | 1 | a0001c0001t0006g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.283+6204C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107442 | ||||||
| chr14:74107452
|
G | A | 1 | a0001c0001t0002g0276 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.283+6214G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107452 | ||||||
| chr14:74107460
|
G | A | 105 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(102): Show | 106 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.283+6222G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107460 | ||||||
| chr14:74107460
|
G | C | 1 | a0001c0001t0002g0148 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.283+6222G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107460 | ||||||
| chr14:74107534
|
T | A | 7 | a0001c0001t0011g0204a0001c0001t0014g0198a0001c0001t0014g0199others(4): Show | 7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+6296T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107534 | ||||||
| chr14:74107538
|
G | A | 1 | a0001c0001t0017g0322 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.283+6300G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107538 | ||||||
| chr14:74107583
|
G | A | 3 | a0001c0001t0011g0204a0001c0001t0014g0203a0001c0001t0029g0202 | 3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.283+6345G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107583 | ||||||
| chr14:74107682
|
T | C | 3 | a0001c0001t0003g0023a0001c0001t0003g0053a0001c0001t0003g0054 | 3 | HG00423.hp2 HG02165.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.283+6444T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107682 | ||||||
| chr14:74107702
|
A | C | 1 | a0001c0001t0001g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.283+6464A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107702 | ||||||
| chr14:74107712
|
G | A | 7 | a0001c0001t0011g0204a0001c0001t0014g0198a0001c0001t0014g0199others(4): Show | 7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+6474G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107712 | ||||||
| chr14:74107858
|
G | T | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+6620G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74107858 | ||||||
| chr14:74108062
|
C | A | 5 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0251others(2): Show | 5 | HG00639.hp1 HG01261.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+6824C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74108062 | ||||||
| chr14:74108202
|
GCTTT | G | 4 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0263others(1): Show | 4 | HG00099.hp1 HG00642.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+6973_283+6976d others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74108202 | |||||
| chr14:74108262
|
A | G | 1 | a0001c0001t0005g0315 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.283+7024A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74108262 | ||||||
| chr14:74108349
|
A | T | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+7111A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74108349 | ||||||
| chr14:74108368
|
C | T | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.283+7130C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74108368 | ||||||
| chr14:74108554
|
T | C | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283+7316T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74108554 | ||||||
| chr14:74108610
|
A | G | 1 | a0001c0001t0001g0335 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.283+7372A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74108610 | ||||||
| chr14:74108672
|
T | C | 3 | a0001c0001t0011g0204a0001c0001t0014g0203a0001c0001t0029g0202 | 3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.283+7434T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74108672 | ||||||
| chr14:74109004
|
G | A | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.283+7766G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74109004 | ||||||
| chr14:74109017
|
A | G | 1 | a0001c0001t0006g0169 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.283+7779A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74109017 | ||||||
| chr14:74109070
|
T | C | 4 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200others(1): Show | 4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+7832T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74109070 | ||||||
| chr14:74109345
|
A | G | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+8107A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74109345 | ||||||
| chr14:74109414
|
C | T | 1 | a0001c0001t0029g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.283+8176C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74109414 | ||||||
| chr14:74109488
|
C | T | 1 | a0001c0001t0040g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.283+8250C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74109488 | ||||||
| chr14:74109694
|
T | C | 1 | a0001c0001t0036g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.283+8456T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74109694 | ||||||
| chr14:74109720
|
T | C | 3 | a0001c0001t0011g0204a0001c0001t0014g0203a0001c0001t0029g0202 | 3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.283+8482T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74109720 | ||||||
| chr14:74110041
|
A | G | 1 | a0001c0001t0001g0335 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.283+8803A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110041 | ||||||
| chr14:74110110
|
T | C | 83 | a0001c0001t0001g0205a0001c0001t0001g0231a0001c0001t0001g0234others(80): Show | 83 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.283+8872T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110110 | ||||||
| chr14:74110299
|
A | T | 1 | a0001c0001t0017g0314 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.283+9061A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110299 | ||||||
| chr14:74110363
|
A | C | 1 | a0001c0001t0002g0189 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.283+9125A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110363 | ||||||
| chr14:74110610
|
C | T | 3 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0034g0119 | 3 | HG01074.hp2 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.283+9372C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110610 | ||||||
| chr14:74110884
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.283+9646T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110884 | ||||||
| chr14:74110897
|
T | C | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+9659T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110897 | ||||||
| chr14:74110898
|
G | A | 10 | a0001c0001t0002g0092a0001c0001t0011g0204a0001c0001t0014g0198others(7): Show | 10 | HG02145.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+9660G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110898 | ||||||
| chr14:74110920
|
C | T | 34 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0002g0117others(31): Show | 34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.283+9682C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110920 | ||||||
| chr14:74110923
|
G | A | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+9685G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110923 | ||||||
| chr14:74110938
|
C | A | 1 | a0001c0001t0002g0276 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.283+9700C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110938 | ||||||
| chr14:74110994
|
C | T | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.283+9756C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74110994 | ||||||
| chr14:74111058
|
A | G | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+9820A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111058 | ||||||
| chr14:74111131
|
C | T | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+9893C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111131 | ||||||
| chr14:74111408
|
C | A | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+10170C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111408 | ||||||
| chr14:74111414
|
G | A | 3 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200 | 3 | HG02809.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.283+10176G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111414 | ||||||
| chr14:74111414
|
G | C | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+10176G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111414 | ||||||
| chr14:74111444
|
A | G | 4 | a0001c0001t0013g0094a0001c0001t0013g0120a0001c0001t0013g0125others(1): Show | 4 | HG02602.hp2 HG03688.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+10206A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111444 | ||||||
| chr14:74111455
|
AT | A | 117 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(114): Show | 119 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.283+10232delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74111455 | |||||
| chr14:74111455
|
ATT | A | 131 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(128): Show | 132 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.283+10231_283+1023 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74111455 | |||||
| chr14:74111508
|
C | T | 1 | a0001c0001t0003g0007 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.283+10270C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111508 | ||||||
| chr14:74111535
|
C | T | 1 | a0001c0001t0016g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.283+10297C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111535 | ||||||
| chr14:74111594
|
G | A | 1 | a0001c0001t0029g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.283+10356G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111594 | ||||||
| chr14:74111606
|
G | GTATT | 31 | a0001c0001t0001g0218a0001c0001t0001g0227a0001c0001t0001g0241others(28): Show | 31 | HG00438.hp2 HG00597.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.283+10410_283+1041 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74111606 | |||||
| chr14:74111606
|
G | GTATTTAT others(1): Show |
51 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0002g0276others(48): Show | 51 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.283+10406_283+1041 others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74111606 | |||||
| chr14:74111606
|
G | GTATTTAT others(5): Show |
4 | a0001c0001t0003g0015a0001c0001t0003g0074a0001c0001t0004g0066others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+10402_283+1041 others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74111606 | |||||
| chr14:74111606
|
GTATT | G | 54 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(51): Show | 55 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.283+10410_283+1041 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74111606 | |||||
| chr14:74111606
|
GTATTTAT others(1): Show |
G | 92 | a0001c0001t0001g0161a0001c0001t0002g0093a0001c0001t0002g0127others(89): Show | 93 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.283+10406_283+1041 others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74111606 | |||||
| chr14:74111606
|
GTATTTAT others(5): Show |
G | 12 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(9): Show | 12 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.283+10402_283+1041 others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74111606 | |||||
| chr14:74111664
|
A | G | 3 | a0001c0001t0003g0015a0001c0001t0004g0066a0001c0001t0004g0067 | 3 | HG01069.hp1 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.283+10426A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111664 | ||||||
| chr14:74111707
|
C | T | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+10469C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111707 | ||||||
| chr14:74111796
|
T | C | 3 | a0001c0001t0002g0001a0001c0001t0002g0170a0001c0001t0006g0178 | 4 | NA18963.hp2 NA18971.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+10558T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111796 | ||||||
| chr14:74111867
|
TTTTTTTT others(1): Show |
T | 34 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0002g0117others(31): Show | 34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.283+10645_283+1065 others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74111867 | |||||
| chr14:74111914
|
C | T | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+10676C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111914 | ||||||
| chr14:74111938
|
T | C | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+10700T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111938 | ||||||
| chr14:74111941
|
C | T | 9 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(6): Show | 9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+10703C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111941 | ||||||
| chr14:74111957
|
C | T | 3 | a0001c0001t0003g0023a0001c0001t0003g0053a0001c0001t0003g0054 | 3 | HG00423.hp2 HG02165.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.283+10719C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111957 | ||||||
| chr14:74111974
|
T | C | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+10736T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74111974 | ||||||
| chr14:74112127
|
A | T | 1 | a0001c0001t0007g0115 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.283+10889A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74112127 | ||||||
| chr14:74112266
|
A | G | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+11028A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74112266 | ||||||
| chr14:74112290
|
T | A | 1 | a0001c0001t0040g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.283+11052T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74112290 | ||||||
| chr14:74112333
|
G | A | 1 | a0001c0001t0029g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.283+11095G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74112333 | ||||||
| chr14:74112376
|
C | T | 8 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(5): Show | 9 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.283+11138C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74112376 | ||||||
| chr14:74112621
|
G | A | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+11383G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74112621 | ||||||
| chr14:74112635
|
C | G | 1 | a0001c0001t0003g0038 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.283+11397C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74112635 | ||||||
| chr14:74112766
|
T | C | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+11528T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74112766 | ||||||
| chr14:74112919
|
A | G | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+11681A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74112919 | ||||||
| chr14:74113025
|
A | AGAG | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+11788_283+1179 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74113025 | |||||
| chr14:74113264
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.283+12026C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74113264 | ||||||
| chr14:74113403
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.283+12165A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74113403 | ||||||
| chr14:74113457
|
G | A | 2 | a0001c0001t0002g0092a0001c0001t0015g0090 | 2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+12219G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74113457 | ||||||
| chr14:74113694
|
T | A | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+12456T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74113694 | ||||||
| chr14:74113868
|
G | A | 73 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(70): Show | 73 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.283+12630G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74113868 | ||||||
| chr14:74113970
|
C | CT | 40 | a0001c0001t0001g0213a0001c0001t0001g0237a0001c0001t0001g0255others(37): Show | 40 | HG00438.hp1 HG00438.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.283+12742dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74113970 | |||||
| chr14:74114174
|
T | TTG | 8 | a0001c0001t0012g0086a0001c0001t0025g0087a0001c0002t0009g0278others(5): Show | 8 | HG01243.hp1 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.283+12936_283+1293 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74114174 | ||||||
| chr14:74114174
|
T | TTGTGTG | 3 | a0001c0001t0011g0204a0001c0001t0014g0203a0001c0001t0029g0202 | 3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.283+12936_283+1293 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74114174 | ||||||
| chr14:74114174
|
TAG | T | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+12937_283+1293 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74114174 | ||||||
| chr14:74114175
|
A | AGT | 34 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0341others(31): Show | 34 | HG00423.hp1 HG00642.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.283+12974_283+1297 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | |||||
| chr14:74114175
|
A | AGTGT | 35 | a0001c0001t0001g0205a0001c0001t0001g0231a0001c0001t0001g0236others(32): Show | 36 | HG00438.hp1 HG01074.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.283+12972_283+1297 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | |||||
| chr14:74114175
|
A | AGTGTGT | 31 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0213others(28): Show | 31 | HG00741.hp2 HG01175.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.283+12970_283+1297 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | |||||
| chr14:74114175
|
A | AGTGTGTG others(1): Show |
16 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0007others(13): Show | 16 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.283+12968_283+1297 others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | |||||
| chr14:74114175
|
A | AGTGTGTG others(3): Show |
41 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0003g0017others(38): Show | 41 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.283+12966_283+1297 others(14): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | |||||
| chr14:74114175
|
A | AGTGTGTG others(5): Show |
10 | a0001c0001t0003g0012a0001c0001t0003g0033a0001c0001t0003g0034others(7): Show | 10 | HG00408.hp2 HG00673.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+12964_283+1297 others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | |||||
| chr14:74114175
|
A | AGTGTGTG others(7): Show |
2 | a0001c0001t0003g0068a0001c0001t0003g0088 | 2 | HG03017.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.283+12962_283+1297 others(18): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | |||||
| chr14:74114175
|
A | AGTGTGTG others(9): Show |
2 | a0001c0001t0001g0152a0001c0001t0016g0051 | 2 | HG01069.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.283+12960_283+1297 others(20): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | |||||
| chr14:74114175
|
A | T | 13 | a0001c0001t0011g0204a0001c0001t0012g0086a0001c0001t0014g0203others(10): Show | 13 | HG01243.hp1 HG02258.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.283+12937A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74114175 | ||||||
| chr14:74114175
|
AGT | A | 49 | a0001c0001t0001g0233a0001c0001t0001g0255a0001c0001t0001g0339others(46): Show | 50 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.283+12974_283+1297 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | |||||
| chr14:74114175
|
AGTGT | A | 42 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217others(39): Show | 42 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.283+12972_283+1297 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | |||||
| chr14:74114175
|
AGTGTGT | A | 6 | a0001c0001t0001g0286a0001c0001t0001g0290a0001c0001t0001g0291others(3): Show | 6 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+12970_283+1297 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114175 | |||||
| chr14:74114492
|
G | A | 1 | a0001c0001t0042g0302 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.283+13254G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74114492 | ||||||
| chr14:74114510
|
C | A | 1 | a0001c0001t0019g0141 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.283+13272C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74114510 | ||||||
| chr14:74114511
|
G | A | 2 | a0001c0001t0003g0053a0001c0001t0006g0156 | 2 | HG02071.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.283+13273G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74114511 | ||||||
| chr14:74114534
|
AC | A | 5 | a0001c0001t0011g0221a0001c0001t0011g0222a0001c0001t0011g0223others(2): Show | 5 | HG01891.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+13298delC | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114534 | |||||
| chr14:74114593
|
T | TAAC | 6 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(3): Show | 6 | HG02258.hp2 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+13373_283+1337 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74114593 | |||||
| chr14:74114603
|
A | C | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+13365A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74114603 | ||||||
| chr14:74114818
|
G | A | 269 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(266): Show | 272 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.283+13580G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74114818 | ||||||
| chr14:74115010
|
A | C | 1 | a0001c0001t0014g0198 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.283+13772A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74115010 | ||||||
| chr14:74115146
|
A | G | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+13908A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74115146 | ||||||
| chr14:74115451
|
A | T | 34 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0002g0117others(31): Show | 34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.283+14213A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74115451 | ||||||
| chr14:74115459
|
G | C | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+14221G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74115459 | ||||||
| chr14:74115476
|
CTG | C | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+14242_283+1424 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74115476 | |||||
| chr14:74115666
|
A | G | 7 | a0001c0001t0005g0295a0001c0001t0005g0300a0001c0001t0005g0301others(4): Show | 7 | NA18967.hp1 NA19003.hp1 NA19010.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+14428A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74115666 | ||||||
| chr14:74115693
|
A | G | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.283+14455A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74115693 | ||||||
| chr14:74115803
|
C | T | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+14565C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74115803 | ||||||
| chr14:74115826
|
C | T | 1 | a0001c0001t0004g0026 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.283+14588C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74115826 | ||||||
| chr14:74116004
|
G | A | 264 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(261): Show | 267 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.283+14766G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74116004 | ||||||
| chr14:74116018
|
A | T | 3 | a0001c0001t0001g0213a0001c0001t0001g0272a0001c0001t0018g0271 | 3 | HG02027.hp2 NA18944.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.283+14780A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74116018 | ||||||
| chr14:74116092
|
T | C | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+14854T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74116092 | ||||||
| chr14:74116192
|
A | G | 7 | a0001c0001t0011g0204a0001c0001t0014g0198a0001c0001t0014g0199others(4): Show | 7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+14954A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74116192 | ||||||
| chr14:74116302
|
CAAAAAAT | C | 26 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0007g0004others(23): Show | 26 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.283+15078_283+1508 others(11): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74116302 | |||||
| chr14:74116309
|
TAAAAAA | T | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.283+15072_283+1507 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74116309 | ||||||
| chr14:74116435
|
G | C | 2 | a0001c0001t0011g0223a0001c0001t0011g0224 | 2 | HG01891.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.283+15197G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74116435 | ||||||
| chr14:74116774
|
A | G | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+15536A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74116774 | ||||||
| chr14:74116790
|
G | A | 3 | a0001c0001t0011g0204a0001c0001t0014g0203a0001c0001t0029g0202 | 3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.283+15552G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74116790 | ||||||
| chr14:74116830
|
G | GT | 7 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289others(4): Show | 7 | HG02559.hp1 HG02738.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+15607dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74116830 | |||||
| chr14:74116835
|
T | G | 1 | a0001c0001t0001g0161 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.283+15597T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74116835 | ||||||
| chr14:74116846
|
C | A | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+15608C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74116846 | ||||||
| chr14:74117128
|
T | C | 1 | a0001c0001t0006g0167 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.283+15890T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74117128 | ||||||
| chr14:74117469
|
A | AT | 13 | a0001c0001t0002g0177a0001c0001t0008g0296a0001c0001t0013g0120others(10): Show | 14 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+16234dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74117469 | |||||
| chr14:74117473
|
C | T | 348 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(345): Show | 351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.283+16235C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74117473 | ||||||
| chr14:74117491
|
GC | G | 12 | a0001c0001t0004g0077a0001c0001t0004g0348a0001c0001t0004g0349others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.283+16254delC | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74117491 | ||||||
| chr14:74117789
|
A | G | 1 | a0001c0001t0001g0338 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.283+16551A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74117789 | ||||||
| chr14:74117855
|
A | C | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+16617A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74117855 | ||||||
| chr14:74117868
|
A | G | 1 | a0001c0001t0001g0289 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.283+16630A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74117868 | ||||||
| chr14:74117927
|
CA | C | 61 | a0001c0001t0001g0152a0001c0001t0001g0161a0001c0001t0002g0001others(58): Show | 62 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.283+16697delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74117927 | |||||
| chr14:74118055
|
C | G | 248 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(245): Show | 251 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.283+16817C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74118055 | ||||||
| chr14:74118120
|
G | A | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+16882G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74118120 | ||||||
| chr14:74118225
|
C | T | 1 | a0001c0001t0007g0114 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.283+16987C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74118225 | ||||||
| chr14:74118234
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.283+16996C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74118234 | ||||||
| chr14:74118399
|
G | A | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+17161G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74118399 | ||||||
| chr14:74118614
|
A | G | 1 | a0001c0001t0001g0342 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.283+17376A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74118614 | ||||||
| chr14:74118874
|
C | T | 1 | a0002c0003t0044g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.283+17636C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74118874 | ||||||
| chr14:74118949
|
A | ACTT | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+17712_283+1771 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74118949 | |||||
| chr14:74119160
|
C | CT | 82 | a0001c0001t0001g0226a0001c0001t0001g0239a0001c0001t0001g0342others(79): Show | 82 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.283+17941dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74119160 | |||||
| chr14:74119160
|
CT | C | 167 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(164): Show | 170 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.283+17941delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74119160 | |||||
| chr14:74119164
|
T | C | 7 | a0001c0001t0001g0205a0001c0001t0001g0231a0001c0001t0001g0234others(4): Show | 7 | HG01081.hp2 HG01884.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+17926T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119164 | ||||||
| chr14:74119247
|
C | T | 1 | a0001c0001t0004g0044 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.283+18009C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119247 | ||||||
| chr14:74119286
|
C | T | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+18048C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119286 | ||||||
| chr14:74119307
|
GC | G | 40 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(37): Show | 41 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.283+18076delC | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74119307 | |||||
| chr14:74119314
|
C | G | 1 | a0001c0001t0025g0087 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.283+18076C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119314 | ||||||
| chr14:74119329
|
A | AT | 5 | a0001c0001t0011g0221a0001c0001t0011g0222a0001c0001t0011g0223others(2): Show | 5 | HG01891.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+18099dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74119329 | |||||
| chr14:74119355
|
A | G | 1 | a0001c0001t0005g0320 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.283+18117A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119355 | ||||||
| chr14:74119374
|
T | C | 1 | a0001c0001t0040g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.283+18136T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119374 | ||||||
| chr14:74119407
|
G | T | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+18169G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119407 | ||||||
| chr14:74119573
|
A | G | 14 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(11): Show | 14 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+18335A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119573 | ||||||
| chr14:74119665
|
G | A | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+18427G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119665 | ||||||
| chr14:74119836
|
C | CT | 20 | a0001c0001t0001g0239a0001c0001t0001g0335a0001c0001t0002g0092others(17): Show | 20 | HG01109.hp2 HG01243.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.283+18615dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74119836 | |||||
| chr14:74119836
|
CT | C | 6 | a0001c0001t0001g0242a0001c0001t0002g0175a0001c0001t0003g0046others(3): Show | 6 | HG01167.hp1 HG01168.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+18615delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74119836 | |||||
| chr14:74119969
|
G | A | 4 | a0001c0001t0004g0348a0001c0001t0004g0349a0001c0001t0004g0350others(1): Show | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+18731G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119969 | ||||||
| chr14:74119984
|
C | A | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+18746C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119984 | ||||||
| chr14:74119984
|
C | T | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.283+18746C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74119984 | ||||||
| chr14:74120307
|
G | C | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+19069G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74120307 | ||||||
| chr14:74120354
|
C | T | 4 | a0001c0001t0004g0348a0001c0001t0004g0349a0001c0001t0004g0350others(1): Show | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+19116C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74120354 | ||||||
| chr14:74120376
|
C | T | 269 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(266): Show | 272 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.283+19138C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74120376 | ||||||
| chr14:74120472
|
AGGCCAGG others(1): Show |
A | 11 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(8): Show | 11 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.283+19236_283+1924 others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74120472 | |||||
| chr14:74120481
|
G | T | 4 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200others(1): Show | 4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+19243G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74120481 | ||||||
| chr14:74120612
|
G | A | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+19374G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74120612 | ||||||
| chr14:74120687
|
G | T | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+19449G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74120687 | ||||||
| chr14:74120703
|
C | T | 22 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0022others(19): Show | 22 | HG00438.hp2 HG00544.hp2 NA18940.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+19465C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74120703 | ||||||
| chr14:74120754
|
C | CA | 81 | a0001c0001t0001g0248a0001c0001t0002g0027a0001c0001t0002g0073others(78): Show | 81 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.283+19534dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74120754 | |||||
| chr14:74120781
|
G | A | 3 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289 | 3 | HG02559.hp1 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.283+19543G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74120781 | ||||||
| chr14:74120795
|
G | A | 2 | a0001c0001t0012g0086a0001c0001t0025g0087 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.283+19557G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74120795 | ||||||
| chr14:74120913
|
G | GA | 14 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(11): Show | 14 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+19685dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74120913 | |||||
| chr14:74121403
|
A | G | 34 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0002g0117others(31): Show | 34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.283+20165A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121403 | ||||||
| chr14:74121445
|
T | C | 10 | a0001c0001t0002g0092a0001c0001t0011g0204a0001c0001t0014g0198others(7): Show | 10 | HG02145.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+20207T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121445 | ||||||
| chr14:74121470
|
C | T | 248 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(245): Show | 251 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.283+20232C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121470 | ||||||
| chr14:74121530
|
G | A | 5 | a0001c0001t0005g0303a0001c0001t0005g0304a0001c0001t0005g0305others(2): Show | 5 | HG02129.hp2 HG02602.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+20292G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121530 | ||||||
| chr14:74121575
|
G | A | 1 | a0001c0001t0002g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.283+20337G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121575 | ||||||
| chr14:74121653
|
T | G | 248 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(245): Show | 251 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.283+20415T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121653 | ||||||
| chr14:74121725
|
CT | C | 238 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(235): Show | 241 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.283+20503delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74121725 | |||||
| chr14:74121725
|
CTT | C | 8 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(5): Show | 8 | HG02258.hp1 HG02572.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+20502_283+2050 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74121725 | |||||
| chr14:74121747
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.283+20509G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121747 | ||||||
| chr14:74121805
|
C | T | 2 | a0001c0002t0009g0283a0001c0002t0009g0284 | 2 | HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.283+20567C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121805 | ||||||
| chr14:74121816
|
C | T | 1 | a0001c0001t0001g0339 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283+20578C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121816 | ||||||
| chr14:74121851
|
A | G | 269 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(266): Show | 272 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.283+20613A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121851 | ||||||
| chr14:74121869
|
G | A | 63 | a0001c0001t0001g0152a0001c0001t0001g0161a0001c0001t0002g0001others(60): Show | 65 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.283+20631G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121869 | ||||||
| chr14:74121895
|
G | A | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+20657G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74121895 | ||||||
| chr14:74122003
|
CTCATAT | C | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+20768_283+2077 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74122003 | |||||
| chr14:74122015
|
T | TGAG | 207 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(204): Show | 209 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.283+20778_283+2078 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74122015 | |||||
| chr14:74122115
|
C | G | 1 | a0001c0001t0001g0259 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.283+20877C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74122115 | ||||||
| chr14:74122153
|
C | T | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+20915C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74122153 | ||||||
| chr14:74122284
|
C | T | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.283+21046C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74122284 | ||||||
| chr14:74122299
|
C | T | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+21061C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74122299 | ||||||
| chr14:74122537
|
G | C | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0006g0194 | 3 | HG01496.hp1 HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.283+21299G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74122537 | ||||||
| chr14:74122741
|
C | G | 106 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(103): Show | 107 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.283+21503C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74122741 | ||||||
| chr14:74122742
|
T | C | 1 | a0001c0001t0007g0004 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.283+21504T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74122742 | ||||||
| chr14:74122877
|
A | G | 1 | a0001c0001t0007g0122 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.283+21639A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74122877 | ||||||
| chr14:74122884
|
CAAACAA | C | 108 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(105): Show | 110 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.283+21663_283+2166 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74122884 | |||||
| chr14:74122901
|
A | AAAAAC | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+21664_283+2166 others(9): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74122901 | |||||
| chr14:74122943
|
C | T | 130 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(127): Show | 132 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.283+21705C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74122943 | ||||||
| chr14:74122999
|
G | A | 1 | a0001c0001t0002g0136 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.283+21761G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74122999 | ||||||
| chr14:74123100
|
T | A | 2 | a0001c0002t0009g0283a0001c0002t0009g0284 | 2 | HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.283+21862T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123100 | ||||||
| chr14:74123328
|
A | C | 1 | a0001c0001t0001g0259 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.283+22090A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123328 | ||||||
| chr14:74123374
|
C | T | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283+22136C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123374 | ||||||
| chr14:74123527
|
T | C | 61 | a0001c0001t0001g0152a0001c0001t0001g0161a0001c0001t0002g0001others(58): Show | 62 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.283+22289T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123527 | ||||||
| chr14:74123664
|
C | T | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+22426C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123664 | ||||||
| chr14:74123668
|
G | A | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+22430G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123668 | ||||||
| chr14:74123672
|
T | C | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+22434T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123672 | ||||||
| chr14:74123680
|
A | G | 2 | a0001c0001t0004g0206a0001c0001t0012g0209 | 2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.283+22442A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123680 | ||||||
| chr14:74123782
|
G | C | 8 | a0001c0001t0004g0077a0001c0001t0012g0078a0001c0001t0012g0081others(5): Show | 8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+22544G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123782 | ||||||
| chr14:74123789
|
G | T | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+22551G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123789 | ||||||
| chr14:74123843
|
T | C | 1 | a0001c0001t0001g0342 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.283+22605T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123843 | ||||||
| chr14:74123890
|
A | G | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+22652A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123890 | ||||||
| chr14:74123972
|
G | T | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283+22734G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74123972 | ||||||
| chr14:74124065
|
A | T | 4 | a0001c0001t0011g0221a0001c0001t0011g0222a0001c0001t0011g0223others(1): Show | 4 | HG01891.hp1 HG02717.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+22827A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74124065 | ||||||
| chr14:74124098
|
A | G | 4 | a0001c0001t0004g0348a0001c0001t0004g0349a0001c0001t0004g0350others(1): Show | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+22860A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74124098 | ||||||
| chr14:74124119
|
G | T | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+22881G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74124119 | ||||||
| chr14:74124292
|
C | G | 1 | a0001c0001t0013g0111 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.283+23054C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74124292 | ||||||
| chr14:74124517
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.283+23279T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74124517 | ||||||
| chr14:74124538
|
T | C | 248 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(245): Show | 251 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.283+23300T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74124538 | ||||||
| chr14:74124637
|
C | G | 12 | a0001c0001t0004g0077a0001c0001t0004g0348a0001c0001t0004g0349others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.283+23399C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74124637 | ||||||
| chr14:74124684
|
C | T | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+23446C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74124684 | ||||||
| chr14:74124810
|
C | CA | 8 | a0001c0001t0001g0227a0001c0001t0001g0231a0001c0001t0001g0346others(5): Show | 8 | HG00438.hp2 HG01123.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.283+23595dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74124810 | |||||
| chr14:74124810
|
C | CAAAA | 11 | a0001c0001t0002g0146a0001c0001t0002g0177a0001c0001t0006g0165others(8): Show | 11 | HG00673.hp1 HG02145.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.283+23592_283+2359 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74124810 | |||||
| chr14:74124810
|
C | CAAAAA | 53 | a0001c0001t0001g0152a0001c0001t0001g0161a0001c0001t0001g0191others(50): Show | 54 | HG00408.hp1 HG00642.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.283+23591_283+2359 others(9): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74124810 | |||||
| chr14:74124810
|
C | CAAAAAA | 29 | a0001c0001t0002g0118a0001c0001t0002g0127a0001c0001t0002g0131others(26): Show | 30 | HG00099.hp2 HG00423.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.283+23590_283+2359 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74124810 | |||||
| chr14:74124810
|
C | CAAAAAAA | 16 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0002g0117others(13): Show | 16 | HG00438.hp1 HG00544.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.283+23589_283+2359 others(11): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74124810 | |||||
| chr14:74124810
|
CA | C | 57 | a0001c0001t0001g0248a0001c0001t0002g0276a0001c0001t0002g0277others(54): Show | 58 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.283+23595delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74124810 | |||||
| chr14:74125321
|
A | G | 77 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(74): Show | 77 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.283+24083A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74125321 | ||||||
| chr14:74125515
|
C | A | 264 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(261): Show | 267 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.283+24277C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74125515 | ||||||
| chr14:74125575
|
A | G | 106 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(103): Show | 107 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.283+24337A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74125575 | ||||||
| chr14:74125601
|
C | G | 1 | a0001c0001t0005g0297 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.283+24363C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74125601 | ||||||
| chr14:74125674
|
G | A | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.283+24436G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74125674 | ||||||
| chr14:74125729
|
T | C | 1 | a0001c0001t0003g0064 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.283+24491T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74125729 | ||||||
| chr14:74125804
|
C | T | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283+24566C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74125804 | ||||||
| chr14:74125861
|
G | A | 3 | a0001c0001t0003g0008a0001c0001t0003g0018a0001c0001t0004g0009 | 3 | HG00597.hp1 HG02083.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.283+24623G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74125861 | ||||||
| chr14:74126036
|
T | TA | 167 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0191others(164): Show | 169 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.283+24812dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74126036 | |||||
| chr14:74126047
|
AAAAG | A | 57 | a0001c0001t0001g0152a0001c0001t0002g0001a0001c0001t0002g0127others(54): Show | 58 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.283+24813_283+2481 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74126047 | |||||
| chr14:74126050
|
AGAAAT | A | 4 | a0001c0001t0001g0161a0001c0001t0002g0093a0001c0001t0002g0157others(1): Show | 4 | HG01516.hp1 HG02071.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+24815_283+2481 others(9): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74126050 | |||||
| chr14:74126055
|
T | A | 57 | a0001c0001t0001g0152a0001c0001t0002g0001a0001c0001t0002g0127others(54): Show | 58 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.283+24817T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74126055 | ||||||
| chr14:74126137
|
T | C | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+24899T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74126137 | ||||||
| chr14:74126227
|
C | G | 12 | a0001c0001t0002g0092a0001c0001t0011g0204a0001c0001t0014g0198others(9): Show | 13 | HG02145.hp2 HG02451.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.283+24989C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74126227 | ||||||
| chr14:74126240
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.283+25002G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74126240 | ||||||
| chr14:74126303
|
A | G | 2 | a0001c0001t0003g0054a0001c0001t0042g0302 | 2 | HG01167.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.283+25065A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74126303 | ||||||
| chr14:74126338
|
G | C | 7 | a0001c0001t0008g0296a0001c0001t0008g0308a0001c0001t0008g0309others(4): Show | 7 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+25100G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74126338 | ||||||
| chr14:74126422
|
T | C | 29 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0007g0004others(26): Show | 29 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.283+25184T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74126422 | ||||||
| chr14:74126470
|
G | A | 1 | a0001c0001t0007g0098 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.283+25232G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74126470 | ||||||
| chr14:74127025
|
T | C | 11 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(8): Show | 11 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.283+25787T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74127025 | ||||||
| chr14:74127307
|
G | A | 8 | a0001c0001t0004g0077a0001c0001t0012g0078a0001c0001t0012g0081others(5): Show | 8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+26069G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74127307 | ||||||
| chr14:74127556
|
C | T | 10 | a0001c0001t0002g0092a0001c0001t0011g0204a0001c0001t0014g0198others(7): Show | 10 | HG02145.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+26318C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74127556 | ||||||
| chr14:74127627
|
A | C | 1 | a0001c0001t0007g0004 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.283+26389A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74127627 | ||||||
| chr14:74127659
|
G | A | 2 | a0001c0001t0003g0013a0001c0001t0004g0014 | 2 | HG00597.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.283+26421G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74127659 | ||||||
| chr14:74127690
|
G | A | 1 | a0001c0001t0043g0249 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.283+26452G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74127690 | ||||||
| chr14:74127743
|
A | T | 1 | a0001c0001t0040g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.283+26505A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74127743 | ||||||
| chr14:74127800
|
T | C | 269 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(266): Show | 272 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.283+26562T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74127800 | ||||||
| chr14:74127885
|
G | T | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+26647G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74127885 | ||||||
| chr14:74127978
|
A | C | 1 | a0001c0001t0002g0276 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.283+26740A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74127978 | ||||||
| chr14:74128016
|
G | A | 1 | a0001c0001t0004g0207 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.283+26778G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74128016 | ||||||
| chr14:74128276
|
C | G | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+27038C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74128276 | ||||||
| chr14:74128707
|
T | C | 247 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(244): Show | 250 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.283+27469T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74128707 | ||||||
| chr14:74128715
|
G | A | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+27477G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74128715 | ||||||
| chr14:74128817
|
G | A | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.283+27579G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74128817 | ||||||
| chr14:74128848
|
G | T | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+27610G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74128848 | ||||||
| chr14:74128869
|
G | C | 3 | a0001c0001t0007g0107a0001c0001t0010g0096a0001c0001t0010g0106 | 3 | HG04115.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.283+27631G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74128869 | ||||||
| chr14:74129042
|
G | T | 3 | a0001c0001t0008g0332a0001c0001t0008g0333a0001c0001t0008g0334 | 3 | HG00323.hp1 HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.283+27804G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74129042 | ||||||
| chr14:74129281
|
A | G | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+28043A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74129281 | ||||||
| chr14:74129344
|
G | T | 4 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200others(1): Show | 4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+28106G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74129344 | ||||||
| chr14:74129412
|
G | A | 45 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0191others(42): Show | 45 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.283+28174G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74129412 | ||||||
| chr14:74129497
|
G | A | 1 | a0001c0001t0011g0222 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.283+28259G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74129497 | ||||||
| chr14:74129731
|
A | C | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+28493A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74129731 | ||||||
| chr14:74130027
|
C | T | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.283+28789C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130027 | ||||||
| chr14:74130128
|
C | G | 76 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(73): Show | 76 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.283+28890C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130128 | ||||||
| chr14:74130238
|
A | G | 1 | a0001c0001t0007g0109 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.283+29000A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130238 | ||||||
| chr14:74130259
|
A | G | 4 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200others(1): Show | 4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+29021A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130259 | ||||||
| chr14:74130270
|
A | ATTTTTTG others(17): Show |
44 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(41): Show | 44 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.283+29039_283+2904 others(28): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130270 | |||||
| chr14:74130270
|
A | ATTTTTTG others(18): Show |
2 | a0001c0001t0003g0074a0001c0001t0004g0036 | 2 | HG02027.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.283+29039_283+2904 others(29): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130270 | |||||
| chr14:74130270
|
A | ATTTTTTG others(18): Show |
1 | a0001c0001t0004g0028 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.283+29039_283+2904 others(29): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130270 | |||||
| chr14:74130277
|
G | GGTTTTTT others(16): Show |
1 | a0001c0001t0025g0087 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.283+29050_283+2905 others(27): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130277 | |||||
| chr14:74130277
|
G | GTTTTTTT others(4): Show |
1 | a0001c0001t0004g0014 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.283+29039_283+2904 others(15): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130277 | ||||||
| chr14:74130277
|
G | GTTTTTTT others(16): Show |
21 | a0001c0001t0003g0008a0001c0001t0003g0012a0001c0001t0003g0013others(18): Show | 21 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.283+29039_283+2904 others(27): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130277 | ||||||
| chr14:74130277
|
G | GTTTTTTT others(18): Show |
4 | a0001c0001t0003g0019a0001c0001t0004g0044a0001c0001t0004g0057others(1): Show | 4 | HG00438.hp2 HG01928.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+29039_283+2904 others(29): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130277 | ||||||
| chr14:74130277
|
G | GTTTTTTT others(17): Show |
1 | a0001c0001t0004g0070 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.283+29039_283+2904 others(28): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130277 | ||||||
| chr14:74130278
|
G | GTGTTTTT others(12): Show |
1 | a0001c0001t0024g0230 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.283+29041_283+2904 others(23): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTGTTTTT others(13): Show |
1 | a0001c0001t0024g0229 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.283+29041_283+2904 others(24): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTTTGTTT others(7): Show |
1 | a0002c0003t0018g0201 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.283+29043_283+2904 others(18): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTTTGTTT others(8): Show |
5 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200others(2): Show | 6 | HG02451.hp2 HG02809.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+29043_283+2904 others(19): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTTTGTTT others(11): Show |
1 | a0001c0001t0014g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.283+29043_283+2904 others(22): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTTTGTTT others(12): Show |
1 | a0001c0001t0011g0204 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.283+29043_283+2904 others(23): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTTTGTTT others(13): Show |
1 | a0001c0001t0029g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.283+29043_283+2904 others(24): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTTTGTTT others(22): Show |
1 | a0001c0001t0015g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283+29043_283+2904 others(33): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTTTTTTT others(3): Show |
32 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0300others(29): Show | 33 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.283+29049_283+2905 others(14): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTTTTTTT others(4): Show |
15 | a0001c0001t0005g0297a0001c0001t0005g0299a0001c0001t0005g0301others(12): Show | 15 | HG01099.hp2 HG01106.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.283+29048_283+2905 others(15): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTTTTTTT others(5): Show |
4 | a0001c0001t0008g0312a0001c0001t0011g0221a0001c0001t0011g0222others(1): Show | 4 | HG01981.hp1 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+29047_283+2905 others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTTTTTTT others(6): Show |
3 | a0001c0001t0011g0223a0001c0001t0011g0224a0001c0001t0011g0225 | 3 | HG01891.hp1 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.283+29046_283+2905 others(17): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTTTTTTT others(8): Show |
2 | a0001c0001t0004g0349a0001c0001t0004g0350 | 2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.283+29044_283+2905 others(19): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTTTTTTT others(9): Show |
6 | a0001c0001t0001g0287a0001c0001t0001g0293a0001c0001t0001g0294others(3): Show | 6 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+29043_283+2905 others(20): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTTTTTTT others(10): Show |
10 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0234others(7): Show | 10 | HG01074.hp1 HG01099.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.283+29042_283+2905 others(21): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTTTTTTT others(11): Show |
24 | a0001c0001t0001g0205a0001c0001t0001g0227a0001c0001t0001g0232others(21): Show | 24 | HG00639.hp1 HG01081.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.283+29041_283+2905 others(22): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTTTTTTT others(12): Show |
17 | a0001c0001t0001g0216a0001c0001t0001g0219a0001c0001t0001g0228others(14): Show | 17 | HG00099.hp1 HG00558.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.283+29058_283+2905 others(23): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTTTTTTT others(13): Show |
14 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0218others(11): Show | 14 | HG01175.hp1 HG01261.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.283+29058_283+2905 others(24): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTTTTTTT others(14): Show |
5 | a0001c0001t0001g0231a0001c0001t0001g0254a0001c0001t0001g0257others(2): Show | 5 | HG01358.hp2 HG03486.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+29058_283+2905 others(25): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTTTTTTT others(15): Show |
1 | a0001c0001t0001g0342 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.283+29058_283+2905 others(26): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTTTTTTT others(21): Show |
1 | a0001c0001t0004g0344 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.283+29058_283+2905 others(32): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTTTTTTT others(22): Show |
1 | a0001c0001t0037g0091 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.283+29058_283+2905 others(33): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | GTTTTTTT others(27): Show |
1 | a0001c0001t0002g0092 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.283+29058_283+2905 others(38): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130278 | |||||
| chr14:74130278
|
G | T | 51 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(48): Show | 51 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.283+29040G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130278 | ||||||
| chr14:74130279
|
T | TTTTTTTT others(15): Show |
1 | a0001c0001t0012g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.283+29050_283+2905 others(26): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130279 | |||||
| chr14:74130280
|
T | TTG | 103 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(100): Show | 104 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.283+29043_283+2904 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130280 | |||||
| chr14:74130436
|
C | T | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+29198C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130436 | ||||||
| chr14:74130467
|
A | T | 1 | a0001c0001t0002g0173 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.283+29229A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130467 | ||||||
| chr14:74130524
|
C | T | 90 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(87): Show | 90 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.283+29286C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130524 | ||||||
| chr14:74130538
|
A | C | 10 | a0001c0001t0001g0217a0001c0001t0001g0226a0001c0001t0001g0241others(7): Show | 10 | HG01358.hp2 NA18947.hp2 NA18962.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+29300A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130538 | ||||||
| chr14:74130588
|
A | AT | 74 | a0001c0001t0001g0191a0001c0001t0001g0205a0001c0001t0001g0213others(71): Show | 74 | HG00544.hp1 HG00597.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.283+29374dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130588 | |||||
| chr14:74130588
|
A | ATT | 93 | a0001c0001t0001g0152a0001c0001t0001g0161a0001c0001t0002g0001others(90): Show | 95 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.283+29373_283+2937 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130588 | |||||
| chr14:74130588
|
A | ATTT | 31 | a0001c0001t0001g0110a0001c0001t0002g0137a0001c0001t0002g0170others(28): Show | 31 | HG00099.hp2 HG00423.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.283+29372_283+2937 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130588 | |||||
| chr14:74130588
|
AT | A | 17 | a0001c0001t0001g0242a0001c0001t0001g0273a0001c0001t0003g0058others(14): Show | 17 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.283+29374delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130588 | |||||
| chr14:74130785
|
C | G | 1 | a0001c0001t0004g0009 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.283+29547C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74130785 | ||||||
| chr14:74130948
|
AT | A | 14 | a0001c0001t0001g0216a0001c0001t0001g0220a0001c0001t0001g0232others(11): Show | 14 | HG00280.hp2 HG00735.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+29715delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130948 | |||||
| chr14:74130954
|
A | ATTAT | 33 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0002g0117others(30): Show | 33 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.283+29734_283+2973 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130954 | |||||
| chr14:74130954
|
A | ATTATTTA others(5): Show |
1 | a0001c0001t0013g0120 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.283+29726_283+2973 others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74130954 | |||||
| chr14:74131008
|
C | G | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+29770C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131008 | ||||||
| chr14:74131124
|
T | C | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+29886T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131124 | ||||||
| chr14:74131131
|
G | A | 12 | a0001c0001t0004g0077a0001c0001t0004g0348a0001c0001t0004g0349others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.283+29893G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131131 | ||||||
| chr14:74131146
|
G | A | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+29908G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131146 | ||||||
| chr14:74131160
|
C | A | 3 | a0001c0001t0011g0204a0001c0001t0014g0203a0001c0001t0029g0202 | 3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.283+29922C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131160 | ||||||
| chr14:74131188
|
G | GTATACTT others(10): Show |
114 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(111): Show | 116 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.283+29954_283+2995 others(21): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74131188 | |||||
| chr14:74131190
|
A | ATACTTTG others(10): Show |
4 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(1): Show | 4 | HG02258.hp1 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+29954_283+2995 others(21): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74131190 | |||||
| chr14:74131264
|
G | A | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+30026G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131264 | ||||||
| chr14:74131319
|
C | CT | 8 | a0001c0001t0001g0228a0001c0001t0003g0072a0001c0001t0004g0029others(5): Show | 8 | HG02055.hp2 HG02135.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+30097dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74131319 | |||||
| chr14:74131319
|
C | CTT | 41 | a0001c0001t0001g0335a0001c0001t0003g0323a0001c0001t0005g0295others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+30096_283+3009 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74131319 | |||||
| chr14:74131319
|
CT | C | 10 | a0001c0001t0002g0073a0001c0001t0011g0204a0001c0001t0011g0221others(7): Show | 10 | HG01891.hp1 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+30097delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74131319 | |||||
| chr14:74131429
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.283+30191C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131429 | ||||||
| chr14:74131486
|
CTT | C | 7 | a0001c0001t0002g0276a0001c0001t0002g0277a0001c0001t0011g0221others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+30252_283+3025 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74131486 | |||||
| chr14:74131612
|
G | A | 76 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(73): Show | 76 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.283+30374G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131612 | ||||||
| chr14:74131614
|
C | T | 1 | a0001c0001t0007g0114 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.283+30376C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131614 | ||||||
| chr14:74131659
|
A | C | 1 | a0001c0001t0002g0181 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.283+30421A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131659 | ||||||
| chr14:74131698
|
T | G | 76 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(73): Show | 76 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.283+30460T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131698 | ||||||
| chr14:74131771
|
G | A | 5 | a0001c0001t0011g0221a0001c0001t0011g0222a0001c0001t0011g0223others(2): Show | 5 | HG01891.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+30533G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131771 | ||||||
| chr14:74131915
|
T | C | 76 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(73): Show | 76 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.283+30677T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131915 | ||||||
| chr14:74131964
|
A | G | 3 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200 | 3 | HG02809.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.283+30726A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74131964 | ||||||
| chr14:74132077
|
T | C | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+30839T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74132077 | ||||||
| chr14:74132461
|
G | A | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+31223G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74132461 | ||||||
| chr14:74132572
|
A | G | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+31334A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74132572 | ||||||
| chr14:74132648
|
A | G | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+31410A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74132648 | ||||||
| chr14:74132710
|
T | C | 1 | a0001c0001t0016g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.283+31472T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74132710 | ||||||
| chr14:74132728
|
C | T | 12 | a0001c0001t0004g0077a0001c0001t0004g0348a0001c0001t0004g0349others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.283+31490C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74132728 | ||||||
| chr14:74132798
|
C | T | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+31560C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74132798 | ||||||
| chr14:74132862
|
T | A | 1 | a0001c0001t0007g0116 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.283+31624T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74132862 | ||||||
| chr14:74133014
|
T | TA | 9 | a0001c0001t0001g0259a0001c0001t0002g0276a0001c0001t0002g0277others(6): Show | 9 | HG01433.hp2 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+31787dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74133014 | |||||
| chr14:74133031
|
C | G | 1 | a0001c0002t0009g0282 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.283+31793C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74133031 | ||||||
| chr14:74133689
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.283+32451A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74133689 | ||||||
| chr14:74133834
|
C | A | 1 | a0001c0001t0006g0183 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.283+32596C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74133834 | ||||||
| chr14:74134093
|
A | C | 5 | a0001c0001t0004g0206a0001c0001t0004g0207a0001c0001t0004g0208others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+32855A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74134093 | ||||||
| chr14:74134128
|
G | A | 2 | a0001c0001t0003g0025a0001c0001t0003g0071 | 2 | NA18954.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.283+32890G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74134128 | ||||||
| chr14:74134146
|
C | G | 76 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(73): Show | 76 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.283+32908C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74134146 | ||||||
| chr14:74134315
|
G | C | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.283+33077G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74134315 | ||||||
| chr14:74134640
|
AT | A | 61 | a0001c0001t0001g0152a0001c0001t0001g0161a0001c0001t0002g0001others(58): Show | 62 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.283+33406delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74134640 | |||||
| chr14:74134688
|
T | C | 7 | a0001c0001t0011g0204a0001c0001t0014g0198a0001c0001t0014g0199others(4): Show | 7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+33450T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74134688 | ||||||
| chr14:74134693
|
T | C | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+33455T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74134693 | ||||||
| chr14:74134795
|
G | A | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283+33557G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74134795 | ||||||
| chr14:74134858
|
A | G | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+33620A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74134858 | ||||||
| chr14:74135027
|
A | G | 7 | a0001c0001t0008g0296a0001c0001t0008g0308a0001c0001t0008g0309others(4): Show | 7 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+33789A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135027 | ||||||
| chr14:74135055
|
T | TTTG | 3 | a0001c0001t0002g0164a0001c0001t0006g0156a0001c0001t0033g0182 | 3 | HG02071.hp1 NA18967.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.283+33831_283+3383 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74135055 | |||||
| chr14:74135055
|
TTTG | T | 4 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200others(1): Show | 4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+33831_283+3383 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74135055 | |||||
| chr14:74135140
|
C | G | 1 | a0001c0001t0001g0248 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.283+33902C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135140 | ||||||
| chr14:74135185
|
C | T | 108 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(105): Show | 110 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.283+33947C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135185 | ||||||
| chr14:74135276
|
G | T | 3 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0034g0119 | 3 | HG01074.hp2 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.283+34038G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135276 | ||||||
| chr14:74135286
|
A | G | 1 | a0001c0001t0011g0221 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.283+34048A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135286 | ||||||
| chr14:74135303
|
T | A | 2 | a0001c0001t0003g0024a0001c0001t0003g0033 | 2 | NA19057.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.283+34065T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135303 | ||||||
| chr14:74135547
|
A | AT | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+34318dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74135547 | |||||
| chr14:74135547
|
AT | A | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+34318delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74135547 | |||||
| chr14:74135556
|
T | A | 3 | a0001c0001t0011g0204a0001c0001t0014g0203a0001c0001t0029g0202 | 3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.283+34318T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135556 | ||||||
| chr14:74135657
|
A | T | 61 | a0001c0001t0001g0152a0001c0001t0001g0161a0001c0001t0002g0001others(58): Show | 62 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.283+34419A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135657 | ||||||
| chr14:74135664
|
T | G | 1 | a0001c0001t0010g0123 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.283+34426T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135664 | ||||||
| chr14:74135690
|
T | C | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+34452T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135690 | ||||||
| chr14:74135727
|
T | A | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34489T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135727 | ||||||
| chr14:74135768
|
T | A | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34530T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135768 | ||||||
| chr14:74135819
|
GT | G | 243 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(240): Show | 246 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.283+34593delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74135819 | |||||
| chr14:74135895
|
T | A | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34657T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74135895 | ||||||
| chr14:74136156
|
C | T | 76 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(73): Show | 76 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.283+34918C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136156 | ||||||
| chr14:74136190
|
T | A | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34952T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136190 | ||||||
| chr14:74136191
|
T | C | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34953T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136191 | ||||||
| chr14:74136193
|
T | A | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34955T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136193 | ||||||
| chr14:74136194
|
T | G | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34956T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136194 | ||||||
| chr14:74136195
|
T | A | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34957T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136195 | ||||||
| chr14:74136198
|
T | G | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34960T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136198 | ||||||
| chr14:74136199
|
T | C | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34961T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136199 | ||||||
| chr14:74136200
|
C | G | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34962C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136200 | ||||||
| chr14:74136201
|
A | T | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34963A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136201 | ||||||
| chr14:74136204
|
G | T | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.283+34966G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136204 | ||||||
| chr14:74136279
|
T | C | 3 | a0001c0001t0011g0222a0001c0001t0011g0223a0001c0001t0011g0224 | 3 | HG01891.hp1 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.283+35041T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136279 | ||||||
| chr14:74136564
|
T | C | 4 | a0001c0001t0013g0094a0001c0001t0013g0120a0001c0001t0013g0125others(1): Show | 4 | HG02602.hp2 HG03688.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+35326T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136564 | ||||||
| chr14:74136685
|
C | T | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.283+35447C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136685 | ||||||
| chr14:74136700
|
A | C | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+35462A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136700 | ||||||
| chr14:74136764
|
T | A | 2 | a0001c0002t0009g0283a0001c0002t0009g0284 | 2 | HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.283+35526T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136764 | ||||||
| chr14:74136797
|
A | T | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+35559A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74136797 | ||||||
| chr14:74137010
|
A | G | 1 | a0001c0001t0003g0053 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.283+35772A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137010 | ||||||
| chr14:74137110
|
G | A | 345 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(342): Show | 348 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(345): Show |
intron_variant | MODIFIER | c.283+35872G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137110 | ||||||
| chr14:74137137
|
G | A | 1 | a0001c0001t0040g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.283+35899G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137137 | ||||||
| chr14:74137155
|
AAT | A | 108 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(105): Show | 109 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.283+35934_283+3593 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137155 | |||||
| chr14:74137169
|
TA | T | 4 | a0001c0001t0002g0276a0001c0001t0002g0277a0001c0001t0008g0327others(1): Show | 4 | HG01346.hp2 HG01884.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+35932delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137169 | ||||||
| chr14:74137169
|
TATA | T | 5 | a0001c0001t0007g0105a0001c0001t0011g0204a0001c0001t0014g0203others(2): Show | 5 | HG02132.hp1 HG02572.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+35932_283+3593 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137169 | ||||||
| chr14:74137170
|
A | T | 2 | a0001c0001t0003g0038a0001c0001t0013g0094 | 2 | HG03688.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.283+35932A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137170 | ||||||
| chr14:74137171
|
TA | T | 47 | a0001c0001t0001g0347a0001c0001t0002g0092a0001c0001t0003g0018others(44): Show | 49 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.283+35934delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137171 | ||||||
| chr14:74137172
|
A | T | 174 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0215others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.283+35934A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137172 | ||||||
| chr14:74137246
|
G | A | 1 | a0001c0001t0002g0179 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.283+36008G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137246 | ||||||
| chr14:74137247
|
C | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0010g0112others(1): Show | 4 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+36009C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137247 | ||||||
| chr14:74137307
|
ATAT | A | 106 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(103): Show | 107 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.283+36073_283+3607 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137307 | |||||
| chr14:74137364
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.283+36126C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137364 | ||||||
| chr14:74137445
|
C | T | 4 | a0001c0001t0002g0166a0001c0001t0006g0167a0001c0001t0020g0132others(1): Show | 4 | HG01167.hp1 HG01169.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+36207C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137445 | ||||||
| chr14:74137485
|
T | G | 348 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(345): Show | 351 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.283+36247T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137485 | ||||||
| chr14:74137495
|
T | G | 3 | a0001c0001t0007g0107a0001c0001t0010g0096a0001c0001t0010g0106 | 3 | HG04115.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.283+36257T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137495 | ||||||
| chr14:74137496
|
C | CTTTTTTT | 4 | a0001c0001t0004g0077a0001c0001t0004g0349a0001c0001t0004g0351others(1): Show | 4 | HG02897.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+36259_283+3626 others(11): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137496 | |||||
| chr14:74137496
|
C | CTTTTTTT others(1): Show |
7 | a0001c0001t0004g0350a0001c0001t0012g0078a0001c0001t0012g0083others(4): Show | 7 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+36259_283+3626 others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137496 | |||||
| chr14:74137498
|
C | CT | 9 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0228others(6): Show | 9 | HG00099.hp1 HG00642.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.283+36278dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | |||||
| chr14:74137498
|
C | CTCT | 8 | a0001c0001t0002g0142a0001c0001t0002g0190a0001c0001t0002g0197others(5): Show | 8 | HG01167.hp1 HG01169.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+36261_283+3626 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | |||||
| chr14:74137498
|
C | CTCTT | 62 | a0001c0001t0001g0152a0001c0001t0001g0161a0001c0001t0001g0191others(59): Show | 63 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.283+36261_283+3626 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | |||||
| chr14:74137498
|
C | CTCTTT | 35 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0002g0117others(32): Show | 35 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.283+36261_283+3626 others(9): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | |||||
| chr14:74137498
|
C | CTTTTTTT others(4): Show |
6 | a0001c0001t0003g0012a0001c0001t0003g0060a0001c0001t0012g0086others(3): Show | 6 | HG01243.hp1 HG01256.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+36268_283+3627 others(15): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | |||||
| chr14:74137498
|
C | CTTTTTTT others(5): Show |
66 | a0001c0001t0002g0027a0001c0001t0003g0005a0001c0001t0003g0007others(63): Show | 66 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.283+36267_283+3627 others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | |||||
| chr14:74137498
|
C | CTTTTTTT others(6): Show |
11 | a0001c0001t0002g0073a0001c0001t0003g0017a0001c0001t0003g0032others(8): Show | 11 | HG02135.hp1 HG03471.hp1 NA18940.hp1 others(8): Show |
intron_variant | MODIFIER | c.283+36266_283+3627 others(17): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | |||||
| chr14:74137498
|
C | CTTTTTTT others(7): Show |
3 | a0001c0001t0002g0092a0001c0001t0004g0070a0001c0001t0039g0031 | 3 | HG03831.hp1 HG06807.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.283+36265_283+3627 others(18): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | |||||
| chr14:74137498
|
C | CTTTTTTT others(8): Show |
4 | a0001c0001t0004g0207a0001c0001t0004g0208a0001c0001t0012g0209others(1): Show | 4 | HG02055.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+36264_283+3627 others(19): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | |||||
| chr14:74137498
|
C | CTTTTTTT others(9): Show |
4 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0210others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+36263_283+3627 others(20): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | |||||
| chr14:74137498
|
C | T | 12 | a0001c0001t0004g0077a0001c0001t0004g0348a0001c0001t0004g0349others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.283+36260C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137498 | ||||||
| chr14:74137498
|
CT | C | 50 | a0001c0001t0001g0205a0001c0001t0001g0231a0001c0001t0001g0234others(47): Show | 51 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.283+36278delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74137498 | |||||
| chr14:74137548
|
G | C | 2 | a0001c0001t0013g0094a0001c0001t0013g0125 | 2 | HG03688.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.283+36310G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137548 | ||||||
| chr14:74137585
|
C | G | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+36347C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137585 | ||||||
| chr14:74137747
|
C | G | 3 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0034g0119 | 3 | HG01074.hp2 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.283+36509C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137747 | ||||||
| chr14:74137788
|
G | A | 4 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200others(1): Show | 4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+36550G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137788 | ||||||
| chr14:74137790
|
G | A | 1 | a0001c0001t0002g0189 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.283+36552G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137790 | ||||||
| chr14:74137871
|
A | T | 3 | a0001c0001t0005g0297a0001c0001t0005g0319a0001c0001t0005g0320 | 3 | HG02071.hp2 HG02165.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.283+36633A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137871 | ||||||
| chr14:74137951
|
T | G | 1 | a0001c0001t0002g0092 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.283+36713T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74137951 | ||||||
| chr14:74138182
|
C | T | 1 | a0001c0001t0011g0222 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.283+36944C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74138182 | ||||||
| chr14:74138445
|
G | C | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.283+37207G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74138445 | ||||||
| chr14:74138465
|
T | A | 1 | a0001c0001t0007g0004 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.283+37227T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74138465 | ||||||
| chr14:74138520
|
A | C | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+37282A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74138520 | ||||||
| chr14:74138522
|
G | A | 9 | a0001c0001t0001g0213a0001c0001t0001g0272a0001c0001t0002g0260others(6): Show | 9 | HG02027.hp2 HG02155.hp1 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+37284G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74138522 | ||||||
| chr14:74138587
|
T | C | 1 | a0001c0001t0010g0123 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.283+37349T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74138587 | ||||||
| chr14:74138627
|
C | A | 4 | a0001c0001t0001g0346a0001c0001t0001g0347a0001c0001t0004g0344others(1): Show | 4 | HG01123.hp1 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+37389C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74138627 | ||||||
| chr14:74138641
|
T | C | 8 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(5): Show | 9 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.283+37403T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74138641 | ||||||
| chr14:74138769
|
C | CA | 233 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(230): Show | 235 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.283+37547dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74138769 | |||||
| chr14:74138769
|
C | CAA | 11 | a0001c0001t0003g0061a0001c0001t0004g0036a0001c0001t0004g0070others(8): Show | 11 | HG01109.hp2 HG02027.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.283+37546_283+3754 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74138769 | |||||
| chr14:74138824
|
T | C | 1 | a0001c0001t0003g0088 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.283+37586T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74138824 | ||||||
| chr14:74138935
|
AT | A | 100 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0213others(97): Show | 101 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.283+37712delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74138935 | |||||
| chr14:74138935
|
ATT | A | 169 | a0001c0001t0001g0152a0001c0001t0001g0161a0001c0001t0001g0191others(166): Show | 171 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.283+37711_283+3771 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74138935 | |||||
| chr14:74139020
|
TA | T | 61 | a0001c0001t0001g0152a0001c0001t0001g0161a0001c0001t0002g0001others(58): Show | 62 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.283+37785delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74139020 | |||||
| chr14:74139217
|
G | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0010g0112others(1): Show | 4 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+37979G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74139217 | ||||||
| chr14:74139669
|
T | C | 3 | a0001c0001t0011g0204a0001c0001t0014g0203a0001c0001t0029g0202 | 3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.283+38431T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74139669 | ||||||
| chr14:74139702
|
G | T | 1 | a0001c0001t0001g0248 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.283+38464G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74139702 | ||||||
| chr14:74139715
|
G | C | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+38477G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74139715 | ||||||
| chr14:74139739
|
T | A | 12 | a0001c0001t0004g0077a0001c0001t0004g0348a0001c0001t0004g0349others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.283+38501T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74139739 | ||||||
| chr14:74140044
|
TTTA | T | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+38810_283+3881 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74140044 | |||||
| chr14:74140079
|
C | CTT | 207 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(204): Show | 209 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.283+38842_283+3884 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74140079 | |||||
| chr14:74140289
|
C | A | 1 | a0001c0001t0012g0081 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.283+39051C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74140289 | ||||||
| chr14:74140305
|
G | A | 34 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0002g0117others(31): Show | 34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.283+39067G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74140305 | ||||||
| chr14:74140582
|
C | T | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.283+39344C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74140582 | ||||||
| chr14:74140621
|
G | C | 118 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(115): Show | 120 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.283+39383G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74140621 | ||||||
| chr14:74140625
|
C | T | 4 | a0001c0001t0003g0034a0001c0001t0004g0026a0001c0002t0009g0002others(1): Show | 5 | HG02451.hp2 HG02970.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+39387C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74140625 | ||||||
| chr14:74140711
|
A | G | 1 | a0001c0001t0001g0293 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.283+39473A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74140711 | ||||||
| chr14:74140927
|
C | T | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+39689C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74140927 | ||||||
| chr14:74141572
|
A | T | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.283+40334A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74141572 | ||||||
| chr14:74142140
|
T | C | 1 | a0001c0001t0037g0091 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.283+40902T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74142140 | ||||||
| chr14:74142317
|
T | A | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.283+41079T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74142317 | ||||||
| chr14:74142630
|
G | A | 2 | a0001c0001t0004g0077a0001c0001t0012g0078 | 2 | HG02486.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.283+41392G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74142630 | ||||||
| chr14:74142643
|
A | G | 1 | a0001c0001t0006g0135 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.283+41405A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74142643 | ||||||
| chr14:74142716
|
T | C | 102 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.283+41478T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74142716 | ||||||
| chr14:74142757
|
A | T | 2 | a0001c0001t0011g0204a0001c0001t0014g0203 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.283+41519A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74142757 | ||||||
| chr14:74142796
|
T | C | 1 | a0001c0001t0007g0247 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.283+41558T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74142796 | ||||||
| chr14:74142898
|
C | G | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.283+41660C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74142898 | ||||||
| chr14:74142991
|
A | G | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+41753A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74142991 | ||||||
| chr14:74143063
|
G | A | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+41825G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143063 | ||||||
| chr14:74143172
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.283+41934C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143172 | ||||||
| chr14:74143287
|
T | C | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG00099.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.283+42049T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143287 | ||||||
| chr14:74143362
|
G | A | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.283+42124G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143362 | ||||||
| chr14:74143395
|
C | G | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+42157C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143395 | ||||||
| chr14:74143524
|
A | G | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+42286A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143524 | ||||||
| chr14:74143564
|
T | C | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.283+42326T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143564 | ||||||
| chr14:74143610
|
A | G | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.283+42372A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143610 | ||||||
| chr14:74143611
|
G | GT | 231 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(228): Show | 232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.283+42382dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74143611 | |||||
| chr14:74143622
|
A | C | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.283+42384A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143622 | ||||||
| chr14:74143772
|
T | G | 5 | a0001c0001t0004g0206a0001c0001t0004g0207a0001c0001t0004g0208others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+42534T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143772 | ||||||
| chr14:74143899
|
C | T | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+42661C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74143899 | ||||||
| chr14:74143988
|
A | AT | 7 | a0001c0001t0002g0276a0001c0001t0002g0277a0001c0001t0011g0221others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+42761dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74143988 | |||||
| chr14:74144127
|
AT | A | 235 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(232): Show | 236 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.283+42904delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74144127 | |||||
| chr14:74144162
|
T | A | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+42924T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144162 | ||||||
| chr14:74144194
|
G | A | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+42956G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144194 | ||||||
| chr14:74144279
|
A | AT | 8 | a0001c0001t0011g0204a0001c0001t0014g0198a0001c0001t0014g0199others(5): Show | 8 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+43054dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74144279 | |||||
| chr14:74144279
|
AT | A | 11 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(8): Show | 11 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.283+43054delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74144279 | |||||
| chr14:74144346
|
C | T | 1 | a0001c0001t0007g0004 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.283+43108C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144346 | ||||||
| chr14:74144386
|
C | G | 6 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(3): Show | 6 | HG02258.hp2 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.283+43148C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144386 | ||||||
| chr14:74144471
|
A | G | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.283+43233A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144471 | ||||||
| chr14:74144487
|
G | T | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.283+43249G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144487 | ||||||
| chr14:74144568
|
A | G | 191 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(188): Show | 191 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.283+43330A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144568 | ||||||
| chr14:74144617
|
A | AAATTAGA others(1): Show |
289 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0191others(286): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.283+43380_283+4338 others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74144617 | |||||
| chr14:74144700
|
A | G | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283+43462A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144700 | ||||||
| chr14:74144754
|
G | A | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+43516G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144754 | ||||||
| chr14:74144784
|
G | A | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.283+43546G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144784 | ||||||
| chr14:74144985
|
G | C | 8 | a0001c0001t0004g0077a0001c0001t0012g0078a0001c0001t0012g0081others(5): Show | 8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+43747G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74144985 | ||||||
| chr14:74145051
|
C | T | 1 | a0002c0003t0044g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.283+43813C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145051 | ||||||
| chr14:74145313
|
T | C | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.283+44075T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145313 | ||||||
| chr14:74145383
|
T | A | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283+44145T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145383 | ||||||
| chr14:74145397
|
T | G | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283+44159T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145397 | ||||||
| chr14:74145452
|
A | G | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.283+44214A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145452 | ||||||
| chr14:74145480
|
T | C | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.283+44242T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145480 | ||||||
| chr14:74145615
|
C | G | 2 | a0001c0001t0006g0156a0001c0002t0009g0281 | 2 | HG02071.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.283+44377C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145615 | ||||||
| chr14:74145695
|
G | C | 3 | a0001c0001t0002g0128a0001c0001t0002g0147a0001c0001t0019g0149 | 3 | NA18954.hp2 NA19055.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.283+44457G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145695 | ||||||
| chr14:74145791
|
C | T | 3 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200 | 3 | HG02809.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.283+44553C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145791 | ||||||
| chr14:74145807
|
C | A | 1 | a0001c0001t0002g0092 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.283+44569C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145807 | ||||||
| chr14:74145966
|
T | C | 4 | a0001c0001t0021g0079a0001c0001t0021g0084a0001c0001t0036g0082others(1): Show | 4 | HG02895.hp1 HG03486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+44728T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74145966 | ||||||
| chr14:74146009
|
T | C | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+44771T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146009 | ||||||
| chr14:74146025
|
T | C | 4 | a0001c0001t0001g0286a0001c0001t0001g0290a0001c0001t0001g0291others(1): Show | 4 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+44787T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146025 | ||||||
| chr14:74146192
|
G | A | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.283+44954G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146192 | ||||||
| chr14:74146257
|
A | G | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283+45019A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146257 | ||||||
| chr14:74146260
|
C | T | 1 | a0001c0001t0003g0033 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.283+45022C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146260 | ||||||
| chr14:74146271
|
A | C | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+45033A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146271 | ||||||
| chr14:74146308
|
A | G | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.283+45070A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146308 | ||||||
| chr14:74146348
|
A | G | 1 | a0001c0001t0005g0297 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.283+45110A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146348 | ||||||
| chr14:74146401
|
C | T | 10 | a0001c0001t0002g0092a0001c0001t0011g0204a0001c0001t0014g0198others(7): Show | 10 | HG02145.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+45163C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146401 | ||||||
| chr14:74146581
|
A | G | 34 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0002g0117others(31): Show | 34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.283+45343A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146581 | ||||||
| chr14:74146663
|
C | T | 2 | a0001c0001t0002g0192a0001c0001t0015g0185 | 2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.283+45425C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146663 | ||||||
| chr14:74146692
|
G | A | 4 | a0001c0001t0001g0346a0001c0001t0001g0347a0001c0001t0004g0344others(1): Show | 4 | HG01123.hp1 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+45454G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74146692 | ||||||
| chr14:74147022
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.283+45784G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147022 | ||||||
| chr14:74147025
|
G | A | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.283+45787G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147025 | ||||||
| chr14:74147126
|
C | T | 1 | a0001c0001t0010g0113 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.283+45888C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147126 | ||||||
| chr14:74147189
|
C | T | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.283+45951C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147189 | ||||||
| chr14:74147190
|
G | A | 7 | a0001c0001t0002g0276a0001c0001t0002g0277a0001c0001t0011g0221others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+45952G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147190 | ||||||
| chr14:74147197
|
G | A | 8 | a0001c0001t0004g0077a0001c0001t0012g0078a0001c0001t0012g0081others(5): Show | 8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+45959G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147197 | ||||||
| chr14:74147260
|
A | G | 1 | a0001c0001t0005g0325 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.283+46022A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147260 | ||||||
| chr14:74147387
|
G | A | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+46149G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147387 | ||||||
| chr14:74147470
|
G | A | 4 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200others(1): Show | 4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+46232G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147470 | ||||||
| chr14:74147796
|
A | G | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283+46558A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147796 | ||||||
| chr14:74147857
|
T | G | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.283+46619T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147857 | ||||||
| chr14:74147863
|
T | C | 81 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(78): Show | 81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.283+46625T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147863 | ||||||
| chr14:74147925
|
G | C | 1 | a0001c0001t0007g0114 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.283+46687G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74147925 | ||||||
| chr14:74148001
|
G | T | 76 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(73): Show | 76 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.283+46763G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148001 | ||||||
| chr14:74148002
|
C | T | 76 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(73): Show | 76 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.283+46764C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148002 | ||||||
| chr14:74148040
|
A | G | 289 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0191others(286): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.283+46802A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148040 | ||||||
| chr14:74148134
|
A | G | 10 | a0001c0001t0002g0129a0001c0001t0002g0133a0001c0001t0002g0134others(7): Show | 10 | NA18940.hp2 NA18944.hp1 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.283+46896A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148134 | ||||||
| chr14:74148195
|
C | G | 1 | a0001c0001t0015g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283+46957C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148195 | ||||||
| chr14:74148213
|
C | T | 2 | a0001c0001t0001g0239a0001c0001t0001g0253 | 2 | NA19072.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.283+46975C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148213 | ||||||
| chr14:74148234
|
T | C | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.283+46996T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148234 | ||||||
| chr14:74148290
|
A | G | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+47052A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148290 | ||||||
| chr14:74148316
|
T | C | 1 | a0001c0001t0007g0116 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.283+47078T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148316 | ||||||
| chr14:74148327
|
A | C | 102 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.283+47089A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148327 | ||||||
| chr14:74148392
|
G | A | 34 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0002g0117others(31): Show | 34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.283+47154G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148392 | ||||||
| chr14:74148558
|
A | G | 4 | a0001c0001t0002g0131a0001c0001t0002g0138a0001c0001t0002g0160others(1): Show | 4 | HG00642.hp1 HG00735.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+47320A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148558 | ||||||
| chr14:74148627
|
T | G | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+47389T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148627 | ||||||
| chr14:74148675
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.283+47437C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148675 | ||||||
| chr14:74148741
|
G | GA | 34 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0002g0117others(31): Show | 34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.283+47513dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74148741 | |||||
| chr14:74148801
|
G | T | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.283+47563G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148801 | ||||||
| chr14:74148915
|
G | C | 1 | a0001c0001t0001g0231 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.283+47677G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74148915 | ||||||
| chr14:74149111
|
A | G | 244 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(241): Show | 246 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.283+47873A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74149111 | ||||||
| chr14:74149206
|
A | T | 76 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(73): Show | 76 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.283+47968A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74149206 | ||||||
| chr14:74149373
|
T | G | 2 | a0001c0001t0021g0079a0001c0001t0021g0084 | 2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.283+48135T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74149373 | ||||||
| chr14:74149596
|
T | A | 34 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0002g0117others(31): Show | 34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.283+48358T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74149596 | ||||||
| chr14:74149647
|
A | G | 1 | a0001c0001t0002g0261 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.283+48409A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74149647 | ||||||
| chr14:74149706
|
T | C | 4 | a0001c0001t0004g0348a0001c0001t0004g0349a0001c0001t0004g0350others(1): Show | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+48468T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74149706 | ||||||
| chr14:74149718
|
A | G | 1 | a0001c0001t0003g0055 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.283+48480A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74149718 | ||||||
| chr14:74149790
|
T | C | 242 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(239): Show | 243 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.283+48552T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74149790 | ||||||
| chr14:74150071
|
T | C | 1 | a0001c0001t0004g0014 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.283+48833T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150071 | ||||||
| chr14:74150405
|
C | A | 5 | a0001c0001t0004g0206a0001c0001t0004g0207a0001c0001t0004g0208others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-48517C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150405 | ||||||
| chr14:74150474
|
A | T | 1 | a0001c0001t0001g0335 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.284-48448A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150474 | ||||||
| chr14:74150519
|
T | C | 6 | a0001c0001t0002g0092a0001c0001t0014g0198a0001c0001t0014g0199others(3): Show | 6 | HG02145.hp2 HG02809.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-48403T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150519 | ||||||
| chr14:74150634
|
T | A | 1 | a0001c0001t0003g0074 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.284-48288T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150634 | ||||||
| chr14:74150646
|
T | C | 3 | a0001c0001t0011g0204a0001c0001t0014g0203a0001c0001t0029g0202 | 3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.284-48276T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150646 | ||||||
| chr14:74150735
|
A | T | 45 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0191others(42): Show | 45 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.284-48187A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150735 | ||||||
| chr14:74150804
|
G | T | 4 | a0001c0001t0001g0346a0001c0001t0001g0347a0001c0001t0004g0344others(1): Show | 4 | HG01123.hp1 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-48118G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150804 | ||||||
| chr14:74150927
|
G | C | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-47995G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150927 | ||||||
| chr14:74150965
|
C | T | 9 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(6): Show | 9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-47957C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150965 | ||||||
| chr14:74150974
|
T | A | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.284-47948T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74150974 | ||||||
| chr14:74151264
|
A | T | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-47658A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74151264 | ||||||
| chr14:74151504
|
TTAAAA | T | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-47417_284-4741 others(9): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74151504 | ||||||
| chr14:74151647
|
T | C | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-47275T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74151647 | ||||||
| chr14:74151982
|
C | T | 1 | a0001c0001t0007g0109 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.284-46940C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74151982 | ||||||
| chr14:74151994
|
C | T | 1 | a0001c0001t0002g0145 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.284-46928C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74151994 | ||||||
| chr14:74152097
|
T | C | 102 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.284-46825T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152097 | ||||||
| chr14:74152124
|
A | G | 1 | a0001c0001t0010g0123 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.284-46798A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152124 | ||||||
| chr14:74152129
|
G | A | 2 | a0001c0001t0011g0204a0001c0001t0014g0203 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.284-46793G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152129 | ||||||
| chr14:74152262
|
C | CA | 82 | a0001c0001t0001g0335a0001c0001t0002g0177a0001c0001t0002g0276others(79): Show | 83 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.284-46645dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74152262 | |||||
| chr14:74152262
|
C | CAA | 73 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(70): Show | 73 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.284-46646_284-4664 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74152262 | |||||
| chr14:74152331
|
TACTG | T | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.284-46590_284-4658 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152331 | ||||||
| chr14:74152447
|
A | G | 1 | a0001c0001t0003g0053 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.284-46475A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152447 | ||||||
| chr14:74152488
|
C | T | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.284-46434C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152488 | ||||||
| chr14:74152506
|
G | A | 5 | a0001c0001t0004g0206a0001c0001t0004g0207a0001c0001t0004g0208others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-46416G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152506 | ||||||
| chr14:74152519
|
C | T | 2 | a0001c0001t0003g0065a0001c0001t0004g0029 | 2 | HG00673.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.284-46403C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152519 | ||||||
| chr14:74152839
|
A | G | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-46083A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152839 | ||||||
| chr14:74152901
|
A | G | 5 | a0001c0001t0011g0221a0001c0001t0011g0222a0001c0001t0011g0223others(2): Show | 5 | HG01891.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-46021A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152901 | ||||||
| chr14:74152959
|
C | CA | 34 | a0001c0001t0001g0097a0001c0001t0001g0161a0001c0001t0001g0191others(31): Show | 34 | HG00673.hp2 HG00735.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.284-45940dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74152959 | |||||
| chr14:74152959
|
C | CAA | 11 | a0001c0001t0001g0205a0001c0001t0001g0231a0001c0001t0001g0234others(8): Show | 11 | HG01081.hp2 HG01109.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.284-45941_284-4594 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74152959 | |||||
| chr14:74152959
|
CA | C | 12 | a0001c0001t0001g0263a0001c0001t0001g0287a0001c0001t0001g0288others(9): Show | 13 | HG00099.hp1 HG00323.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.284-45940delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74152959 | |||||
| chr14:74152959
|
CAA | C | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-45941_284-4594 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74152959 | |||||
| chr14:74152961
|
A | C | 1 | a0002c0003t0044g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.284-45961A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74152961 | ||||||
| chr14:74153164
|
G | T | 2 | a0001c0001t0017g0321a0001c0001t0017g0322 | 2 | HG00280.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.284-45758G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74153164 | ||||||
| chr14:74153401
|
T | C | 1 | a0001c0001t0015g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.284-45521T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74153401 | ||||||
| chr14:74153408
|
CT | C | 13 | a0001c0001t0003g0017a0001c0001t0003g0023a0001c0001t0003g0053others(10): Show | 13 | HG00423.hp2 HG02165.hp1 NA18975.hp2 others(10): Show |
intron_variant | MODIFIER | c.284-45513delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74153408 | ||||||
| chr14:74153548
|
A | AT | 21 | a0001c0001t0001g0286a0001c0001t0001g0335a0001c0001t0002g0197others(18): Show | 21 | HG01074.hp1 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.284-45360dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74153548 | |||||
| chr14:74153548
|
AT | A | 11 | a0001c0001t0002g0092a0001c0001t0003g0016a0001c0001t0005g0299others(8): Show | 11 | HG00280.hp1 HG01167.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-45360delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74153548 | |||||
| chr14:74153629
|
A | T | 2 | a0001c0001t0012g0086a0001c0001t0025g0087 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.284-45293A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74153629 | ||||||
| chr14:74153764
|
G | A | 1 | a0001c0001t0017g0322 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.284-45158G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74153764 | ||||||
| chr14:74153791
|
G | A | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284-45131G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74153791 | ||||||
| chr14:74153873
|
A | C | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-45049A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74153873 | ||||||
| chr14:74153961
|
A | G | 3 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289 | 3 | HG02559.hp1 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.284-44961A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74153961 | ||||||
| chr14:74154008
|
C | G | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-44914C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154008 | ||||||
| chr14:74154041
|
G | A | 1 | a0001c0001t0006g0156 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.284-44881G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154041 | ||||||
| chr14:74154173
|
G | C | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.284-44749G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154173 | ||||||
| chr14:74154174
|
T | C | 1 | a0001c0001t0006g0165 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.284-44748T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154174 | ||||||
| chr14:74154176
|
A | G | 5 | a0001c0001t0011g0221a0001c0001t0011g0222a0001c0001t0011g0223others(2): Show | 5 | HG01891.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-44746A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154176 | ||||||
| chr14:74154249
|
A | AAT | 7 | a0001c0001t0002g0276a0001c0001t0002g0277a0001c0001t0011g0221others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-44672_284-4467 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74154249 | |||||
| chr14:74154583
|
T | C | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-44339T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154583 | ||||||
| chr14:74154711
|
G | A | 2 | a0001c0001t0012g0086a0001c0001t0025g0087 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.284-44211G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154711 | ||||||
| chr14:74154736
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.284-44186T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154736 | ||||||
| chr14:74154753
|
A | C | 2 | a0001c0001t0002g0192a0001c0001t0015g0185 | 2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.284-44169A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154753 | ||||||
| chr14:74154845
|
T | C | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-44077T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154845 | ||||||
| chr14:74154882
|
T | C | 1 | a0001c0001t0002g0157 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.284-44040T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74154882 | ||||||
| chr14:74155131
|
G | A | 6 | a0001c0001t0002g0128a0001c0001t0002g0144a0001c0001t0002g0145others(3): Show | 6 | NA18946.hp1 NA18954.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-43791G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74155131 | ||||||
| chr14:74155354
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.284-43568C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74155354 | ||||||
| chr14:74155412
|
C | T | 1 | a0001c0001t0003g0042 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.284-43510C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74155412 | ||||||
| chr14:74155575
|
T | C | 9 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(6): Show | 9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-43347T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74155575 | ||||||
| chr14:74155588
|
T | C | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-43334T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74155588 | ||||||
| chr14:74155631
|
C | G | 244 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(241): Show | 246 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.284-43291C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74155631 | ||||||
| chr14:74155790
|
G | A | 3 | a0001c0001t0011g0222a0001c0001t0011g0223a0001c0001t0011g0224 | 3 | HG01891.hp1 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.284-43132G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74155790 | ||||||
| chr14:74155950
|
C | T | 1 | a0001c0001t0003g0019 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.284-42972C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74155950 | ||||||
| chr14:74156415
|
G | C | 12 | a0001c0001t0004g0077a0001c0001t0004g0348a0001c0001t0004g0349others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-42507G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74156415 | ||||||
| chr14:74156493
|
T | G | 1 | a0001c0001t0003g0064 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.284-42429T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74156493 | ||||||
| chr14:74156494
|
G | T | 1 | a0001c0001t0003g0064 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.284-42428G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74156494 | ||||||
| chr14:74156496
|
T | C | 1 | a0001c0001t0003g0064 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.284-42426T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74156496 | ||||||
| chr14:74156550
|
A | G | 12 | a0001c0001t0004g0077a0001c0001t0004g0348a0001c0001t0004g0349others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-42372A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74156550 | ||||||
| chr14:74156717
|
A | T | 1 | a0001c0001t0007g0247 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.284-42205A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74156717 | ||||||
| chr14:74156854
|
A | T | 12 | a0001c0001t0004g0077a0001c0001t0004g0348a0001c0001t0004g0349others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-42068A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74156854 | ||||||
| chr14:74156988
|
A | G | 81 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(78): Show | 81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.284-41934A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74156988 | ||||||
| chr14:74157002
|
T | G | 1 | a0001c0001t0007g0103 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.284-41920T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157002 | ||||||
| chr14:74157035
|
C | CTT | 182 | a0001c0001t0001g0205a0001c0001t0001g0214a0001c0001t0001g0215others(179): Show | 182 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.284-41874_284-4187 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74157035 | |||||
| chr14:74157035
|
C | CTTT | 44 | a0001c0001t0001g0213a0001c0001t0001g0264a0001c0001t0003g0323others(41): Show | 45 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.284-41875_284-4187 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74157035 | |||||
| chr14:74157102
|
G | A | 1 | a0001c0001t0007g0108 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.284-41820G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157102 | ||||||
| chr14:74157222
|
A | G | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-41700A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157222 | ||||||
| chr14:74157455
|
A | ATT | 9 | a0001c0001t0001g0214a0001c0001t0001g0218a0001c0001t0001g0256others(6): Show | 9 | HG00558.hp1 HG01192.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.284-41466_284-4146 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74157455 | |||||
| chr14:74157457
|
A | AT | 13 | a0001c0001t0001g0205a0001c0001t0001g0231a0001c0001t0001g0234others(10): Show | 13 | HG01081.hp2 HG01884.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.284-41464dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74157457 | |||||
| chr14:74157457
|
A | ATT | 49 | a0001c0001t0001g0213a0001c0001t0001g0216a0001c0001t0001g0217others(46): Show | 49 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.284-41464_284-4146 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74157457 | |||||
| chr14:74157457
|
A | T | 12 | a0001c0001t0001g0214a0001c0001t0001g0218a0001c0001t0001g0256others(9): Show | 12 | HG00558.hp1 HG01192.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-41465A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157457 | ||||||
| chr14:74157458
|
TA | T | 3 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200 | 3 | HG02809.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.284-41463delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157458 | ||||||
| chr14:74157459
|
A | AT | 9 | a0001c0001t0004g0210a0001c0001t0004g0348a0001c0001t0004g0349others(6): Show | 9 | HG01109.hp2 HG01891.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-41457dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74157459 | |||||
| chr14:74157459
|
A | ATAT | 22 | a0001c0001t0002g0276a0001c0001t0003g0323a0001c0001t0005g0297others(19): Show | 23 | HG00280.hp1 HG00639.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.284-41462_284-4146 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74157459 | |||||
| chr14:74157459
|
A | ATT | 17 | a0001c0001t0001g0215a0001c0001t0001g0220a0001c0001t0001g0250others(14): Show | 17 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.284-41458_284-4145 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74157459 | |||||
| chr14:74157459
|
A | ATTT | 10 | a0001c0001t0002g0277a0001c0001t0005g0300a0001c0001t0005g0301others(7): Show | 10 | HG01123.hp2 HG01978.hp1 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-41459_284-4145 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74157459 | |||||
| chr14:74157459
|
A | T | 128 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0205others(125): Show | 128 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.284-41463A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157459 | ||||||
| chr14:74157460
|
T | TA | 84 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(81): Show | 84 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.284-41462_284-4146 others(5): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157460 | ||||||
| chr14:74157460
|
T | TATA | 9 | a0001c0001t0005g0303a0001c0001t0005g0304a0001c0001t0005g0305others(6): Show | 9 | HG00323.hp1 HG00741.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.284-41462_284-4146 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157460 | ||||||
| chr14:74157461
|
T | A | 1 | a0001c0001t0003g0064 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.284-41461T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157461 | ||||||
| chr14:74157493
|
G | T | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.284-41429G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157493 | ||||||
| chr14:74157660
|
G | A | 1 | a0001c0001t0029g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.284-41262G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157660 | ||||||
| chr14:74157705
|
G | A | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-41217G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157705 | ||||||
| chr14:74157894
|
T | C | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-41028T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157894 | ||||||
| chr14:74157952
|
A | G | 2 | a0001c0001t0001g0338a0001c0001t0001g0340 | 2 | HG01106.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.284-40970A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157952 | ||||||
| chr14:74157955
|
C | G | 1 | a0001c0001t0001g0255 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.284-40967C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74157955 | ||||||
| chr14:74158117
|
A | AT | 12 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(9): Show | 12 | HG00323.hp1 HG02071.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-40804dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74158117 | |||||
| chr14:74158118
|
TA | T | 4 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200others(1): Show | 4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-40803delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158118 | ||||||
| chr14:74158119
|
A | AT | 28 | a0001c0001t0005g0299a0001c0001t0005g0303a0001c0001t0005g0304others(25): Show | 29 | HG00280.hp1 HG00639.hp2 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.284-40802dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74158119 | |||||
| chr14:74158119
|
A | ATT | 25 | a0001c0001t0001g0205a0001c0001t0001g0215a0001c0001t0001g0231others(22): Show | 25 | HG01074.hp1 HG01081.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.284-40802_284-4080 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74158119 | |||||
| chr14:74158119
|
A | ATTT | 16 | a0001c0001t0001g0213a0001c0001t0001g0272a0001c0001t0001g0338others(13): Show | 16 | HG01106.hp1 HG01243.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.284-40802_284-4080 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74158119 | |||||
| chr14:74158119
|
A | T | 18 | a0001c0001t0001g0341a0001c0001t0002g0195a0001c0001t0002g0196others(15): Show | 18 | HG00323.hp1 HG01496.hp1 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.284-40803A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158119 | ||||||
| chr14:74158121
|
A | ATT | 64 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(61): Show | 64 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.284-40800_284-4079 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74158121 | |||||
| chr14:74158121
|
A | T | 130 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0191others(127): Show | 131 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.284-40801A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158121 | ||||||
| chr14:74158123
|
A | ATTTT | 72 | a0001c0001t0001g0214a0001c0001t0002g0027a0001c0001t0002g0073others(69): Show | 72 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.284-40798_284-4079 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74158123 | |||||
| chr14:74158123
|
A | T | 205 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0191others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.284-40799A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158123 | ||||||
| chr14:74158124
|
TA | T | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-40797delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158124 | ||||||
| chr14:74158125
|
A | T | 291 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0161others(288): Show | 292 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.284-40797A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158125 | ||||||
| chr14:74158127
|
T | A | 1 | a0001c0001t0035g0180 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.284-40795T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158127 | ||||||
| chr14:74158184
|
G | A | 1 | a0001c0001t0005g0310 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.284-40738G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158184 | ||||||
| chr14:74158254
|
C | T | 3 | a0001c0001t0003g0008a0001c0001t0003g0018a0001c0001t0004g0009 | 3 | HG00597.hp1 HG02083.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.284-40668C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158254 | ||||||
| chr14:74158260
|
C | T | 143 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(140): Show | 144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-40662C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158260 | ||||||
| chr14:74158273
|
C | T | 3 | a0001c0001t0022g0056a0001c0001t0022g0075a0001c0001t0039g0031 | 3 | NA18991.hp2 NA19009.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.284-40649C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158273 | ||||||
| chr14:74158306
|
T | G | 81 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(78): Show | 81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.284-40616T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158306 | ||||||
| chr14:74158402
|
C | T | 1 | a0001c0001t0001g0342 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.284-40520C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158402 | ||||||
| chr14:74158429
|
C | T | 2 | a0001c0001t0003g0018a0001c0001t0004g0009 | 2 | HG00597.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.284-40493C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158429 | ||||||
| chr14:74158481
|
TG | T | 81 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(78): Show | 81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.284-40440delG | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158481 | ||||||
| chr14:74158486
|
A | G | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.284-40436A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158486 | ||||||
| chr14:74158531
|
T | C | 1 | a0001c0001t0007g0109 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.284-40391T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158531 | ||||||
| chr14:74158571
|
C | T | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-40351C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158571 | ||||||
| chr14:74158776
|
C | T | 81 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(78): Show | 81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.284-40146C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158776 | ||||||
| chr14:74158777
|
C | T | 1 | a0001c0001t0005g0299 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.284-40145C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158777 | ||||||
| chr14:74158782
|
G | A | 1 | a0001c0001t0012g0081 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.284-40140G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158782 | ||||||
| chr14:74158873
|
C | T | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-40049C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158873 | ||||||
| chr14:74158991
|
C | T | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.284-39931C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74158991 | ||||||
| chr14:74159040
|
G | C | 1 | a0001c0001t0015g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.284-39882G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159040 | ||||||
| chr14:74159070
|
T | C | 7 | a0001c0001t0002g0276a0001c0001t0002g0277a0001c0001t0011g0221others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-39852T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159070 | ||||||
| chr14:74159168
|
T | TATTA | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-39753_284-3975 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74159168 | |||||
| chr14:74159348
|
T | C | 7 | a0001c0001t0011g0204a0001c0001t0014g0198a0001c0001t0014g0199others(4): Show | 7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-39574T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159348 | ||||||
| chr14:74159428
|
C | T | 1 | a0001c0001t0002g0166 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.284-39494C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159428 | ||||||
| chr14:74159503
|
C | T | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-39419C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159503 | ||||||
| chr14:74159566
|
TG | T | 3 | a0001c0001t0001g0110a0001c0001t0010g0113a0001c0001t0010g0126 | 3 | HG00099.hp2 HG00741.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.284-39355delG | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159566 | ||||||
| chr14:74159567
|
G | T | 2 | a0001c0001t0001g0097a0001c0001t0010g0112 | 2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.284-39355G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159567 | ||||||
| chr14:74159567
|
GT | G | 271 | a0001c0001t0001g0191a0001c0001t0001g0205a0001c0001t0001g0213others(268): Show | 272 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.284-39335delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74159567 | |||||
| chr14:74159567
|
GTT | G | 9 | a0001c0001t0011g0204a0001c0001t0014g0198a0001c0001t0014g0199others(6): Show | 10 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-39336_284-3933 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74159567 | |||||
| chr14:74159574
|
T | G | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG01891.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.284-39348T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159574 | ||||||
| chr14:74159575
|
T | G | 230 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(227): Show | 231 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.284-39347T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159575 | ||||||
| chr14:74159576
|
T | G | 1 | a0001c0001t0007g0004 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.284-39346T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159576 | ||||||
| chr14:74159588
|
G | A | 6 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(3): Show | 6 | HG02258.hp2 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-39334G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159588 | ||||||
| chr14:74159791
|
C | T | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284-39131C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159791 | ||||||
| chr14:74159841
|
T | G | 244 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(241): Show | 246 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.284-39081T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159841 | ||||||
| chr14:74159862
|
G | A | 1 | a0001c0001t0005g0320 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.284-39060G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159862 | ||||||
| chr14:74159904
|
C | A | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-39018C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74159904 | ||||||
| chr14:74160055
|
A | G | 102 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.284-38867A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160055 | ||||||
| chr14:74160070
|
C | G | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-38852C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160070 | ||||||
| chr14:74160118
|
G | A | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-38804G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160118 | ||||||
| chr14:74160191
|
A | G | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-38731A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160191 | ||||||
| chr14:74160261
|
G | A | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-38661G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160261 | ||||||
| chr14:74160337
|
T | G | 8 | a0001c0001t0004g0077a0001c0001t0012g0078a0001c0001t0012g0081others(5): Show | 8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-38585T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160337 | ||||||
| chr14:74160439
|
C | T | 77 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(74): Show | 77 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.284-38483C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160439 | ||||||
| chr14:74160632
|
C | T | 42 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(39): Show | 43 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.284-38290C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160632 | ||||||
| chr14:74160732
|
T | C | 2 | a0001c0001t0002g0192a0001c0001t0015g0185 | 2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.284-38190T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160732 | ||||||
| chr14:74160918
|
A | G | 1 | a0001c0001t0008g0311 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.284-38004A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160918 | ||||||
| chr14:74160931
|
C | T | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.284-37991C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160931 | ||||||
| chr14:74160981
|
C | G | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-37941C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160981 | ||||||
| chr14:74160987
|
T | C | 1 | a0001c0001t0011g0225 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.284-37935T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74160987 | ||||||
| chr14:74161010
|
A | T | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-37912A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74161010 | ||||||
| chr14:74161295
|
C | T | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.284-37627C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74161295 | ||||||
| chr14:74161477
|
G | A | 1 | a0001c0001t0034g0119 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.284-37445G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74161477 | ||||||
| chr14:74161486
|
C | T | 1 | a0001c0001t0008g0312 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.284-37436C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74161486 | ||||||
| chr14:74161495
|
G | A | 3 | a0001c0001t0011g0204a0001c0001t0014g0203a0001c0001t0029g0202 | 3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.284-37427G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74161495 | ||||||
| chr14:74161700
|
G | C | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-37222G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74161700 | ||||||
| chr14:74161936
|
G | C | 74 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(71): Show | 74 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.284-36986G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74161936 | ||||||
| chr14:74162104
|
T | G | 1 | a0001c0001t0002g0189 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.284-36818T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162104 | ||||||
| chr14:74162282
|
C | T | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.284-36640C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162282 | ||||||
| chr14:74162292
|
A | G | 5 | a0001c0001t0003g0059a0001c0001t0003g0060a0001c0001t0003g0061others(2): Show | 5 | HG00323.hp2 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-36630A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162292 | ||||||
| chr14:74162443
|
C | T | 29 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0007g0004others(26): Show | 29 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.284-36479C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162443 | ||||||
| chr14:74162462
|
A | G | 102 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.284-36460A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162462 | ||||||
| chr14:74162475
|
C | CA | 53 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0233others(50): Show | 53 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.284-36427dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74162475 | |||||
| chr14:74162475
|
C | CAA | 77 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(74): Show | 77 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.284-36428_284-3642 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74162475 | |||||
| chr14:74162475
|
CA | C | 50 | a0001c0001t0001g0152a0001c0001t0002g0196a0001c0001t0003g0015others(47): Show | 51 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.284-36427delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74162475 | |||||
| chr14:74162477
|
A | C | 3 | a0001c0002t0009g0282a0001c0002t0009g0283a0001c0002t0009g0284 | 3 | HG02622.hp1 HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.284-36445A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162477 | ||||||
| chr14:74162478
|
A | C | 5 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-36444A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162478 | ||||||
| chr14:74162479
|
A | C | 3 | a0001c0002t0009g0282a0001c0002t0009g0283a0001c0002t0009g0284 | 3 | HG02622.hp1 HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.284-36443A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162479 | ||||||
| chr14:74162480
|
A | C | 5 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-36442A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162480 | ||||||
| chr14:74162513
|
C | T | 1 | a0001c0001t0025g0087 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.284-36409C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162513 | ||||||
| chr14:74162528
|
T | C | 1 | a0001c0001t0001g0253 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.284-36394T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162528 | ||||||
| chr14:74162563
|
GA | G | 6 | a0001c0001t0001g0240a0001c0001t0002g0260a0001c0001t0002g0261others(3): Show | 6 | HG02040.hp2 HG02155.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-36350delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74162563 | |||||
| chr14:74162630
|
G | C | 9 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(6): Show | 9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-36292G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162630 | ||||||
| chr14:74162780
|
C | T | 244 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(241): Show | 246 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.284-36142C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162780 | ||||||
| chr14:74162957
|
C | T | 1 | a0001c0001t0001g0339 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-35965C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162957 | ||||||
| chr14:74162965
|
T | G | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-35957T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74162965 | ||||||
| chr14:74162998
|
TTAAG | T | 5 | a0001c0001t0011g0221a0001c0001t0011g0222a0001c0001t0011g0223others(2): Show | 5 | HG01891.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-35919_284-3591 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74162998 | |||||
| chr14:74163151
|
A | T | 1 | a0001c0001t0001g0238 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.284-35771A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163151 | ||||||
| chr14:74163331
|
C | A | 1 | a0001c0001t0007g0109 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.284-35591C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163331 | ||||||
| chr14:74163362
|
G | A | 1 | a0001c0001t0041g0298 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.284-35560G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163362 | ||||||
| chr14:74163362
|
G | T | 6 | a0001c0001t0001g0286a0001c0001t0001g0290a0001c0001t0001g0291others(3): Show | 6 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-35560G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163362 | ||||||
| chr14:74163467
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.284-35455A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163467 | ||||||
| chr14:74163472
|
C | G | 3 | a0001c0001t0002g0195a0001c0001t0002g0196a0001c0001t0006g0194 | 3 | HG01496.hp1 HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.284-35450C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163472 | ||||||
| chr14:74163496
|
G | A | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-35426G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163496 | ||||||
| chr14:74163635
|
T | A | 16 | a0001c0001t0004g0077a0001c0001t0004g0348a0001c0001t0004g0349others(13): Show | 16 | HG00438.hp1 HG01109.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.284-35287T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163635 | ||||||
| chr14:74163801
|
G | A | 9 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(6): Show | 9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-35121G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163801 | ||||||
| chr14:74163814
|
G | A | 2 | a0001c0001t0001g0338a0001c0001t0001g0340 | 2 | HG01106.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.284-35108G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163814 | ||||||
| chr14:74163881
|
A | C | 45 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217others(42): Show | 45 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.284-35041A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163881 | ||||||
| chr14:74163892
|
C | T | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-35030C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74163892 | ||||||
| chr14:74163984
|
A | AT | 82 | a0001c0001t0001g0097a0001c0001t0001g0205a0001c0001t0001g0213others(79): Show | 82 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.284-34923dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74163984 | |||||
| chr14:74164138
|
T | C | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.284-34784T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164138 | ||||||
| chr14:74164253
|
T | C | 102 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.284-34669T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164253 | ||||||
| chr14:74164287
|
G | GT | 235 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(232): Show | 236 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.284-34626dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74164287 | |||||
| chr14:74164297
|
G | C | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-34625G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164297 | ||||||
| chr14:74164384
|
A | G | 6 | a0001c0001t0002g0128a0001c0001t0002g0144a0001c0001t0002g0145others(3): Show | 6 | NA18946.hp1 NA18954.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-34538A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164384 | ||||||
| chr14:74164407
|
C | T | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.284-34515C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164407 | ||||||
| chr14:74164420
|
G | A | 1 | a0002c0003t0044g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.284-34502G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164420 | ||||||
| chr14:74164434
|
A | G | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-34488A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164434 | ||||||
| chr14:74164477
|
G | A | 2 | a0001c0001t0012g0086a0001c0001t0025g0087 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.284-34445G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164477 | ||||||
| chr14:74164613
|
C | T | 5 | a0001c0001t0004g0206a0001c0001t0004g0207a0001c0001t0004g0208others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-34309C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164613 | ||||||
| chr14:74164664
|
C | G | 74 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(71): Show | 74 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.284-34258C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164664 | ||||||
| chr14:74164700
|
T | C | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-34222T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164700 | ||||||
| chr14:74164786
|
A | G | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-34136A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164786 | ||||||
| chr14:74164919
|
A | C | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.284-34003A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164919 | ||||||
| chr14:74164987
|
A | G | 9 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(6): Show | 9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-33935A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74164987 | ||||||
| chr14:74165054
|
A | C | 122 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(119): Show | 123 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.284-33868A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165054 | ||||||
| chr14:74165082
|
A | C | 1 | a0001c0001t0003g0088 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.284-33840A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165082 | ||||||
| chr14:74165107
|
G | A | 4 | a0001c0001t0021g0079a0001c0001t0021g0084a0001c0001t0036g0082others(1): Show | 4 | HG02895.hp1 HG03486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-33815G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165107 | ||||||
| chr14:74165117
|
T | C | 9 | a0001c0001t0005g0303a0001c0001t0005g0304a0001c0001t0005g0305others(6): Show | 9 | HG00323.hp1 HG00741.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.284-33805T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165117 | ||||||
| chr14:74165217
|
G | A | 7 | a0001c0001t0011g0204a0001c0001t0014g0198a0001c0001t0014g0199others(4): Show | 7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-33705G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165217 | ||||||
| chr14:74165237
|
T | C | 1 | a0001c0001t0002g0181 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.284-33685T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165237 | ||||||
| chr14:74165267
|
AG | A | 9 | a0001c0001t0001g0205a0001c0001t0001g0231a0001c0001t0001g0234others(6): Show | 10 | HG01081.hp2 HG01884.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-33650delG | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165267 | |||||
| chr14:74165327
|
C | T | 1 | a0001c0001t0006g0165 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.284-33595C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165327 | ||||||
| chr14:74165444
|
G | T | 38 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(35): Show | 39 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.284-33478G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165444 | ||||||
| chr14:74165513
|
C | CTT | 9 | a0001c0001t0003g0008a0001c0001t0004g0077a0001c0001t0012g0078others(6): Show | 9 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-33395_284-3339 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | |||||
| chr14:74165513
|
C | CTTTTCTT others(6): Show |
8 | a0001c0001t0001g0191a0001c0001t0002g0190a0001c0001t0002g0192others(5): Show | 8 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-33405_284-3340 others(17): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | |||||
| chr14:74165513
|
C | CTTTTCTT others(7): Show |
3 | a0001c0001t0001g0097a0001c0001t0002g0189a0001c0001t0010g0113 | 3 | HG00099.hp2 HG01175.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.284-33405_284-3340 others(18): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | |||||
| chr14:74165513
|
C | CTTTTCTT others(8): Show |
2 | a0001c0001t0001g0110a0001c0001t0010g0112 | 2 | HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.284-33405_284-3340 others(19): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | |||||
| chr14:74165513
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0004g0009 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.284-33402_284-3340 others(17): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | |||||
| chr14:74165513
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0005g0310 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.284-33403_284-3339 others(14): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | |||||
| chr14:74165513
|
C | CTTTTTTT others(4): Show |
38 | a0001c0001t0002g0073a0001c0001t0003g0069a0001c0001t0003g0323others(35): Show | 39 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.284-33404_284-3339 others(15): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | |||||
| chr14:74165513
|
C | CTTTTTTT others(5): Show |
96 | a0001c0001t0001g0335a0001c0001t0002g0027a0001c0001t0002g0092others(93): Show | 97 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.284-33405_284-3339 others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | |||||
| chr14:74165513
|
C | CTTTTTTT others(6): Show |
28 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0003g0015others(25): Show | 28 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.284-33406_284-3339 others(17): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | |||||
| chr14:74165513
|
C | CTTTTTTT others(7): Show |
10 | a0001c0001t0003g0033a0001c0001t0007g0098a0001c0001t0007g0115others(7): Show | 10 | HG02647.hp2 HG03017.hp1 HG03688.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-33407_284-3339 others(18): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | |||||
| chr14:74165513
|
C | CTTTTTTT others(8): Show |
9 | a0001c0001t0007g0095a0001c0001t0007g0107a0001c0001t0010g0096others(6): Show | 9 | HG01081.hp1 HG02809.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.284-33408_284-3339 others(19): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | |||||
| chr14:74165513
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0014g0198 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.284-33394_284-3339 others(20): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165513 | |||||
| chr14:74165526
|
T | TTTGAGAC others(4): Show |
1 | a0001c0001t0043g0249 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.284-33394_284-3338 others(15): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165526 | |||||
| chr14:74165589
|
A | G | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.284-33333A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165589 | ||||||
| chr14:74165853
|
A | G | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-33069A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165853 | ||||||
| chr14:74165894
|
A | AT | 15 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0002g0092others(12): Show | 16 | HG02145.hp2 HG02258.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.284-33014dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165894 | |||||
| chr14:74165894
|
AT | A | 16 | a0001c0001t0001g0191a0001c0001t0001g0236a0001c0001t0001g0268others(13): Show | 16 | HG00323.hp2 HG01081.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.284-33014delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74165894 | |||||
| chr14:74165984
|
C | T | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-32938C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74165984 | ||||||
| chr14:74166235
|
A | G | 1 | a0001c0001t0035g0180 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.284-32687A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74166235 | ||||||
| chr14:74166252
|
C | T | 1 | a0001c0001t0016g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.284-32670C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74166252 | ||||||
| chr14:74166457
|
C | T | 2 | a0001c0001t0012g0086a0001c0001t0025g0087 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.284-32465C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74166457 | ||||||
| chr14:74166502
|
C | T | 2 | a0001c0001t0003g0034a0001c0001t0004g0026 | 2 | NA18956.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.284-32420C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74166502 | ||||||
| chr14:74166503
|
G | A | 12 | a0001c0001t0004g0077a0001c0001t0004g0348a0001c0001t0004g0349others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-32419G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74166503 | ||||||
| chr14:74166583
|
A | C | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-32339A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74166583 | ||||||
| chr14:74166906
|
G | A | 34 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0002g0117others(31): Show | 34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.284-32016G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74166906 | ||||||
| chr14:74166907
|
C | T | 34 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0002g0117others(31): Show | 34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.284-32015C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74166907 | ||||||
| chr14:74167044
|
G | A | 1 | a0002c0003t0044g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.284-31878G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74167044 | ||||||
| chr14:74167107
|
T | C | 1 | a0001c0001t0003g0323 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.284-31815T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74167107 | ||||||
| chr14:74167112
|
C | CT | 94 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0258others(91): Show | 96 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.284-31790dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74167112 | |||||
| chr14:74167112
|
C | CTT | 97 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(94): Show | 97 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.284-31791_284-3179 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74167112 | |||||
| chr14:74167112
|
C | CTTTT | 68 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(65): Show | 68 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.284-31793_284-3179 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74167112 | |||||
| chr14:74167133
|
A | G | 1 | a0001c0001t0003g0061 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.284-31789A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74167133 | ||||||
| chr14:74167162
|
G | C | 242 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(239): Show | 243 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.284-31760G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74167162 | ||||||
| chr14:74167208
|
A | G | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-31714A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74167208 | ||||||
| chr14:74167527
|
A | C | 2 | a0001c0001t0017g0321a0001c0001t0017g0322 | 2 | HG00280.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.284-31395A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74167527 | ||||||
| chr14:74167950
|
G | A | 1 | a0001c0001t0003g0033 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.284-30972G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74167950 | ||||||
| chr14:74167966
|
A | AT | 223 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(220): Show | 224 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.284-30952dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74167966 | |||||
| chr14:74167978
|
GGTTT | G | 9 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(6): Show | 9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-30939_284-3093 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74167978 | |||||
| chr14:74168049
|
G | A | 241 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(238): Show | 242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.284-30873G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168049 | ||||||
| chr14:74168104
|
A | G | 1 | a0001c0001t0001g0340 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.284-30818A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168104 | ||||||
| chr14:74168397
|
G | A | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-30525G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168397 | ||||||
| chr14:74168464
|
C | T | 1 | a0001c0001t0004g0009 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.284-30458C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168464 | ||||||
| chr14:74168467
|
G | C | 5 | a0001c0001t0004g0206a0001c0001t0004g0207a0001c0001t0004g0208others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-30455G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168467 | ||||||
| chr14:74168476
|
G | C | 2 | a0001c0001t0004g0206a0001c0001t0012g0209 | 2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.284-30446G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168476 | ||||||
| chr14:74168669
|
G | GA | 9 | a0001c0001t0011g0204a0001c0001t0014g0198a0001c0001t0014g0199others(6): Show | 9 | HG02145.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.284-30243dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74168669 | |||||
| chr14:74168708
|
T | A | 1 | a0001c0001t0028g0101 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.284-30214T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168708 | ||||||
| chr14:74168741
|
C | A | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-30181C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168741 | ||||||
| chr14:74168840
|
G | A | 1 | a0001c0001t0003g0045 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.284-30082G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168840 | ||||||
| chr14:74168873
|
C | T | 7 | a0001c0001t0011g0204a0001c0001t0014g0198a0001c0001t0014g0199others(4): Show | 7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-30049C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168873 | ||||||
| chr14:74168916
|
G | A | 2 | a0001c0001t0002g0137a0001c0001t0002g0150 | 2 | HG01358.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.284-30006G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168916 | ||||||
| chr14:74168926
|
G | A | 1 | a0001c0001t0001g0347 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.284-29996G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168926 | ||||||
| chr14:74168932
|
C | T | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-29990C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168932 | ||||||
| chr14:74168948
|
G | A | 76 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(73): Show | 76 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.284-29974G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74168948 | ||||||
| chr14:74169046
|
T | G | 45 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0191others(42): Show | 45 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.284-29876T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74169046 | ||||||
| chr14:74169180
|
T | C | 1 | a0001c0001t0001g0335 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.284-29742T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74169180 | ||||||
| chr14:74169329
|
C | T | 1 | a0001c0001t0003g0323 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.284-29593C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74169329 | ||||||
| chr14:74169387
|
G | T | 1 | a0001c0001t0003g0045 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.284-29535G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74169387 | ||||||
| chr14:74169696
|
A | AC | 9 | a0001c0001t0001g0215a0001c0001t0001g0238a0001c0001t0003g0065others(6): Show | 9 | HG00673.hp2 HG01978.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.284-29221dupC | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74169696 | |||||
| chr14:74169701
|
C | T | 1 | a0001c0001t0002g0151 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.284-29221C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74169701 | ||||||
| chr14:74169705
|
T | A | 1 | a0001c0001t0002g0151 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.284-29217T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74169705 | ||||||
| chr14:74169827
|
A | T | 1 | a0001c0001t0002g0151 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.284-29095A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74169827 | ||||||
| chr14:74169879
|
T | G | 10 | a0001c0001t0002g0092a0001c0001t0011g0204a0001c0001t0014g0198others(7): Show | 10 | HG02145.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-29043T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74169879 | ||||||
| chr14:74169934
|
G | T | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-28988G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74169934 | ||||||
| chr14:74169983
|
A | G | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-28939A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74169983 | ||||||
| chr14:74170075
|
G | A | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-28847G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74170075 | ||||||
| chr14:74170129
|
G | C | 1 | a0001c0001t0001g0342 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.284-28793G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74170129 | ||||||
| chr14:74170170
|
A | G | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-28752A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74170170 | ||||||
| chr14:74170215
|
C | G | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.284-28707C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74170215 | ||||||
| chr14:74170475
|
G | A | 289 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0191others(286): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.284-28447G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74170475 | ||||||
| chr14:74170506
|
CA | C | 148 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(145): Show | 149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.284-28405delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74170506 | |||||
| chr14:74170741
|
G | A | 143 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(140): Show | 144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-28181G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74170741 | ||||||
| chr14:74170881
|
A | T | 1 | a0001c0001t0013g0120 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.284-28041A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74170881 | ||||||
| chr14:74170881
|
AT | A | 141 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(138): Show | 142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.284-28036delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74170881 | |||||
| chr14:74170882
|
T | A | 100 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0002g0092others(97): Show | 100 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.284-28040T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74170882 | ||||||
| chr14:74170932
|
A | G | 1 | a0001c0001t0002g0276 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.284-27990A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74170932 | ||||||
| chr14:74170995
|
A | G | 3 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200 | 3 | HG02809.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.284-27927A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74170995 | ||||||
| chr14:74171018
|
C | CAA | 91 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0002g0276others(88): Show | 92 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.284-27888_284-2788 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74171018 | |||||
| chr14:74171138
|
CTT | C | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-27782_284-2778 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74171138 | |||||
| chr14:74171363
|
T | TA | 21 | a0001c0001t0001g0215a0001c0001t0001g0335a0001c0001t0001g0341others(18): Show | 21 | HG00642.hp1 HG01109.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.284-27544dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74171363 | |||||
| chr14:74171464
|
G | A | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-27458G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74171464 | ||||||
| chr14:74171697
|
ATAT | A | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-27220_284-2721 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74171697 | |||||
| chr14:74171705
|
TTA | T | 143 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(140): Show | 144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-27215_284-2721 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74171705 | |||||
| chr14:74171736
|
C | CT | 53 | a0001c0001t0001g0191a0001c0001t0002g0117a0001c0001t0002g0118others(50): Show | 53 | HG00438.hp1 HG00544.hp1 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.284-27166dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74171736 | |||||
| chr14:74171736
|
C | CTT | 95 | a0001c0001t0001g0335a0001c0001t0002g0027a0001c0001t0002g0073others(92): Show | 96 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.284-27167_284-2716 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74171736 | |||||
| chr14:74171736
|
C | CTTT | 56 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0003g0323others(53): Show | 57 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.284-27168_284-2716 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74171736 | |||||
| chr14:74171736
|
C | CTTTT | 6 | a0001c0001t0005g0299a0001c0001t0005g0319a0001c0001t0008g0296others(3): Show | 6 | HG01243.hp1 HG02165.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-27169_284-2716 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74171736 | |||||
| chr14:74171736
|
CTTTTTTT | C | 81 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(78): Show | 81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.284-27172_284-2716 others(11): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74171736 | |||||
| chr14:74171765
|
G | A | 1 | a0001c0001t0013g0111 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.284-27157G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74171765 | ||||||
| chr14:74171789
|
A | G | 1 | a0001c0001t0004g0349 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.284-27133A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74171789 | ||||||
| chr14:74171802
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.284-27120G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74171802 | ||||||
| chr14:74171846
|
C | G | 1 | a0001c0001t0004g0029 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.284-27076C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74171846 | ||||||
| chr14:74172095
|
G | T | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-26827G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74172095 | ||||||
| chr14:74172096
|
T | C | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-26826T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74172096 | ||||||
| chr14:74172197
|
T | C | 1 | a0002c0003t0044g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.284-26725T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74172197 | ||||||
| chr14:74172422
|
T | C | 1 | a0001c0001t0025g0087 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.284-26500T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74172422 | ||||||
| chr14:74172615
|
T | C | 3 | a0001c0001t0001g0220a0001c0001t0001g0266a0001c0001t0001g0267 | 3 | HG00280.hp2 HG01255.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.284-26307T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74172615 | ||||||
| chr14:74172769
|
C | G | 7 | a0001c0001t0002g0276a0001c0001t0002g0277a0001c0001t0011g0221others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-26153C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74172769 | ||||||
| chr14:74172902
|
T | C | 1 | a0001c0001t0007g0004 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.284-26020T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74172902 | ||||||
| chr14:74172909
|
C | G | 9 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0272others(6): Show | 9 | HG01192.hp1 HG02027.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-26013C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74172909 | ||||||
| chr14:74173052
|
G | C | 4 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200others(1): Show | 4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-25870G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74173052 | ||||||
| chr14:74173265
|
G | T | 102 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.284-25657G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74173265 | ||||||
| chr14:74173327
|
A | C | 1 | a0001c0001t0041g0298 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.284-25595A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74173327 | ||||||
| chr14:74173434
|
G | A | 84 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(81): Show | 84 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.284-25488G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74173434 | ||||||
| chr14:74173477
|
G | A | 4 | a0001c0001t0002g0131a0001c0001t0002g0138a0001c0001t0002g0160others(1): Show | 4 | HG00642.hp1 HG00735.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-25445G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74173477 | ||||||
| chr14:74173659
|
A | T | 1 | a0001c0001t0040g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.284-25263A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74173659 | ||||||
| chr14:74173809
|
T | C | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.284-25113T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74173809 | ||||||
| chr14:74173889
|
C | A | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-25033C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74173889 | ||||||
| chr14:74173900
|
G | T | 8 | a0001c0001t0004g0077a0001c0001t0012g0078a0001c0001t0012g0081others(5): Show | 8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-25022G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74173900 | ||||||
| chr14:74173998
|
C | T | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-24924C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74173998 | ||||||
| chr14:74174269
|
A | G | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-24653A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74174269 | ||||||
| chr14:74174283
|
C | T | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284-24639C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74174283 | ||||||
| chr14:74174357
|
T | G | 3 | a0001c0001t0011g0204a0001c0001t0014g0203a0001c0001t0029g0202 | 3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.284-24565T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74174357 | ||||||
| chr14:74174504
|
T | C | 1 | a0001c0001t0002g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.284-24418T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74174504 | ||||||
| chr14:74174508
|
G | A | 1 | a0001c0001t0005g0328 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.284-24414G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74174508 | ||||||
| chr14:74174535
|
T | C | 3 | a0001c0001t0011g0204a0001c0001t0014g0203a0001c0001t0029g0202 | 3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.284-24387T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74174535 | ||||||
| chr14:74174550
|
G | A | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-24372G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74174550 | ||||||
| chr14:74174650
|
G | A | 1 | a0001c0001t0005g0304 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.284-24272G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74174650 | ||||||
| chr14:74174770
|
A | T | 2 | a0001c0001t0012g0086a0001c0001t0025g0087 | 2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.284-24152A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74174770 | ||||||
| chr14:74174789
|
G | GA | 138 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0002g0092others(135): Show | 139 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.284-24123dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74174789 | |||||
| chr14:74174789
|
G | GAA | 103 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.284-24124_284-2412 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74174789 | |||||
| chr14:74174871
|
A | G | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-24051A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74174871 | ||||||
| chr14:74175020
|
A | AAATAAT | 4 | a0001c0001t0001g0346a0001c0001t0001g0347a0001c0001t0004g0344others(1): Show | 4 | HG01123.hp1 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-23883_284-2387 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175020 | |||||
| chr14:74175020
|
A | AAATAATA others(5): Show |
14 | a0001c0001t0001g0232a0001c0001t0002g0277a0001c0001t0011g0222others(11): Show | 14 | HG01891.hp1 HG02258.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-23889_284-2387 others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175020 | |||||
| chr14:74175020
|
A | AAATAATA others(8): Show |
16 | a0001c0001t0002g0276a0001c0001t0003g0024a0001c0001t0003g0033others(13): Show | 16 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.284-23892_284-2387 others(19): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175020 | |||||
| chr14:74175020
|
A | AAATAATA others(11): Show |
142 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(139): Show | 142 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.284-23895_284-2387 others(22): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175020 | |||||
| chr14:74175020
|
A | AAATAATA others(14): Show |
49 | a0001c0001t0001g0226a0001c0001t0001g0258a0001c0001t0001g0287others(46): Show | 50 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.284-23898_284-2387 others(25): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175020 | |||||
| chr14:74175020
|
A | AAATAATA others(17): Show |
14 | a0001c0001t0001g0235a0001c0001t0001g0342a0001c0001t0003g0025others(11): Show | 14 | HG00558.hp1 HG01943.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-23901_284-2387 others(28): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175020 | |||||
| chr14:74175020
|
A | AAATAATA others(23): Show |
1 | a0001c0001t0002g0092 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.284-23878_284-2387 others(34): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175020 | |||||
| chr14:74175020
|
AAAT | A | 47 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0191others(44): Show | 48 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.284-23880_284-2387 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175020 | |||||
| chr14:74175040
|
A | G | 1 | a0001c0001t0040g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.284-23882A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175040 | ||||||
| chr14:74175072
|
A | G | 1 | a0001c0001t0001g0335 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.284-23850A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175072 | ||||||
| chr14:74175083
|
T | C | 1 | a0001c0001t0007g0103 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.284-23839T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175083 | ||||||
| chr14:74175220
|
A | G | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG00099.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.284-23702A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175220 | ||||||
| chr14:74175242
|
C | CTGTA | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-23679_284-2367 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175242 | |||||
| chr14:74175529
|
C | CA | 5 | a0001c0001t0001g0240a0001c0001t0008g0312a0001c0001t0034g0119others(2): Show | 6 | HG01074.hp2 HG01981.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-23381dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175529 | |||||
| chr14:74175529
|
CA | C | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-23381delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175529 | |||||
| chr14:74175566
|
G | A | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-23356G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175566 | ||||||
| chr14:74175577
|
G | A | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-23345G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175577 | ||||||
| chr14:74175586
|
A | G | 81 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(78): Show | 81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.284-23336A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175586 | ||||||
| chr14:74175711
|
T | C | 1 | a0001c0001t0016g0048 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.284-23211T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175711 | ||||||
| chr14:74175711
|
T | TAC | 34 | a0001c0001t0002g0128a0001c0001t0002g0140a0001c0001t0002g0144others(31): Show | 34 | HG00280.hp1 HG00323.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.284-23172_284-2317 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | |||||
| chr14:74175711
|
T | TACAC | 39 | a0001c0001t0001g0152a0001c0001t0002g0001a0001c0001t0002g0131others(36): Show | 41 | HG00408.hp1 HG00408.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.284-23174_284-2317 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | |||||
| chr14:74175711
|
T | TACACAC | 36 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0002g0137others(33): Show | 36 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.284-23176_284-2317 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | |||||
| chr14:74175711
|
T | TACACACA others(1): Show |
16 | a0001c0001t0003g0007a0001c0001t0003g0024a0001c0001t0003g0025others(13): Show | 16 | HG00438.hp2 HG02027.hp1 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.284-23178_284-2317 others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | |||||
| chr14:74175711
|
T | TACACACA others(3): Show |
9 | a0001c0001t0001g0097a0001c0001t0003g0038a0001c0001t0004g0037others(6): Show | 9 | HG00099.hp2 HG00738.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.284-23180_284-2317 others(14): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | |||||
| chr14:74175711
|
T | TACACACA others(5): Show |
3 | a0001c0001t0004g0349a0001c0001t0004g0350a0001c0001t0004g0351 | 3 | HG03195.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.284-23182_284-2317 others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | |||||
| chr14:74175711
|
T | TACACACA others(7): Show |
1 | a0001c0001t0004g0348 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.284-23184_284-2317 others(18): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | |||||
| chr14:74175711
|
TAC | T | 12 | a0001c0001t0001g0228a0001c0001t0001g0240a0001c0001t0001g0255others(9): Show | 12 | HG01106.hp1 HG02040.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-23172_284-2317 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | |||||
| chr14:74175711
|
TACAC | T | 56 | a0001c0001t0001g0205a0001c0001t0001g0215a0001c0001t0001g0216others(53): Show | 56 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.284-23174_284-2317 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | |||||
| chr14:74175711
|
TACACAC | T | 10 | a0001c0001t0001g0227a0001c0001t0001g0339a0001c0001t0002g0276others(7): Show | 10 | HG01516.hp2 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.284-23176_284-2317 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | |||||
| chr14:74175711
|
TACACACA others(3): Show |
T | 2 | a0001c0001t0023g0337a0001c0001t0023g0343 | 2 | HG01255.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.284-23180_284-2317 others(14): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175711 | |||||
| chr14:74175732
|
ACACACAC others(13): Show |
A | 10 | a0001c0002t0009g0002a0001c0002t0009g0193a0001c0002t0009g0278others(7): Show | 11 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-23188_284-2316 others(24): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175732 | |||||
| chr14:74175746
|
ACACACC | A | 7 | a0001c0001t0001g0335a0001c0001t0004g0077a0001c0001t0004g0206others(4): Show | 7 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-23174_284-2316 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175746 | |||||
| chr14:74175748
|
A | ACACACAC others(4): Show |
2 | a0001c0001t0007g0099a0001c0001t0010g0123 | 2 | HG00544.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.284-23171_284-2317 others(15): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175748 | |||||
| chr14:74175748
|
A | ACACACAC others(11): Show |
1 | a0001c0001t0006g0100 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.284-23171_284-2317 others(22): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175748 | |||||
| chr14:74175748
|
A | ACACACAC others(9): Show |
1 | a0001c0001t0013g0094 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.284-23171_284-2317 others(20): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175748 | |||||
| chr14:74175748
|
A | ACACACAC others(7): Show |
3 | a0001c0001t0007g0098a0001c0001t0007g0122a0001c0001t0027g0124 | 3 | HG02698.hp1 HG03017.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.284-23171_284-2317 others(18): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175748 | |||||
| chr14:74175748
|
A | ACACACAC others(5): Show |
8 | a0001c0001t0007g0004a0001c0001t0007g0095a0001c0001t0007g0108others(5): Show | 8 | HG00438.hp1 HG03704.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.284-23171_284-2317 others(16): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175748 | |||||
| chr14:74175748
|
A | ACACACAC others(3): Show |
12 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0006g0102others(9): Show | 12 | HG01074.hp2 HG01081.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-23171_284-2317 others(14): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175748 | |||||
| chr14:74175748
|
A | C | 1 | a0001c0001t0001g0253 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.284-23174A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175748 | ||||||
| chr14:74175748
|
ACACC | A | 11 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0012g0078others(8): Show | 11 | HG01192.hp1 HG02027.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-23172_284-2316 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175748 | |||||
| chr14:74175750
|
A | C | 33 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217others(30): Show | 33 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.284-23172A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175750 | ||||||
| chr14:74175750
|
ACC | A | 14 | a0001c0001t0001g0272a0001c0001t0002g0260a0001c0001t0002g0261others(11): Show | 14 | HG01243.hp2 HG01257.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.284-23168_284-2316 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74175750 | |||||
| chr14:74175751
|
C | CACACACA others(4): Show |
1 | a0001c0001t0001g0110 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.284-23171_284-2317 others(15): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175751 | ||||||
| chr14:74175752
|
C | A | 113 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(110): Show | 114 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.284-23170C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175752 | ||||||
| chr14:74175753
|
C | A | 3 | a0001c0001t0003g0046a0001c0001t0003g0074a0001c0001t0006g0211 | 3 | NA18950.hp1 NA19012.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.284-23169C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175753 | ||||||
| chr14:74175848
|
C | T | 1 | a0001c0001t0040g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.284-23074C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74175848 | ||||||
| chr14:74176031
|
G | A | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-22891G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74176031 | ||||||
| chr14:74176089
|
A | G | 34 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0002g0117others(31): Show | 34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.284-22833A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74176089 | ||||||
| chr14:74176224
|
G | T | 4 | a0001c0001t0004g0348a0001c0001t0004g0349a0001c0001t0004g0350others(1): Show | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-22698G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74176224 | ||||||
| chr14:74176227
|
A | G | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-22695A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74176227 | ||||||
| chr14:74176297
|
A | G | 8 | a0001c0001t0004g0077a0001c0001t0012g0078a0001c0001t0012g0081others(5): Show | 8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-22625A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74176297 | ||||||
| chr14:74176301
|
G | A | 1 | a0001c0001t0004g0009 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.284-22621G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74176301 | ||||||
| chr14:74176540
|
A | C | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-22382A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74176540 | ||||||
| chr14:74176853
|
T | C | 231 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(228): Show | 232 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.284-22069T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74176853 | ||||||
| chr14:74176963
|
G | A | 3 | a0001c0001t0001g0287a0001c0001t0001g0288a0001c0001t0001g0289 | 3 | HG02559.hp1 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.284-21959G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74176963 | ||||||
| chr14:74177030
|
C | T | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-21892C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74177030 | ||||||
| chr14:74177218
|
G | A | 4 | a0001c0001t0001g0346a0001c0001t0001g0347a0001c0001t0004g0344others(1): Show | 4 | HG01123.hp1 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-21704G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74177218 | ||||||
| chr14:74177249
|
C | T | 5 | a0001c0001t0003g0059a0001c0001t0003g0060a0001c0001t0003g0061others(2): Show | 5 | HG00323.hp2 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-21673C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74177249 | ||||||
| chr14:74177376
|
T | C | 9 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(6): Show | 9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-21546T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74177376 | ||||||
| chr14:74177418
|
A | G | 34 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0002g0117others(31): Show | 34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.284-21504A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74177418 | ||||||
| chr14:74177480
|
AAT | A | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-21440_284-2143 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74177480 | |||||
| chr14:74177531
|
A | G | 1 | a0001c0001t0004g0207 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.284-21391A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74177531 | ||||||
| chr14:74177743
|
G | A | 1 | a0001c0001t0029g0202 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.284-21179G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74177743 | ||||||
| chr14:74177808
|
C | T | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284-21114C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74177808 | ||||||
| chr14:74177904
|
A | G | 10 | a0001c0001t0001g0217a0001c0001t0001g0226a0001c0001t0001g0241others(7): Show | 10 | HG01358.hp2 NA18947.hp2 NA18962.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-21018A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74177904 | ||||||
| chr14:74178119
|
G | A | 76 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(73): Show | 76 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.284-20803G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74178119 | ||||||
| chr14:74178355
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.284-20567A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74178355 | ||||||
| chr14:74178460
|
A | AT | 53 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0216others(50): Show | 53 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.284-20447dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74178460 | |||||
| chr14:74178476
|
G | A | 1 | a0001c0001t0042g0302 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.284-20446G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74178476 | ||||||
| chr14:74178542
|
C | A | 3 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200 | 3 | HG02809.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.284-20380C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74178542 | ||||||
| chr14:74178568
|
G | A | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-20354G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74178568 | ||||||
| chr14:74178572
|
G | A | 8 | a0001c0001t0004g0077a0001c0001t0012g0078a0001c0001t0012g0081others(5): Show | 8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-20350G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74178572 | ||||||
| chr14:74178632
|
AT | A | 244 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(241): Show | 246 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.284-20283delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74178632 | |||||
| chr14:74178878
|
C | G | 1 | a0001c0001t0008g0331 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.284-20044C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74178878 | ||||||
| chr14:74179223
|
T | C | 1 | a0001c0001t0037g0091 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.284-19699T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179223 | ||||||
| chr14:74179374
|
T | G | 102 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.284-19548T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179374 | ||||||
| chr14:74179406
|
T | G | 3 | a0001c0001t0011g0204a0001c0001t0014g0203a0001c0001t0029g0202 | 3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.284-19516T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179406 | ||||||
| chr14:74179469
|
C | T | 12 | a0001c0001t0004g0077a0001c0001t0004g0348a0001c0001t0004g0349others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-19453C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179469 | ||||||
| chr14:74179503
|
T | C | 74 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(71): Show | 74 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.284-19419T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179503 | ||||||
| chr14:74179520
|
G | A | 143 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(140): Show | 144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-19402G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179520 | ||||||
| chr14:74179562
|
G | A | 12 | a0001c0001t0004g0077a0001c0001t0004g0348a0001c0001t0004g0349others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-19360G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179562 | ||||||
| chr14:74179655
|
CA | C | 135 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(132): Show | 136 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.284-19253delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74179655 | |||||
| chr14:74179655
|
CAA | C | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-19254_284-1925 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74179655 | |||||
| chr14:74179673
|
AAAAAAG | A | 76 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(73): Show | 76 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.284-19243_284-1923 others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74179673 | |||||
| chr14:74179674
|
AAAAAG | A | 67 | a0001c0001t0001g0205a0001c0001t0001g0231a0001c0001t0001g0234others(64): Show | 68 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.284-19243_284-1923 others(9): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74179674 | |||||
| chr14:74179692
|
A | C | 1 | a0001c0001t0001g0339 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-19230A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179692 | ||||||
| chr14:74179696
|
C | A | 7 | a0001c0001t0011g0204a0001c0001t0014g0198a0001c0001t0014g0199others(4): Show | 7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-19226C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179696 | ||||||
| chr14:74179700
|
G | A | 2 | a0001c0001t0003g0034a0001c0001t0004g0026 | 2 | NA18956.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.284-19222G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179700 | ||||||
| chr14:74179890
|
A | G | 1 | a0002c0003t0044g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.284-19032A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179890 | ||||||
| chr14:74179896
|
T | C | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-19026T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179896 | ||||||
| chr14:74179912
|
A | C | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.284-19010A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179912 | ||||||
| chr14:74179972
|
C | T | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-18950C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74179972 | ||||||
| chr14:74180002
|
C | T | 4 | a0001c0001t0002g0166a0001c0001t0006g0167a0001c0001t0020g0132others(1): Show | 4 | HG01167.hp1 HG01169.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-18920C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180002 | ||||||
| chr14:74180129
|
C | T | 45 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217others(42): Show | 45 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.284-18793C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180129 | ||||||
| chr14:74180191
|
A | G | 74 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(71): Show | 74 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.284-18731A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180191 | ||||||
| chr14:74180219
|
A | T | 81 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(78): Show | 81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.284-18703A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180219 | ||||||
| chr14:74180262
|
A | AT | 17 | a0001c0001t0002g0147a0001c0001t0004g0077a0001c0001t0004g0206others(14): Show | 17 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.284-18639dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74180262 | |||||
| chr14:74180262
|
A | ATT | 79 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(76): Show | 79 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.284-18640_284-1863 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74180262 | |||||
| chr14:74180262
|
A | ATTT | 11 | a0001c0001t0001g0218a0001c0001t0001g0220a0001c0001t0001g0226others(8): Show | 11 | HG00099.hp1 HG00735.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-18641_284-1863 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74180262 | |||||
| chr14:74180262
|
AT | A | 123 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0002g0092others(120): Show | 124 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.284-18639delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74180262 | |||||
| chr14:74180271
|
T | G | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-18651T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180271 | ||||||
| chr14:74180359
|
G | A | 3 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200 | 3 | HG02809.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.284-18563G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180359 | ||||||
| chr14:74180394
|
T | C | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284-18528T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180394 | ||||||
| chr14:74180422
|
T | C | 244 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(241): Show | 246 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.284-18500T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180422 | ||||||
| chr14:74180432
|
AT | A | 9 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0272others(6): Show | 9 | HG01192.hp1 HG02027.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-18479delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74180432 | |||||
| chr14:74180460
|
T | C | 143 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(140): Show | 144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-18462T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180460 | ||||||
| chr14:74180501
|
A | G | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-18421A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180501 | ||||||
| chr14:74180715
|
A | G | 143 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(140): Show | 144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-18207A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180715 | ||||||
| chr14:74180879
|
C | T | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-18043C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74180879 | ||||||
| chr14:74181033
|
A | G | 1 | a0001c0001t0012g0083 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.284-17889A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74181033 | ||||||
| chr14:74181056
|
T | C | 143 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(140): Show | 144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-17866T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74181056 | ||||||
| chr14:74181080
|
C | T | 1 | a0001c0001t0005g0305 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.284-17842C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74181080 | ||||||
| chr14:74181107
|
C | CA | 10 | a0001c0001t0002g0129a0001c0001t0002g0146a0001c0001t0002g0175others(7): Show | 10 | HG01168.hp2 HG02027.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.284-17794dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74181107 | |||||
| chr14:74181107
|
CA | C | 25 | a0001c0001t0002g0092a0001c0001t0003g0060a0001c0001t0011g0204others(22): Show | 26 | HG01243.hp1 HG01243.hp2 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.284-17794delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74181107 | |||||
| chr14:74181107
|
CAA | C | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-17795_284-1779 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74181107 | |||||
| chr14:74181107
|
CAAAA | C | 132 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(129): Show | 133 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.284-17797_284-1779 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74181107 | |||||
| chr14:74181123
|
A | G | 7 | a0001c0001t0011g0204a0001c0001t0014g0198a0001c0001t0014g0199others(4): Show | 7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-17799A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74181123 | ||||||
| chr14:74181128
|
A | G | 143 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(140): Show | 144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-17794A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74181128 | ||||||
| chr14:74181201
|
A | G | 143 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(140): Show | 144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-17721A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74181201 | ||||||
| chr14:74181237
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.284-17685A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74181237 | ||||||
| chr14:74181259
|
T | C | 143 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(140): Show | 144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-17663T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74181259 | ||||||
| chr14:74181435
|
C | CA | 43 | a0001c0001t0002g0173a0001c0001t0002g0192a0001c0001t0003g0323others(40): Show | 44 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.284-17471dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74181435 | |||||
| chr14:74181512
|
G | T | 2 | a0001c0001t0001g0239a0001c0001t0001g0253 | 2 | NA19072.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.284-17410G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74181512 | ||||||
| chr14:74181548
|
C | G | 1 | a0001c0001t0007g0105 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.284-17374C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74181548 | ||||||
| chr14:74181650
|
TACAG | T | 102 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.284-17269_284-1726 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74181650 | |||||
| chr14:74182037
|
G | T | 1 | a0001c0001t0001g0256 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.284-16885G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182037 | ||||||
| chr14:74182157
|
CATG | C | 143 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(140): Show | 144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-16764_284-1676 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182157 | ||||||
| chr14:74182403
|
A | G | 289 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0191others(286): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.284-16519A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182403 | ||||||
| chr14:74182426
|
A | G | 143 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(140): Show | 144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-16496A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182426 | ||||||
| chr14:74182447
|
A | C | 1 | a0001c0001t0005g0330 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.284-16475A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182447 | ||||||
| chr14:74182454
|
G | A | 143 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(140): Show | 144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-16468G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182454 | ||||||
| chr14:74182477
|
T | C | 2 | a0001c0001t0003g0034a0001c0001t0004g0026 | 2 | NA18956.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.284-16445T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182477 | ||||||
| chr14:74182499
|
A | AGCCAAGT others(27): Show |
41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-16398_284-1639 others(38): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74182499 | |||||
| chr14:74182561
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.284-16361A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182561 | ||||||
| chr14:74182577
|
C | T | 143 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(140): Show | 144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-16345C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182577 | ||||||
| chr14:74182659
|
T | G | 81 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(78): Show | 81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.284-16263T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182659 | ||||||
| chr14:74182828
|
C | T | 76 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(73): Show | 76 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.284-16094C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182828 | ||||||
| chr14:74182877
|
C | A | 1 | a0001c0001t0001g0339 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.284-16045C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74182877 | ||||||
| chr14:74183102
|
TC | T | 148 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(145): Show | 149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.284-15819delC | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183102 | ||||||
| chr14:74183103
|
C | T | 140 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0191others(137): Show | 141 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.284-15819C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183103 | ||||||
| chr14:74183108
|
T | C | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-15814T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183108 | ||||||
| chr14:74183157
|
A | G | 143 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(140): Show | 144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.284-15765A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183157 | ||||||
| chr14:74183252
|
C | CA | 73 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(70): Show | 73 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.284-15669dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74183252 | |||||
| chr14:74183254
|
C | T | 2 | a0001c0001t0002g0195a0001c0001t0002g0196 | 2 | HG01496.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.284-15668C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183254 | ||||||
| chr14:74183282
|
G | A | 4 | a0001c0001t0004g0348a0001c0001t0004g0349a0001c0001t0004g0350others(1): Show | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-15640G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183282 | ||||||
| chr14:74183290
|
G | A | 1 | a0001c0001t0008g0307 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.284-15632G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183290 | ||||||
| chr14:74183608
|
T | A | 1 | a0001c0001t0002g0181 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.284-15314T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183608 | ||||||
| chr14:74183635
|
T | C | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-15287T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183635 | ||||||
| chr14:74183657
|
C | T | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-15265C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183657 | ||||||
| chr14:74183765
|
C | G | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-15157C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183765 | ||||||
| chr14:74183795
|
C | T | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.284-15127C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74183795 | ||||||
| chr14:74184282
|
T | C | 2 | a0001c0001t0003g0065a0001c0001t0004g0029 | 2 | HG00673.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.284-14640T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74184282 | ||||||
| chr14:74184305
|
G | A | 7 | a0001c0001t0001g0205a0001c0001t0001g0231a0001c0001t0001g0234others(4): Show | 7 | HG01081.hp2 HG01884.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-14617G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74184305 | ||||||
| chr14:74184363
|
G | A | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-14559G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74184363 | ||||||
| chr14:74184374
|
T | C | 4 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200others(1): Show | 4 | HG02809.hp1 HG02809.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-14548T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74184374 | ||||||
| chr14:74184411
|
A | G | 102 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.284-14511A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74184411 | ||||||
| chr14:74184535
|
C | T | 7 | a0001c0001t0011g0204a0001c0001t0014g0198a0001c0001t0014g0199others(4): Show | 7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-14387C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74184535 | ||||||
| chr14:74184559
|
C | G | 1 | a0001c0001t0019g0149 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.284-14363C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74184559 | ||||||
| chr14:74184627
|
G | A | 244 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(241): Show | 246 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.284-14295G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74184627 | ||||||
| chr14:74184738
|
C | T | 130 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(127): Show | 131 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.284-14184C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74184738 | ||||||
| chr14:74184930
|
A | C | 89 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(86): Show | 89 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.284-13992A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74184930 | ||||||
| chr14:74185038
|
T | C | 3 | a0001c0001t0011g0204a0001c0001t0014g0203a0001c0001t0029g0202 | 3 | HG02572.hp1 HG02647.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.284-13884T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185038 | ||||||
| chr14:74185068
|
A | T | 1 | a0001c0001t0002g0134 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.284-13854A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185068 | ||||||
| chr14:74185209
|
A | G | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-13713A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185209 | ||||||
| chr14:74185210
|
A | G | 1 | a0001c0001t0003g0061 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.284-13712A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185210 | ||||||
| chr14:74185309
|
C | CT | 81 | a0001c0001t0001g0205a0001c0001t0001g0215a0001c0001t0001g0216others(78): Show | 81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.284-13590dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74185309 | |||||
| chr14:74185309
|
C | CTT | 35 | a0001c0001t0001g0214a0001c0001t0001g0248a0001c0001t0001g0272others(32): Show | 35 | HG00735.hp2 HG01074.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.284-13591_284-1359 others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74185309 | |||||
| chr14:74185309
|
C | CTTT | 98 | a0001c0001t0001g0213a0001c0001t0001g0335a0001c0001t0002g0073others(95): Show | 99 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.284-13592_284-1359 others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74185309 | |||||
| chr14:74185309
|
C | CTTTT | 21 | a0001c0001t0002g0027a0001c0001t0003g0016a0001c0001t0003g0019others(18): Show | 21 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.284-13593_284-1359 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74185309 | |||||
| chr14:74185309
|
C | CTTTTT | 9 | a0001c0001t0004g0036a0001c0001t0005g0318a0001c0001t0005g0328others(6): Show | 9 | HG02027.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.284-13594_284-1359 others(9): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74185309 | |||||
| chr14:74185313
|
T | C | 8 | a0001c0001t0002g0130a0001c0001t0002g0166a0001c0001t0006g0154others(5): Show | 8 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-13609T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185313 | ||||||
| chr14:74185372
|
T | C | 1 | a0001c0001t0037g0091 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.284-13550T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185372 | ||||||
| chr14:74185504
|
G | A | 130 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(127): Show | 131 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.284-13418G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185504 | ||||||
| chr14:74185564
|
C | T | 1 | a0001c0001t0014g0198 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.284-13358C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185564 | ||||||
| chr14:74185572
|
G | C | 10 | a0001c0001t0001g0217a0001c0001t0001g0226a0001c0001t0001g0241others(7): Show | 10 | HG01358.hp2 NA18947.hp2 NA18962.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-13350G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185572 | ||||||
| chr14:74185602
|
C | T | 1 | a0001c0001t0017g0322 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.284-13320C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185602 | ||||||
| chr14:74185750
|
T | C | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-13172T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185750 | ||||||
| chr14:74185823
|
G | A | 45 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217others(42): Show | 45 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.284-13099G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185823 | ||||||
| chr14:74185839
|
A | G | 73 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(70): Show | 73 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.284-13083A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185839 | ||||||
| chr14:74185908
|
A | C | 1 | a0001c0001t0001g0248 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.284-13014A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185908 | ||||||
| chr14:74185990
|
G | T | 7 | a0001c0001t0008g0296a0001c0001t0008g0308a0001c0001t0008g0309others(4): Show | 7 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-12932G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74185990 | ||||||
| chr14:74186010
|
C | T | 1 | a0001c0001t0002g0027 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.284-12912C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74186010 | ||||||
| chr14:74186164
|
A | G | 4 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(1): Show | 4 | HG02258.hp1 HG02630.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-12758A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74186164 | ||||||
| chr14:74186206
|
C | T | 9 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0272others(6): Show | 9 | HG01192.hp1 HG02027.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-12716C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74186206 | ||||||
| chr14:74186229
|
C | T | 289 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0191others(286): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.284-12693C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74186229 | ||||||
| chr14:74186295
|
AAAAC | A | 5 | a0001c0001t0001g0286a0001c0001t0001g0290a0001c0001t0001g0291others(2): Show | 5 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-12607_284-1260 others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74186295 | |||||
| chr14:74186428
|
A | G | 1 | a0001c0001t0004g0036 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.284-12494A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74186428 | ||||||
| chr14:74186453
|
G | A | 1 | a0001c0001t0025g0087 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.284-12469G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74186453 | ||||||
| chr14:74186783
|
G | A | 10 | a0001c0001t0002g0092a0001c0001t0011g0204a0001c0001t0014g0198others(7): Show | 10 | HG02145.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-12139G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74186783 | ||||||
| chr14:74186877
|
A | G | 1 | a0001c0001t0013g0120 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.284-12045A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74186877 | ||||||
| chr14:74186933
|
G | T | 2 | a0001c0001t0017g0321a0001c0001t0017g0322 | 2 | HG00280.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.284-11989G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74186933 | ||||||
| chr14:74186948
|
A | G | 232 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(229): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.284-11974A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74186948 | ||||||
| chr14:74187037
|
A | C | 1 | a0001c0001t0002g0261 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.284-11885A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74187037 | ||||||
| chr14:74187238
|
G | T | 4 | a0001c0001t0004g0348a0001c0001t0004g0349a0001c0001t0004g0350others(1): Show | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-11684G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74187238 | ||||||
| chr14:74187447
|
C | A | 1 | a0001c0001t0002g0153 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.284-11475C>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74187447 | ||||||
| chr14:74187450
|
A | G | 76 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(73): Show | 76 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.284-11472A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74187450 | ||||||
| chr14:74187489
|
C | T | 242 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(239): Show | 243 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.284-11433C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74187489 | ||||||
| chr14:74187549
|
T | C | 5 | a0001c0001t0001g0152a0001c0001t0002g0137a0001c0001t0002g0150others(2): Show | 5 | HG01069.hp2 HG01346.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-11373T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74187549 | ||||||
| chr14:74187803
|
T | C | 1 | a0001c0001t0004g0070 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.284-11119T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74187803 | ||||||
| chr14:74188027
|
A | G | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-10895A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188027 | ||||||
| chr14:74188174
|
A | G | 1 | a0001c0002t0009g0282 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.284-10748A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188174 | ||||||
| chr14:74188418
|
T | C | 244 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(241): Show | 246 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.284-10504T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188418 | ||||||
| chr14:74188440
|
A | AT | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-10475dupT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74188440 | |||||
| chr14:74188447
|
T | A | 3 | a0001c0001t0013g0094a0001c0001t0013g0125a0001c0001t0028g0101 | 3 | HG02602.hp2 HG03688.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.284-10475T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188447 | ||||||
| chr14:74188519
|
A | G | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-10403A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188519 | ||||||
| chr14:74188571
|
C | T | 94 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(91): Show | 94 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.284-10351C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188571 | ||||||
| chr14:74188671
|
C | T | 3 | a0001c0001t0014g0198a0001c0001t0014g0199a0001c0001t0014g0200 | 3 | HG02809.hp2 HG03041.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.284-10251C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188671 | ||||||
| chr14:74188714
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.284-10208G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188714 | ||||||
| chr14:74188761
|
A | G | 1 | a0001c0001t0007g0004 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.284-10161A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188761 | ||||||
| chr14:74188880
|
T | G | 3 | a0001c0001t0002g0164a0001c0001t0006g0156a0001c0001t0033g0182 | 3 | HG02071.hp1 NA18967.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.284-10042T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188880 | ||||||
| chr14:74188955
|
C | T | 102 | a0001c0001t0001g0205a0001c0001t0001g0213a0001c0001t0001g0214others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.284-9967C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74188955 | ||||||
| chr14:74189025
|
G | C | 1 | a0001c0001t0004g0070 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.284-9897G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189025 | ||||||
| chr14:74189175
|
C | T | 8 | a0001c0001t0004g0077a0001c0001t0012g0078a0001c0001t0012g0081others(5): Show | 8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-9747C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189175 | ||||||
| chr14:74189193
|
T | C | 7 | a0001c0001t0011g0204a0001c0001t0014g0198a0001c0001t0014g0199others(4): Show | 7 | HG02572.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-9729T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189193 | ||||||
| chr14:74189249
|
T | C | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-9673T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189249 | ||||||
| chr14:74189359
|
T | A | 1 | a0001c0001t0003g0035 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.284-9563T>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189359 | ||||||
| chr14:74189477
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.284-9445C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189477 | ||||||
| chr14:74189497
|
A | G | 8 | a0001c0001t0001g0217a0001c0001t0001g0226a0001c0001t0001g0241others(5): Show | 8 | NA18947.hp2 NA18962.hp2 NA18984.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-9425A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189497 | ||||||
| chr14:74189626
|
A | G | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.284-9296A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189626 | ||||||
| chr14:74189710
|
A | G | 2 | a0001c0001t0012g0081a0001c0001t0012g0083 | 2 | HG01243.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.284-9212A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189710 | ||||||
| chr14:74189938
|
G | A | 2 | a0001c0001t0006g0100a0001c0001t0006g0102 | 2 | HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.284-8984G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189938 | ||||||
| chr14:74189963
|
A | C | 1 | a0001c0001t0001g0263 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.284-8959A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74189963 | ||||||
| chr14:74190230
|
T | C | 1 | a0001c0001t0027g0124 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.284-8692T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74190230 | ||||||
| chr14:74190345
|
G | A | 4 | a0001c0001t0004g0348a0001c0001t0004g0349a0001c0001t0004g0350others(1): Show | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-8577G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74190345 | ||||||
| chr14:74190360
|
T | C | 233 | a0001c0001t0001g0161a0001c0001t0001g0205a0001c0001t0001g0213others(230): Show | 234 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.284-8562T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74190360 | ||||||
| chr14:74190389
|
C | CTT | 13 | a0001c0001t0001g0243a0001c0001t0001g0263a0001c0001t0001g0274others(10): Show | 13 | HG00099.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.284-8514_284-8513d others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74190389 | |||||
| chr14:74190389
|
C | CTTT | 81 | a0001c0001t0001g0161a0001c0001t0001g0205a0001c0001t0001g0213others(78): Show | 81 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.284-8515_284-8513d others(5): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74190389 | |||||
| chr14:74190389
|
C | CTTTT | 7 | a0001c0001t0001g0287a0001c0001t0001g0289a0001c0001t0001g0292others(4): Show | 7 | HG01175.hp1 HG01891.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-8516_284-8513d others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74190389 | |||||
| chr14:74190389
|
C | CTTTTT | 11 | a0001c0001t0002g0276a0001c0001t0002g0277a0001c0001t0011g0221others(8): Show | 11 | HG01243.hp2 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.284-8517_284-8513d others(7): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74190389 | |||||
| chr14:74190389
|
C | CTTTTTT | 6 | a0001c0001t0004g0348a0001c0001t0004g0349a0001c0001t0004g0350others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-8518_284-8513d others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74190389 | |||||
| chr14:74190389
|
C | CTTTTTTT others(1): Show |
59 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(56): Show | 59 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.284-8520_284-8513d others(10): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74190389 | |||||
| chr14:74190389
|
C | CTTTTTTT others(2): Show |
6 | a0001c0001t0003g0007a0001c0001t0003g0012a0001c0001t0003g0022others(3): Show | 6 | HG00408.hp2 HG00544.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-8521_284-8513d others(11): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74190389 | |||||
| chr14:74190389
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0003g0076a0001c0001t0004g0036a0001c0001t0015g0041others(1): Show | 4 | HG01943.hp2 HG02027.hp1 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-8522_284-8513d others(12): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74190389 | |||||
| chr14:74190389
|
C | T | 1 | a0001c0001t0002g0146 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.284-8533C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74190389 | ||||||
| chr14:74190389
|
CTTT | C | 39 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(36): Show | 40 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.284-8515_284-8513d others(5): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74190389 | |||||
| chr14:74190519
|
G | C | 1 | a0001c0001t0015g0185 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.284-8403G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74190519 | ||||||
| chr14:74190597
|
G | C | 1 | a0001c0001t0001g0237 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.284-8325G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74190597 | ||||||
| chr14:74190828
|
T | C | 11 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(8): Show | 11 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.284-8094T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74190828 | ||||||
| chr14:74191263
|
G | A | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-7659G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74191263 | ||||||
| chr14:74191326
|
C | T | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-7596C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74191326 | ||||||
| chr14:74191719
|
C | T | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-7203C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74191719 | ||||||
| chr14:74191727
|
G | A | 7 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(4): Show | 7 | HG01106.hp1 HG01255.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-7195G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74191727 | ||||||
| chr14:74191734
|
C | T | 1 | a0001c0001t0005g0326 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.284-7188C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74191734 | ||||||
| chr14:74191790
|
C | T | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-7132C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74191790 | ||||||
| chr14:74191801
|
T | C | 1 | a0001c0001t0003g0018 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.284-7121T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74191801 | ||||||
| chr14:74191949
|
T | G | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-6973T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74191949 | ||||||
| chr14:74192086
|
AC | A | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-6834delC | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74192086 | |||||
| chr14:74192231
|
A | C | 1 | a0001c0001t0013g0094 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.284-6691A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74192231 | ||||||
| chr14:74192265
|
G | A | 4 | a0001c0001t0001g0286a0001c0001t0001g0290a0001c0001t0001g0291others(1): Show | 4 | HG01074.hp1 HG01099.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-6657G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74192265 | ||||||
| chr14:74192268
|
GTTGTTTT others(12): Show |
G | 1 | a0001c0001t0002g0145 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.284-6638_284-6620d others(21): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74192268 | |||||
| chr14:74192442
|
C | G | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-6480C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74192442 | ||||||
| chr14:74192497
|
G | A | 2 | a0001c0001t0002g0276a0001c0001t0002g0277 | 2 | HG01884.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.284-6425G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74192497 | ||||||
| chr14:74192505
|
C | T | 1 | a0001c0001t0002g0261 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.284-6417C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74192505 | ||||||
| chr14:74192608
|
G | C | 1 | a0001c0001t0002g0093 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.284-6314G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74192608 | ||||||
| chr14:74192677
|
A | G | 2 | a0001c0001t0004g0047a0001c0001t0004g0049 | 2 | NA18942.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.284-6245A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74192677 | ||||||
| chr14:74192934
|
G | T | 145 | a0001c0001t0001g0161a0001c0001t0001g0205a0001c0001t0001g0213others(142): Show | 146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.284-5988G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74192934 | ||||||
| chr14:74192987
|
T | G | 145 | a0001c0001t0001g0161a0001c0001t0001g0205a0001c0001t0001g0213others(142): Show | 146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.284-5935T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74192987 | ||||||
| chr14:74193038
|
G | A | 1 | a0001c0001t0011g0221 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.284-5884G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193038 | ||||||
| chr14:74193087
|
A | C | 47 | a0001c0001t0001g0161a0001c0001t0001g0215a0001c0001t0001g0216others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.284-5835A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193087 | ||||||
| chr14:74193240
|
G | A | 1 | a0001c0001t0002g0192 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.284-5682G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193240 | ||||||
| chr14:74193247
|
C | CA | 134 | a0001c0001t0001g0161a0001c0001t0001g0205a0001c0001t0001g0213others(131): Show | 135 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.284-5661dupA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74193247 | |||||
| chr14:74193247
|
C | CAA | 11 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(8): Show | 11 | HG01891.hp1 HG02055.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.284-5662_284-5661d others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74193247 | |||||
| chr14:74193247
|
CA | C | 101 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0002g0092others(98): Show | 102 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.284-5661delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74193247 | |||||
| chr14:74193286
|
T | C | 145 | a0001c0001t0001g0161a0001c0001t0001g0205a0001c0001t0001g0213others(142): Show | 146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.284-5636T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193286 | ||||||
| chr14:74193401
|
G | A | 1 | a0001c0001t0007g0109 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.284-5521G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193401 | ||||||
| chr14:74193417
|
TA | T | 138 | a0001c0001t0001g0161a0001c0001t0001g0205a0001c0001t0001g0213others(135): Show | 139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.284-5491delA | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74193417 | |||||
| chr14:74193422
|
A | G | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-5500A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193422 | ||||||
| chr14:74193515
|
A | G | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-5407A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193515 | ||||||
| chr14:74193599
|
G | A | 145 | a0001c0001t0001g0161a0001c0001t0001g0205a0001c0001t0001g0213others(142): Show | 146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.284-5323G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193599 | ||||||
| chr14:74193617
|
T | G | 41 | a0001c0001t0003g0323a0001c0001t0005g0295a0001c0001t0005g0297others(38): Show | 42 | HG00280.hp1 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.284-5305T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193617 | ||||||
| chr14:74193668
|
T | C | 1 | a0001c0001t0011g0221 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.284-5254T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193668 | ||||||
| chr14:74193805
|
A | G | 145 | a0001c0001t0001g0161a0001c0001t0001g0205a0001c0001t0001g0213others(142): Show | 146 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.284-5117A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193805 | ||||||
| chr14:74193964
|
T | C | 2 | a0001c0001t0003g0059a0001c0001t0003g0060 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.284-4958T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74193964 | ||||||
| chr14:74194021
|
A | C | 245 | a0001c0001t0001g0161a0001c0001t0001g0205a0001c0001t0001g0213others(242): Show | 246 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.284-4901A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194021 | ||||||
| chr14:74194095
|
T | C | 8 | a0001c0001t0004g0077a0001c0001t0012g0078a0001c0001t0012g0081others(5): Show | 8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-4827T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194095 | ||||||
| chr14:74194228
|
T | G | 7 | a0001c0001t0002g0276a0001c0001t0002g0277a0001c0001t0011g0221others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-4694T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194228 | ||||||
| chr14:74194314
|
G | A | 1 | a0001c0001t0004g0208 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.284-4608G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194314 | ||||||
| chr14:74194656
|
C | T | 1 | a0001c0001t0005g0326 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.284-4266C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194656 | ||||||
| chr14:74194714
|
G | A | 2 | a0001c0002t0009g0002a0001c0002t0009g0193 | 3 | HG02451.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.284-4208G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194714 | ||||||
| chr14:74194734
|
C | T | 2 | a0001c0001t0002g0138a0001c0001t0006g0176 | 2 | HG00642.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.284-4188C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194734 | ||||||
| chr14:74194791
|
G | C | 1 | a0001c0001t0018g0085 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284-4131G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194791 | ||||||
| chr14:74194794
|
G | A | 103 | a0001c0001t0001g0161a0001c0001t0001g0205a0001c0001t0001g0213others(100): Show | 103 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.284-4128G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194794 | ||||||
| chr14:74194795
|
C | T | 3 | a0001c0001t0002g0092a0001c0001t0015g0090a0001c0001t0037g0091 | 3 | HG02145.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.284-4127C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194795 | ||||||
| chr14:74194796
|
G | A | 1 | a0001c0001t0002g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.284-4126G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194796 | ||||||
| chr14:74194947
|
C | T | 1 | a0001c0001t0002g0144 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.284-3975C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194947 | ||||||
| chr14:74194978
|
G | A | 3 | a0001c0001t0003g0008a0001c0001t0003g0018a0001c0001t0004g0009 | 3 | HG00597.hp1 HG02083.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.284-3944G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74194978 | ||||||
| chr14:74195058
|
A | C | 46 | a0001c0001t0001g0161a0001c0001t0001g0215a0001c0001t0001g0216others(43): Show | 46 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.284-3864A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74195058 | ||||||
| chr14:74195070
|
G | A | 6 | a0001c0001t0001g0335a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.284-3852G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74195070 | ||||||
| chr14:74195468
|
A | C | 1 | a0001c0001t0003g0323 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.284-3454A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74195468 | ||||||
| chr14:74195477
|
G | A | 8 | a0001c0001t0004g0077a0001c0001t0012g0078a0001c0001t0012g0081others(5): Show | 8 | HG01243.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-3445G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74195477 | ||||||
| chr14:74195556
|
A | ACG | 12 | a0001c0001t0004g0077a0001c0001t0004g0348a0001c0001t0004g0349others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-3366_284-3365i others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74195556 | ||||||
| chr14:74195556
|
A | ATG | 240 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0161others(237): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.284-3347_284-3346d others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74195556 | |||||
| chr14:74195556
|
A | ATGTG | 9 | a0001c0001t0011g0204a0001c0001t0011g0223a0001c0001t0011g0224others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.284-3349_284-3346d others(6): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74195556 | |||||
| chr14:74195556
|
A | ATGTGTG | 12 | a0001c0001t0002g0276a0001c0001t0002g0277a0001c0001t0005g0303others(9): Show | 12 | HG00323.hp1 HG00741.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.284-3351_284-3346d others(8): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74195556 | |||||
| chr14:74195575
|
T | TGC | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-3343_284-3342d others(4): Show |
LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr14 | 74195575 | |||||
| chr14:74195579
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.284-3343C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74195579 | ||||||
| chr14:74195616
|
G | A | 1 | a0001c0001t0006g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.284-3306G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74195616 | ||||||
| chr14:74195713
|
A | T | 1 | a0001c0001t0001g0290 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.284-3209A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74195713 | ||||||
| chr14:74195775
|
T | G | 245 | a0001c0001t0001g0161a0001c0001t0001g0205a0001c0001t0001g0213others(242): Show | 247 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.284-3147T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74195775 | ||||||
| chr14:74196671
|
CT | C | 9 | a0001c0001t0001g0191a0001c0001t0002g0189a0001c0001t0002g0190others(6): Show | 9 | HG01109.hp1 HG01496.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-2250delT | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74196671 | ||||||
| chr14:74196692
|
T | C | 3 | a0001c0001t0003g0032a0001c0001t0003g0038a0001c0001t0003g0052 | 3 | NA18960.hp1 NA18961.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.284-2230T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74196692 | ||||||
| chr14:74196693
|
G | A | 3 | a0001c0001t0003g0032a0001c0001t0003g0038a0001c0001t0003g0052 | 3 | NA18960.hp1 NA18961.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.284-2229G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74196693 | ||||||
| chr14:74196718
|
C | T | 8 | a0001c0002t0009g0278a0001c0002t0009g0279a0001c0002t0009g0280others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284-2204C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74196718 | ||||||
| chr14:74196755
|
C | T | 4 | a0001c0001t0004g0348a0001c0001t0004g0349a0001c0001t0004g0350others(1): Show | 4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-2167C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74196755 | ||||||
| chr14:74196782
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.284-2140T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74196782 | ||||||
| chr14:74196839
|
A | C | 1 | a0001c0001t0012g0078 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.284-2083A>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74196839 | ||||||
| chr14:74196848
|
G | A | 5 | a0001c0001t0011g0221a0001c0001t0011g0222a0001c0001t0011g0223others(2): Show | 5 | HG01891.hp1 HG02717.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-2074G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74196848 | ||||||
| chr14:74196895
|
G | A | 34 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0002g0117others(31): Show | 34 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.284-2027G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74196895 | ||||||
| chr14:74197163
|
T | C | 1 | a0001c0001t0001g0294 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.284-1759T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197163 | ||||||
| chr14:74197266
|
A | G | 75 | a0001c0001t0002g0027a0001c0001t0002g0073a0001c0001t0003g0005others(72): Show | 75 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.284-1656A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197266 | ||||||
| chr14:74197291
|
G | A | 3 | a0001c0001t0004g0206a0001c0001t0012g0209a0001c0001t0045g0188 | 3 | HG02055.hp2 HG02976.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.284-1631G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197291 | ||||||
| chr14:74197303
|
C | G | 1 | a0001c0001t0003g0035 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.284-1619C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197303 | ||||||
| chr14:74197303
|
C | T | 1 | a0001c0001t0005g0324 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.284-1619C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197303 | ||||||
| chr14:74197315
|
G | A | 1 | a0001c0001t0040g0184 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.284-1607G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197315 | ||||||
| chr14:74197513
|
A | G | 2 | a0001c0001t0011g0204a0001c0001t0014g0203 | 2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.284-1409A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197513 | ||||||
| chr14:74197794
|
A | G | 1 | a0001c0001t0002g0134 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.284-1128A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197794 | ||||||
| chr14:74197795
|
C | G | 2 | a0001c0001t0001g0251a0001c0001t0029g0202 | 2 | HG00639.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.284-1127C>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197795 | ||||||
| chr14:74197961
|
A | G | 1 | a0001c0001t0023g0343 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.284-961A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197961 | ||||||
| chr14:74197998
|
C | T | 24 | a0001c0001t0002g0276a0001c0001t0002g0277a0001c0001t0003g0059others(21): Show | 24 | HG00558.hp1 HG01167.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.284-924C>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74197998 | ||||||
| chr14:74198007
|
T | C | 16 | a0001c0001t0002g0189a0001c0001t0003g0088a0001c0001t0015g0090others(13): Show | 17 | HG02145.hp2 HG02280.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.284-915T>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74198007 | ||||||
| chr14:74198117
|
A | T | 1 | a0001c0001t0005g0315 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.284-805A>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74198117 | ||||||
| chr14:74198268
|
A | G | 7 | a0001c0001t0001g0205a0001c0001t0001g0236a0001c0001t0001g0238others(4): Show | 7 | HG01081.hp2 HG02145.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.284-654A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74198268 | ||||||
| chr14:74198418
|
G | T | 11 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0192others(8): Show | 11 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.284-504G>T | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74198418 | ||||||
| chr14:74198637
|
T | G | 11 | a0001c0001t0002g0136a0001c0001t0003g0016a0001c0001t0003g0040others(8): Show | 11 | HG01928.hp1 HG01943.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.284-285T>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74198637 | ||||||
| chr14:74198690
|
G | C | 36 | a0001c0001t0002g0117a0001c0001t0002g0118a0001c0001t0006g0100others(33): Show | 36 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.284-232G>C | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74198690 | ||||||
| chr14:74198700
|
A | G | 1 | a0001c0001t0003g0035 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.284-222A>G | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74198700 | ||||||
| chr14:74198840
|
G | A | 114 | a0001c0001t0001g0097a0001c0001t0001g0110a0001c0001t0001g0152others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.284-82G>A | LIN52 | ENSG00000205659.12 | transcript | ENST00000555028.7 | protein_coding | 5/5 | chr14 | 74198840 |