Item | Value |
---|---|
geneid | 23336 |
ensemblid | ENSG00000182253.15 |
hgncid | 24466 |
symbol | SYNM |
name | synemin |
refseq_nuc | NM_145728.3 |
refseq_prot | NP_663780.2 |
ensembl_nuc | ENST00000336292.11 |
ensembl_prot | ENSP00000336775.7 |
mane_status | MANE Select |
chr | chr15 |
start | 99105080 |
end | 99135593 |
strand | + |
ver | v1.2 |
region | chr15:99105080-99135593 |
region5000 | chr15:99100080-99140593 |
regionname0 | SYNM_chr15_99105080_99135593 |
regionname5000 | SYNM_chr15_99100080_99140593 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1565 | 120 | 27 | 20 | 49 | 6 | 18 | 33 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0002 | 1/0 | 1565 | 91 | 22 | 14 | 43 | 3 | 8 | 34 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0003 | 0/0 | 1565 | 66 | 5 | 4 | 50 | 2 | 5 | 42 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0004 | 0/0 | 1565 | 26 | 4 | 5 | 12 | 0 | 5 | 10 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0005 | 0/0 | 1565 | 15 | 3 | 2 | 7 | 1 | 2 | 6 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0006 | 0/0 | 1565 | 10 | 7 | 2 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0007 | 0/0 | 1565 | 8 | 0 | 2 | 3 | 2 | 1 | 3 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0008 | 0/1 | 1565 | 8 | 0 | 7 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0009 | 0/0 | 1565 | 7 | 0 | 4 | 0 | 0 | 3 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0010 | 0/0 | 1565 | 6 | 3 | 1 | 0 | 0 | 2 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0011 | 0/0 | 1565 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0012 | 0/0 | 1565 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0013 | 0/0 | 1565 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0014 | 0/0 | 1565 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0015 | 0/0 | 1565 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0016 | 0/0 | 1565 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0017 | 0/0 | 1565 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0018 | 0/0 | 1565 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0019 | 0/0 | 1565 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0020 | 0/0 | 1565 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0021 | 0/0 | 1565 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0022 | 0/0 | 1565 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0023 | 0/0 | 1572 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1567): Show |
chr15 | 99100080 | 99140593 |
a0024 | 0/0 | 1565 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0025 | 0/0 | 1565 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0026 | 0/0 | 1565 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0027 | 0/0 | 1565 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0028 | 0/0 | 1565 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0029 | 0/0 | 1565 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0030 | 0/0 | 1565 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0031 | 0/0 | 1565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0032 | 0/0 | 1565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0033 | 0/0 | 1565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0034 | 0/0 | 1565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0035 | 0/0 | 1565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0036 | 0/0 | 1565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0037 | 0/0 | 1565 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0038 | 0/0 | 1565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0039 | 0/0 | 1565 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0040 | 0/0 | 1565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0041 | 0/0 | 1565 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0042 | 0/0 | 1565 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0043 | 0/0 | 1565 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0044 | 0/0 | 1565 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0045 | 0/0 | 1565 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
a0046 | 0/0 | 1565 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | MLSWR others(1560): Show |
chr15 | 99100080 | 99140593 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4695 | 97 | 15 | 20 | 42 | 6 | 14 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0001c0007 | 0/0 | 4695 | 14 | 8 | 0 | 3 | 0 | 3 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0001c0018 | 0/0 | 4695 | 3 | 3 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0001c0025 | 0/0 | 4695 | 2 | 0 | 0 | 2 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0001c0030 | 0/0 | 4695 | 2 | 0 | 0 | 2 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0001c0043 | 0/0 | 4695 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0001c0061 | 0/0 | 4695 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0002c0002 | 1/0 | 4695 | 68 | 2 | 13 | 43 | 3 | 6 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0002c0005 | 0/0 | 4695 | 17 | 16 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0002c0019 | 0/0 | 4695 | 3 | 3 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0002c0034 | 0/0 | 4695 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0002c0048 | 0/0 | 4695 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0002c0064 | 0/0 | 4695 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0003c0003 | 0/0 | 4695 | 63 | 5 | 4 | 47 | 2 | 5 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0003c0024 | 0/0 | 4695 | 2 | 0 | 0 | 2 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0003c0063 | 0/0 | 4695 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0004c0004 | 0/0 | 4695 | 23 | 2 | 5 | 12 | 0 | 4 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0004c0021 | 0/0 | 4695 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0004c0038 | 0/0 | 4695 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0005c0006 | 0/0 | 4695 | 15 | 3 | 2 | 7 | 1 | 2 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0006c0016 | 0/0 | 4695 | 4 | 2 | 2 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0006c0022 | 0/0 | 4695 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0006c0039 | 0/0 | 4695 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0006c0040 | 0/0 | 4695 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0006c0044 | 0/0 | 4695 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0006c0056 | 0/0 | 4695 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0007c0010 | 0/0 | 4695 | 6 | 0 | 1 | 3 | 1 | 1 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0007c0052 | 0/0 | 4695 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0007c0069 | 0/0 | 4695 | 1 | 0 | 0 | 0 | 1 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0008c0011 | 0/0 | 4695 | 6 | 0 | 6 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0008c0029 | 0/1 | 4695 | 2 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0009c0008 | 0/0 | 4695 | 7 | 0 | 4 | 0 | 0 | 3 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0010c0012 | 0/0 | 4695 | 6 | 3 | 1 | 0 | 0 | 2 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0011c0009 | 0/0 | 4695 | 6 | 6 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0012c0015 | 0/0 | 4695 | 5 | 0 | 0 | 5 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0013c0014 | 0/0 | 4695 | 5 | 0 | 0 | 5 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0014c0013 | 0/0 | 4695 | 5 | 0 | 0 | 5 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0015c0027 | 0/0 | 4695 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0015c0066 | 0/0 | 4695 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0015c0067 | 0/0 | 4695 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0016c0023 | 0/0 | 4695 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0016c0033 | 0/0 | 4695 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0017c0017 | 0/0 | 4695 | 3 | 3 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0018c0020 | 0/0 | 4695 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0019c0028 | 0/0 | 4695 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0020c0026 | 0/0 | 4695 | 2 | 0 | 0 | 2 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0021c0049 | 0/0 | 4695 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0022c0045 | 0/0 | 4695 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0023c0071 | 0/0 | 4716 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4711): Show |
chr15 | 99100080 | 99140593 | ||
a0024c0068 | 0/0 | 4695 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0025c0055 | 0/0 | 4695 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0026c0053 | 0/0 | 4695 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0027c0051 | 0/0 | 4695 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0028c0046 | 0/0 | 4695 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0029c0050 | 0/0 | 4695 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0030c0057 | 0/0 | 4695 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0031c0062 | 0/0 | 4695 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0032c0036 | 0/0 | 4695 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0033c0058 | 0/0 | 4695 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0034c0035 | 0/0 | 4695 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0035c0041 | 0/0 | 4695 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0036c0031 | 0/0 | 4695 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0037c0054 | 0/0 | 4695 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0038c0042 | 0/0 | 4695 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0039c0072 | 0/0 | 4695 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0040c0070 | 0/0 | 4695 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0041c0037 | 0/0 | 4695 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0042c0032 | 0/0 | 4695 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0043c0059 | 0/0 | 4695 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0044c0047 | 0/0 | 4695 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0045c0060 | 0/0 | 4695 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 | ||
a0046c0065 | 0/0 | 4695 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | ATGCT others(4690): Show |
chr15 | 99100080 | 99140593 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7353 | 82 | 13 | 18 | 32 | 5 | 14 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0001c0001t0003 | 0/0 | 7353 | 3 | 0 | 0 | 3 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0001c0001t0009 | 0/0 | 7353 | 5 | 0 | 0 | 5 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0001c0001t0015 | 0/0 | 7353 | 3 | 2 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0001c0001t0026 | 0/0 | 7353 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0001c0001t0028 | 0/0 | 7353 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0001c0001t0029 | 0/0 | 7353 | 1 | 0 | 0 | 0 | 1 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0001c0001t0032 | 0/0 | 7353 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0001c0007t0001 | 0/0 | 7353 | 7 | 2 | 0 | 2 | 0 | 3 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0001c0007t0009 | 0/0 | 7353 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0001c0007t0010 | 0/0 | 7353 | 6 | 6 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0001c0018t0001 | 0/0 | 7353 | 3 | 3 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0001c0025t0001 | 0/0 | 7353 | 2 | 0 | 0 | 2 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0001c0030t0001 | 0/0 | 7353 | 2 | 0 | 0 | 2 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0001c0043t0001 | 0/0 | 7353 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0001c0061t0001 | 0/0 | 7353 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0002c0002t0001 | 0/0 | 7353 | 12 | 0 | 3 | 8 | 1 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0002c0002t0002 | 1/0 | 7353 | 48 | 2 | 8 | 30 | 2 | 5 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0002c0002t0013 | 0/0 | 7353 | 4 | 0 | 0 | 4 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0002c0002t0014 | 0/0 | 7353 | 3 | 0 | 2 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0002c0002t0033 | 0/0 | 7353 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0002c0005t0001 | 0/0 | 7353 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0002c0005t0007 | 0/0 | 7370 | 7 | 7 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0002c0005t0008 | 0/0 | 7370 | 8 | 7 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0002c0005t0011 | 0/0 | 7370 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0002c0019t0011 | 0/0 | 7370 | 3 | 3 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0002c0034t0002 | 0/0 | 7353 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0002c0048t0002 | 0/0 | 7353 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0002c0064t0023 | 0/0 | 7353 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0003c0003t0001 | 0/0 | 7353 | 5 | 3 | 1 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0003c0003t0003 | 0/0 | 7353 | 53 | 2 | 3 | 42 | 2 | 4 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0003c0003t0012 | 0/0 | 7353 | 4 | 0 | 0 | 4 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0003c0003t0025 | 0/0 | 7353 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0003c0024t0003 | 0/0 | 7353 | 2 | 0 | 0 | 2 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0003c0063t0003 | 0/0 | 7353 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0004c0004t0005 | 0/0 | 7370 | 19 | 2 | 4 | 12 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0004c0004t0018 | 0/0 | 7370 | 3 | 0 | 1 | 0 | 0 | 2 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0004c0004t0034 | 0/0 | 7370 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0004c0021t0005 | 0/0 | 7370 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0004c0038t0005 | 0/0 | 7370 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0005c0006t0004 | 0/0 | 7370 | 15 | 3 | 2 | 7 | 1 | 2 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0006c0016t0001 | 0/0 | 7353 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0006c0016t0002 | 0/0 | 7353 | 3 | 2 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0006c0022t0008 | 0/0 | 7370 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0006c0039t0007 | 0/0 | 7370 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0006c0040t0030 | 0/0 | 7357 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7352): Show |
chr15 | 99100080 | 99140593 |
a0006c0044t0002 | 0/0 | 7353 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0006c0056t0008 | 0/0 | 7370 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0007c0010t0006 | 0/0 | 7370 | 6 | 0 | 1 | 3 | 1 | 1 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0007c0052t0006 | 0/0 | 7370 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0007c0069t0002 | 0/0 | 7353 | 1 | 0 | 0 | 0 | 1 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0008c0011t0004 | 0/0 | 7370 | 4 | 0 | 4 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0008c0011t0020 | 0/0 | 7370 | 2 | 0 | 2 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0008c0029t0004 | 0/1 | 7370 | 2 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0009c0008t0002 | 0/0 | 7353 | 7 | 0 | 4 | 0 | 0 | 3 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0010c0012t0001 | 0/0 | 7353 | 3 | 0 | 1 | 0 | 0 | 2 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0010c0012t0016 | 0/0 | 7353 | 3 | 3 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0011c0009t0001 | 0/0 | 7353 | 6 | 6 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0012c0015t0001 | 0/0 | 7353 | 4 | 0 | 0 | 4 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0012c0015t0009 | 0/0 | 7353 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0013c0014t0002 | 0/0 | 7353 | 5 | 0 | 0 | 5 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0014c0013t0006 | 0/0 | 7370 | 5 | 0 | 0 | 5 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0015c0027t0017 | 0/0 | 7370 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0015c0066t0031 | 0/0 | 7370 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0015c0067t0017 | 0/0 | 7370 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0016c0023t0007 | 0/0 | 7370 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0016c0023t0021 | 0/0 | 7370 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0016c0033t0021 | 0/0 | 7370 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0017c0017t0004 | 0/0 | 7370 | 3 | 3 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0018c0020t0019 | 0/0 | 7370 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0019c0028t0007 | 0/0 | 7370 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0020c0026t0002 | 0/0 | 7353 | 2 | 0 | 0 | 2 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0021c0049t0001 | 0/0 | 7353 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0022c0045t0003 | 0/0 | 7353 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0023c0071t0007 | 0/0 | 7391 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7386): Show |
chr15 | 99100080 | 99140593 |
a0024c0068t0007 | 0/0 | 7370 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0025c0055t0001 | 0/0 | 7353 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0026c0053t0001 | 0/0 | 7353 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0027c0051t0006 | 0/0 | 7370 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0028c0046t0003 | 0/0 | 7353 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0029c0050t0004 | 0/0 | 7370 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0030c0057t0003 | 0/0 | 7353 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0031c0062t0004 | 0/0 | 7370 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0032c0036t0024 | 0/0 | 7370 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0033c0058t0001 | 0/0 | 7353 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0034c0035t0011 | 0/0 | 7370 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7365): Show |
chr15 | 99100080 | 99140593 |
a0035c0041t0001 | 0/0 | 7353 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0036c0031t0001 | 0/0 | 7353 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0037c0054t0003 | 0/0 | 7353 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0038c0042t0001 | 0/0 | 7353 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0039c0072t0002 | 0/0 | 7353 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0040c0070t0001 | 0/0 | 7353 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0041c0037t0022 | 0/0 | 7353 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0042c0032t0003 | 0/0 | 7353 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0043c0059t0001 | 0/0 | 7353 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0044c0047t0002 | 0/0 | 7353 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0045c0060t0027 | 0/0 | 7353 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
a0046c0065t0001 | 0/0 | 7353 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | AGTCT others(7348): Show |
chr15 | 99100080 | 99140593 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 18 | 0 | 9 | 1 | 4 | 4 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0005 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0019 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0048 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0009g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0009g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0009g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0015g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0026g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0028g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0029g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0001t0032g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0007t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0007t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0007t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0007t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0007t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0007t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0007t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0007t0009g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0007t0010g0023 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0007t0010g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0007t0010g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0018t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0025t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0025t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0030t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0030t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0043t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0001c0061t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0001g0006 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0001 | 0/0 | 15 | 0 | 1 | 14 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0014 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0116 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0013g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0013g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0014g0001 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0002t0033g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0005t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0005t0007g0009 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0005t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0005t0008g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0005t0008g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0005t0008g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0005t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0005t0011g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0019t0011g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0019t0011g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0034t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0048t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0002c0064t0023g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0003 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0004 | 0/0 | 12 | 0 | 0 | 10 | 1 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0012g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0012g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0003t0025g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0024t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0024t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0003c0063t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0004c0004t0005g0021 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0004c0004t0005g0022 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0004c0004t0005g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0004c0004t0005g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0004c0004t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0004c0004t0005g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0004c0004t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0004c0004t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0004c0004t0005g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0004c0004t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0004c0004t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0004c0004t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0004c0004t0018g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0004c0004t0018g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0004c0004t0018g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0004c0004t0034g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0004c0021t0005g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0004c0038t0005g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0005c0006t0004g0011 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0005c0006t0004g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0005c0006t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0005c0006t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0005c0006t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0005c0006t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0005c0006t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0005c0006t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0005c0006t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0005c0006t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0006c0016t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0006c0016t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0006c0016t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0006c0022t0008g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0006c0022t0008g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0006c0039t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0006c0040t0030g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0006c0044t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0006c0056t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0007c0010t0006g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0007c0010t0006g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0007c0010t0006g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0007c0010t0006g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0007c0052t0006g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0007c0069t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0008c0011t0004g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0008c0011t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0008c0011t0020g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0008c0029t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0008c0029t0004g0162 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0009c0008t0002g0008 | 0/0 | 6 | 0 | 4 | 0 | 0 | 2 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0009c0008t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0010c0012t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0010c0012t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0010c0012t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0010c0012t0016g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0010c0012t0016g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0011c0009t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0011c0009t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0011c0009t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0011c0009t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0012c0015t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0012c0015t0009g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0013c0014t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0013c0014t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0014c0013t0006g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0014c0013t0006g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0014c0013t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0015c0027t0017g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0015c0027t0017g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0015c0066t0031g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0015c0067t0017g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0016c0023t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0016c0023t0021g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0016c0033t0021g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0017c0017t0004g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0017c0017t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0018c0020t0019g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0018c0020t0019g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0019c0028t0007g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0020c0026t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0021c0049t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0022c0045t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0023c0071t0007g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0024c0068t0007g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0025c0055t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0026c0053t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0027c0051t0006g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0028c0046t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0029c0050t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0030c0057t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0031c0062t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0032c0036t0024g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0033c0058t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0034c0035t0011g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0035c0041t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0036c0031t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0037c0054t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0038c0042t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0039c0072t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0040c0070t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0041c0037t0022g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0042c0032t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0043c0059t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0044c0047t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0045c0060t0027g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
a0046c0065t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0007 | c0069 | t0002 | g0175 | EUR | GBR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00099 | hp2 | a0003 | c0003 | t0003 | g0099 | EUR | GBR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00140 | hp2 | a0005 | c0006 | t0004 | g0063 | EUR | GBR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00280 | hp1 | a0002 | c0002 | t0002 | g0166 | EUR | FIN | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0013 | EUR | FIN | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00323 | hp1 | a0007 | c0010 | t0006 | g0030 | EUR | FIN | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00423 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | CHS | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00423 | hp2 | a0001 | c0001 | t0032 | g0046 | EAS | CHS | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | CHS | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00544 | hp1 | a0021 | c0049 | t0001 | g0075 | EAS | CHS | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00544 | hp2 | a0001 | c0030 | t0001 | g0130 | EAS | CHS | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00558 | hp2 | a0004 | c0004 | t0005 | g0050 | EAS | CHS | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0113 | EAS | CHS | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00597 | hp2 | a0022 | c0045 | t0003 | g0003 | EAS | CHS | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00621 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | CHS | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00621 | hp2 | a0001 | c0001 | t0009 | g0223 | EAS | CHS | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00639 | hp2 | a0006 | c0016 | t0002 | g0121 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00642 | hp1 | a0004 | c0004 | t0005 | g0022 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | CHS | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00733 | hp1 | a0023 | c0071 | t0007 | g0192 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00735 | hp1 | a0024 | c0068 | t0007 | g0122 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00735 | hp2 | a0009 | c0008 | t0002 | g0008 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00738 | hp1 | a0008 | c0029 | t0004 | g0133 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00741 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG00741 | hp2 | a0008 | c0011 | t0004 | g0010 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01069 | hp1 | a0009 | c0008 | t0002 | g0008 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01069 | hp2 | a0004 | c0004 | t0005 | g0051 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01071 | hp1 | a0004 | c0004 | t0005 | g0051 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01071 | hp2 | a0001 | c0001 | t0026 | g0002 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01074 | hp2 | a0002 | c0002 | t0014 | g0001 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01081 | hp1 | a0003 | c0003 | t0003 | g0034 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0014 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01099 | hp1 | a0025 | c0055 | t0001 | g0220 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01109 | hp1 | a0001 | c0001 | t0015 | g0018 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01109 | hp2 | a0010 | c0012 | t0001 | g0008 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01167 | hp1 | a0002 | c0002 | t0014 | g0001 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0125 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01168 | hp1 | a0003 | c0003 | t0003 | g0035 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01169 | hp1 | a0003 | c0003 | t0003 | g0035 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01243 | hp1 | a0002 | c0005 | t0008 | g0012 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01243 | hp2 | a0026 | c0053 | t0001 | g0204 | AMR | PUR | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01255 | hp2 | a0005 | c0006 | t0004 | g0057 | AMR | CLM | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0026 | AMR | CLM | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0117 | AMR | CLM | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01261 | hp2 | a0027 | c0051 | t0006 | g0201 | AMR | CLM | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01346 | hp1 | a0007 | c0010 | t0006 | g0030 | AMR | CLM | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01346 | hp2 | a0009 | c0008 | t0002 | g0008 | AMR | CLM | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0014 | AMR | CLM | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01361 | hp1 | a0002 | c0002 | t0002 | g0026 | AMR | CLM | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01361 | hp2 | a0007 | c0052 | t0006 | g0030 | AMR | CLM | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0026 | AMR | CLM | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01496 | hp2 | a0003 | c0003 | t0001 | g0219 | AMR | CLM | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01515 | hp1 | a0003 | c0003 | t0003 | g0004 | EUR | IBS | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01884 | hp1 | a0002 | c0019 | t0011 | g0124 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01884 | hp2 | a0010 | c0012 | t0016 | g0037 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01891 | hp1 | a0015 | c0066 | t0031 | g0174 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01891 | hp2 | a0011 | c0009 | t0001 | g0055 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01943 | hp2 | a0008 | c0011 | t0020 | g0010 | AMR | PEL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01952 | hp2 | a0002 | c0002 | t0002 | g0106 | AMR | PEL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01975 | hp1 | a0006 | c0016 | t0001 | g0150 | AMR | PEL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01975 | hp2 | a0008 | c0011 | t0004 | g0010 | AMR | PEL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01978 | hp1 | a0008 | c0011 | t0004 | g0010 | AMR | PEL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01978 | hp2 | a0004 | c0004 | t0005 | g0186 | AMR | PEL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01981 | hp1 | a0028 | c0046 | t0003 | g0086 | AMR | PEL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01993 | hp1 | a0005 | c0006 | t0004 | g0190 | AMR | PEL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01993 | hp2 | a0008 | c0011 | t0004 | g0058 | AMR | PEL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02004 | hp1 | a0029 | c0050 | t0004 | g0191 | AMR | PEL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02015 | hp1 | a0003 | c0003 | t0003 | g0004 | EAS | KHV | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02027 | hp1 | a0003 | c0003 | t0003 | g0004 | EAS | KHV | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02040 | hp1 | a0004 | c0004 | t0005 | g0021 | EAS | KHV | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02040 | hp2 | a0003 | c0003 | t0003 | g0098 | EAS | KHV | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02055 | hp1 | a0006 | c0040 | t0030 | g0085 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02055 | hp2 | a0011 | c0009 | t0001 | g0205 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02056 | hp1 | a0005 | c0006 | t0004 | g0011 | EAS | KHV | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02056 | hp2 | a0001 | c0030 | t0001 | g0129 | EAS | KHV | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02071 | hp1 | a0006 | c0044 | t0002 | g0097 | EAS | KHV | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02074 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | KHV | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02083 | hp1 | a0030 | c0057 | t0003 | g0002 | EAS | KHV | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0119 | EAS | KHV | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02129 | hp1 | a0003 | c0003 | t0003 | g0072 | EAS | KHV | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02132 | hp1 | a0001 | c0025 | t0001 | g0139 | EAS | KHV | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02135 | hp1 | a0001 | c0025 | t0001 | g0154 | EAS | KHV | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0110 | EAS | KHV | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02145 | hp1 | a0002 | c0005 | t0007 | g0009 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02145 | hp2 | a0001 | c0001 | t0015 | g0018 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | CDX | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | CDX | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02257 | hp1 | a0011 | c0009 | t0001 | g0054 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02258 | hp1 | a0002 | c0005 | t0008 | g0012 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02258 | hp2 | a0002 | c0005 | t0007 | g0009 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02273 | hp1 | a0008 | c0011 | t0020 | g0010 | AMR | PEL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02280 | hp2 | a0031 | c0062 | t0004 | g0144 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02451 | hp1 | a0016 | c0023 | t0007 | g0214 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02451 | hp2 | a0015 | c0027 | t0017 | g0173 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02572 | hp1 | a0006 | c0016 | t0002 | g0001 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02572 | hp2 | a0032 | c0036 | t0024 | g0102 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02602 | hp1 | a0002 | c0034 | t0002 | g0001 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02602 | hp2 | a0003 | c0003 | t0003 | g0004 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02622 | hp1 | a0033 | c0058 | t0001 | g0137 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02622 | hp2 | a0001 | c0018 | t0001 | g0027 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02630 | hp2 | a0002 | c0005 | t0008 | g0070 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02647 | hp1 | a0001 | c0007 | t0010 | g0023 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02683 | hp1 | a0004 | c0004 | t0018 | g0181 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02683 | hp2 | a0007 | c0010 | t0006 | g0202 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02698 | hp1 | a0001 | c0007 | t0001 | g0028 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02698 | hp2 | a0004 | c0004 | t0005 | g0180 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02717 | hp1 | a0016 | c0023 | t0021 | g0215 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02717 | hp2 | a0002 | c0005 | t0008 | g0012 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02723 | hp2 | a0019 | c0028 | t0007 | g0013 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02735 | hp2 | a0005 | c0006 | t0004 | g0011 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02738 | hp1 | a0002 | c0064 | t0023 | g0039 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0040 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02809 | hp1 | a0006 | c0022 | t0008 | g0211 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02809 | hp2 | a0003 | c0003 | t0003 | g0034 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02818 | hp1 | a0001 | c0007 | t0001 | g0218 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02818 | hp2 | a0034 | c0035 | t0011 | g0178 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02886 | hp1 | a0006 | c0039 | t0007 | g0209 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02886 | hp2 | a0035 | c0041 | t0001 | g0208 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02895 | hp1 | a0017 | c0017 | t0004 | g0053 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02895 | hp2 | a0001 | c0007 | t0010 | g0023 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02896 | hp1 | a0002 | c0019 | t0011 | g0047 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02896 | hp2 | a0003 | c0003 | t0001 | g0036 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02897 | hp1 | a0002 | c0019 | t0011 | g0047 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02897 | hp2 | a0017 | c0017 | t0004 | g0053 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02922 | hp1 | a0011 | c0009 | t0001 | g0054 | AFR | ESN | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02922 | hp2 | a0002 | c0005 | t0007 | g0210 | AFR | ESN | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02965 | hp2 | a0005 | c0006 | t0004 | g0031 | AFR | ESN | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02970 | hp1 | a0002 | c0005 | t0007 | g0009 | AFR | ESN | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02970 | hp2 | a0010 | c0012 | t0016 | g0037 | AFR | ESN | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02976 | hp1 | a0002 | c0005 | t0001 | g0177 | AFR | ESN | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02976 | hp2 | a0002 | c0005 | t0008 | g0069 | AFR | ESN | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03017 | hp2 | a0003 | c0003 | t0003 | g0078 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03041 | hp1 | a0011 | c0009 | t0001 | g0206 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03041 | hp2 | a0017 | c0017 | t0004 | g0120 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03098 | hp1 | a0036 | c0031 | t0001 | g0200 | AFR | MSL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03130 | hp1 | a0002 | c0005 | t0008 | g0012 | AFR | ESN | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03130 | hp2 | a0002 | c0005 | t0007 | g0009 | AFR | ESN | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03139 | hp1 | a0002 | c0005 | t0008 | g0032 | AFR | ESN | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03139 | hp2 | a0004 | c0004 | t0005 | g0221 | AFR | ESN | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03195 | hp1 | a0001 | c0018 | t0001 | g0027 | AFR | ESN | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03195 | hp2 | a0010 | c0012 | t0016 | g0168 | AFR | ESN | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03209 | hp1 | a0001 | c0018 | t0001 | g0027 | AFR | MSL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03209 | hp2 | a0001 | c0007 | t0001 | g0213 | AFR | MSL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03225 | hp1 | a0015 | c0067 | t0017 | g0172 | AFR | MSL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03225 | hp2 | a0005 | c0006 | t0004 | g0064 | AFR | MSL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03239 | hp1 | a0037 | c0054 | t0003 | g0062 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03239 | hp2 | a0005 | c0006 | t0004 | g0011 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03453 | hp1 | a0004 | c0021 | t0005 | g0049 | AFR | MSL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03453 | hp2 | a0038 | c0042 | t0001 | g0199 | AFR | MSL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03486 | hp1 | a0004 | c0004 | t0005 | g0184 | AFR | MSL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03486 | hp2 | a0001 | c0043 | t0001 | g0193 | AFR | MSL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03490 | hp1 | a0010 | c0012 | t0001 | g0001 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03492 | hp2 | a0004 | c0038 | t0005 | g0022 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03516 | hp1 | a0002 | c0048 | t0002 | g0071 | AFR | ESN | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03516 | hp2 | a0003 | c0003 | t0001 | g0101 | AFR | ESN | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03540 | hp1 | a0003 | c0003 | t0003 | g0100 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03540 | hp2 | a0006 | c0022 | t0008 | g0207 | AFR | GWD | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03579 | hp1 | a0005 | c0006 | t0004 | g0031 | AFR | MSL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03654 | hp1 | a0039 | c0072 | t0002 | g0001 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03654 | hp2 | a0010 | c0012 | t0001 | g0115 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0039 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03688 | hp1 | a0001 | c0007 | t0001 | g0217 | SAS | STU | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | STU | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03704 | hp2 | a0009 | c0008 | t0002 | g0008 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03710 | hp1 | a0003 | c0003 | t0001 | g0004 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03831 | hp1 | a0001 | c0007 | t0001 | g0094 | SAS | BEB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03831 | hp2 | a0004 | c0004 | t0034 | g0188 | SAS | BEB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0040 | SAS | BEB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03942 | hp2 | a0009 | c0008 | t0002 | g0123 | SAS | BEB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG04115 | hp2 | a0009 | c0008 | t0002 | g0008 | SAS | STU | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG04184 | hp1 | a0004 | c0004 | t0018 | g0185 | SAS | BEB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0013 | SAS | BEB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG04204 | hp1 | a0003 | c0003 | t0003 | g0092 | SAS | STU | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG04228 | hp1 | a0001 | c0061 | t0001 | g0143 | SAS | STU | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG04228 | hp2 | a0003 | c0003 | t0003 | g0084 | SAS | STU | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18522 | hp1 | a0041 | c0037 | t0022 | g0067 | AFR | YRI | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18522 | hp2 | a0001 | c0001 | t0015 | g0018 | AFR | YRI | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18612 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18747 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | CHB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18906 | hp1 | a0018 | c0020 | t0019 | g0066 | AFR | YRI | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18906 | hp2 | a0004 | c0021 | t0005 | g0049 | AFR | YRI | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18939 | hp1 | a0003 | c0003 | t0003 | g0068 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18939 | hp2 | a0020 | c0026 | t0002 | g0038 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18940 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18942 | hp1 | a0042 | c0032 | t0003 | g0004 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18943 | hp2 | a0003 | c0003 | t0003 | g0033 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18946 | hp2 | a0005 | c0006 | t0004 | g0059 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18947 | hp1 | a0003 | c0003 | t0012 | g0003 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18947 | hp2 | a0002 | c0002 | t0013 | g0015 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18948 | hp1 | a0001 | c0007 | t0001 | g0081 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18948 | hp2 | a0043 | c0059 | t0001 | g0005 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18949 | hp2 | a0003 | c0003 | t0003 | g0195 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18951 | hp1 | a0003 | c0024 | t0003 | g0087 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18952 | hp1 | a0003 | c0003 | t0003 | g0083 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18952 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18954 | hp1 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18956 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18956 | hp2 | a0012 | c0015 | t0001 | g0020 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18959 | hp1 | a0007 | c0010 | t0006 | g0203 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18959 | hp2 | a0003 | c0003 | t0003 | g0096 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18960 | hp1 | a0005 | c0006 | t0004 | g0061 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18961 | hp1 | a0003 | c0003 | t0003 | g0076 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18961 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18964 | hp2 | a0013 | c0014 | t0002 | g0016 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18965 | hp2 | a0003 | c0003 | t0025 | g0004 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18969 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18969 | hp2 | a0005 | c0006 | t0004 | g0060 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18970 | hp1 | a0001 | c0001 | t0009 | g0024 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18970 | hp2 | a0014 | c0013 | t0006 | g0025 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18971 | hp1 | a0013 | c0014 | t0002 | g0016 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18971 | hp2 | a0001 | c0001 | t0009 | g0024 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18972 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18973 | hp1 | a0044 | c0047 | t0002 | g0003 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18973 | hp2 | a0001 | c0007 | t0001 | g0080 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18974 | hp1 | a0003 | c0003 | t0003 | g0033 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18975 | hp1 | a0002 | c0002 | t0013 | g0015 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18978 | hp1 | a0045 | c0060 | t0027 | g0149 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18978 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18979 | hp2 | a0014 | c0013 | t0006 | g0025 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18980 | hp1 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18980 | hp2 | a0004 | c0004 | t0005 | g0021 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18981 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18982 | hp2 | a0001 | c0001 | t0009 | g0222 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18983 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18983 | hp2 | a0004 | c0004 | t0005 | g0050 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18984 | hp2 | a0007 | c0010 | t0006 | g0052 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18986 | hp1 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18988 | hp1 | a0004 | c0004 | t0005 | g0021 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18988 | hp2 | a0003 | c0003 | t0003 | g0088 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18989 | hp2 | a0014 | c0013 | t0006 | g0025 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18990 | hp1 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18991 | hp1 | a0046 | c0065 | t0001 | g0007 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18991 | hp2 | a0003 | c0003 | t0012 | g0074 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18993 | hp1 | a0012 | c0015 | t0001 | g0020 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18993 | hp2 | a0003 | c0003 | t0003 | g0194 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18994 | hp1 | a0012 | c0015 | t0001 | g0020 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18994 | hp2 | a0005 | c0006 | t0004 | g0056 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18997 | hp1 | a0014 | c0013 | t0006 | g0082 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18998 | hp2 | a0020 | c0026 | t0002 | g0038 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19000 | hp1 | a0012 | c0015 | t0009 | g0159 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19000 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19001 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19002 | hp1 | a0004 | c0004 | t0005 | g0022 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19002 | hp2 | a0003 | c0003 | t0003 | g0103 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19003 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19003 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19004 | hp1 | a0003 | c0024 | t0003 | g0004 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19004 | hp2 | a0005 | c0006 | t0004 | g0011 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19005 | hp1 | a0003 | c0003 | t0003 | g0189 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19006 | hp2 | a0004 | c0004 | t0005 | g0187 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19007 | hp1 | a0012 | c0015 | t0001 | g0020 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19007 | hp2 | a0003 | c0003 | t0012 | g0003 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19012 | hp1 | a0007 | c0010 | t0006 | g0052 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19030 | hp1 | a0015 | c0027 | t0017 | g0171 | AFR | LWK | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19030 | hp2 | a0001 | c0007 | t0010 | g0023 | AFR | LWK | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19043 | hp1 | a0002 | c0005 | t0008 | g0032 | AFR | LWK | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19043 | hp2 | a0001 | c0007 | t0010 | g0023 | AFR | LWK | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19054 | hp1 | a0003 | c0063 | t0003 | g0003 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19054 | hp2 | a0004 | c0004 | t0005 | g0022 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19055 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19055 | hp2 | a0003 | c0003 | t0003 | g0079 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19056 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19057 | hp1 | a0005 | c0006 | t0004 | g0011 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19057 | hp2 | a0003 | c0003 | t0012 | g0003 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19058 | hp1 | a0004 | c0004 | t0005 | g0179 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19060 | hp2 | a0003 | c0003 | t0003 | g0091 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19064 | hp1 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19064 | hp2 | a0002 | c0002 | t0013 | g0041 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19066 | hp2 | a0003 | c0003 | t0003 | g0003 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19067 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19067 | hp2 | a0004 | c0004 | t0005 | g0021 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19068 | hp1 | a0013 | c0014 | t0002 | g0016 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19070 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19072 | hp1 | a0001 | c0001 | t0028 | g0153 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19072 | hp2 | a0003 | c0003 | t0003 | g0004 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19076 | hp1 | a0001 | c0001 | t0009 | g0024 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19076 | hp2 | a0003 | c0003 | t0003 | g0183 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19077 | hp1 | a0013 | c0014 | t0002 | g0016 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19077 | hp2 | a0004 | c0004 | t0005 | g0196 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19080 | hp1 | a0003 | c0003 | t0003 | g0095 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19080 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19081 | hp1 | a0002 | c0002 | t0033 | g0001 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19081 | hp2 | a0003 | c0003 | t0003 | g0077 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19082 | hp2 | a0002 | c0002 | t0013 | g0041 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19083 | hp1 | a0004 | c0004 | t0005 | g0182 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19083 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19085 | hp1 | a0014 | c0013 | t0006 | g0089 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19085 | hp2 | a0013 | c0014 | t0002 | g0132 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19090 | hp2 | a0001 | c0007 | t0009 | g0090 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19240 | hp1 | a0001 | c0007 | t0010 | g0198 | AFR | YRI | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA19240 | hp2 | a0002 | c0005 | t0007 | g0009 | AFR | YRI | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA20129 | hp1 | a0003 | c0003 | t0001 | g0036 | AFR | ASW | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA20129 | hp2 | a0006 | c0016 | t0002 | g0001 | AFR | ASW | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0014 | EUR | TSI | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA20805 | hp1 | a0001 | c0001 | t0029 | g0138 | EUR | TSI | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA20905 | hp1 | a0002 | c0002 | t0014 | g0001 | SAS | GIH | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA20905 | hp2 | a0002 | c0002 | t0002 | g0014 | SAS | GIH | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01123 | hp1 | a0004 | c0004 | t0018 | g0073 | AMR | CLM | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG01123 | hp2 | a0009 | c0008 | t0002 | g0008 | AMR | CLM | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02109 | hp1 | a0011 | c0009 | t0001 | g0055 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02109 | hp2 | a0016 | c0033 | t0021 | g0216 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02486 | hp2 | a0002 | c0005 | t0007 | g0009 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02559 | hp1 | a0018 | c0020 | t0019 | g0065 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG02559 | hp2 | a0019 | c0028 | t0007 | g0013 | AFR | ACB | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03471 | hp1 | a0006 | c0056 | t0008 | g0170 | AFR | MSL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG06807 | hp1 | a0001 | c0007 | t0010 | g0197 | AFR | USA | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
HG06807 | hp2 | a0040 | c0070 | t0001 | g0002 | AFR | USA | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA18955 | hp2 | a0003 | c0003 | t0003 | g0093 | EAS | JPT | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0109 | AFR | USA | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA20300 | hp2 | a0002 | c0005 | t0011 | g0212 | AFR | USA | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0108 | AFR | LWK | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
homoSapiens | chm13v2 | a0008 | c0029 | t0004 | g0162 | REF | REF | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0116 | REF | REF | SYNM_chr15_99100080_99140593 | SYNM | chr15 | 99100080 | 99140593 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:99105222 | C | G | 1 | a0039 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.23C>G | p.Thr8Arg | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/4 | 143/7353 | 23/4698 | 8/1565 | chr15 | 99105222 | |||
chr15:99105358 | G | GGCCGAGG others(14): Show |
1 | a0023 | 1 | HG00733.hp1 | disruptive_inframe_insertion | MODERATE | c.167_187dupGGCAGGCC others(13): Show |
p.Gly56_Glu62dup | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/4 | 308/7353 | 188/4698 | 63/1565 | INFO_REALIGN_3_PRIME | chr15 | 99105358 | ||
chr15:99105365 | G | C | 1 | a0036 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.166G>C | p.Gly56Arg | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/4 | 286/7353 | 166/4698 | 56/1565 | chr15 | 99105365 | |||
chr15:99105547 | G | C | 1 | a0042 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.348G>C | p.Gln116His | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/4 | 468/7353 | 348/4698 | 116/1565 | chr15 | 99105547 | |||
chr15:99105770 | G | C | 2 | a0032 a0034 |
2 | HG02572.hp2 HG02818.hp2 |
missense_variant | MODERATE | c.571G>C | p.Val191Leu | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/4 | 691/7353 | 571/4698 | 191/1565 | chr15 | 99105770 | |||
chr15:99105808 | G | C | 2 | a0018 a0041 |
3 | HG02559.hp1 NA18522.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.609G>C | p.Glu203Asp | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/4 | 729/7353 | 609/4698 | 203/1565 | chr15 | 99105808 | |||
chr15:99105891 | C | T | 1 | a0012 | 5 | NA18956.hp2 NA18993.hp1 NA18994.hp1 others(2): Show |
missense_variant | MODERATE | c.692C>T | p.Ala231Val | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/4 | 812/7353 | 692/4698 | 231/1565 | chr15 | 99105891 | |||
chr15:99105914 | C | T | 1 | a0013 | 5 | NA18964.hp2 NA18971.hp1 NA19068.hp1 others(2): Show |
missense_variant | MODERATE | c.715C>T | p.Arg239Cys | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/4 | 835/7353 | 715/4698 | 239/1565 | chr15 | 99105914 | |||
chr15:99105996 | C | T | 1 | a0040 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.797C>T | p.Ala266Val | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/4 | 917/7353 | 797/4698 | 266/1565 | chr15 | 99105996 | |||
chr15:99113595 | T | C | 25 | a0001 a0003 a0004 others(22): Show |
254 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(251): Show |
missense_variant | MODERATE | c.815T>C | p.Val272Ala | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/4 | 935/7353 | 815/4698 | 272/1565 | chr15 | 99113595 | |||
chr15:99126774 | G | A | 2 | a0004 a0018 |
28 | HG00558.hp2 HG00642.hp1 HG01069.hp2 others(25): Show |
missense_variant | MODERATE | c.988G>A | p.Val330Ile | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/4 | 1108/7353 | 988/4698 | 330/1565 | chr15 | 99126774 | |||
chr15:99129423 | A | T | 11 | a0003 a0017 a0022 others(8): Show |
78 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(75): Show |
missense_variant | MODERATE | c.1063A>T | p.Arg355Trp | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 1183/7353 | 1063/4698 | 355/1565 | chr15 | 99129423 | |||
chr15:99129778 | G | A | 1 | a0020 | 2 | NA18939.hp2 NA18998.hp2 |
missense_variant | MODERATE | c.1418G>A | p.Arg473Gln | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 1538/7353 | 1418/4698 | 473/1565 | chr15 | 99129778 | |||
chr15:99129822 | C | T | 1 | a0025 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.1462C>T | p.Arg488Trp | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 1582/7353 | 1462/4698 | 488/1565 | chr15 | 99129822 | |||
chr15:99129975 | T | C | 1 | a0022 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.1615T>C | p.Trp539Arg | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 1735/7353 | 1615/4698 | 539/1565 | chr15 | 99129975 | |||
chr15:99130060 | C | T | 11 | a0005 a0007 a0008 others(8): Show |
48 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(45): Show |
missense_variant | MODERATE | c.1700C>T | p.Pro567Leu | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 1820/7353 | 1700/4698 | 567/1565 | chr15 | 99130060 | |||
chr15:99130195 | A | C | 1 | a0008 | 7 | HG00738.hp1 HG00741.hp2 HG01943.hp2 others(4): Show |
missense_variant | MODERATE | c.1835A>C | p.Glu612Ala | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 1955/7353 | 1835/4698 | 612/1565 | chr15 | 99130195 | |||
chr15:99130272 | G | A | 1 | a0015 | 4 | HG01891.hp1 HG02451.hp2 HG03225.hp1 others(1): Show |
missense_variant | MODERATE | c.1912G>A | p.Val638Ile | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 2032/7353 | 1912/4698 | 638/1565 | chr15 | 99130272 | |||
chr15:99130599 | G | A | 1 | a0011 | 6 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(3): Show |
missense_variant | MODERATE | c.2239G>A | p.Glu747Lys | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 2359/7353 | 2239/4698 | 747/1565 | chr15 | 99130599 | |||
chr15:99130614 | C | A | 1 | a0021 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.2254C>A | p.Pro752Thr | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 2374/7353 | 2254/4698 | 752/1565 | chr15 | 99130614 | |||
chr15:99130642 | C | T | 3 | a0007 a0014 a0027 |
14 | HG00099.hp1 HG00323.hp1 HG01261.hp2 others(11): Show |
missense_variant | MODERATE | c.2282C>T | p.Pro761Leu | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 2402/7353 | 2282/4698 | 761/1565 | chr15 | 99130642 | |||
chr15:99130711 | T | C | 1 | a0035 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.2351T>C | p.Val784Ala | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 2471/7353 | 2351/4698 | 784/1565 | chr15 | 99130711 | |||
chr15:99131128 | T | C | 1 | a0030 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.2768T>C | p.Ile923Thr | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 2888/7353 | 2768/4698 | 923/1565 | chr15 | 99131128 | |||
chr15:99131287 | A | G | 1 | a0008 | 7 | HG00738.hp1 HG00741.hp2 HG01943.hp2 others(4): Show |
missense_variant | MODERATE | c.2927A>G | p.Gln976Arg | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 3047/7353 | 2927/4698 | 976/1565 | chr15 | 99131287 | |||
chr15:99131386 | T | C | 1 | a0027 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.3026T>C | p.Val1009Ala | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 3146/7353 | 3026/4698 | 1009/1565 | chr15 | 99131386 | |||
chr15:99131412 | G | T | 2 | a0035 a0038 |
2 | HG02886.hp2 HG03453.hp2 |
stop_gained | HIGH | c.3052G>T | p.Glu1018* | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 3172/7353 | 3052/4698 | 1018/1565 | chr15 | 99131412 | |||
chr15:99131413 | A | T | 2 | a0035 a0038 |
2 | HG02886.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.3053A>T | p.Glu1018Val | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 3173/7353 | 3053/4698 | 1018/1565 | chr15 | 99131413 | |||
chr15:99131536 | C | T | 1 | a0009 | 7 | HG00735.hp2 HG01069.hp1 HG01123.hp2 others(4): Show |
missense_variant | MODERATE | c.3176C>T | p.Pro1059Leu | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 3296/7353 | 3176/4698 | 1059/1565 | chr15 | 99131536 | |||
chr15:99131560 | G | C | 3 | a0007 a0014 a0027 |
14 | HG00099.hp1 HG00323.hp1 HG01261.hp2 others(11): Show |
missense_variant | MODERATE | c.3200G>C | p.Arg1067Pro | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 3320/7353 | 3200/4698 | 1067/1565 | chr15 | 99131560 | |||
chr15:99131571 | C | T | 1 | a0037 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.3211C>T | p.Arg1071Trp | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 3331/7353 | 3211/4698 | 1071/1565 | chr15 | 99131571 | |||
chr15:99131590 | C | T | 5 | a0005 a0008 a0017 others(2): Show |
27 | HG00140.hp2 HG00738.hp1 HG00741.hp2 others(24): Show |
missense_variant | MODERATE | c.3230C>T | p.Ser1077Leu | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 3350/7353 | 3230/4698 | 1077/1565 | chr15 | 99131590 | |||
chr15:99131601 | G | A | 1 | a0011 | 6 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(3): Show |
missense_variant | MODERATE | c.3241G>A | p.Glu1081Lys | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 3361/7353 | 3241/4698 | 1081/1565 | chr15 | 99131601 | |||
chr15:99131748 | G | A | 2 | a0019 a0024 |
3 | HG00735.hp1 HG02559.hp2 HG02723.hp2 |
missense_variant | MODERATE | c.3388G>A | p.Gly1130Ser | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 3508/7353 | 3388/4698 | 1130/1565 | chr15 | 99131748 | |||
chr15:99132028 | T | C | 1 | a0024 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.3668T>C | p.Phe1223Ser | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 3788/7353 | 3668/4698 | 1223/1565 | chr15 | 99132028 | |||
chr15:99132084 | G | C | 1 | a0046 | 1 | NA18991.hp1 | missense_variant | MODERATE | c.3724G>C | p.Ala1242Pro | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 3844/7353 | 3724/4698 | 1242/1565 | chr15 | 99132084 | |||
chr15:99132240 | G | A | 1 | a0008 | 7 | HG00738.hp1 HG00741.hp2 HG01943.hp2 others(4): Show |
missense_variant | MODERATE | c.3880G>A | p.Asp1294Asn | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 4000/7353 | 3880/4698 | 1294/1565 | chr15 | 99132240 | |||
chr15:99132339 | C | T | 1 | a0025 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.3979C>T | p.His1327Tyr | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 4099/7353 | 3979/4698 | 1327/1565 | chr15 | 99132339 | |||
chr15:99132394 | G | C | 12 | a0005 a0007 a0008 others(9): Show |
48 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(45): Show |
missense_variant | MODERATE | c.4034G>C | p.Gly1345Ala | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 4154/7353 | 4034/4698 | 1345/1565 | chr15 | 99132394 | |||
chr15:99132439 | C | T | 1 | a0045 | 1 | NA18978.hp1 | missense_variant | MODERATE | c.4079C>T | p.Ser1360Leu | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 4199/7353 | 4079/4698 | 1360/1565 | chr15 | 99132439 | |||
chr15:99132517 | A | G | 17 | a0001 a0003 a0010 others(14): Show |
210 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(207): Show |
missense_variant | MODERATE | c.4157A>G | p.Glu1386Gly | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 4277/7353 | 4157/4698 | 1386/1565 | chr15 | 99132517 | |||
chr15:99132765 | G | A | 1 | a0029 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.4405G>A | p.Val1469Ile | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 4525/7353 | 4405/4698 | 1469/1565 | chr15 | 99132765 | |||
chr15:99132776 | C | G | 1 | a0043 | 1 | NA18948.hp2 | missense_variant | MODERATE | c.4416C>G | p.Ile1472Met | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 4536/7353 | 4416/4698 | 1472/1565 | chr15 | 99132776 | |||
chr15:99132814 | C | G | 1 | a0028 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.4454C>G | p.Ser1485Cys | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 4574/7353 | 4454/4698 | 1485/1565 | chr15 | 99132814 | |||
chr15:99132850 | A | G | 1 | a0033 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.4490A>G | p.Asn1497Ser | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 4610/7353 | 4490/4698 | 1497/1565 | chr15 | 99132850 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:99105607 | G | A | 41 | a0001c0007 a0001c0043 a0002c0005 others(38): Show |
194 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(191): Show |
synonymous_variant | LOW | c.408G>A | p.Arg136Arg | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/4 | 528/7353 | 408/4698 | 136/1565 | chr15 | 99105607 | |||
chr15:99105656 | A | C | 40 | a0001c0007 a0001c0030 a0001c0043 others(37): Show |
194 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(191): Show |
synonymous_variant | LOW | c.457A>C | p.Arg153Arg | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/4 | 577/7353 | 457/4698 | 153/1565 | chr15 | 99105656 | |||
chr15:99129767 | C | T | 1 | a0001c0018 | 3 | HG02622.hp2 HG03195.hp1 HG03209.hp1 |
synonymous_variant | LOW | c.1407C>T | p.Arg469Arg | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 1527/7353 | 1407/4698 | 469/1565 | chr15 | 99129767 | |||
chr15:99129812 | G | A | 1 | a0006c0039 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.1452G>A | p.Ser484Ser | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 1572/7353 | 1452/4698 | 484/1565 | chr15 | 99129812 | |||
chr15:99129956 | C | T | 8 | a0003c0003 a0003c0024 a0003c0063 others(5): Show |
71 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(68): Show |
synonymous_variant | LOW | c.1596C>T | p.Ser532Ser | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 1716/7353 | 1596/4698 | 532/1565 | chr15 | 99129956 | |||
chr15:99130073 | C | T | 12 | a0003c0003 a0003c0024 a0003c0063 others(9): Show |
77 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(74): Show |
synonymous_variant | LOW | c.1713C>T | p.Ser571Ser | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 1833/7353 | 1713/4698 | 571/1565 | chr15 | 99130073 | |||
chr15:99130154 | G | A | 1 | a0032c0036 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.1794G>A | p.Thr598Thr | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 1914/7353 | 1794/4698 | 598/1565 | chr15 | 99130154 | |||
chr15:99130313 | T | C | 28 | a0002c0005 a0002c0019 a0002c0048 others(25): Show |
101 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(98): Show |
synonymous_variant | LOW | c.1953T>C | p.Thr651Thr | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 2073/7353 | 1953/4698 | 651/1565 | chr15 | 99130313 | |||
chr15:99130361 | A | G | 1 | a0007c0052 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.2001A>G | p.Lys667Lys | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 2121/7353 | 2001/4698 | 667/1565 | chr15 | 99130361 | |||
chr15:99130556 | C | T | 4 | a0004c0021 a0017c0017 a0026c0053 others(1): Show |
7 | HG01243.hp2 HG02280.hp2 HG02895.hp1 others(4): Show |
synonymous_variant | LOW | c.2196C>T | p.Leu732Leu | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 2316/7353 | 2196/4698 | 732/1565 | chr15 | 99130556 | |||
chr15:99130784 | T | C | 59 | a0001c0001 a0001c0007 a0001c0018 others(56): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
synonymous_variant | LOW | c.2424T>C | p.Pro808Pro | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 2544/7353 | 2424/4698 | 808/1565 | chr15 | 99130784 | |||
chr15:99130910 | C | T | 3 | a0001c0043 a0006c0039 a0015c0067 |
3 | HG02886.hp1 HG03225.hp1 HG03486.hp2 |
synonymous_variant | LOW | c.2550C>T | p.Tyr850Tyr | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 2670/7353 | 2550/4698 | 850/1565 | chr15 | 99130910 | |||
chr15:99130961 | T | C | 1 | a0015c0027 | 2 | HG02451.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.2601T>C | p.Asp867Asp | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 2721/7353 | 2601/4698 | 867/1565 | chr15 | 99130961 | |||
chr15:99131267 | C | T | 1 | a0001c0061 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.2907C>T | p.Ser969Ser | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 3027/7353 | 2907/4698 | 969/1565 | chr15 | 99131267 | |||
chr15:99131405 | C | T | 2 | a0035c0041 a0038c0042 |
2 | HG02886.hp2 HG03453.hp2 |
synonymous_variant | LOW | c.3045C>T | p.Asp1015Asp | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 3165/7353 | 3045/4698 | 1015/1565 | chr15 | 99131405 | |||
chr15:99131528 | G | A | 1 | a0002c0064 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.3168G>A | p.Ala1056Ala | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 3288/7353 | 3168/4698 | 1056/1565 | chr15 | 99131528 | |||
chr15:99131555 | T | C | 53 | a0001c0001 a0001c0007 a0001c0018 others(50): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
synonymous_variant | LOW | c.3195T>C | p.Phe1065Phe | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 3315/7353 | 3195/4698 | 1065/1565 | chr15 | 99131555 | |||
chr15:99132113 | A | C | 1 | a0004c0038 | 1 | HG03492.hp2 | synonymous_variant | LOW | c.3753A>C | p.Ala1251Ala | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 3873/7353 | 3753/4698 | 1251/1565 | chr15 | 99132113 | |||
chr15:99132446 | A | G | 1 | a0003c0024 | 2 | NA18951.hp1 NA19004.hp1 |
synonymous_variant | LOW | c.4086A>G | p.Arg1362Arg | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 4206/7353 | 4086/4698 | 1362/1565 | chr15 | 99132446 | |||
chr15:99132644 | G | A | 2 | a0019c0028 a0024c0068 |
3 | HG00735.hp1 HG02559.hp2 HG02723.hp2 |
synonymous_variant | LOW | c.4284G>A | p.Val1428Val | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 4404/7353 | 4284/4698 | 1428/1565 | chr15 | 99132644 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:99105102 | C | T | 1 | a0001c0007t0010 | 6 | HG02647.hp1 HG02895.hp2 HG06807.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-98C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/4 | 98 | chr15 | 99105102 | ||||||
chr15:99105105 | C | T | 1 | a0004c0004t0034 | 1 | HG03831.hp2 | 5_prime_UTR_variant | MODIFIER | c.-95C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/4 | 95 | chr15 | 99105105 | ||||||
chr15:99105142 | G | C | 2 | a0018c0020t0019 a0041c0037t0022 |
3 | HG02559.hp1 NA18522.hp1 NA18906.hp1 |
5_prime_UTR_variant | MODIFIER | c.-58G>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/4 | 58 | chr15 | 99105142 | ||||||
chr15:99133138 | C | T | 1 | a0002c0002t0013 | 4 | NA18947.hp2 NA18975.hp1 NA19064.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*80C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 80 | chr15 | 99133138 | ||||||
chr15:99133219 | C | T | 3 | a0001c0001t0009 a0001c0007t0009 a0012c0015t0009 |
7 | HG00621.hp2 NA18970.hp1 NA18971.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*161C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 161 | chr15 | 99133219 | ||||||
chr15:99133299 | T | C | 1 | a0002c0002t0014 | 3 | HG01074.hp2 HG01167.hp1 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*241T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 241 | chr15 | 99133299 | ||||||
chr15:99133417 | G | C | 1 | a0002c0064t0023 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*359G>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 359 | chr15 | 99133417 | ||||||
chr15:99133722 | A | G | 1 | a0002c0002t0033 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*664A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 664 | chr15 | 99133722 | ||||||
chr15:99133773 | G | A | 1 | a0032c0036t0024 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*715G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 715 | chr15 | 99133773 | ||||||
chr15:99133817 | A | G | 1 | a0001c0001t0032 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*759A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 759 | chr15 | 99133817 | ||||||
chr15:99133841 | T | TTTCTGTT others(10): Show |
36 | a0002c0005t0007 a0002c0005t0008 a0002c0005t0011 others(33): Show |
105 | HG00140.hp2 HG00323.hp1 HG00558.hp2 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*788_*789insTTATAG others(11): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 789 | INFO_REALIGN_3_PRIME | chr15 | 99133841 | |||||
chr15:99133862 | A | G | 1 | a0001c0001t0029 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*804A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 804 | chr15 | 99133862 | ||||||
chr15:99133881 | C | T | 9 | a0002c0005t0008 a0004c0004t0005 a0004c0004t0018 others(6): Show |
39 | HG00558.hp2 HG00642.hp1 HG01069.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*823C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 823 | chr15 | 99133881 | ||||||
chr15:99134041 | T | C | 10 | a0005c0006t0004 a0007c0010t0006 a0007c0052t0006 others(7): Show |
38 | HG00140.hp2 HG00323.hp1 HG00738.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*983T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 983 | chr15 | 99134041 | ||||||
chr15:99134242 | A | C | 1 | a0001c0001t0028 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1184A>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 1184 | chr15 | 99134242 | ||||||
chr15:99134263 | C | A | 7 | a0005c0006t0004 a0008c0011t0004 a0008c0011t0020 others(4): Show |
27 | HG00140.hp2 HG00738.hp1 HG00741.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1205C>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 1205 | chr15 | 99134263 | ||||||
chr15:99134545 | G | A | 29 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0032 others(26): Show |
119 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*1487G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 1487 | chr15 | 99134545 | ||||||
chr15:99134558 | C | T | 3 | a0015c0027t0017 a0015c0066t0031 a0015c0067t0017 |
4 | HG01891.hp1 HG02451.hp2 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1500C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 1500 | chr15 | 99134558 | ||||||
chr15:99134609 | C | T | 1 | a0003c0003t0012 | 4 | NA18947.hp1 NA18991.hp2 NA19007.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1551C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 1551 | chr15 | 99134609 | ||||||
chr15:99134704 | G | A | 1 | a0001c0001t0026 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1646G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 1646 | chr15 | 99134704 | ||||||
chr15:99134707 | A | G | 1 | a0010c0012t0016 | 3 | HG01884.hp2 HG02970.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1649A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 1649 | chr15 | 99134707 | ||||||
chr15:99134799 | T | C | 7 | a0005c0006t0004 a0008c0011t0004 a0008c0011t0020 others(4): Show |
27 | HG00140.hp2 HG00738.hp1 HG00741.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1741T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 1741 | chr15 | 99134799 | ||||||
chr15:99134823 | A | G | 82 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0009 others(79): Show |
338 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(335): Show |
3_prime_UTR_variant | MODIFIER | c.*1765A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 1765 | chr15 | 99134823 | ||||||
chr15:99135062 | C | T | 22 | a0001c0001t0015 a0002c0005t0007 a0002c0005t0011 others(19): Show |
56 | HG00558.hp2 HG00642.hp1 HG00733.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2004C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 2004 | chr15 | 99135062 | ||||||
chr15:99135147 | ACTTTGGG others(6): Show |
A | 1 | a0006c0040t0030 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2093_*2105delTGGG others(9): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 2093 | INFO_REALIGN_3_PRIME | chr15 | 99135147 | |||||
chr15:99135264 | C | T | 1 | a0045c0060t0027 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2206C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 2206 | chr15 | 99135264 | ||||||
chr15:99135322 | C | T | 1 | a0003c0003t0025 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2264C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 2264 | chr15 | 99135322 | ||||||
chr15:99135436 | G | A | 2 | a0016c0023t0021 a0016c0033t0021 |
2 | HG02109.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2378G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 2378 | chr15 | 99135436 | ||||||
chr15:99135454 | C | G | 1 | a0004c0004t0018 | 3 | HG01123.hp1 HG02683.hp1 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2396C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 4/4 | 2396 | chr15 | 99135454 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:99106012 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0009g0024 a0001c0001t0009g0222 others(1): Show |
6 | HG00621.hp2 NA18960.hp2 NA18970.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.810+3C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99106012 | |||||||
chr15:99106013 | C | A | 13 | a0005c0006t0004g0011 a0005c0006t0004g0031 a0005c0006t0004g0056 others(10): Show |
21 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(18): Show |
splice_region_variant&intron_variant | LOW | c.810+4C>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99106013 | |||||||
chr15:99106032 | C | A | 3 | a0018c0020t0019g0065 a0018c0020t0019g0066 a0041c0037t0022g0067 |
3 | HG02559.hp1 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.810+23C>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99106032 | |||||||
chr15:99106094 | C | T | 32 | a0001c0007t0001g0213 a0001c0007t0001g0217 a0001c0007t0001g0218 others(29): Show |
40 | HG00323.hp1 HG01099.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.810+85C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99106094 | |||||||
chr15:99106126 | A | C | 1 | a0004c0004t0005g0196 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.810+117A>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99106126 | |||||||
chr15:99106142 | G | T | 4 | a0001c0001t0001g0024 a0001c0001t0009g0024 a0001c0001t0009g0222 others(1): Show |
6 | HG00621.hp2 NA18960.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.810+133G>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99106142 | |||||||
chr15:99106165 | G | A | 3 | a0018c0020t0019g0065 a0018c0020t0019g0066 a0041c0037t0022g0067 |
3 | HG02559.hp1 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.810+156G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99106165 | |||||||
chr15:99106181 | TC | T | 3 | a0001c0007t0010g0023 a0001c0007t0010g0197 a0001c0007t0010g0198 |
6 | HG02647.hp1 HG02895.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.810+174delC | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr15 | 99106181 | ||||||
chr15:99106319 | A | G | 1 | a0004c0004t0005g0221 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.810+310A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99106319 | |||||||
chr15:99106457 | A | G | 1 | a0003c0003t0003g0195 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.810+448A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99106457 | |||||||
chr15:99106548 | C | G | 1 | a0003c0003t0003g0194 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.810+539C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99106548 | |||||||
chr15:99106606 | C | G | 1 | a0025c0055t0001g0220 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.810+597C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99106606 | |||||||
chr15:99106620 | G | A | 1 | a0003c0003t0003g0068 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.810+611G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99106620 | |||||||
chr15:99106632 | C | T | 2 | a0001c0043t0001g0193 a0023c0071t0007g0192 |
2 | HG00733.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.810+623C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99106632 | |||||||
chr15:99106702 | C | T | 20 | a0003c0003t0003g0183 a0003c0003t0003g0189 a0004c0004t0005g0021 others(17): Show |
28 | HG00558.hp2 HG00642.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.810+693C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99106702 | |||||||
chr15:99106767 | CTA | C | 15 | a0003c0003t0001g0219 a0005c0006t0004g0011 a0005c0006t0004g0031 others(12): Show |
23 | HG00140.hp2 HG00741.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.810+760_810+761del others(2): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr15 | 99106767 | ||||||
chr15:99106967 | A | T | 1 | a0001c0001t0001g0048 | 2 | HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.810+958A>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99106967 | |||||||
chr15:99107077 | C | T | 1 | a0034c0035t0011g0178 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.810+1068C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107077 | |||||||
chr15:99107094 | G | A | 5 | a0002c0005t0008g0012 a0002c0005t0008g0032 a0002c0005t0008g0069 others(2): Show |
9 | HG01243.hp1 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.810+1085G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107094 | |||||||
chr15:99107154 | T | G | 1 | a0038c0042t0001g0199 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.810+1145T>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107154 | |||||||
chr15:99107225 | T | C | 1 | a0034c0035t0011g0178 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.810+1216T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107225 | |||||||
chr15:99107274 | G | T | 32 | a0001c0007t0001g0213 a0001c0007t0001g0217 a0001c0007t0001g0218 others(29): Show |
40 | HG00323.hp1 HG01099.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.810+1265G>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107274 | |||||||
chr15:99107276 | A | C | 2 | a0002c0005t0001g0177 a0002c0005t0007g0009 |
7 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.810+1267A>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107276 | |||||||
chr15:99107328 | T | G | 2 | a0002c0005t0001g0177 a0002c0005t0007g0009 |
7 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.810+1319T>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107328 | |||||||
chr15:99107335 | G | C | 1 | a0036c0031t0001g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.810+1326G>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107335 | |||||||
chr15:99107364 | A | C | 1 | a0001c0001t0001g0176 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.810+1355A>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107364 | |||||||
chr15:99107400 | T | G | 115 | a0001c0007t0001g0080 a0001c0007t0001g0081 a0001c0007t0001g0094 others(112): Show |
170 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.810+1391T>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107400 | |||||||
chr15:99107449 | C | G | 1 | a0003c0003t0003g0103 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.810+1440C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107449 | |||||||
chr15:99107548 | C | T | 1 | a0007c0069t0002g0175 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.810+1539C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107548 | |||||||
chr15:99107611 | C | CT | 10 | a0001c0007t0001g0213 a0001c0007t0001g0217 a0001c0007t0001g0218 others(7): Show |
13 | HG02109.hp2 HG02451.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.810+1605dupT | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr15 | 99107611 | ||||||
chr15:99107777 | C | G | 8 | a0001c0001t0001g0169 a0002c0019t0011g0047 a0006c0056t0008g0170 others(5): Show |
9 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.810+1768C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107777 | |||||||
chr15:99107848 | C | T | 1 | a0036c0031t0001g0200 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.810+1839C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107848 | |||||||
chr15:99107927 | G | GT | 119 | a0001c0007t0001g0080 a0001c0007t0001g0081 a0001c0007t0001g0094 others(116): Show |
178 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.810+1929dupT | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr15 | 99107927 | ||||||
chr15:99107939 | G | T | 2 | a0002c0005t0001g0177 a0002c0005t0007g0009 |
7 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.810+1930G>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107939 | |||||||
chr15:99107942 | TTTTGTTT others(20): Show |
T | 2 | a0002c0005t0001g0177 a0002c0005t0007g0009 |
7 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.810+1937_810+1963d others(29): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr15 | 99107942 | ||||||
chr15:99107944 | T | G | 1 | a0005c0006t0004g0056 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.810+1935T>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107944 | |||||||
chr15:99107946 | G | T | 1 | a0005c0006t0004g0056 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.810+1937G>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107946 | |||||||
chr15:99107951 | G | T | 114 | a0001c0007t0001g0080 a0001c0007t0001g0081 a0001c0007t0001g0094 others(111): Show |
169 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.810+1942G>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107951 | |||||||
chr15:99107952 | T | TG | 3 | a0003c0003t0003g0003 a0003c0003t0012g0003 a0032c0036t0024g0102 |
4 | HG02572.hp2 NA18952.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.810+1943_810+1944i others(3): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107952 | |||||||
chr15:99107953 | T | G | 113 | a0001c0007t0001g0080 a0001c0007t0001g0081 a0001c0007t0001g0094 others(110): Show |
165 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.810+1944T>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107953 | |||||||
chr15:99107957 | TTTTTGG | T | 10 | a0001c0043t0001g0193 a0002c0005t0008g0012 a0002c0005t0008g0032 others(7): Show |
15 | HG00733.hp1 HG01243.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.810+1977_810+1982d others(8): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr15 | 99107957 | ||||||
chr15:99107957 | TTTTTGGT others(5): Show |
T | 8 | a0001c0001t0001g0169 a0002c0019t0011g0047 a0006c0056t0008g0170 others(5): Show |
9 | HG01891.hp1 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.810+1971_810+1982d others(14): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr15 | 99107957 | ||||||
chr15:99107958 | T | G | 1 | a0005c0006t0004g0056 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.810+1949T>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107958 | |||||||
chr15:99107958 | TTTTGG | T | 110 | a0001c0007t0001g0080 a0001c0007t0001g0081 a0001c0007t0001g0094 others(107): Show |
162 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.810+1953_810+1957d others(7): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr15 | 99107958 | ||||||
chr15:99107958 | TTTTGGTT others(4): Show |
T | 2 | a0001c0007t0001g0218 a0002c0005t0011g0212 |
2 | HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.810+1953_810+1963d others(13): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr15 | 99107958 | ||||||
chr15:99107962 | G | T | 1 | a0005c0006t0004g0056 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.810+1953G>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107962 | |||||||
chr15:99107963 | G | T | 1 | a0005c0006t0004g0056 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.810+1954G>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107963 | |||||||
chr15:99107980 | G | C | 5 | a0002c0005t0008g0012 a0002c0005t0008g0032 a0002c0005t0008g0069 others(2): Show |
9 | HG01243.hp1 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.810+1971G>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99107980 | |||||||
chr15:99108043 | C | A | 11 | a0005c0006t0004g0011 a0005c0006t0004g0056 a0005c0006t0004g0057 others(8): Show |
18 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.810+2034C>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99108043 | |||||||
chr15:99108147 | G | A | 1 | a0003c0003t0003g0072 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.810+2138G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99108147 | |||||||
chr15:99108221 | G | A | 2 | a0001c0001t0001g0105 a0002c0002t0002g0104 |
2 | NA18967.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.810+2212G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99108221 | |||||||
chr15:99108274 | A | AT | 9 | a0001c0001t0001g0176 a0002c0002t0001g0167 a0002c0005t0007g0210 others(6): Show |
9 | HG02004.hp1 HG02809.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.810+2275dupT | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr15 | 99108274 | ||||||
chr15:99108365 | T | C | 1 | a0006c0022t0008g0207 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.810+2356T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99108365 | |||||||
chr15:99108367 | A | C | 4 | a0011c0009t0001g0054 a0011c0009t0001g0055 a0011c0009t0001g0205 others(1): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.810+2358A>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99108367 | |||||||
chr15:99108436 | A | T | 1 | a0002c0002t0002g0166 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.810+2427A>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99108436 | |||||||
chr15:99108490 | T | C | 6 | a0007c0010t0006g0030 a0007c0010t0006g0052 a0007c0010t0006g0202 others(3): Show |
8 | HG00323.hp1 HG01261.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.810+2481T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99108490 | |||||||
chr15:99108633 | C | T | 1 | a0007c0010t0006g0203 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.810+2624C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99108633 | |||||||
chr15:99108659 | C | T | 1 | a0032c0036t0024g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.810+2650C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99108659 | |||||||
chr15:99108757 | C | G | 3 | a0018c0020t0019g0065 a0018c0020t0019g0066 a0041c0037t0022g0067 |
3 | HG02559.hp1 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.810+2748C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99108757 | |||||||
chr15:99108791 | G | A | 1 | a0002c0002t0002g0106 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.810+2782G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99108791 | |||||||
chr15:99108961 | A | T | 1 | a0005c0006t0004g0063 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.810+2952A>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99108961 | |||||||
chr15:99109041 | C | T | 196 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(193): Show |
313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.810+3032C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99109041 | |||||||
chr15:99109100 | T | C | 7 | a0002c0005t0001g0177 a0002c0005t0007g0009 a0006c0056t0008g0170 others(4): Show |
12 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.810+3091T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99109100 | |||||||
chr15:99109170 | T | A | 1 | a0001c0001t0001g0128 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.810+3161T>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99109170 | |||||||
chr15:99109192 | A | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(74): Show |
136 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.810+3183A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99109192 | |||||||
chr15:99109270 | C | G | 7 | a0002c0005t0001g0177 a0002c0005t0007g0009 a0006c0056t0008g0170 others(4): Show |
12 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.810+3261C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99109270 | |||||||
chr15:99109419 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.810+3410C>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99109419 | |||||||
chr15:99109643 | C | G | 1 | a0032c0036t0024g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.810+3634C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99109643 | |||||||
chr15:99109682 | G | T | 1 | a0001c0001t0001g0165 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.810+3673G>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99109682 | |||||||
chr15:99109808 | T | C | 2 | a0001c0030t0001g0129 a0001c0030t0001g0130 |
2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.811-3783T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99109808 | |||||||
chr15:99109884 | T | C | 21 | a0001c0001t0001g0131 a0001c0018t0001g0027 a0003c0003t0003g0183 others(18): Show |
31 | HG00558.hp2 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.811-3707T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99109884 | |||||||
chr15:99109996 | C | G | 1 | a0001c0001t0001g0164 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.811-3595C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99109996 | |||||||
chr15:99110083 | C | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(192): Show |
313 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(310): Show |
intron_variant | MODIFIER | c.811-3508C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99110083 | |||||||
chr15:99110090 | G | A | 1 | a0007c0010t0006g0203 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.811-3501G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99110090 | |||||||
chr15:99110098 | T | G | 1 | a0003c0003t0012g0074 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.811-3493T>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99110098 | |||||||
chr15:99110099 | G | A | 1 | a0003c0003t0012g0074 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.811-3492G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99110099 | |||||||
chr15:99110158 | A | T | 1 | a0001c0001t0001g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.811-3433A>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99110158 | |||||||
chr15:99110207 | T | C | 1 | a0002c0002t0001g0167 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.811-3384T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99110207 | |||||||
chr15:99110211 | G | A | 1 | a0003c0003t0003g0033 | 2 | NA18943.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.811-3380G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99110211 | |||||||
chr15:99110338 | A | G | 191 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(188): Show |
305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.811-3253A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99110338 | |||||||
chr15:99110460 | T | G | 118 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(115): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.811-3131T>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99110460 | |||||||
chr15:99110469 | G | A | 1 | a0006c0022t0008g0207 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.811-3122G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99110469 | |||||||
chr15:99110634 | C | A | 1 | a0002c0002t0001g0167 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.811-2957C>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99110634 | |||||||
chr15:99110635 | A | C | 1 | a0002c0002t0001g0167 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.811-2956A>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99110635 | |||||||
chr15:99110636 | C | A | 1 | a0002c0002t0001g0167 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.811-2955C>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99110636 | |||||||
chr15:99110707 | A | G | 3 | a0001c0007t0001g0213 a0017c0017t0004g0053 a0026c0053t0001g0204 |
4 | HG01243.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.811-2884A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99110707 | |||||||
chr15:99110709 | G | A | 58 | a0001c0007t0001g0080 a0001c0007t0001g0081 a0001c0007t0001g0094 others(55): Show |
91 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.811-2882G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99110709 | |||||||
chr15:99110935 | G | A | 2 | a0003c0003t0003g0076 a0003c0003t0003g0077 |
2 | NA18961.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.811-2656G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99110935 | |||||||
chr15:99110966 | C | T | 195 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(192): Show |
310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.811-2625C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99110966 | |||||||
chr15:99110968 | G | T | 1 | a0003c0003t0012g0074 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.811-2623G>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99110968 | |||||||
chr15:99111225 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.811-2366A>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99111225 | |||||||
chr15:99111311 | A | G | 73 | a0001c0001t0001g0005 a0001c0001t0001g0158 a0001c0001t0001g0160 others(70): Show |
121 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.811-2280A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99111311 | |||||||
chr15:99111312 | T | A | 1 | a0002c0002t0002g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.811-2279T>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99111312 | |||||||
chr15:99111321 | T | A | 1 | a0003c0003t0012g0074 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.811-2270T>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99111321 | |||||||
chr15:99111594 | G | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0018 others(104): Show |
163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.811-1997G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99111594 | |||||||
chr15:99111627 | C | T | 2 | a0007c0010t0006g0052 a0007c0010t0006g0203 |
3 | NA18959.hp1 NA18984.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.811-1964C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99111627 | |||||||
chr15:99111644 | A | G | 4 | a0015c0027t0017g0171 a0015c0027t0017g0173 a0015c0066t0031g0174 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-1947A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99111644 | |||||||
chr15:99111745 | T | TA | 85 | a0001c0001t0001g0005 a0001c0001t0001g0158 a0001c0001t0001g0160 others(82): Show |
144 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.811-1840dupA | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr15 | 99111745 | ||||||
chr15:99111918 | G | A | 2 | a0003c0003t0001g0219 a0023c0071t0007g0192 |
2 | HG00733.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.811-1673G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99111918 | |||||||
chr15:99111922 | G | T | 4 | a0002c0005t0007g0210 a0006c0022t0008g0207 a0006c0022t0008g0211 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-1669G>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99111922 | |||||||
chr15:99111955 | T | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(189): Show |
307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.811-1636T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99111955 | |||||||
chr15:99111966 | T | C | 2 | a0002c0005t0001g0177 a0002c0005t0007g0009 |
7 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.811-1625T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99111966 | |||||||
chr15:99112009 | A | G | 1 | a0006c0039t0007g0209 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.811-1582A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99112009 | |||||||
chr15:99112047 | C | A | 200 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(197): Show |
315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.811-1544C>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99112047 | |||||||
chr15:99112117 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.811-1474C>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99112117 | |||||||
chr15:99112189 | A | G | 15 | a0001c0001t0001g0169 a0001c0007t0001g0213 a0001c0007t0001g0217 others(12): Show |
18 | HG02109.hp2 HG02451.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.811-1402A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99112189 | |||||||
chr15:99112218 | G | A | 58 | a0001c0001t0001g0005 a0001c0001t0001g0158 a0001c0001t0001g0160 others(55): Show |
103 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.811-1373G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99112218 | |||||||
chr15:99112246 | T | C | 1 | a0003c0003t0003g0078 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.811-1345T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99112246 | |||||||
chr15:99112451 | C | T | 73 | a0001c0001t0001g0005 a0001c0001t0001g0158 a0001c0001t0001g0160 others(70): Show |
121 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.811-1140C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99112451 | |||||||
chr15:99112476 | A | C | 4 | a0015c0027t0017g0171 a0015c0027t0017g0173 a0015c0066t0031g0174 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-1115A>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99112476 | |||||||
chr15:99112515 | T | C | 1 | a0003c0003t0003g0079 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.811-1076T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99112515 | |||||||
chr15:99112581 | C | T | 7 | a0006c0022t0008g0207 a0006c0022t0008g0211 a0006c0056t0008g0170 others(4): Show |
7 | HG01891.hp1 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.811-1010C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99112581 | |||||||
chr15:99112636 | G | A | 1 | a0005c0006t0004g0057 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.811-955G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99112636 | |||||||
chr15:99112750 | G | A | 1 | a0002c0005t0008g0070 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.811-841G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99112750 | |||||||
chr15:99112890 | C | T | 17 | a0002c0005t0001g0177 a0002c0005t0007g0009 a0002c0005t0007g0210 others(14): Show |
28 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.811-701C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99112890 | |||||||
chr15:99113165 | A | C | 7 | a0002c0002t0001g0006 a0002c0002t0001g0125 a0002c0002t0001g0126 others(4): Show |
17 | HG01167.hp2 HG01169.hp2 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.811-426A>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99113165 | |||||||
chr15:99113264 | A | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(197): Show |
315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.811-327A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99113264 | |||||||
chr15:99113298 | C | T | 13 | a0002c0005t0001g0177 a0002c0005t0007g0009 a0002c0005t0007g0210 others(10): Show |
24 | HG01243.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.811-293C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99113298 | |||||||
chr15:99113306 | A | G | 154 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(151): Show |
247 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.811-285A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99113306 | |||||||
chr15:99113371 | T | A | 39 | a0002c0005t0001g0177 a0002c0005t0007g0009 a0002c0005t0007g0210 others(36): Show |
61 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.811-220T>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99113371 | |||||||
chr15:99113461 | C | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(89): Show |
151 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.811-130C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99113461 | |||||||
chr15:99113507 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.811-84A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 1/3 | chr15 | 99113507 | |||||||
chr15:99113968 | A | G | 7 | a0007c0010t0006g0030 a0007c0010t0006g0052 a0007c0010t0006g0202 others(4): Show |
9 | HG00323.hp1 HG00544.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.935+253A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99113968 | |||||||
chr15:99114000 | T | C | 1 | a0001c0007t0010g0197 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.935+285T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114000 | |||||||
chr15:99114020 | G | GGAACT | 115 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(112): Show |
183 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.935+307_935+311dup others(5): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 99114020 | ||||||
chr15:99114040 | C | T | 8 | a0001c0001t0001g0169 a0001c0007t0001g0213 a0001c0007t0001g0217 others(5): Show |
11 | HG02615.hp2 HG02647.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.935+325C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114040 | |||||||
chr15:99114095 | ATG | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(78): Show |
135 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.935+384_935+385del others(2): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 99114095 | ||||||
chr15:99114196 | G | T | 37 | a0002c0005t0001g0177 a0002c0005t0007g0009 a0002c0005t0007g0210 others(34): Show |
56 | HG00558.hp2 HG00642.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.935+481G>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114196 | |||||||
chr15:99114204 | C | G | 1 | a0002c0019t0011g0124 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.935+489C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114204 | |||||||
chr15:99114273 | A | G | 2 | a0016c0023t0021g0215 a0016c0033t0021g0216 |
2 | HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.935+558A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114273 | |||||||
chr15:99114285 | CAG | C | 8 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0107 others(5): Show |
13 | HG00621.hp2 HG00733.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.935+571_935+572del others(2): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114285 | |||||||
chr15:99114350 | C | A | 27 | a0002c0005t0001g0177 a0002c0005t0007g0009 a0002c0005t0007g0210 others(24): Show |
42 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.935+635C>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114350 | |||||||
chr15:99114403 | A | G | 166 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(163): Show |
266 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.935+688A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114403 | |||||||
chr15:99114491 | T | C | 33 | a0002c0005t0008g0012 a0002c0005t0008g0032 a0002c0005t0008g0069 others(30): Show |
47 | HG00558.hp2 HG00642.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.935+776T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114491 | |||||||
chr15:99114537 | C | A | 1 | a0025c0055t0001g0220 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.935+822C>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114537 | |||||||
chr15:99114675 | G | A | 95 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(92): Show |
157 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.935+960G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114675 | |||||||
chr15:99114702 | G | A | 3 | a0002c0005t0001g0177 a0002c0005t0007g0009 a0002c0005t0007g0210 |
8 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.935+987G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114702 | |||||||
chr15:99114723 | C | T | 1 | a0001c0025t0001g0154 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.935+1008C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114723 | |||||||
chr15:99114726 | T | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(123): Show |
202 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.935+1011T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114726 | |||||||
chr15:99114739 | C | T | 32 | a0002c0005t0008g0012 a0002c0005t0008g0032 a0002c0005t0008g0069 others(29): Show |
46 | HG00558.hp2 HG00642.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.935+1024C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114739 | |||||||
chr15:99114747 | C | T | 1 | a0037c0054t0003g0062 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.935+1032C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114747 | |||||||
chr15:99114759 | C | T | 20 | a0003c0003t0003g0183 a0004c0004t0005g0021 a0004c0004t0005g0022 others(17): Show |
28 | HG00558.hp2 HG00642.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.935+1044C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114759 | |||||||
chr15:99114773 | C | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(123): Show |
201 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.935+1058C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114773 | |||||||
chr15:99114777 | A | AC | 126 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(123): Show |
201 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.935+1065dupC | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 99114777 | ||||||
chr15:99114784 | T | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(123): Show |
201 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.935+1069T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114784 | |||||||
chr15:99114829 | G | A | 200 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(197): Show |
315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.935+1114G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114829 | |||||||
chr15:99114879 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.935+1164G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114879 | |||||||
chr15:99114903 | T | A | 1 | a0002c0005t0008g0069 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.935+1188T>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114903 | |||||||
chr15:99114948 | C | T | 3 | a0002c0005t0001g0177 a0002c0005t0007g0009 a0002c0005t0007g0210 |
8 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.935+1233C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99114948 | |||||||
chr15:99115063 | A | T | 66 | a0001c0001t0003g0157 a0001c0007t0001g0094 a0001c0007t0009g0090 others(63): Show |
104 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.935+1348A>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115063 | |||||||
chr15:99115067 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.935+1352C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115067 | |||||||
chr15:99115136 | C | G | 1 | a0021c0049t0001g0075 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.935+1421C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115136 | |||||||
chr15:99115138 | A | G | 20 | a0003c0003t0003g0183 a0004c0004t0005g0021 a0004c0004t0005g0022 others(17): Show |
28 | HG00558.hp2 HG00642.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.935+1423A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115138 | |||||||
chr15:99115146 | G | A | 4 | a0015c0027t0017g0171 a0015c0027t0017g0173 a0015c0066t0031g0174 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.935+1431G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115146 | |||||||
chr15:99115228 | C | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(93): Show |
158 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.935+1513C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115228 | |||||||
chr15:99115287 | A | C | 1 | a0015c0066t0031g0174 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.935+1572A>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115287 | |||||||
chr15:99115355 | C | G | 1 | a0001c0001t0028g0153 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.935+1640C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115355 | |||||||
chr15:99115407 | AT | A | 128 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(125): Show |
206 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.935+1702delT | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 99115407 | ||||||
chr15:99115417 | T | C | 68 | a0001c0001t0001g0135 a0001c0001t0003g0157 a0001c0007t0001g0094 others(65): Show |
105 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.935+1702T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115417 | |||||||
chr15:99115418 | C | A | 68 | a0001c0001t0001g0135 a0001c0001t0003g0157 a0001c0007t0001g0094 others(65): Show |
105 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.935+1703C>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115418 | |||||||
chr15:99115419 | A | ATT | 123 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(120): Show |
196 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.935+1711_935+1712d others(4): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 99115419 | ||||||
chr15:99115419 | A | T | 68 | a0001c0001t0001g0135 a0001c0001t0003g0157 a0001c0007t0001g0094 others(65): Show |
105 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.935+1704A>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115419 | |||||||
chr15:99115467 | C | CTT | 7 | a0004c0004t0005g0179 a0004c0004t0005g0180 a0011c0009t0001g0054 others(4): Show |
9 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.935+1753_935+1754i others(4): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 99115467 | ||||||
chr15:99115467 | C | CTTT | 25 | a0002c0005t0008g0012 a0002c0005t0008g0032 a0002c0005t0008g0069 others(22): Show |
37 | HG00558.hp2 HG00642.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.935+1753_935+1754i others(5): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 99115467 | ||||||
chr15:99115469 | A | AT | 88 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(85): Show |
146 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.935+1767dupT | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 99115469 | ||||||
chr15:99115469 | A | T | 32 | a0002c0005t0008g0012 a0002c0005t0008g0032 a0002c0005t0008g0069 others(29): Show |
46 | HG00558.hp2 HG00642.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.935+1754A>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115469 | |||||||
chr15:99115469 | AT | A | 7 | a0002c0005t0001g0177 a0002c0005t0007g0009 a0015c0027t0017g0171 others(4): Show |
12 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.935+1767delT | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 99115469 | ||||||
chr15:99115469 | ATT | A | 64 | a0001c0001t0003g0157 a0001c0007t0001g0094 a0001c0007t0009g0090 others(61): Show |
98 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.935+1766_935+1767d others(4): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 99115469 | ||||||
chr15:99115501 | A | G | 128 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(125): Show |
204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.935+1786A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115501 | |||||||
chr15:99115503 | C | G | 28 | a0002c0005t0008g0012 a0002c0005t0008g0032 a0002c0005t0008g0069 others(25): Show |
40 | HG00558.hp2 HG00642.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.935+1788C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115503 | |||||||
chr15:99115530 | G | A | 2 | a0035c0041t0001g0208 a0038c0042t0001g0199 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.935+1815G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115530 | |||||||
chr15:99115542 | G | T | 1 | a0009c0008t0002g0123 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.935+1827G>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115542 | |||||||
chr15:99115682 | G | A | 4 | a0011c0009t0001g0054 a0011c0009t0001g0055 a0011c0009t0001g0205 others(1): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.935+1967G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115682 | |||||||
chr15:99115716 | C | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(78): Show |
135 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.935+2001C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115716 | |||||||
chr15:99115717 | G | A | 64 | a0001c0001t0003g0157 a0001c0007t0001g0094 a0001c0007t0009g0090 others(61): Show |
98 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.935+2002G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115717 | |||||||
chr15:99115725 | G | C | 1 | a0001c0001t0009g0222 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.935+2010G>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115725 | |||||||
chr15:99115729 | T | G | 1 | a0002c0002t0002g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.935+2014T>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115729 | |||||||
chr15:99115797 | G | A | 1 | a0001c0001t0029g0138 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.935+2082G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115797 | |||||||
chr15:99115825 | A | G | 1 | a0002c0002t0002g0014 | 4 | HG01081.hp2 HG01358.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.935+2110A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115825 | |||||||
chr15:99115842 | C | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(78): Show |
135 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.935+2127C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115842 | |||||||
chr15:99115860 | T | A | 1 | a0003c0003t0003g0083 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.935+2145T>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115860 | |||||||
chr15:99115984 | C | T | 4 | a0015c0027t0017g0171 a0015c0027t0017g0173 a0015c0066t0031g0174 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.935+2269C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99115984 | |||||||
chr15:99116206 | G | A | 1 | a0002c0002t0002g0110 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.935+2491G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99116206 | |||||||
chr15:99116372 | G | A | 20 | a0003c0003t0003g0183 a0004c0004t0005g0021 a0004c0004t0005g0022 others(17): Show |
28 | HG00558.hp2 HG00642.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.935+2657G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99116372 | |||||||
chr15:99116378 | G | A | 2 | a0012c0015t0001g0020 a0012c0015t0009g0159 |
5 | NA18956.hp2 NA18993.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.935+2663G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99116378 | |||||||
chr15:99116394 | A | T | 63 | a0001c0001t0003g0157 a0001c0007t0001g0094 a0001c0007t0009g0090 others(60): Show |
102 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.935+2679A>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99116394 | |||||||
chr15:99116396 | ACTGCCCC others(790): Show |
A | 63 | a0001c0001t0003g0157 a0001c0007t0001g0094 a0001c0007t0009g0090 others(60): Show |
102 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.935+2685_935+3481d others(2): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 99116396 | ||||||
chr15:99116509 | T | G | 1 | a0001c0001t0001g0029 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.935+2794T>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99116509 | |||||||
chr15:99116529 | T | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(110): Show |
181 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.935+2814T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99116529 | |||||||
chr15:99116541 | C | T | 5 | a0002c0005t0008g0012 a0002c0005t0008g0032 a0002c0005t0008g0069 others(2): Show |
9 | HG01243.hp1 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.935+2826C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99116541 | |||||||
chr15:99116556 | G | A | 4 | a0002c0005t0001g0177 a0002c0005t0007g0009 a0002c0005t0007g0210 others(1): Show |
9 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.935+2841G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99116556 | |||||||
chr15:99116581 | G | A | 6 | a0001c0001t0001g0169 a0001c0007t0001g0213 a0001c0007t0010g0023 others(3): Show |
9 | HG02615.hp2 HG02647.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.935+2866G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99116581 | |||||||
chr15:99116582 | G | A | 6 | a0001c0001t0001g0169 a0001c0007t0001g0213 a0001c0007t0010g0023 others(3): Show |
9 | HG02615.hp2 HG02647.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.935+2867G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99116582 | |||||||
chr15:99116620 | G | T | 1 | a0033c0058t0001g0137 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.935+2905G>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99116620 | |||||||
chr15:99116629 | A | G | 81 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(78): Show |
135 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.935+2914A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99116629 | |||||||
chr15:99116641 | C | T | 32 | a0002c0005t0008g0012 a0002c0005t0008g0032 a0002c0005t0008g0069 others(29): Show |
46 | HG00558.hp2 HG00642.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.935+2926C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99116641 | |||||||
chr15:99116722 | T | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(110): Show |
181 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.935+3007T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99116722 | |||||||
chr15:99116736 | T | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(110): Show |
181 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.935+3021T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99116736 | |||||||
chr15:99116894 | A | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(110): Show |
181 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.935+3179A>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99116894 | |||||||
chr15:99116922 | G | A | 10 | a0007c0010t0006g0030 a0007c0010t0006g0052 a0007c0010t0006g0202 others(7): Show |
12 | HG00323.hp1 HG00544.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.935+3207G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99116922 | |||||||
chr15:99117007 | T | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(110): Show |
181 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.935+3292T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99117007 | |||||||
chr15:99117053 | C | T | 5 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0031c0062t0004g0144 others(2): Show |
6 | HG01261.hp1 HG02280.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.935+3338C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99117053 | |||||||
chr15:99117174 | A | G | 1 | a0004c0004t0005g0051 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.935+3459A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99117174 | |||||||
chr15:99117202 | C | T | 1 | a0041c0037t0022g0067 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.935+3487C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99117202 | |||||||
chr15:99117208 | G | A | 15 | a0005c0006t0004g0011 a0005c0006t0004g0031 a0005c0006t0004g0056 others(12): Show |
23 | HG00140.hp2 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.935+3493G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99117208 | |||||||
chr15:99117243 | G | A | 3 | a0001c0025t0001g0139 a0001c0025t0001g0154 a0003c0003t0003g0084 |
3 | HG02132.hp1 HG02135.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.935+3528G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99117243 | |||||||
chr15:99117298 | G | A | 5 | a0002c0005t0008g0012 a0002c0005t0008g0032 a0002c0005t0008g0069 others(2): Show |
9 | HG01243.hp1 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.935+3583G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99117298 | |||||||
chr15:99117311 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.935+3596C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99117311 | |||||||
chr15:99117312 | G | A | 3 | a0017c0017t0004g0053 a0025c0055t0001g0220 a0026c0053t0001g0204 |
4 | HG01099.hp1 HG01243.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.935+3597G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99117312 | |||||||
chr15:99117328 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(117): Show |
194 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.935+3613C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99117328 | |||||||
chr15:99117362 | G | A | 1 | a0001c0001t0001g0019 | 4 | HG00733.hp2 HG01168.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.935+3647G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99117362 | |||||||
chr15:99117409 | C | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(78): Show |
135 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.935+3694C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99117409 | |||||||
chr15:99117444 | G | C | 1 | a0016c0023t0007g0214 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.935+3729G>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99117444 | |||||||
chr15:99117562 | A | T | 4 | a0002c0005t0001g0177 a0002c0005t0007g0009 a0002c0005t0007g0210 others(1): Show |
9 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.935+3847A>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99117562 | |||||||
chr15:99117570 | A | G | 1 | a0024c0068t0007g0122 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.935+3855A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99117570 | |||||||
chr15:99117584 | A | G | 1 | a0005c0006t0004g0061 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.935+3869A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99117584 | |||||||
chr15:99117590 | C | T | 1 | a0018c0020t0019g0066 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.935+3875C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99117590 | |||||||
chr15:99117611 | C | G | 3 | a0011c0009t0001g0054 a0011c0009t0001g0055 a0011c0009t0001g0206 |
5 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.935+3896C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99117611 | |||||||
chr15:99117724 | C | CCGGGGCC others(29): Show |
1 | a0034c0035t0011g0178 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.935+4050_935+4085d others(38): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 99117724 | ||||||
chr15:99117724 | CCGGGGCC others(29): Show |
C | 80 | a0001c0001t0001g0156 a0001c0001t0003g0157 a0001c0007t0001g0094 others(77): Show |
125 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.935+4050_935+4085d others(38): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 99117724 | ||||||
chr15:99117977 | T | C | 4 | a0011c0009t0001g0054 a0011c0009t0001g0055 a0011c0009t0001g0205 others(1): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.935+4262T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99117977 | |||||||
chr15:99118049 | T | C | 89 | a0001c0001t0001g0024 a0001c0001t0001g0169 a0001c0001t0003g0157 others(86): Show |
136 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.935+4334T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99118049 | |||||||
chr15:99118115 | C | A | 55 | a0001c0001t0001g0140 a0001c0001t0003g0157 a0001c0007t0001g0094 others(52): Show |
88 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.935+4400C>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99118115 | |||||||
chr15:99118124 | G | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(78): Show |
138 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.935+4409G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99118124 | |||||||
chr15:99118127 | A | G | 39 | a0001c0001t0001g0131 a0002c0005t0007g0009 a0002c0005t0007g0210 others(36): Show |
53 | HG00558.hp2 HG00642.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.935+4412A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99118127 | |||||||
chr15:99118208 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0015g0018 |
4 | HG01109.hp1 HG02145.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.935+4493A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99118208 | |||||||
chr15:99118209 | C | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(120): Show |
197 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(194): Show |
intron_variant | MODIFIER | c.935+4494C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99118209 | |||||||
chr15:99118234 | G | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(84): Show |
147 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.935+4519G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99118234 | |||||||
chr15:99118264 | T | C | 1 | a0004c0004t0018g0181 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.935+4549T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99118264 | |||||||
chr15:99118289 | C | T | 2 | a0001c0001t0009g0222 a0001c0001t0009g0223 |
2 | HG00621.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.935+4574C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99118289 | |||||||
chr15:99118343 | G | C | 1 | a0001c0007t0001g0213 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.935+4628G>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99118343 | |||||||
chr15:99118344 | C | G | 1 | a0001c0007t0001g0213 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.935+4629C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99118344 | |||||||
chr15:99118360 | T | G | 1 | a0006c0040t0030g0085 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.935+4645T>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99118360 | |||||||
chr15:99118416 | G | A | 1 | a0002c0002t0002g0112 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.935+4701G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99118416 | |||||||
chr15:99118655 | A | G | 1 | a0006c0016t0002g0121 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.935+4940A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99118655 | |||||||
chr15:99118675 | C | G | 2 | a0003c0003t0001g0219 a0023c0071t0007g0192 |
2 | HG00733.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.935+4960C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99118675 | |||||||
chr15:99118893 | C | T | 8 | a0002c0005t0001g0177 a0002c0005t0007g0009 a0002c0005t0007g0210 others(5): Show |
14 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.935+5178C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99118893 | |||||||
chr15:99118894 | G | A | 64 | a0001c0001t0003g0157 a0001c0007t0001g0094 a0001c0007t0009g0090 others(61): Show |
103 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.935+5179G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99118894 | |||||||
chr15:99118907 | C | T | 7 | a0002c0005t0001g0177 a0002c0005t0007g0009 a0002c0005t0007g0210 others(4): Show |
13 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.935+5192C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99118907 | |||||||
chr15:99118941 | A | T | 31 | a0002c0005t0008g0012 a0002c0005t0008g0032 a0002c0005t0008g0069 others(28): Show |
45 | HG00558.hp2 HG00642.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.935+5226A>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99118941 | |||||||
chr15:99119228 | G | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(127): Show |
207 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.935+5513G>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99119228 | |||||||
chr15:99119236 | T | C | 115 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(112): Show |
184 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.935+5521T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99119236 | |||||||
chr15:99119272 | G | A | 1 | a0002c0002t0002g0114 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.935+5557G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99119272 | |||||||
chr15:99119299 | G | A | 1 | a0002c0002t0001g0125 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.935+5584G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99119299 | |||||||
chr15:99119313 | A | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(117): Show |
190 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.935+5598A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99119313 | |||||||
chr15:99119365 | C | G | 1 | a0003c0003t0003g0035 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.935+5650C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99119365 | |||||||
chr15:99119405 | G | A | 4 | a0011c0009t0001g0054 a0011c0009t0001g0055 a0011c0009t0001g0205 others(1): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.935+5690G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99119405 | |||||||
chr15:99119428 | C | T | 1 | a0033c0058t0001g0137 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.935+5713C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99119428 | |||||||
chr15:99119611 | C | T | 24 | a0003c0003t0003g0183 a0004c0004t0005g0021 a0004c0004t0005g0022 others(21): Show |
32 | HG00558.hp2 HG00642.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.935+5896C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99119611 | |||||||
chr15:99119685 | A | G | 1 | a0002c0005t0011g0212 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.935+5970A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99119685 | |||||||
chr15:99119728 | C | G | 1 | a0001c0001t0001g0161 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.935+6013C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99119728 | |||||||
chr15:99119793 | G | T | 1 | a0001c0007t0001g0218 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.935+6078G>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99119793 | |||||||
chr15:99119867 | C | T | 1 | a0001c0025t0001g0139 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.935+6152C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99119867 | |||||||
chr15:99119972 | G | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(201): Show |
321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.935+6257G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99119972 | |||||||
chr15:99120007 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.935+6292A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99120007 | |||||||
chr15:99120073 | T | A | 24 | a0003c0003t0003g0183 a0004c0004t0005g0021 a0004c0004t0005g0022 others(21): Show |
32 | HG00558.hp2 HG00642.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.935+6358T>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99120073 | |||||||
chr15:99120079 | T | C | 72 | a0001c0001t0003g0157 a0001c0007t0001g0094 a0001c0007t0009g0090 others(69): Show |
113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.935+6364T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99120079 | |||||||
chr15:99120092 | G | A | 1 | a0020c0026t0002g0038 | 2 | NA18939.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.935+6377G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99120092 | |||||||
chr15:99120375 | A | G | 8 | a0001c0007t0001g0213 a0011c0009t0001g0054 a0011c0009t0001g0055 others(5): Show |
11 | HG01099.hp1 HG01243.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.936-6347A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99120375 | |||||||
chr15:99120393 | G | A | 4 | a0001c0001t0001g0134 a0002c0002t0002g0039 a0002c0064t0023g0039 others(1): Show |
4 | HG02738.hp1 HG03654.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.936-6329G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99120393 | |||||||
chr15:99120420 | G | C | 9 | a0001c0001t0001g0169 a0001c0007t0001g0217 a0001c0007t0001g0218 others(6): Show |
12 | HG02615.hp2 HG02647.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.936-6302G>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99120420 | |||||||
chr15:99120439 | T | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(201): Show |
321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.936-6283T>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99120439 | |||||||
chr15:99120459 | C | G | 76 | a0001c0001t0003g0157 a0001c0007t0001g0094 a0001c0007t0009g0090 others(73): Show |
119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.936-6263C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99120459 | |||||||
chr15:99120595 | C | T | 1 | a0002c0002t0013g0041 | 2 | NA19064.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.936-6127C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99120595 | |||||||
chr15:99120657 | T | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(94): Show |
160 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.936-6065T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99120657 | |||||||
chr15:99120718 | A | G | 3 | a0006c0022t0008g0207 a0006c0022t0008g0211 a0006c0056t0008g0170 |
3 | HG02809.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.936-6004A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99120718 | |||||||
chr15:99120752 | C | T | 14 | a0005c0006t0004g0011 a0005c0006t0004g0031 a0005c0006t0004g0056 others(11): Show |
22 | HG00140.hp2 HG00738.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.936-5970C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99120752 | |||||||
chr15:99120800 | C | T | 4 | a0011c0009t0001g0054 a0011c0009t0001g0055 a0011c0009t0001g0205 others(1): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.936-5922C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99120800 | |||||||
chr15:99120825 | G | A | 1 | a0028c0046t0003g0086 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.936-5897G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99120825 | |||||||
chr15:99120951 | C | T | 4 | a0011c0009t0001g0054 a0011c0009t0001g0055 a0011c0009t0001g0205 others(1): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.936-5771C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99120951 | |||||||
chr15:99121058 | G | C | 1 | a0002c0002t0002g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.936-5664G>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99121058 | |||||||
chr15:99121207 | T | C | 4 | a0011c0009t0001g0054 a0011c0009t0001g0055 a0011c0009t0001g0205 others(1): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.936-5515T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99121207 | |||||||
chr15:99121376 | A | G | 1 | a0002c0002t0002g0119 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.936-5346A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99121376 | |||||||
chr15:99121389 | C | T | 4 | a0011c0009t0001g0054 a0011c0009t0001g0055 a0011c0009t0001g0205 others(1): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.936-5333C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99121389 | |||||||
chr15:99121403 | C | T | 41 | a0002c0002t0001g0013 a0002c0002t0002g0001 a0002c0002t0002g0007 others(38): Show |
79 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.936-5319C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99121403 | |||||||
chr15:99121451 | A | G | 205 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(202): Show |
322 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.936-5271A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99121451 | |||||||
chr15:99121510 | C | T | 4 | a0011c0009t0001g0054 a0011c0009t0001g0055 a0011c0009t0001g0205 others(1): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.936-5212C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99121510 | |||||||
chr15:99121511 | A | G | 4 | a0011c0009t0001g0054 a0011c0009t0001g0055 a0011c0009t0001g0205 others(1): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.936-5211A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99121511 | |||||||
chr15:99121533 | G | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(155): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.936-5189G>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99121533 | |||||||
chr15:99121542 | C | T | 42 | a0001c0001t0003g0157 a0001c0007t0001g0094 a0001c0007t0009g0090 others(39): Show |
71 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.936-5180C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99121542 | |||||||
chr15:99121556 | T | G | 1 | a0004c0021t0005g0049 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.936-5166T>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99121556 | |||||||
chr15:99121620 | G | C | 4 | a0011c0009t0001g0054 a0011c0009t0001g0055 a0011c0009t0001g0205 others(1): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.936-5102G>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99121620 | |||||||
chr15:99121707 | G | A | 4 | a0011c0009t0001g0054 a0011c0009t0001g0055 a0011c0009t0001g0205 others(1): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.936-5015G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99121707 | |||||||
chr15:99121712 | G | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(155): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.936-5010G>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99121712 | |||||||
chr15:99121721 | G | C | 204 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(201): Show |
321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.936-5001G>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99121721 | |||||||
chr15:99121756 | A | C | 6 | a0001c0001t0001g0029 a0001c0001t0001g0105 a0001c0001t0001g0134 others(3): Show |
8 | HG00673.hp2 NA18612.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.936-4966A>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99121756 | |||||||
chr15:99121784 | A | G | 1 | a0004c0004t0034g0188 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.936-4938A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99121784 | |||||||
chr15:99121843 | CAG | C | 15 | a0005c0006t0004g0011 a0005c0006t0004g0031 a0005c0006t0004g0056 others(12): Show |
23 | HG00140.hp2 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.936-4878_936-4877d others(4): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99121843 | |||||||
chr15:99121844 | A | T | 1 | a0001c0001t0001g0024 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.936-4878A>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99121844 | |||||||
chr15:99121990 | A | G | 20 | a0003c0003t0003g0183 a0004c0004t0005g0021 a0004c0004t0005g0022 others(17): Show |
28 | HG00558.hp2 HG00642.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.936-4732A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99121990 | |||||||
chr15:99122004 | G | A | 4 | a0004c0004t0005g0021 a0004c0004t0005g0050 a0004c0004t0005g0179 others(1): Show |
8 | HG00558.hp2 HG02040.hp1 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.936-4718G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99122004 | |||||||
chr15:99122031 | C | T | 8 | a0002c0002t0001g0006 a0002c0002t0001g0125 a0002c0002t0001g0126 others(5): Show |
18 | HG01167.hp2 HG01169.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.936-4691C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99122031 | |||||||
chr15:99122049 | G | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(84): Show |
142 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.936-4673G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99122049 | |||||||
chr15:99122123 | T | G | 11 | a0002c0005t0001g0177 a0002c0005t0007g0009 a0002c0005t0007g0210 others(8): Show |
17 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.936-4599T>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99122123 | |||||||
chr15:99122212 | AG | A | 5 | a0002c0002t0001g0006 a0002c0002t0001g0125 a0002c0002t0001g0126 others(2): Show |
12 | HG01167.hp2 HG01169.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.936-4509delG | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99122212 | |||||||
chr15:99122226 | T | G | 6 | a0001c0007t0001g0213 a0010c0012t0016g0037 a0010c0012t0016g0168 others(3): Show |
8 | HG01099.hp1 HG01243.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.936-4496T>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99122226 | |||||||
chr15:99122369 | G | A | 1 | a0037c0054t0003g0062 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.936-4353G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99122369 | |||||||
chr15:99122497 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.936-4225T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99122497 | |||||||
chr15:99122630 | G | T | 21 | a0002c0005t0001g0177 a0002c0005t0007g0009 a0002c0005t0007g0210 others(18): Show |
31 | HG00323.hp1 HG00544.hp1 HG01261.hp2 others(28): Show |
intron_variant | MODIFIER | c.936-4092G>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99122630 | |||||||
chr15:99122641 | G | C | 67 | a0001c0001t0003g0157 a0001c0007t0001g0094 a0003c0003t0001g0004 others(64): Show |
104 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.936-4081G>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99122641 | |||||||
chr15:99122676 | C | T | 15 | a0005c0006t0004g0011 a0005c0006t0004g0031 a0005c0006t0004g0056 others(12): Show |
23 | HG00140.hp2 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.936-4046C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99122676 | |||||||
chr15:99122709 | C | T | 5 | a0015c0027t0017g0171 a0015c0027t0017g0173 a0015c0066t0031g0174 others(2): Show |
5 | HG01099.hp1 HG01891.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.936-4013C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99122709 | |||||||
chr15:99122710 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0142 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.936-4012G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99122710 | |||||||
chr15:99122878 | G | A | 1 | a0003c0003t0003g0091 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.936-3844G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99122878 | |||||||
chr15:99122929 | T | C | 189 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(186): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.936-3793T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99122929 | |||||||
chr15:99123025 | C | T | 85 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(82): Show |
140 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.936-3697C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99123025 | |||||||
chr15:99123068 | C | G | 1 | a0018c0020t0019g0066 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.936-3654C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99123068 | |||||||
chr15:99123076 | C | T | 3 | a0002c0005t0011g0212 a0002c0019t0011g0047 a0002c0019t0011g0124 |
4 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.936-3646C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99123076 | |||||||
chr15:99123276 | G | C | 1 | a0011c0009t0001g0054 | 2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.936-3446G>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99123276 | |||||||
chr15:99123302 | G | GT | 7 | a0003c0003t0001g0219 a0005c0006t0004g0060 a0008c0011t0004g0010 others(4): Show |
10 | HG00733.hp1 HG00738.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.936-3420_936-3419i others(3): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99123302 | |||||||
chr15:99123303 | G | GT | 82 | a0001c0001t0003g0157 a0001c0007t0001g0094 a0002c0002t0002g0118 others(79): Show |
126 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.936-3406dupT | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 99123303 | ||||||
chr15:99123303 | G | GTT | 82 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(79): Show |
137 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.936-3407_936-3406d others(4): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 99123303 | ||||||
chr15:99123303 | G | GTTT | 28 | a0002c0005t0001g0177 a0002c0005t0007g0009 a0002c0005t0007g0210 others(25): Show |
42 | HG00558.hp2 HG00642.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.936-3408_936-3406d others(5): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr15 | 99123303 | ||||||
chr15:99123303 | G | T | 9 | a0001c0030t0001g0130 a0001c0043t0001g0193 a0003c0003t0001g0219 others(6): Show |
12 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.936-3419G>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99123303 | |||||||
chr15:99123304 | T | G | 3 | a0002c0002t0002g0026 a0002c0002t0002g0106 a0002c0002t0002g0109 |
5 | HG01256.hp2 HG01361.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.936-3418T>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99123304 | |||||||
chr15:99123355 | G | A | 1 | a0025c0055t0001g0220 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.936-3367G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99123355 | |||||||
chr15:99123534 | G | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0127 a0001c0001t0001g0131 |
6 | HG02257.hp2 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.936-3188G>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99123534 | |||||||
chr15:99123549 | C | T | 57 | a0001c0001t0003g0157 a0001c0007t0001g0094 a0001c0007t0001g0213 others(54): Show |
91 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.936-3173C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99123549 | |||||||
chr15:99123550 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.936-3172G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99123550 | |||||||
chr15:99123658 | A | C | 4 | a0015c0027t0017g0171 a0015c0027t0017g0173 a0015c0066t0031g0174 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.936-3064A>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99123658 | |||||||
chr15:99123832 | G | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(143): Show |
227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.936-2890G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99123832 | |||||||
chr15:99123840 | G | A | 32 | a0003c0003t0001g0219 a0005c0006t0004g0011 a0005c0006t0004g0031 others(29): Show |
44 | HG00323.hp1 HG00733.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.936-2882G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99123840 | |||||||
chr15:99123917 | A | C | 3 | a0001c0007t0001g0213 a0017c0017t0004g0053 a0026c0053t0001g0204 |
4 | HG01243.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.936-2805A>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99123917 | |||||||
chr15:99123919 | G | A | 2 | a0014c0013t0006g0082 a0014c0013t0006g0089 |
2 | NA18997.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.936-2803G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99123919 | |||||||
chr15:99123941 | G | A | 8 | a0002c0002t0001g0006 a0002c0002t0001g0125 a0002c0002t0001g0126 others(5): Show |
18 | HG01167.hp2 HG01169.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.936-2781G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99123941 | |||||||
chr15:99123969 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(52): Show |
99 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.936-2753C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99123969 | |||||||
chr15:99123979 | A | G | 1 | a0013c0014t0002g0016 | 4 | NA18964.hp2 NA18971.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.936-2743A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99123979 | |||||||
chr15:99124102 | A | G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(217): Show |
353 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.936-2620A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99124102 | |||||||
chr15:99124162 | C | T | 2 | a0001c0007t0001g0217 a0001c0007t0001g0218 |
2 | HG02818.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.936-2560C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99124162 | |||||||
chr15:99124163 | G | A | 1 | a0004c0004t0005g0184 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.936-2559G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99124163 | |||||||
chr15:99124214 | T | G | 1 | a0004c0004t0005g0051 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.936-2508T>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99124214 | |||||||
chr15:99124346 | G | A | 43 | a0001c0001t0003g0157 a0001c0007t0001g0094 a0003c0003t0001g0004 others(40): Show |
72 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.936-2376G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99124346 | |||||||
chr15:99124435 | T | C | 85 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(82): Show |
140 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.936-2287T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99124435 | |||||||
chr15:99124441 | G | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(142): Show |
226 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.936-2281G>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99124441 | |||||||
chr15:99124522 | G | A | 1 | a0003c0003t0003g0093 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.936-2200G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99124522 | |||||||
chr15:99124574 | T | C | 1 | a0003c0003t0001g0219 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.936-2148T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99124574 | |||||||
chr15:99124586 | G | A | 4 | a0001c0007t0001g0213 a0017c0017t0004g0053 a0025c0055t0001g0220 others(1): Show |
5 | HG01099.hp1 HG01243.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.936-2136G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99124586 | |||||||
chr15:99124831 | G | A | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(65): Show |
120 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.936-1891G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99124831 | |||||||
chr15:99125373 | C | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(142): Show |
226 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.936-1349C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99125373 | |||||||
chr15:99125492 | G | A | 54 | a0001c0001t0003g0157 a0001c0007t0001g0094 a0001c0007t0001g0213 others(51): Show |
88 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.936-1230G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99125492 | |||||||
chr15:99125523 | G | A | 2 | a0035c0041t0001g0208 a0038c0042t0001g0199 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.936-1199G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99125523 | |||||||
chr15:99125580 | A | T | 1 | a0027c0051t0006g0201 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.936-1142A>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99125580 | |||||||
chr15:99125660 | G | A | 2 | a0035c0041t0001g0208 a0038c0042t0001g0199 |
2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.936-1062G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99125660 | |||||||
chr15:99125888 | G | A | 212 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(209): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.936-834G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99125888 | |||||||
chr15:99126124 | A | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(117): Show |
188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.936-598A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99126124 | |||||||
chr15:99126138 | C | T | 31 | a0002c0005t0001g0177 a0002c0005t0007g0009 a0002c0005t0007g0210 others(28): Show |
45 | HG00558.hp2 HG00642.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.936-584C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99126138 | |||||||
chr15:99126183 | C | T | 1 | a0002c0005t0011g0212 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.936-539C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99126183 | |||||||
chr15:99126243 | C | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(80): Show |
138 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.936-479C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99126243 | |||||||
chr15:99126421 | G | A | 1 | a0011c0009t0001g0206 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.936-301G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99126421 | |||||||
chr15:99126432 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.936-290C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99126432 | |||||||
chr15:99126444 | C | G | 2 | a0002c0002t0002g0007 a0046c0065t0001g0007 |
7 | HG00438.hp1 NA18945.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.936-278C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 2/3 | chr15 | 99126444 | |||||||
chr15:99126907 | C | T | 7 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0018t0001g0027 others(4): Show |
12 | HG01261.hp1 HG01884.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1006+115C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | chr15 | 99126907 | |||||||
chr15:99127209 | T | C | 15 | a0005c0006t0004g0011 a0005c0006t0004g0031 a0005c0006t0004g0056 others(12): Show |
23 | HG00140.hp2 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1006+417T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | chr15 | 99127209 | |||||||
chr15:99127297 | G | T | 4 | a0015c0027t0017g0171 a0015c0027t0017g0173 a0015c0066t0031g0174 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1006+505G>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | chr15 | 99127297 | |||||||
chr15:99127319 | G | C | 66 | a0002c0005t0001g0177 a0002c0005t0007g0009 a0002c0005t0007g0210 others(63): Show |
96 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1006+527G>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | chr15 | 99127319 | |||||||
chr15:99127398 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1006+606G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | chr15 | 99127398 | |||||||
chr15:99127467 | G | A | 1 | a0001c0001t0001g0044 | 2 | NA18962.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1006+675G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | chr15 | 99127467 | |||||||
chr15:99127481 | C | T | 48 | a0001c0001t0003g0157 a0003c0003t0001g0004 a0003c0003t0001g0036 others(45): Show |
78 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.1006+689C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | chr15 | 99127481 | |||||||
chr15:99127521 | C | G | 34 | a0003c0003t0001g0219 a0005c0006t0004g0011 a0005c0006t0004g0031 others(31): Show |
46 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.1006+729C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | chr15 | 99127521 | |||||||
chr15:99127657 | T | C | 1 | a0002c0002t0001g0167 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1006+865T>C | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | chr15 | 99127657 | |||||||
chr15:99128001 | C | CTTCA | 25 | a0001c0001t0001g0028 a0001c0001t0001g0134 a0001c0001t0001g0147 others(22): Show |
37 | HG00673.hp2 HG00733.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1006+1240_1006+124 others(8): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr15 | 99128001 | ||||||
chr15:99128001 | C | CTTCATTC others(1): Show |
18 | a0001c0001t0001g0169 a0001c0007t0001g0217 a0001c0007t0001g0218 others(15): Show |
23 | HG00558.hp2 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.1006+1236_1006+124 others(12): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr15 | 99128001 | ||||||
chr15:99128001 | C | CTTCATTC others(5): Show |
11 | a0002c0048t0002g0071 a0004c0004t0005g0021 a0004c0004t0005g0022 others(8): Show |
17 | HG00642.hp1 HG01123.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.1006+1232_1006+124 others(16): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr15 | 99128001 | ||||||
chr15:99128001 | C | CTTCATTC others(9): Show |
1 | a0004c0004t0005g0187 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1006+1228_1006+124 others(20): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr15 | 99128001 | ||||||
chr15:99128001 | CTTCA | C | 6 | a0001c0001t0001g0146 a0015c0027t0017g0171 a0015c0027t0017g0173 others(3): Show |
6 | HG01099.hp2 HG01891.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1006+1240_1006+124 others(8): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr15 | 99128001 | ||||||
chr15:99128001 | CTTCATTC others(1): Show |
C | 15 | a0005c0006t0004g0011 a0005c0006t0004g0031 a0005c0006t0004g0056 others(12): Show |
23 | HG00140.hp2 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1006+1236_1006+124 others(12): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr15 | 99128001 | ||||||
chr15:99128005 | A | ATTCG | 16 | a0003c0003t0003g0003 a0003c0003t0003g0068 a0003c0003t0003g0088 others(13): Show |
30 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1006+1216_1006+121 others(8): Show |
SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr15 | 99128005 | ||||||
chr15:99128009 | A | G | 27 | a0001c0001t0003g0157 a0003c0003t0001g0004 a0003c0003t0001g0036 others(24): Show |
42 | HG00099.hp2 HG01081.hp1 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.1006+1217A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | chr15 | 99128009 | |||||||
chr15:99128284 | G | A | 4 | a0011c0009t0001g0054 a0011c0009t0001g0055 a0011c0009t0001g0205 others(1): Show |
6 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007-1083G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | chr15 | 99128284 | |||||||
chr15:99128295 | A | T | 32 | a0005c0006t0004g0011 a0005c0006t0004g0031 a0005c0006t0004g0056 others(29): Show |
44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.1007-1072A>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | chr15 | 99128295 | |||||||
chr15:99128319 | G | A | 2 | a0002c0002t0001g0125 a0002c0002t0001g0126 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1007-1048G>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | chr15 | 99128319 | |||||||
chr15:99128695 | C | T | 20 | a0004c0004t0005g0021 a0004c0004t0005g0022 a0004c0004t0005g0050 others(17): Show |
28 | HG00558.hp2 HG00642.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.1007-672C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | chr15 | 99128695 | |||||||
chr15:99128783 | C | G | 3 | a0002c0005t0001g0177 a0002c0005t0007g0009 a0002c0005t0007g0210 |
8 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1007-584C>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | chr15 | 99128783 | |||||||
chr15:99129065 | T | A | 2 | a0001c0007t0001g0217 a0001c0007t0001g0218 |
2 | HG02818.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1007-302T>A | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | chr15 | 99129065 | |||||||
chr15:99129111 | A | G | 2 | a0001c0030t0001g0129 a0001c0030t0001g0130 |
2 | HG00544.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.1007-256A>G | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | chr15 | 99129111 | |||||||
chr15:99129148 | C | T | 30 | a0002c0005t0001g0177 a0002c0005t0007g0009 a0002c0005t0007g0210 others(27): Show |
44 | HG00558.hp2 HG00642.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.1007-219C>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | chr15 | 99129148 | |||||||
chr15:99129340 | A | T | 1 | a0003c0003t0003g0195 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1007-27A>T | SYNM | ENSG00000182253.15 | transcript | ENST00000336292.11 | protein_coding | 3/3 | chr15 | 99129340 |