Item | Value |
---|---|
geneid | 23025 |
ensemblid | ENSG00000130477.16 |
hgncid | 23150 |
symbol | UNC13A |
name | unc-13 homolog A |
refseq_nuc | NM_001080421.3 |
refseq_prot | NP_001073890.2 |
ensembl_nuc | ENST00000519716.7 |
ensembl_prot | ENSP00000429562.2 |
mane_status | MANE Select |
chr | chr19 |
start | 17601336 |
end | 17688354 |
strand | - |
ver | v1.2 |
region | chr19:17601336-17688354 |
region5000 | chr19:17596336-17693354 |
regionname0 | UNC13A_chr19_17601336_17688354 |
regionname5000 | UNC13A_chr19_17596336_17693354 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1703 | 252 | 79 | 44 | 93 | 6 | 29 | 58 | UNC13A_chr19_17596336_17693354 | UNC13A | MSLLC others(1698): Show |
chr19 | 17596336 | 17693354 |
a0002 | 0/0 | 1703 | 52 | 12 | 16 | 5 | 9 | 10 | 5 | UNC13A_chr19_17596336_17693354 | UNC13A | MSLLC others(1698): Show |
chr19 | 17596336 | 17693354 |
a0003 | 0/0 | 1703 | 6 | 0 | 6 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | MSLLC others(1698): Show |
chr19 | 17596336 | 17693354 |
a0004 | 0/0 | 1703 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | MSLLC others(1698): Show |
chr19 | 17596336 | 17693354 |
a0005 | 0/1 | 1703 | 2 | 0 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | MSLLC others(1698): Show |
chr19 | 17596336 | 17693354 |
a0006 | 0/0 | 1703 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | MSLLC others(1698): Show |
chr19 | 17596336 | 17693354 |
a0007 | 0/0 | 1703 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | MSLLC others(1698): Show |
chr19 | 17596336 | 17693354 |
a0008 | 0/0 | 1703 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | MSLLC others(1698): Show |
chr19 | 17596336 | 17693354 |
a0009 | 0/0 | 1703 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | MSLLC others(1698): Show |
chr19 | 17596336 | 17693354 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 5109 | 54 | 0 | 11 | 35 | 1 | 6 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0002 | 0/0 | 5109 | 53 | 27 | 8 | 11 | 2 | 5 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0003 | 0/0 | 5109 | 46 | 2 | 7 | 25 | 2 | 10 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0004 | 0/0 | 5109 | 23 | 6 | 4 | 9 | 0 | 4 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0007 | 0/0 | 5109 | 10 | 9 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0008 | 0/0 | 5109 | 9 | 7 | 2 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0011 | 0/0 | 5109 | 5 | 3 | 2 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0014 | 0/0 | 5109 | 3 | 0 | 0 | 3 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0015 | 0/0 | 5109 | 3 | 1 | 1 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0016 | 0/0 | 5109 | 3 | 2 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0020 | 0/0 | 5109 | 2 | 0 | 2 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0021 | 0/0 | 5109 | 2 | 2 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0022 | 0/0 | 5109 | 2 | 2 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0023 | 0/0 | 5109 | 2 | 2 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0024 | 0/0 | 5109 | 2 | 2 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0027 | 0/0 | 5109 | 2 | 2 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0028 | 0/0 | 5109 | 2 | 0 | 0 | 2 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0029 | 0/0 | 5109 | 2 | 0 | 0 | 0 | 1 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0030 | 0/0 | 5109 | 2 | 0 | 2 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0031 | 0/0 | 5109 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0032 | 0/0 | 5109 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0042 | 0/0 | 5109 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0044 | 0/0 | 5109 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0045 | 0/0 | 5109 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0046 | 0/0 | 5109 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0047 | 0/0 | 5109 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0050 | 0/0 | 5109 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0052 | 0/0 | 5109 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0053 | 0/0 | 5109 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0054 | 0/0 | 5109 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0055 | 0/0 | 5109 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0056 | 0/0 | 5109 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0057 | 0/0 | 5109 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0058 | 0/0 | 5109 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0060 | 0/0 | 5109 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0061 | 0/0 | 5109 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0063 | 0/0 | 5109 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0064 | 0/0 | 5109 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0066 | 0/0 | 5109 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0067 | 0/0 | 5109 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0069 | 0/0 | 5109 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0070 | 0/0 | 5109 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0071 | 0/0 | 5109 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0001c0072 | 0/0 | 5109 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0002c0005 | 0/0 | 5109 | 13 | 5 | 3 | 0 | 0 | 5 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0002c0006 | 0/0 | 5109 | 11 | 0 | 4 | 2 | 3 | 2 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0002c0009 | 0/0 | 5109 | 5 | 0 | 3 | 0 | 1 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0002c0012 | 0/0 | 5109 | 4 | 0 | 2 | 0 | 2 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0002c0013 | 0/0 | 5109 | 3 | 0 | 1 | 0 | 0 | 2 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0002c0017 | 0/0 | 5109 | 2 | 0 | 1 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0002c0018 | 0/0 | 5109 | 2 | 0 | 0 | 0 | 2 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0002c0019 | 0/0 | 5109 | 2 | 2 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0002c0026 | 0/0 | 5109 | 2 | 0 | 0 | 2 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0002c0033 | 0/0 | 5109 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0002c0034 | 0/0 | 5109 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0002c0036 | 0/0 | 5109 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0002c0038 | 0/0 | 5109 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0002c0039 | 0/0 | 5109 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0002c0040 | 0/0 | 5109 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0002c0041 | 0/0 | 5109 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0002c0059 | 0/0 | 5109 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0003c0010 | 0/0 | 5109 | 5 | 0 | 5 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0003c0037 | 0/0 | 5109 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0004c0048 | 0/0 | 5109 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0004c0049 | 0/0 | 5109 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0004c0065 | 0/0 | 5109 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0005c0051 | 0/0 | 5109 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0005c0062 | 0/1 | 5109 | 1 | 0 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0006c0025 | 0/0 | 5109 | 2 | 0 | 0 | 0 | 0 | 2 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0007c0068 | 0/0 | 5109 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0008c0035 | 0/0 | 5109 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 | ||
a0009c0043 | 0/0 | 5109 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | ATGTC others(5104): Show |
chr19 | 17596336 | 17693354 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 9985 | 42 | 0 | 9 | 26 | 1 | 5 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0001t0003 | 0/0 | 9984 | 4 | 0 | 0 | 4 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0001c0001t0004 | 0/0 | 9986 | 2 | 0 | 0 | 1 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0001t0007 | 0/0 | 9984 | 2 | 0 | 0 | 2 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0001c0001t0009 | 0/0 | 9986 | 2 | 0 | 1 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0001t0034 | 0/0 | 9984 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0001c0001t0046 | 0/0 | 9985 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0001 | 0/0 | 9985 | 9 | 2 | 2 | 5 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0003 | 0/0 | 9984 | 4 | 2 | 0 | 0 | 0 | 2 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0004 | 0/0 | 9986 | 4 | 0 | 0 | 3 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0005 | 0/0 | 9987 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9982): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0007 | 0/0 | 9984 | 3 | 0 | 0 | 2 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0008 | 0/0 | 9983 | 3 | 3 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9978): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0009 | 0/0 | 9986 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0010 | 0/0 | 9985 | 3 | 2 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0011 | 0/0 | 9988 | 4 | 4 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9983): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0012 | 0/0 | 9984 | 4 | 0 | 2 | 0 | 0 | 2 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0015 | 0/0 | 9983 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9978): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0017 | 0/0 | 9986 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0018 | 0/0 | 9984 | 2 | 1 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0019 | 0/0 | 9988 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9983): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0020 | 0/0 | 9987 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9982): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0025 | 0/0 | 9985 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0027 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0028 | 0/0 | 9983 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9978): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0029 | 0/0 | 9983 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9978): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0031 | 0/0 | 9985 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0032 | 0/0 | 9989 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9984): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0038 | 0/0 | 9985 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0039 | 0/0 | 9985 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0042 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0044 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0001c0002t0045 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0003t0001 | 0/0 | 9985 | 35 | 0 | 6 | 18 | 1 | 10 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0003t0003 | 0/0 | 9984 | 4 | 1 | 0 | 3 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0001c0003t0007 | 0/0 | 9984 | 2 | 0 | 0 | 2 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0001c0003t0016 | 0/0 | 9987 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9982): Show |
chr19 | 17596336 | 17693354 |
a0001c0003t0017 | 0/0 | 9986 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0003t0037 | 0/0 | 9985 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0003t0040 | 0/0 | 9985 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0003t0048 | 0/0 | 9985 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0004t0001 | 0/0 | 9985 | 11 | 0 | 4 | 4 | 0 | 3 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0004t0003 | 0/0 | 9984 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0001c0004t0004 | 0/0 | 9986 | 2 | 0 | 0 | 2 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0004t0007 | 0/0 | 9984 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0001c0004t0009 | 0/0 | 9986 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0004t0010 | 0/0 | 9985 | 2 | 2 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0004t0011 | 0/0 | 9988 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9983): Show |
chr19 | 17596336 | 17693354 |
a0001c0004t0018 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0001c0004t0021 | 0/0 | 9985 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0004t0041 | 0/0 | 9984 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0001c0004t0049 | 0/0 | 9985 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0007t0001 | 0/0 | 9985 | 3 | 3 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0007t0003 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0001c0007t0005 | 0/0 | 9987 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9982): Show |
chr19 | 17596336 | 17693354 |
a0001c0007t0008 | 0/0 | 9983 | 2 | 2 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9978): Show |
chr19 | 17596336 | 17693354 |
a0001c0007t0015 | 0/0 | 9983 | 2 | 2 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9978): Show |
chr19 | 17596336 | 17693354 |
a0001c0007t0025 | 0/0 | 9985 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0008t0002 | 0/0 | 9986 | 8 | 6 | 2 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0008t0026 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0011t0001 | 0/0 | 9985 | 3 | 2 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0011t0010 | 0/0 | 9985 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0011t0020 | 0/0 | 9987 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9982): Show |
chr19 | 17596336 | 17693354 |
a0001c0014t0001 | 0/0 | 9985 | 3 | 0 | 0 | 3 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0015t0006 | 0/0 | 9983 | 2 | 1 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9978): Show |
chr19 | 17596336 | 17693354 |
a0001c0015t0022 | 0/0 | 9983 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9978): Show |
chr19 | 17596336 | 17693354 |
a0001c0016t0002 | 0/0 | 9986 | 3 | 2 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0020t0001 | 0/0 | 9985 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0020t0005 | 0/0 | 9987 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9982): Show |
chr19 | 17596336 | 17693354 |
a0001c0021t0014 | 0/0 | 9986 | 2 | 2 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0022t0008 | 0/0 | 9983 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9978): Show |
chr19 | 17596336 | 17693354 |
a0001c0022t0024 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0023t0001 | 0/0 | 9985 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0023t0047 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0001c0024t0001 | 0/0 | 9985 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0024t0019 | 0/0 | 9988 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9983): Show |
chr19 | 17596336 | 17693354 |
a0001c0027t0002 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0027t0014 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0028t0002 | 0/0 | 9986 | 2 | 0 | 0 | 2 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0029t0006 | 0/0 | 9983 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9978): Show |
chr19 | 17596336 | 17693354 |
a0001c0029t0022 | 0/0 | 9983 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9978): Show |
chr19 | 17596336 | 17693354 |
a0001c0030t0001 | 0/0 | 9985 | 2 | 0 | 2 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0031t0001 | 0/0 | 9985 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0032t0008 | 0/0 | 9983 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9978): Show |
chr19 | 17596336 | 17693354 |
a0001c0042t0001 | 0/0 | 9985 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0044t0001 | 0/0 | 9985 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0045t0035 | 0/0 | 9946 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9941): Show |
chr19 | 17596336 | 17693354 |
a0001c0046t0001 | 0/0 | 9985 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0047t0001 | 0/0 | 9985 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0050t0033 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0001c0052t0002 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0053t0023 | 0/0 | 9985 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0054t0009 | 0/0 | 9986 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0055t0001 | 0/0 | 9985 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0056t0002 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0057t0024 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0058t0001 | 0/0 | 9985 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0060t0002 | 0/0 | 9986 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0061t0001 | 0/0 | 9985 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0063t0002 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0064t0001 | 0/0 | 9985 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0066t0019 | 0/0 | 9988 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9983): Show |
chr19 | 17596336 | 17693354 |
a0001c0067t0004 | 0/0 | 9986 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0069t0001 | 0/0 | 9985 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0070t0001 | 0/0 | 9985 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0001c0071t0002 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0001c0072t0003 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0002c0005t0001 | 0/0 | 9985 | 5 | 3 | 1 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0002c0005t0003 | 0/0 | 9984 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0002c0005t0004 | 0/0 | 9986 | 4 | 0 | 1 | 0 | 0 | 3 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0002c0005t0006 | 0/0 | 9983 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9978): Show |
chr19 | 17596336 | 17693354 |
a0002c0005t0009 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0002c0005t0020 | 0/0 | 9987 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9982): Show |
chr19 | 17596336 | 17693354 |
a0002c0006t0001 | 0/0 | 9985 | 6 | 0 | 3 | 1 | 0 | 2 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0002c0006t0003 | 0/0 | 9984 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0002c0006t0006 | 0/0 | 9983 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9978): Show |
chr19 | 17596336 | 17693354 |
a0002c0006t0016 | 0/0 | 9987 | 2 | 0 | 0 | 0 | 2 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9982): Show |
chr19 | 17596336 | 17693354 |
a0002c0006t0017 | 0/0 | 9986 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0002c0009t0005 | 0/0 | 9987 | 4 | 0 | 3 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9982): Show |
chr19 | 17596336 | 17693354 |
a0002c0009t0043 | 0/0 | 9988 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9983): Show |
chr19 | 17596336 | 17693354 |
a0002c0012t0001 | 0/0 | 9985 | 3 | 0 | 1 | 0 | 2 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0002c0012t0006 | 0/0 | 9983 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9978): Show |
chr19 | 17596336 | 17693354 |
a0002c0013t0002 | 0/0 | 9986 | 3 | 0 | 1 | 0 | 0 | 2 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0002c0017t0001 | 0/0 | 9985 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0002c0017t0013 | 0/0 | 9983 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9978): Show |
chr19 | 17596336 | 17693354 |
a0002c0018t0002 | 0/0 | 9986 | 2 | 0 | 0 | 0 | 2 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0002c0019t0003 | 0/0 | 9984 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0002c0019t0008 | 0/0 | 9983 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9978): Show |
chr19 | 17596336 | 17693354 |
a0002c0026t0002 | 0/0 | 9986 | 2 | 0 | 0 | 2 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0002c0033t0030 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0002c0034t0002 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0002c0036t0002 | 0/0 | 9986 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0002c0038t0023 | 0/0 | 9985 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0002c0039t0021 | 0/0 | 9985 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0002c0040t0014 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0002c0041t0036 | 0/0 | 9987 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9982): Show |
chr19 | 17596336 | 17693354 |
a0002c0059t0009 | 0/0 | 9986 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0003c0010t0001 | 0/0 | 9985 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0003c0010t0006 | 0/0 | 9983 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9978): Show |
chr19 | 17596336 | 17693354 |
a0003c0010t0013 | 0/0 | 9983 | 3 | 0 | 3 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9978): Show |
chr19 | 17596336 | 17693354 |
a0003c0037t0001 | 0/0 | 9985 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0004c0048t0005 | 0/0 | 9987 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9982): Show |
chr19 | 17596336 | 17693354 |
a0004c0049t0006 | 0/0 | 9983 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9978): Show |
chr19 | 17596336 | 17693354 |
a0004c0065t0005 | 0/0 | 9987 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9982): Show |
chr19 | 17596336 | 17693354 |
a0005c0051t0001 | 0/0 | 9985 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0005c0062t0003 | 0/1 | 9984 | 1 | 0 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9979): Show |
chr19 | 17596336 | 17693354 |
a0006c0025t0001 | 0/0 | 9985 | 2 | 0 | 0 | 0 | 0 | 2 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0007c0068t0002 | 0/0 | 9986 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9981): Show |
chr19 | 17596336 | 17693354 |
a0008c0035t0001 | 0/0 | 9985 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
a0009c0043t0001 | 0/0 | 9985 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | GCCCC others(9980): Show |
chr19 | 17596336 | 17693354 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0007g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0007g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0009g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0009g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0034g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0001t0046g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0004g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0005g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0007g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0007g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0007g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0008g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0009g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0010g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0010g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0011g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0011g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0011g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0011g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0012g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0012g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0012g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0012g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0015g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0017g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0018g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0018g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0019g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0020g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0025g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0027g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0028g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0029g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0031g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0032g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0038g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0039g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0042g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0044g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0002t0045g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0007g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0007g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0016g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0017g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0037g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0040g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0003t0048g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0007g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0009g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0010g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0011g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0018g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0021g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0041g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0004t0049g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0007t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0007t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0007t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0007t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0007t0005g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0007t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0007t0008g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0007t0015g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0007t0015g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0007t0025g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0008t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0008t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0008t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0008t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0008t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0008t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0008t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0008t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0008t0026g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0011t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0011t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0011t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0011t0010g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0011t0020g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0014t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0014t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0014t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0015t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0015t0006g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0015t0022g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0016t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0016t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0016t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0020t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0020t0005g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0021t0014g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0021t0014g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0022t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0022t0024g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0023t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0023t0047g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0024t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0024t0019g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0027t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0027t0014g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0028t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0028t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0029t0006g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0029t0022g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0030t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0030t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0031t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0032t0008g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0042t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0044t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0045t0035g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0046t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0047t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0050t0033g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0052t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0053t0023g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0054t0009g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0055t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0056t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0057t0024g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0058t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0060t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0061t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0063t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0064t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0066t0019g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0067t0004g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0069t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0070t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0071t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0001c0072t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0005t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0005t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0005t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0005t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0005t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0005t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0005t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0005t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0005t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0005t0004g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0005t0006g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0005t0009g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0005t0020g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0006t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0006t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0006t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0006t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0006t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0006t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0006t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0006t0006g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0006t0016g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0006t0016g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0006t0017g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0009t0005g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0009t0005g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0009t0005g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0009t0005g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0009t0043g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0012t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0012t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0012t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0012t0006g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0013t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0013t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0013t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0017t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0017t0013g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0018t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0018t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0019t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0019t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0026t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0026t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0033t0030g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0034t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0036t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0038t0023g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0039t0021g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0040t0014g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0041t0036g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0002c0059t0009g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0003c0010t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0003c0010t0006g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0003c0010t0013g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0003c0010t0013g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0003c0010t0013g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0003c0037t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0004c0048t0005g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0004c0049t0006g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0004c0065t0005g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0005c0051t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0005c0062t0003g0032 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0006c0025t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0006c0025t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0007c0068t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0008c0035t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
a0009c0043t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0004 | g0224 | EUR | GBR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00099 | hp2 | a0002 | c0017 | t0001 | g0086 | EUR | GBR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00140 | hp1 | a0001 | c0029 | t0006 | g0243 | EUR | GBR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00140 | hp2 | a0002 | c0006 | t0006 | g0278 | EUR | GBR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00280 | hp1 | a0002 | c0006 | t0016 | g0289 | EUR | FIN | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00280 | hp2 | a0004 | c0049 | t0006 | g0293 | EUR | FIN | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00423 | hp1 | a0005 | c0051 | t0001 | g0259 | EAS | CHS | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00423 | hp2 | a0001 | c0004 | t0009 | g0186 | EAS | CHS | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00438 | hp1 | a0001 | c0003 | t0003 | g0109 | EAS | CHS | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00544 | hp2 | a0001 | c0001 | t0007 | g0223 | EAS | CHS | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00558 | hp1 | a0001 | c0002 | t0004 | g0139 | EAS | CHS | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00558 | hp2 | a0001 | c0004 | t0004 | g0272 | EAS | CHS | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00597 | hp1 | a0001 | c0003 | t0001 | g0110 | EAS | CHS | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00609 | hp1 | a0001 | c0003 | t0007 | g0248 | EAS | CHS | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00609 | hp2 | a0001 | c0003 | t0001 | g0247 | EAS | CHS | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00639 | hp1 | a0001 | c0064 | t0001 | g0048 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00639 | hp2 | a0002 | c0036 | t0002 | g0004 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00642 | hp1 | a0003 | c0037 | t0001 | g0282 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00733 | hp1 | a0002 | c0013 | t0002 | g0307 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00733 | hp2 | a0004 | c0065 | t0005 | g0134 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00735 | hp1 | a0001 | c0002 | t0018 | g0269 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00735 | hp2 | a0001 | c0044 | t0001 | g0301 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00738 | hp1 | a0003 | c0010 | t0013 | g0019 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00738 | hp2 | a0001 | c0003 | t0001 | g0040 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00741 | hp1 | a0001 | c0007 | t0005 | g0173 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG00741 | hp2 | a0002 | c0012 | t0001 | g0124 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01070 | hp1 | a0002 | c0009 | t0005 | g0007 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01070 | hp2 | a0003 | c0010 | t0013 | g0016 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01081 | hp1 | a0002 | c0006 | t0001 | g0281 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01081 | hp2 | a0001 | c0003 | t0001 | g0009 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01109 | hp1 | a0001 | c0003 | t0001 | g0288 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01109 | hp2 | a0001 | c0002 | t0010 | g0069 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01167 | hp1 | a0002 | c0006 | t0001 | g0013 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01167 | hp2 | a0001 | c0008 | t0002 | g0071 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01168 | hp1 | a0002 | c0009 | t0005 | g0006 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01168 | hp2 | a0001 | c0003 | t0016 | g0149 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01169 | hp1 | a0002 | c0009 | t0005 | g0008 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01169 | hp2 | a0001 | c0008 | t0002 | g0095 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01175 | hp1 | a0001 | c0002 | t0009 | g0176 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01175 | hp2 | a0001 | c0054 | t0009 | g0290 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01192 | hp1 | a0001 | c0002 | t0017 | g0028 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01192 | hp2 | a0001 | c0003 | t0001 | g0255 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01243 | hp1 | a0002 | c0017 | t0013 | g0023 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01243 | hp2 | a0002 | c0006 | t0017 | g0309 | AMR | PUR | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01256 | hp1 | a0003 | c0010 | t0006 | g0306 | AMR | CLM | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01256 | hp2 | a0001 | c0030 | t0001 | g0246 | AMR | CLM | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01258 | hp1 | a0001 | c0003 | t0001 | g0305 | AMR | CLM | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01258 | hp2 | a0001 | c0030 | t0001 | g0122 | AMR | CLM | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01261 | hp1 | a0004 | c0048 | t0005 | g0177 | AMR | CLM | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01261 | hp2 | a0001 | c0001 | t0009 | g0146 | AMR | CLM | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01346 | hp1 | a0001 | c0004 | t0001 | g0256 | AMR | CLM | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01346 | hp2 | a0002 | c0005 | t0001 | g0285 | AMR | CLM | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01358 | hp1 | a0001 | c0003 | t0001 | g0128 | AMR | CLM | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01358 | hp2 | a0003 | c0010 | t0013 | g0161 | AMR | CLM | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01361 | hp1 | a0001 | c0011 | t0001 | g0089 | AMR | CLM | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01433 | hp1 | a0001 | c0015 | t0006 | g0303 | AMR | CLM | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01496 | hp1 | a0001 | c0046 | t0001 | g0280 | AMR | CLM | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01496 | hp2 | a0001 | c0020 | t0005 | g0076 | AMR | CLM | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01515 | hp1 | a0002 | c0006 | t0016 | g0296 | EUR | IBS | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01515 | hp2 | a0002 | c0018 | t0002 | g0159 | EUR | IBS | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01516 | hp1 | a0002 | c0012 | t0001 | g0175 | EUR | IBS | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01516 | hp2 | a0002 | c0009 | t0043 | g0226 | EUR | IBS | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01517 | hp1 | a0002 | c0012 | t0001 | g0169 | EUR | IBS | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01517 | hp2 | a0002 | c0018 | t0002 | g0258 | EUR | IBS | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01884 | hp1 | a0001 | c0008 | t0002 | g0286 | AFR | ACB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01884 | hp2 | a0001 | c0002 | t0011 | g0039 | AFR | ACB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0113 | AMR | PEL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01928 | hp2 | a0003 | c0010 | t0001 | g0070 | AMR | PEL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01934 | hp1 | a0002 | c0012 | t0006 | g0181 | AMR | PEL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01943 | hp2 | a0001 | c0004 | t0001 | g0219 | AMR | PEL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01975 | hp2 | a0001 | c0002 | t0012 | g0291 | AMR | PEL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01978 | hp1 | a0001 | c0004 | t0001 | g0114 | AMR | PEL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01978 | hp2 | a0002 | c0006 | t0001 | g0021 | AMR | PEL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01981 | hp2 | a0002 | c0041 | t0036 | g0279 | AMR | PEL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02004 | hp1 | a0001 | c0004 | t0001 | g0191 | AMR | PEL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02004 | hp2 | a0001 | c0002 | t0012 | g0017 | AMR | PEL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02015 | hp1 | a0001 | c0004 | t0007 | g0151 | EAS | KHV | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | KHV | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02027 | hp1 | a0001 | c0003 | t0001 | g0152 | EAS | KHV | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02027 | hp2 | a0001 | c0004 | t0001 | g0238 | EAS | KHV | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02055 | hp1 | a0001 | c0002 | t0044 | g0093 | AFR | ACB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02055 | hp2 | a0002 | c0005 | t0009 | g0180 | AFR | ACB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02056 | hp1 | a0001 | c0004 | t0041 | g0111 | EAS | KHV | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02056 | hp2 | a0001 | c0031 | t0001 | g0116 | EAS | KHV | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02074 | hp1 | a0001 | c0001 | t0009 | g0160 | EAS | KHV | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02074 | hp2 | a0001 | c0004 | t0004 | g0188 | EAS | KHV | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02080 | hp1 | a0001 | c0003 | t0001 | g0101 | EAS | KHV | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02080 | hp2 | a0001 | c0003 | t0037 | g0147 | EAS | KHV | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02083 | hp2 | a0001 | c0003 | t0001 | g0204 | EAS | KHV | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02145 | hp1 | a0001 | c0002 | t0019 | g0092 | AFR | ACB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02145 | hp2 | a0001 | c0007 | t0003 | g0072 | AFR | ACB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0266 | AMR | PEL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02155 | hp1 | a0001 | c0004 | t0001 | g0135 | EAS | CDX | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02165 | hp1 | a0001 | c0002 | t0007 | g0257 | EAS | CDX | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02165 | hp2 | a0001 | c0069 | t0001 | g0261 | EAS | CDX | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02257 | hp1 | a0001 | c0053 | t0023 | g0053 | AFR | ACB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02257 | hp2 | a0001 | c0004 | t0010 | g0056 | AFR | ACB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02258 | hp1 | a0001 | c0002 | t0003 | g0068 | AFR | ACB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02258 | hp2 | a0001 | c0052 | t0002 | g0058 | AFR | ACB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02273 | hp1 | a0001 | c0020 | t0001 | g0005 | AMR | PEL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02280 | hp1 | a0001 | c0002 | t0020 | g0025 | AFR | ACB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02280 | hp2 | a0001 | c0002 | t0011 | g0287 | AFR | ACB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02293 | hp1 | a0002 | c0005 | t0004 | g0144 | AMR | PEL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02293 | hp2 | a0001 | c0001 | t0034 | g0304 | AMR | PEL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02451 | hp1 | a0001 | c0066 | t0019 | g0043 | AFR | ACB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02451 | hp2 | a0001 | c0016 | t0002 | g0091 | AFR | ACB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | KHV | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02572 | hp1 | a0001 | c0002 | t0011 | g0184 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02572 | hp2 | a0001 | c0002 | t0038 | g0037 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02602 | hp1 | a0002 | c0005 | t0001 | g0140 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02602 | hp2 | a0001 | c0029 | t0022 | g0148 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02630 | hp1 | a0001 | c0008 | t0002 | g0075 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02630 | hp2 | a0001 | c0022 | t0008 | g0185 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02647 | hp1 | a0001 | c0057 | t0024 | g0233 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02647 | hp2 | a0001 | c0007 | t0008 | g0063 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02683 | hp1 | a0001 | c0002 | t0012 | g0077 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02683 | hp2 | a0002 | c0005 | t0003 | g0168 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02717 | hp1 | a0001 | c0071 | t0002 | g0311 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02717 | hp2 | a0001 | c0055 | t0001 | g0102 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02723 | hp1 | a0001 | c0002 | t0008 | g0046 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02723 | hp2 | a0001 | c0002 | t0010 | g0033 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02735 | hp1 | a0001 | c0003 | t0001 | g0066 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02738 | hp1 | a0006 | c0025 | t0001 | g0029 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02738 | hp2 | a0001 | c0004 | t0003 | g0030 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02809 | hp1 | a0001 | c0056 | t0002 | g0155 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02809 | hp2 | a0002 | c0019 | t0008 | g0036 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02818 | hp1 | a0001 | c0007 | t0008 | g0212 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02818 | hp2 | a0001 | c0007 | t0001 | g0062 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02886 | hp1 | a0001 | c0022 | t0024 | g0061 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02886 | hp2 | a0001 | c0072 | t0003 | g0312 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02895 | hp1 | a0001 | c0002 | t0045 | g0164 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02895 | hp2 | a0001 | c0021 | t0014 | g0319 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02896 | hp1 | a0001 | c0008 | t0002 | g0034 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02896 | hp2 | a0001 | c0008 | t0002 | g0276 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02897 | hp1 | a0001 | c0008 | t0002 | g0277 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02897 | hp2 | a0001 | c0021 | t0014 | g0318 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02922 | hp1 | a0001 | c0008 | t0026 | g0083 | AFR | ESN | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02922 | hp2 | a0001 | c0004 | t0021 | g0073 | AFR | ESN | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02965 | hp1 | a0001 | c0002 | t0010 | g0097 | AFR | ESN | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02965 | hp2 | a0001 | c0002 | t0025 | g0315 | AFR | ESN | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02970 | hp1 | a0001 | c0007 | t0001 | g0042 | AFR | ESN | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02970 | hp2 | a0001 | c0002 | t0008 | g0284 | AFR | ESN | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02976 | hp1 | a0002 | c0005 | t0001 | g0067 | AFR | ESN | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02976 | hp2 | a0001 | c0011 | t0001 | g0300 | AFR | ESN | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03017 | hp1 | a0001 | c0015 | t0022 | g0153 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03041 | hp1 | a0001 | c0002 | t0018 | g0103 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03041 | hp2 | a0001 | c0003 | t0003 | g0162 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03098 | hp1 | a0001 | c0023 | t0001 | g0045 | AFR | MSL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03098 | hp2 | a0001 | c0002 | t0032 | g0098 | AFR | MSL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03130 | hp1 | a0002 | c0005 | t0020 | g0088 | AFR | ESN | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03130 | hp2 | a0001 | c0004 | t0010 | g0242 | AFR | ESN | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03139 | hp1 | a0001 | c0002 | t0028 | g0047 | AFR | ESN | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03139 | hp2 | a0001 | c0007 | t0001 | g0052 | AFR | ESN | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03195 | hp1 | a0001 | c0027 | t0014 | g0314 | AFR | ESN | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03195 | hp2 | a0002 | c0005 | t0001 | g0051 | AFR | ESN | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0308 | AFR | MSL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03209 | hp2 | a0001 | c0002 | t0015 | g0054 | AFR | MSL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03225 | hp1 | a0001 | c0023 | t0047 | g0275 | AFR | MSL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03225 | hp2 | a0001 | c0002 | t0031 | g0298 | AFR | MSL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03239 | hp1 | a0002 | c0006 | t0001 | g0283 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03239 | hp2 | a0001 | c0002 | t0003 | g0131 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03453 | hp1 | a0002 | c0039 | t0021 | g0026 | AFR | MSL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03453 | hp2 | a0001 | c0032 | t0008 | g0163 | AFR | MSL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03486 | hp1 | a0001 | c0003 | t0040 | g0024 | AFR | MSL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03486 | hp2 | a0001 | c0002 | t0011 | g0064 | AFR | MSL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03490 | hp2 | a0001 | c0004 | t0001 | g0020 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03491 | hp1 | a0001 | c0002 | t0012 | g0299 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03491 | hp2 | a0002 | c0005 | t0004 | g0118 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03492 | hp1 | a0002 | c0005 | t0004 | g0119 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03492 | hp2 | a0001 | c0004 | t0001 | g0123 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03516 | hp1 | a0001 | c0002 | t0042 | g0038 | AFR | ESN | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03516 | hp2 | a0001 | c0063 | t0002 | g0104 | AFR | ESN | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03540 | hp1 | a0002 | c0040 | t0014 | g0316 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03540 | hp2 | a0002 | c0019 | t0003 | g0074 | AFR | GWD | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03579 | hp1 | a0001 | c0007 | t0025 | g0320 | AFR | MSL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03579 | hp2 | a0001 | c0016 | t0002 | g0065 | AFR | MSL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03669 | hp1 | a0001 | c0002 | t0007 | g0018 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03669 | hp2 | a0006 | c0025 | t0001 | g0087 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03688 | hp1 | a0001 | c0002 | t0003 | g0127 | SAS | STU | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | STU | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03704 | hp1 | a0001 | c0067 | t0004 | g0265 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03704 | hp2 | a0002 | c0013 | t0002 | g0200 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03710 | hp1 | a0001 | c0003 | t0001 | g0294 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03710 | hp2 | a0001 | c0003 | t0001 | g0292 | SAS | PJL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03831 | hp1 | a0001 | c0047 | t0001 | g0050 | SAS | BEB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03831 | hp2 | a0002 | c0009 | t0005 | g0182 | SAS | BEB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03834 | hp1 | a0008 | c0035 | t0001 | g0002 | SAS | BEB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03834 | hp2 | a0001 | c0003 | t0001 | g0210 | SAS | BEB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG04115 | hp1 | a0001 | c0004 | t0001 | g0010 | SAS | STU | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0012 | SAS | STU | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG04184 | hp1 | a0002 | c0013 | t0002 | g0078 | SAS | BEB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG04184 | hp2 | a0001 | c0003 | t0001 | g0205 | SAS | BEB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | STU | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG04199 | hp2 | a0002 | c0005 | t0004 | g0220 | SAS | STU | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG04204 | hp1 | a0001 | c0003 | t0001 | g0015 | SAS | STU | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG04204 | hp2 | a0001 | c0003 | t0001 | g0014 | SAS | STU | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG04228 | hp1 | a0001 | c0003 | t0001 | g0079 | SAS | STU | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG04228 | hp2 | a0002 | c0006 | t0001 | g0302 | SAS | STU | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18522 | hp1 | a0001 | c0011 | t0001 | g0156 | AFR | YRI | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18522 | hp2 | a0001 | c0004 | t0018 | g0060 | AFR | YRI | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18612 | hp1 | a0001 | c0003 | t0001 | g0154 | EAS | CHB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18612 | hp2 | a0001 | c0001 | t0046 | g0197 | EAS | CHB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18906 | hp1 | a0001 | c0007 | t0015 | g0041 | AFR | YRI | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18906 | hp2 | a0001 | c0070 | t0001 | g0313 | AFR | YRI | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18944 | hp1 | a0001 | c0014 | t0001 | g0125 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18944 | hp2 | a0001 | c0003 | t0001 | g0112 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18947 | hp2 | a0001 | c0003 | t0003 | g0264 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18948 | hp1 | a0001 | c0003 | t0001 | g0208 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18948 | hp2 | a0001 | c0003 | t0007 | g0206 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18951 | hp1 | a0001 | c0003 | t0001 | g0240 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18952 | hp1 | a0001 | c0014 | t0001 | g0254 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18962 | hp1 | a0001 | c0014 | t0001 | g0081 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18964 | hp2 | a0001 | c0004 | t0001 | g0211 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18969 | hp1 | a0001 | c0003 | t0001 | g0228 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18970 | hp2 | a0001 | c0060 | t0002 | g0192 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18977 | hp2 | a0001 | c0016 | t0002 | g0260 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18983 | hp2 | a0001 | c0004 | t0001 | g0150 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18990 | hp1 | a0001 | c0003 | t0001 | g0198 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18991 | hp1 | a0001 | c0003 | t0003 | g0133 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18991 | hp2 | a0001 | c0045 | t0035 | g0183 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18993 | hp1 | a0002 | c0026 | t0002 | g0251 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18993 | hp2 | a0002 | c0006 | t0001 | g0241 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18994 | hp1 | a0002 | c0059 | t0009 | g0121 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18994 | hp2 | a0001 | c0002 | t0004 | g0215 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18995 | hp2 | a0001 | c0002 | t0039 | g0234 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18998 | hp1 | a0001 | c0003 | t0001 | g0130 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA18998 | hp2 | a0002 | c0026 | t0002 | g0263 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19000 | hp1 | a0001 | c0003 | t0001 | g0138 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19000 | hp2 | a0001 | c0001 | t0007 | g0232 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19004 | hp1 | a0001 | c0061 | t0001 | g0239 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19010 | hp2 | a0001 | c0003 | t0001 | g0213 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19011 | hp2 | a0001 | c0058 | t0001 | g0105 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19012 | hp1 | a0001 | c0042 | t0001 | g0214 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19030 | hp1 | a0001 | c0050 | t0033 | g0085 | AFR | LWK | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19030 | hp2 | a0001 | c0007 | t0015 | g0094 | AFR | LWK | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19043 | hp1 | a0002 | c0034 | t0002 | g0099 | AFR | LWK | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19043 | hp2 | a0001 | c0024 | t0019 | g0100 | AFR | LWK | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19056 | hp1 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19056 | hp2 | a0001 | c0002 | t0007 | g0172 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19062 | hp1 | a0001 | c0028 | t0002 | g0082 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19062 | hp2 | a0001 | c0003 | t0001 | g0222 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19063 | hp2 | a0009 | c0043 | t0001 | g0202 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19064 | hp2 | a0001 | c0002 | t0004 | g0227 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19070 | hp1 | a0001 | c0003 | t0001 | g0217 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19070 | hp2 | a0001 | c0028 | t0002 | g0196 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19074 | hp1 | a0001 | c0003 | t0001 | g0031 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19074 | hp2 | a0001 | c0003 | t0048 | g0158 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19077 | hp1 | a0002 | c0006 | t0003 | g0267 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19079 | hp2 | a0001 | c0003 | t0001 | g0218 | EAS | JPT | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19240 | hp1 | a0001 | c0015 | t0006 | g0090 | AFR | YRI | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA19240 | hp2 | a0001 | c0004 | t0011 | g0055 | AFR | YRI | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA20129 | hp1 | a0001 | c0027 | t0002 | g0044 | AFR | ASW | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA20129 | hp2 | a0001 | c0002 | t0008 | g0027 | AFR | ASW | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA20752 | hp1 | a0001 | c0002 | t0005 | g0120 | EUR | TSI | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA20752 | hp2 | a0001 | c0003 | t0001 | g0142 | EUR | TSI | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA20805 | hp1 | a0001 | c0003 | t0017 | g0049 | EUR | TSI | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | TSI | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA20905 | hp1 | a0001 | c0003 | t0001 | g0117 | SAS | GIH | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA20905 | hp2 | a0001 | c0003 | t0001 | g0129 | SAS | GIH | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01123 | hp1 | a0002 | c0005 | t0006 | g0310 | AMR | CLM | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG01123 | hp2 | a0001 | c0011 | t0010 | g0059 | AMR | CLM | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02486 | hp1 | a0002 | c0005 | t0001 | g0273 | AFR | ACB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02486 | hp2 | a0007 | c0068 | t0002 | g0003 | AFR | ACB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02559 | hp1 | a0001 | c0002 | t0027 | g0295 | AFR | ACB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG02559 | hp2 | a0001 | c0008 | t0002 | g0274 | AFR | ACB | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03471 | hp1 | a0002 | c0038 | t0023 | g0084 | AFR | MSL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG03471 | hp2 | a0001 | c0024 | t0001 | g0057 | AFR | MSL | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG06807 | hp1 | a0002 | c0033 | t0030 | g0141 | AFR | USA | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
HG06807 | hp2 | a0001 | c0004 | t0049 | g0317 | AFR | USA | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA20300 | hp1 | a0001 | c0002 | t0003 | g0096 | AFR | USA | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA20300 | hp2 | a0001 | c0002 | t0029 | g0167 | AFR | USA | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA21309 | hp1 | a0001 | c0011 | t0020 | g0035 | AFR | LWK | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0157 | AFR | LWK | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
homoSapiens | chm13v2 | a0005 | c0062 | t0003 | g0032 | REF | REF | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0108 | REF | REF | UNC13A_chr19_17596336_17693354 | UNC13A | chr19 | 17596336 | 17693354 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:17620722 | C | A | 1 | a0009 | 1 | NA19063.hp2 | missense_variant&splice_region_variant | MODERATE | c.4243G>T | p.Gly1415Cys | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/44 | 4398/9985 | 4243/5112 | 1415/1703 | chr19 | 17620722 | |||
chr19:17621845 | T | G | 1 | a0009 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.4229A>C | p.Lys1410Thr | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 37/44 | 4384/9985 | 4229/5112 | 1410/1703 | chr19 | 17621845 | |||
chr19:17629268 | G | A | 1 | a0008 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.3725C>T | p.Ser1242Phe | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 31/44 | 3880/9985 | 3725/5112 | 1242/1703 | chr19 | 17629268 | |||
chr19:17632813 | C | A | 2 | a0003 a0004 |
9 | HG00280.hp2 HG00642.hp1 HG00733.hp2 others(6): Show |
missense_variant | MODERATE | c.3397G>T | p.Ala1133Ser | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/44 | 3552/9985 | 3397/5112 | 1133/1703 | chr19 | 17632813 | |||
chr19:17636139 | G | C | 1 | a0005 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.3100C>G | p.Leu1034Val | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/44 | 3255/9985 | 3100/5112 | 1034/1703 | chr19 | 17636139 | |||
chr19:17655928 | G | A | 1 | a0006 | 2 | HG02738.hp1 HG03669.hp2 |
missense_variant | MODERATE | c.1238C>T | p.Ala413Val | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 10/44 | 1393/9985 | 1238/5112 | 413/1703 | chr19 | 17655928 | |||
chr19:17656091 | C | T | 3 | a0002 a0003 a0008 |
59 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(56): Show |
missense_variant | MODERATE | c.1075G>A | p.Ala359Thr | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 10/44 | 1230/9985 | 1075/5112 | 359/1703 | chr19 | 17656091 | |||
chr19:17672466 | G | A | 1 | a0007 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.182C>T | p.Thr61Met | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/44 | 337/9985 | 182/5112 | 61/1703 | chr19 | 17672466 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:17606087 | G | T | 18 | a0001c0008 a0001c0016 a0001c0021 others(15): Show |
35 | HG00639.hp2 HG00733.hp1 HG01167.hp2 others(32): Show |
synonymous_variant | LOW | c.5079C>A | p.Ser1693Ser | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 5234/9985 | 5079/5112 | 1693/1703 | chr19 | 17606087 | |||
chr19:17610023 | G | A | 1 | a0001c0045 | 1 | NA18991.hp2 | synonymous_variant | LOW | c.4728C>T | p.Pro1576Pro | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/44 | 4883/9985 | 4728/5112 | 1576/1703 | chr19 | 17610023 | |||
chr19:17610038 | G | C | 1 | a0001c0046 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.4713C>G | p.Val1571Val | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/44 | 4868/9985 | 4713/5112 | 1571/1703 | chr19 | 17610038 | |||
chr19:17617745 | G | A | 1 | a0001c0067 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.4515C>T | p.Thr1505Thr | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/44 | 4670/9985 | 4515/5112 | 1505/1703 | chr19 | 17617745 | |||
chr19:17617763 | C | T | 7 | a0001c0015 a0001c0029 a0001c0064 others(4): Show |
15 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(12): Show |
synonymous_variant | LOW | c.4497G>A | p.Ser1499Ser | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/44 | 4652/9985 | 4497/5112 | 1499/1703 | chr19 | 17617763 | |||
chr19:17626677 | G | A | 3 | a0001c0044 a0002c0012 a0003c0037 |
6 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(3): Show |
synonymous_variant | LOW | c.4029C>T | p.Asp1343Asp | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/44 | 4184/9985 | 4029/5112 | 1343/1703 | chr19 | 17626677 | |||
chr19:17627908 | T | C | 2 | a0001c0027 a0002c0034 |
3 | HG03195.hp1 NA19043.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.3786A>G | p.Leu1262Leu | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 32/44 | 3941/9985 | 3786/5112 | 1262/1703 | chr19 | 17627908 | |||
chr19:17629306 | G | A | 4 | a0001c0044 a0001c0050 a0002c0012 others(1): Show |
7 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(4): Show |
synonymous_variant | LOW | c.3687C>T | p.Leu1229Leu | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 31/44 | 3842/9985 | 3687/5112 | 1229/1703 | chr19 | 17629306 | |||
chr19:17630238 | A | G | 40 | a0001c0002 a0001c0004 a0001c0007 others(37): Show |
164 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(161): Show |
synonymous_variant | LOW | c.3576T>C | p.Val1192Val | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 30/44 | 3731/9985 | 3576/5112 | 1192/1703 | chr19 | 17630238 | |||
chr19:17630241 | A | G | 10 | a0001c0011 a0001c0021 a0001c0023 others(7): Show |
16 | HG01123.hp2 HG01361.hp1 HG02257.hp1 others(13): Show |
synonymous_variant | LOW | c.3573T>C | p.Asp1191Asp | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 30/44 | 3728/9985 | 3573/5112 | 1191/1703 | chr19 | 17630241 | |||
chr19:17630735 | G | A | 1 | a0001c0047 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.3444C>T | p.Phe1148Phe | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 29/44 | 3599/9985 | 3444/5112 | 1148/1703 | chr19 | 17630735 | |||
chr19:17633118 | G | A | 1 | a0001c0024 | 2 | HG03471.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.3291C>T | p.Tyr1097Tyr | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 27/44 | 3446/9985 | 3291/5112 | 1097/1703 | chr19 | 17633118 | |||
chr19:17636104 | G | A | 1 | a0001c0050 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.3135C>T | p.Leu1045Leu | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/44 | 3290/9985 | 3135/5112 | 1045/1703 | chr19 | 17636104 | |||
chr19:17636131 | C | T | 4 | a0001c0020 a0001c0054 a0002c0009 others(1): Show |
9 | HG01070.hp1 HG01168.hp1 HG01169.hp1 others(6): Show |
synonymous_variant | LOW | c.3108G>A | p.Glu1036Glu | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/44 | 3263/9985 | 3108/5112 | 1036/1703 | chr19 | 17636131 | |||
chr19:17640526 | G | A | 6 | a0001c0022 a0001c0024 a0001c0052 others(3): Show |
8 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(5): Show |
synonymous_variant | LOW | c.2772C>T | p.Ala924Ala | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 22/44 | 2927/9985 | 2772/5112 | 924/1703 | chr19 | 17640526 | |||
chr19:17640550 | G | A | 1 | a0001c0067 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.2748C>T | p.Asn916Asn | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 22/44 | 2903/9985 | 2748/5112 | 916/1703 | chr19 | 17640550 | |||
chr19:17641512 | C | T | 1 | a0001c0042 | 1 | NA19012.hp1 | synonymous_variant | LOW | c.2517G>A | p.Val839Val | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 21/44 | 2672/9985 | 2517/5112 | 839/1703 | chr19 | 17641512 | |||
chr19:17642938 | G | A | 2 | a0001c0056 a0001c0057 |
2 | HG02647.hp1 HG02809.hp1 |
synonymous_variant | LOW | c.2379C>T | p.Ala793Ala | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 20/44 | 2534/9985 | 2379/5112 | 793/1703 | chr19 | 17642938 | |||
chr19:17648480 | G | C | 13 | a0001c0007 a0001c0023 a0001c0024 others(10): Show |
27 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(24): Show |
synonymous_variant | LOW | c.1767C>G | p.Val589Val | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 16/44 | 1922/9985 | 1767/5112 | 589/1703 | chr19 | 17648480 | |||
chr19:17648492 | G | A | 1 | a0001c0030 | 2 | HG01256.hp2 HG01258.hp2 |
synonymous_variant | LOW | c.1755C>T | p.Thr585Thr | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 16/44 | 1910/9985 | 1755/5112 | 585/1703 | chr19 | 17648492 | |||
chr19:17656011 | C | T | 3 | a0001c0014 a0001c0060 a0001c0061 |
5 | NA18944.hp1 NA18952.hp1 NA18962.hp1 others(2): Show |
synonymous_variant | LOW | c.1155G>A | p.Glu385Glu | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 10/44 | 1310/9985 | 1155/5112 | 385/1703 | chr19 | 17656011 | |||
chr19:17656224 | C | T | 1 | a0001c0058 | 1 | NA19011.hp2 | synonymous_variant | LOW | c.942G>A | p.Ser314Ser | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 10/44 | 1097/9985 | 942/5112 | 314/1703 | chr19 | 17656224 | |||
chr19:17658196 | C | T | 1 | a0001c0032 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.633G>A | p.Pro211Pro | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/44 | 788/9985 | 633/5112 | 211/1703 | chr19 | 17658196 | |||
chr19:17666699 | C | G | 52 | a0001c0002 a0001c0003 a0001c0007 others(49): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
synonymous_variant | LOW | c.474G>C | p.Ser158Ser | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/44 | 629/9985 | 474/5112 | 158/1703 | chr19 | 17666699 | |||
chr19:17666699 | C | T | 1 | a0001c0031 | 1 | HG02056.hp2 | synonymous_variant | LOW | c.474G>A | p.Ser158Ser | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/44 | 629/9985 | 474/5112 | 158/1703 | chr19 | 17666699 | |||
chr19:17676031 | G | A | 1 | a0001c0069 | 1 | HG02165.hp2 | synonymous_variant | LOW | c.33C>T | p.Ala11Ala | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/44 | 188/9985 | 33/5112 | 11/1703 | chr19 | 17676031 | |||
chr19:17688193 | G | A | 3 | a0001c0070 a0001c0071 a0001c0072 |
3 | HG02717.hp1 HG02886.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.7C>T | p.Leu3Leu | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/44 | 162/9985 | 7/5112 | 3/1703 | chr19 | 17688193 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:17601343 | G | A | 1 | a0001c0003t0040 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4711C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 4711 | chr19 | 17601343 | ||||||
chr19:17601507 | CAG | C | 6 | a0001c0002t0008 a0001c0002t0044 a0001c0007t0008 others(3): Show |
9 | HG02055.hp1 HG02630.hp2 HG02647.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4545_*4546delCT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 4545 | chr19 | 17601507 | ||||||
chr19:17601565 | T | C | 20 | a0001c0008t0002 a0001c0008t0026 a0001c0016t0002 others(17): Show |
35 | HG00639.hp2 HG00733.hp1 HG01167.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*4489A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 4489 | chr19 | 17601565 | ||||||
chr19:17601615 | C | T | 2 | a0001c0002t0018 a0001c0004t0018 |
3 | HG00735.hp1 HG03041.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4439G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 4439 | chr19 | 17601615 | ||||||
chr19:17601902 | C | T | 10 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0017 others(7): Show |
18 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4152G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 4152 | chr19 | 17601902 | ||||||
chr19:17602127 | C | T | 13 | a0001c0002t0005 a0001c0002t0019 a0001c0002t0020 others(10): Show |
16 | HG00733.hp2 HG00741.hp1 HG01070.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3927G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 3927 | chr19 | 17602127 | ||||||
chr19:17602165 | C | T | 13 | a0001c0002t0005 a0001c0002t0019 a0001c0002t0020 others(10): Show |
16 | HG00733.hp2 HG00741.hp1 HG01070.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3889G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 3889 | chr19 | 17602165 | ||||||
chr19:17602247 | G | A | 13 | a0001c0002t0005 a0001c0002t0019 a0001c0002t0020 others(10): Show |
16 | HG00733.hp2 HG00741.hp1 HG01070.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3807C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 3807 | chr19 | 17602247 | ||||||
chr19:17602252 | T | C | 13 | a0001c0002t0005 a0001c0002t0019 a0001c0002t0020 others(10): Show |
16 | HG00733.hp2 HG00741.hp1 HG01070.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3802A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 3802 | chr19 | 17602252 | ||||||
chr19:17602352 | CCCTCTGT others(33): Show |
C | 1 | a0001c0045t0035 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3662_*3701delCTGA others(36): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 3662 | chr19 | 17602352 | ||||||
chr19:17602493 | G | A | 2 | a0001c0053t0023 a0002c0038t0023 |
2 | HG02257.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3561C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 3561 | chr19 | 17602493 | ||||||
chr19:17602570 | C | T | 1 | a0001c0002t0039 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3484G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 3484 | chr19 | 17602570 | ||||||
chr19:17602594 | C | T | 10 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0017 others(7): Show |
18 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3460G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 3460 | chr19 | 17602594 | ||||||
chr19:17602669 | C | G | 1 | a0001c0002t0012 | 4 | HG01975.hp2 HG02004.hp2 HG02683.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3385G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 3385 | chr19 | 17602669 | ||||||
chr19:17602687 | C | T | 1 | a0001c0050t0033 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3367G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 3367 | chr19 | 17602687 | ||||||
chr19:17602706 | C | A | 5 | a0001c0002t0011 a0001c0002t0032 a0001c0002t0042 others(2): Show |
8 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3348G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 3348 | chr19 | 17602706 | ||||||
chr19:17602735 | C | T | 3 | a0001c0002t0015 a0001c0002t0029 a0001c0007t0015 |
4 | HG03209.hp2 NA18906.hp1 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3319G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 3319 | chr19 | 17602735 | ||||||
chr19:17602858 | A | G | 5 | a0001c0002t0010 a0001c0002t0027 a0001c0004t0010 others(2): Show |
8 | HG01109.hp2 HG01123.hp2 HG02257.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3196T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 3196 | chr19 | 17602858 | ||||||
chr19:17603021 | G | A | 4 | a0001c0002t0015 a0001c0002t0028 a0001c0002t0029 others(1): Show |
5 | HG03139.hp1 HG03209.hp2 NA18906.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3033C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 3033 | chr19 | 17603021 | ||||||
chr19:17603055 | C | T | 2 | a0002c0017t0013 a0003c0010t0013 |
4 | HG00738.hp1 HG01070.hp2 HG01243.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2999G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 2999 | chr19 | 17603055 | ||||||
chr19:17603125 | G | T | 13 | a0001c0002t0005 a0001c0002t0019 a0001c0002t0020 others(10): Show |
16 | HG00733.hp2 HG00741.hp1 HG01070.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2929C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 2929 | chr19 | 17603125 | ||||||
chr19:17603175 | A | C | 18 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0034 others(15): Show |
32 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2879T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 2879 | chr19 | 17603175 | ||||||
chr19:17603219 | A | AAC | 33 | a0001c0001t0004 a0001c0002t0004 a0001c0002t0017 others(30): Show |
57 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*2833_*2834dupGT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 2834 | chr19 | 17603219 | ||||||
chr19:17603219 | A | AACAC | 3 | a0001c0002t0011 a0001c0002t0032 a0001c0004t0011 |
6 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2831_*2834dupGTGT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 2834 | chr19 | 17603219 | ||||||
chr19:17603544 | C | T | 1 | a0001c0004t0041 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2510G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 2510 | chr19 | 17603544 | ||||||
chr19:17603583 | T | C | 2 | a0001c0015t0022 a0001c0029t0022 |
2 | HG02602.hp2 HG03017.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2471A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 2471 | chr19 | 17603583 | ||||||
chr19:17603645 | G | A | 2 | a0001c0002t0042 a0001c0023t0047 |
2 | HG03225.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2409C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 2409 | chr19 | 17603645 | ||||||
chr19:17603744 | T | G | 4 | a0001c0001t0007 a0001c0002t0007 a0001c0003t0007 others(1): Show |
8 | HG00544.hp2 HG00609.hp1 HG02015.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2310A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 2310 | chr19 | 17603744 | ||||||
chr19:17603777 | A | G | 91 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(88): Show |
144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*2277T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 2277 | chr19 | 17603777 | ||||||
chr19:17603797 | A | AT | 11 | a0001c0001t0009 a0001c0002t0009 a0001c0002t0027 others(8): Show |
12 | HG00423.hp2 HG01175.hp1 HG01175.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2256dupA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 2256 | chr19 | 17603797 | ||||||
chr19:17603797 | AT | A | 64 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(61): Show |
108 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*2256delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 2256 | chr19 | 17603797 | ||||||
chr19:17603797 | ATT | A | 11 | a0001c0015t0006 a0001c0015t0022 a0001c0029t0006 others(8): Show |
14 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2255_*2256delAA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 2255 | chr19 | 17603797 | ||||||
chr19:17603872 | T | C | 7 | a0001c0002t0010 a0001c0002t0027 a0001c0004t0010 others(4): Show |
10 | HG01109.hp2 HG01123.hp2 HG02257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2182A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 2182 | chr19 | 17603872 | ||||||
chr19:17603879 | A | G | 1 | a0001c0002t0031 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2175T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 2175 | chr19 | 17603879 | ||||||
chr19:17603880 | C | T | 7 | a0001c0002t0005 a0001c0007t0005 a0001c0020t0005 others(4): Show |
10 | HG00733.hp2 HG00741.hp1 HG01070.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2174G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 2174 | chr19 | 17603880 | ||||||
chr19:17603928 | C | CA | 13 | a0001c0002t0005 a0001c0002t0019 a0001c0002t0020 others(10): Show |
16 | HG00733.hp2 HG00741.hp1 HG01070.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2125dupT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 2125 | chr19 | 17603928 | ||||||
chr19:17604168 | G | C | 11 | a0001c0015t0006 a0001c0015t0022 a0001c0029t0006 others(8): Show |
14 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1886C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 1886 | chr19 | 17604168 | ||||||
chr19:17604169 | C | A | 11 | a0001c0015t0006 a0001c0015t0022 a0001c0029t0006 others(8): Show |
14 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1885G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 1885 | chr19 | 17604169 | ||||||
chr19:17604259 | G | C | 2 | a0001c0004t0021 a0002c0039t0021 |
2 | HG02922.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1795C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 1795 | chr19 | 17604259 | ||||||
chr19:17604374 | T | C | 16 | a0001c0002t0011 a0001c0002t0031 a0001c0002t0032 others(13): Show |
22 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1680A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 1680 | chr19 | 17604374 | ||||||
chr19:17604393 | C | T | 1 | a0001c0001t0034 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1661G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 1661 | chr19 | 17604393 | ||||||
chr19:17604466 | C | A | 1 | a0001c0023t0047 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1588G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 1588 | chr19 | 17604466 | ||||||
chr19:17604818 | G | C | 2 | a0001c0022t0024 a0001c0057t0024 |
2 | HG02647.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1236C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 1236 | chr19 | 17604818 | ||||||
chr19:17604861 | T | TTC | 13 | a0001c0002t0005 a0001c0002t0019 a0001c0002t0020 others(10): Show |
16 | HG00733.hp2 HG00741.hp1 HG01070.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1191_*1192dupGA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 1192 | chr19 | 17604861 | ||||||
chr19:17605047 | G | A | 6 | a0001c0002t0008 a0001c0002t0044 a0001c0007t0008 others(3): Show |
9 | HG02055.hp1 HG02630.hp2 HG02647.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1007C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 1007 | chr19 | 17605047 | ||||||
chr19:17605049 | G | C | 1 | a0001c0002t0012 | 4 | HG01975.hp2 HG02004.hp2 HG02683.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1005C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 1005 | chr19 | 17605049 | ||||||
chr19:17605106 | G | A | 5 | a0001c0001t0004 a0001c0002t0004 a0001c0004t0004 others(2): Show |
13 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*948C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 948 | chr19 | 17605106 | ||||||
chr19:17605181 | A | G | 1 | a0001c0008t0026 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*873T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 873 | chr19 | 17605181 | ||||||
chr19:17605211 | C | T | 1 | a0001c0002t0012 | 4 | HG01975.hp2 HG02004.hp2 HG02683.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*843G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 843 | chr19 | 17605211 | ||||||
chr19:17605414 | TC | T | 1 | a0001c0002t0012 | 4 | HG01975.hp2 HG02004.hp2 HG02683.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*639delG | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 639 | chr19 | 17605414 | ||||||
chr19:17605416 | G | A | 1 | a0001c0002t0029 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*638C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 638 | chr19 | 17605416 | ||||||
chr19:17605444 | G | C | 1 | a0001c0002t0045 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*610C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 610 | chr19 | 17605444 | ||||||
chr19:17605527 | G | A | 11 | a0001c0015t0006 a0001c0015t0022 a0001c0029t0006 others(8): Show |
14 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*527C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 527 | chr19 | 17605527 | ||||||
chr19:17605664 | G | A | 1 | a0001c0001t0046 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*390C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 390 | chr19 | 17605664 | ||||||
chr19:17605749 | T | C | 1 | a0001c0023t0047 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*305A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 305 | chr19 | 17605749 | ||||||
chr19:17605773 | A | G | 17 | a0001c0002t0011 a0001c0002t0012 a0001c0002t0031 others(14): Show |
26 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*281T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 281 | chr19 | 17605773 | ||||||
chr19:17605813 | GT | G | 4 | a0001c0002t0015 a0001c0002t0028 a0001c0002t0029 others(1): Show |
5 | HG03139.hp1 HG03209.hp2 NA18906.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*240delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 240 | chr19 | 17605813 | ||||||
chr19:17605864 | G | A | 1 | a0002c0033t0030 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*190C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 190 | chr19 | 17605864 | ||||||
chr19:17605939 | G | A | 1 | a0001c0003t0048 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*115C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 115 | chr19 | 17605939 | ||||||
chr19:17605985 | C | T | 31 | a0001c0002t0010 a0001c0002t0015 a0001c0002t0027 others(28): Show |
50 | HG00639.hp2 HG00733.hp1 HG01109.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*69G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 44/44 | 69 | chr19 | 17605985 | ||||||
chr19:17688215 | G | A | 6 | a0001c0002t0025 a0001c0004t0049 a0001c0007t0025 others(3): Show |
7 | HG02895.hp2 HG02897.hp2 HG02965.hp2 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-16C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/44 | chr19 | 17688215 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:17606429 | C | T | 7 | a0001c0002t0010g0033 a0001c0002t0010g0069 a0001c0002t0010g0097 others(4): Show |
7 | HG01109.hp2 HG01123.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.4812-75G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17606429 | |||||||
chr19:17606503 | C | G | 8 | a0001c0002t0011g0039 a0001c0002t0011g0064 a0001c0002t0011g0184 others(5): Show |
8 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.4812-149G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17606503 | |||||||
chr19:17606517 | C | T | 8 | a0001c0002t0011g0039 a0001c0002t0011g0064 a0001c0002t0011g0184 others(5): Show |
8 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.4812-163G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17606517 | |||||||
chr19:17606519 | A | G | 14 | a0001c0001t0004g0012 a0001c0001t0004g0244 a0001c0002t0004g0139 others(11): Show |
14 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.4812-165T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17606519 | |||||||
chr19:17606577 | GTTC | G | 5 | a0001c0002t0025g0315 a0002c0005t0001g0051 a0002c0005t0001g0067 others(2): Show |
5 | HG02055.hp2 HG02486.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.4812-226_4812-224d others(5): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17606577 | |||||||
chr19:17606671 | C | A | 1 | a0001c0007t0001g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4812-317G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17606671 | |||||||
chr19:17606672 | CCT | C | 10 | a0001c0002t0010g0033 a0001c0002t0010g0069 a0001c0002t0010g0097 others(7): Show |
10 | HG01109.hp2 HG01123.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.4812-320_4812-319d others(4): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17606672 | |||||||
chr19:17606797 | C | A | 4 | a0001c0002t0012g0017 a0001c0002t0012g0077 a0001c0002t0012g0291 others(1): Show |
4 | HG01975.hp2 HG02004.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.4812-443G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17606797 | |||||||
chr19:17606891 | C | T | 8 | a0001c0001t0007g0223 a0001c0001t0007g0232 a0001c0002t0007g0018 others(5): Show |
8 | HG00544.hp2 HG00609.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.4812-537G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17606891 | |||||||
chr19:17606953 | C | T | 1 | a0001c0007t0001g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4812-599G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17606953 | |||||||
chr19:17607157 | T | C | 16 | a0001c0002t0005g0120 a0001c0002t0019g0092 a0001c0002t0020g0025 others(13): Show |
16 | HG00733.hp2 HG00741.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.4812-803A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17607157 | |||||||
chr19:17607246 | CATTTTTA others(3): Show |
C | 3 | a0001c0001t0004g0012 a0001c0067t0004g0265 a0002c0006t0001g0281 |
3 | HG01081.hp1 HG03704.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.4812-902_4812-893d others(12): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17607246 | |||||||
chr19:17607365 | G | A | 1 | a0001c0003t0001g0255 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4812-1011C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17607365 | |||||||
chr19:17607460 | C | CG | 85 | a0001c0001t0001g0107 a0001c0001t0001g0137 a0001c0001t0001g0143 others(82): Show |
85 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.4812-1107dupC | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17607460 | |||||||
chr19:17607460 | C | CGG | 41 | a0001c0001t0003g0126 a0001c0001t0003g0203 a0001c0001t0003g0225 others(38): Show |
41 | HG00140.hp1 HG00609.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.4812-1108_4812-110 others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17607460 | |||||||
chr19:17607460 | C | CGGG | 19 | a0001c0001t0001g0011 a0001c0001t0034g0304 a0001c0002t0010g0069 others(16): Show |
19 | HG01109.hp2 HG01123.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.4812-1109_4812-110 others(7): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17607460 | |||||||
chr19:17607489 | C | G | 137 | a0001c0001t0003g0126 a0001c0001t0003g0203 a0001c0001t0003g0225 others(134): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.4812-1135G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17607489 | |||||||
chr19:17607568 | G | A | 7 | a0001c0002t0011g0039 a0001c0002t0011g0064 a0001c0002t0011g0184 others(4): Show |
7 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.4812-1214C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17607568 | |||||||
chr19:17607865 | C | A | 3 | a0001c0007t0005g0173 a0002c0009t0005g0182 a0004c0065t0005g0134 |
3 | HG00733.hp2 HG00741.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.4812-1511G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17607865 | |||||||
chr19:17607876 | C | CT | 64 | a0001c0001t0003g0203 a0001c0001t0003g0225 a0001c0001t0003g0271 others(61): Show |
64 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.4812-1523dupA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17607876 | |||||||
chr19:17607876 | C | CTT | 22 | a0001c0001t0007g0232 a0001c0002t0005g0120 a0001c0002t0012g0017 others(19): Show |
22 | HG00733.hp2 HG00741.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.4812-1524_4812-152 others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17607876 | |||||||
chr19:17607876 | CT | C | 13 | a0001c0001t0001g0245 a0001c0002t0018g0103 a0001c0003t0001g0040 others(10): Show |
13 | HG00738.hp2 HG01517.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.4812-1523delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17607876 | |||||||
chr19:17607919 | G | A | 16 | a0001c0002t0005g0120 a0001c0002t0019g0092 a0001c0002t0020g0025 others(13): Show |
16 | HG00733.hp2 HG00741.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.4812-1565C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17607919 | |||||||
chr19:17607920 | C | T | 1 | a0001c0003t0001g0101 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.4812-1566G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17607920 | |||||||
chr19:17607926 | C | T | 1 | a0001c0004t0001g0238 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.4812-1572G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17607926 | |||||||
chr19:17608265 | A | T | 49 | a0001c0002t0010g0033 a0001c0002t0010g0069 a0001c0002t0010g0097 others(46): Show |
49 | HG00639.hp2 HG00733.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.4811+1675T>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17608265 | |||||||
chr19:17608300 | T | C | 6 | a0001c0002t0011g0039 a0001c0002t0011g0064 a0001c0002t0011g0184 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.4811+1640A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17608300 | |||||||
chr19:17608356 | TATAA | T | 5 | a0001c0002t0015g0054 a0001c0002t0028g0047 a0001c0002t0029g0167 others(2): Show |
5 | HG03139.hp1 HG03209.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.4811+1580_4811+158 others(8): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17608356 | |||||||
chr19:17608358 | TAA | T | 7 | a0001c0001t0001g0252 a0001c0003t0001g0031 a0001c0003t0001g0152 others(4): Show |
7 | HG01256.hp2 HG01258.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.4811+1580_4811+158 others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17608358 | |||||||
chr19:17608362 | T | C | 7 | a0001c0001t0001g0252 a0001c0003t0001g0031 a0001c0003t0001g0152 others(4): Show |
7 | HG01256.hp2 HG01258.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.4811+1578A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17608362 | |||||||
chr19:17608373 | T | G | 1 | a0001c0020t0005g0076 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4811+1567A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17608373 | |||||||
chr19:17608375 | TG | T | 8 | a0001c0002t0011g0039 a0001c0002t0011g0064 a0001c0002t0011g0184 others(5): Show |
8 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.4811+1564delC | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17608375 | |||||||
chr19:17608377 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.4811+1563A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17608377 | |||||||
chr19:17608380 | A | G | 1 | a0001c0023t0001g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4811+1560T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17608380 | |||||||
chr19:17608383 | AAT | A | 115 | a0001c0001t0003g0126 a0001c0001t0003g0203 a0001c0001t0003g0225 others(112): Show |
115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.4811+1555_4811+155 others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17608383 | |||||||
chr19:17608385 | T | TATATATA others(16): Show |
16 | a0001c0002t0005g0120 a0001c0002t0019g0092 a0001c0002t0020g0025 others(13): Show |
16 | HG00733.hp2 HG00741.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.4811+1554_4811+155 others(27): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17608385 | |||||||
chr19:17608429 | T | A | 1 | a0001c0004t0009g0186 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.4811+1511A>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17608429 | |||||||
chr19:17608443 | A | C | 1 | a0001c0045t0035g0183 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.4811+1497T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17608443 | |||||||
chr19:17608470 | A | G | 1 | a0001c0004t0001g0219 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.4811+1470T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17608470 | |||||||
chr19:17608484 | T | TATATA | 16 | a0001c0002t0005g0120 a0001c0002t0019g0092 a0001c0002t0020g0025 others(13): Show |
16 | HG00733.hp2 HG00741.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.4811+1451_4811+145 others(9): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17608484 | |||||||
chr19:17608515 | TTATATAA | T | 7 | a0001c0001t0001g0022 a0001c0001t0001g0171 a0001c0003t0001g0117 others(4): Show |
7 | HG01109.hp1 HG01175.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.4811+1418_4811+142 others(11): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17608515 | |||||||
chr19:17608581 | G | A | 16 | a0001c0002t0005g0120 a0001c0002t0019g0092 a0001c0002t0020g0025 others(13): Show |
16 | HG00733.hp2 HG00741.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.4811+1359C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17608581 | |||||||
chr19:17608717 | C | T | 1 | a0001c0001t0046g0197 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.4811+1223G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17608717 | |||||||
chr19:17608725 | C | T | 89 | a0001c0001t0003g0126 a0001c0001t0003g0203 a0001c0001t0003g0225 others(86): Show |
89 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.4811+1215G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17608725 | |||||||
chr19:17608959 | C | CT | 52 | a0001c0001t0003g0225 a0001c0002t0010g0033 a0001c0002t0010g0069 others(49): Show |
52 | HG00438.hp1 HG00639.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.4811+980dupA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17608959 | |||||||
chr19:17609013 | A | G | 1 | a0001c0002t0038g0037 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4811+927T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17609013 | |||||||
chr19:17609050 | C | T | 2 | a0001c0002t0003g0131 a0002c0006t0001g0021 |
2 | HG01978.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.4811+890G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17609050 | |||||||
chr19:17609089 | C | T | 1 | a0001c0002t0038g0037 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4811+851G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17609089 | |||||||
chr19:17609103 | G | A | 5 | a0001c0002t0001g0308 a0001c0007t0001g0042 a0001c0007t0001g0052 others(2): Show |
5 | HG02970.hp1 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.4811+837C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17609103 | |||||||
chr19:17609124 | A | AT | 35 | a0001c0001t0001g0199 a0001c0001t0007g0232 a0001c0002t0001g0308 others(32): Show |
35 | HG00733.hp2 HG01070.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.4811+815dupA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17609124 | |||||||
chr19:17609124 | A | ATTT | 18 | a0001c0001t0004g0012 a0001c0001t0004g0244 a0001c0002t0004g0139 others(15): Show |
18 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(15): Show |
intron_variant | MODIFIER | c.4811+813_4811+815d others(5): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17609124 | |||||||
chr19:17609124 | A | ATTTT | 9 | a0001c0002t0011g0039 a0001c0002t0011g0064 a0001c0002t0011g0184 others(6): Show |
9 | HG01884.hp2 HG01981.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.4811+812_4811+815d others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17609124 | |||||||
chr19:17609124 | AT | A | 66 | a0001c0002t0010g0033 a0001c0002t0010g0069 a0001c0002t0010g0097 others(63): Show |
66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.4811+815delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17609124 | |||||||
chr19:17609278 | C | T | 1 | a0003c0010t0006g0306 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.4811+662G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17609278 | |||||||
chr19:17609355 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.4811+585G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17609355 | |||||||
chr19:17609407 | C | T | 88 | a0001c0001t0003g0126 a0001c0001t0003g0203 a0001c0001t0003g0225 others(85): Show |
88 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.4811+533G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17609407 | |||||||
chr19:17609410 | A | C | 16 | a0001c0002t0005g0120 a0001c0002t0019g0092 a0001c0002t0020g0025 others(13): Show |
16 | HG00733.hp2 HG00741.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.4811+530T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17609410 | |||||||
chr19:17609429 | C | A | 40 | a0001c0001t0003g0126 a0001c0001t0003g0203 a0001c0001t0003g0225 others(37): Show |
40 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.4811+511G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17609429 | |||||||
chr19:17609434 | C | T | 40 | a0001c0001t0003g0126 a0001c0001t0003g0203 a0001c0001t0003g0225 others(37): Show |
40 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.4811+506G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17609434 | |||||||
chr19:17609547 | C | T | 4 | a0001c0001t0001g0145 a0001c0003t0001g0228 a0001c0014t0001g0125 others(1): Show |
4 | HG00673.hp1 NA18944.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.4811+393G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17609547 | |||||||
chr19:17609628 | C | T | 1 | a0001c0002t0001g0106 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.4811+312G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 43/43 | chr19 | 17609628 | |||||||
chr19:17610236 | C | A | 16 | a0001c0002t0005g0120 a0001c0002t0019g0092 a0001c0002t0020g0025 others(13): Show |
16 | HG00733.hp2 HG00741.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.4652-137G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 42/43 | chr19 | 17610236 | |||||||
chr19:17610327 | G | A | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4652-228C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 42/43 | chr19 | 17610327 | |||||||
chr19:17610517 | T | C | 7 | a0001c0002t0010g0033 a0001c0002t0010g0069 a0001c0002t0010g0097 others(4): Show |
7 | HG01109.hp2 HG01123.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.4652-418A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 42/43 | chr19 | 17610517 | |||||||
chr19:17610566 | G | C | 19 | a0001c0001t0004g0012 a0001c0001t0004g0244 a0001c0002t0004g0139 others(16): Show |
19 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.4652-467C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 42/43 | chr19 | 17610566 | |||||||
chr19:17610655 | C | T | 24 | a0001c0001t0003g0126 a0001c0001t0003g0203 a0001c0001t0003g0271 others(21): Show |
24 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.4652-556G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 42/43 | chr19 | 17610655 | |||||||
chr19:17610658 | C | T | 137 | a0001c0001t0003g0126 a0001c0001t0003g0203 a0001c0001t0003g0271 others(134): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.4652-559G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 42/43 | chr19 | 17610658 | |||||||
chr19:17610808 | T | G | 1 | a0002c0006t0006g0278 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4652-709A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 42/43 | chr19 | 17610808 | |||||||
chr19:17610909 | T | C | 16 | a0001c0002t0005g0120 a0001c0002t0019g0092 a0001c0002t0020g0025 others(13): Show |
16 | HG00733.hp2 HG00741.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.4652-810A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 42/43 | chr19 | 17610909 | |||||||
chr19:17610910 | G | A | 11 | a0001c0001t0001g0115 a0001c0001t0001g0136 a0001c0001t0001g0189 others(8): Show |
11 | HG01081.hp2 HG01192.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.4652-811C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 42/43 | chr19 | 17610910 | |||||||
chr19:17610926 | C | T | 1 | a0001c0002t0004g0139 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.4652-827G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 42/43 | chr19 | 17610926 | |||||||
chr19:17610940 | G | C | 24 | a0001c0001t0003g0126 a0001c0001t0003g0203 a0001c0001t0003g0271 others(21): Show |
24 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.4651+823C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 42/43 | chr19 | 17610940 | |||||||
chr19:17610947 | C | T | 16 | a0001c0002t0005g0120 a0001c0002t0019g0092 a0001c0002t0020g0025 others(13): Show |
16 | HG00733.hp2 HG00741.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.4651+816G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 42/43 | chr19 | 17610947 | |||||||
chr19:17611050 | C | T | 45 | a0001c0002t0010g0033 a0001c0002t0010g0069 a0001c0002t0010g0097 others(42): Show |
45 | HG00639.hp2 HG00733.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.4651+713G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 42/43 | chr19 | 17611050 | |||||||
chr19:17611390 | G | A | 3 | a0001c0003t0001g0294 a0001c0064t0001g0048 a0002c0006t0001g0283 |
3 | HG00639.hp1 HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.4651+373C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 42/43 | chr19 | 17611390 | |||||||
chr19:17611602 | A | G | 1 | a0001c0047t0001g0050 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4651+161T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 42/43 | chr19 | 17611602 | |||||||
chr19:17611658 | T | C | 1 | a0001c0004t0041g0111 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4651+105A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 42/43 | chr19 | 17611658 | |||||||
chr19:17611878 | G | A | 1 | a0002c0039t0021g0026 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4559-23C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17611878 | |||||||
chr19:17611918 | C | A | 1 | a0001c0022t0008g0185 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4559-63G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17611918 | |||||||
chr19:17611949 | G | A | 18 | a0001c0001t0001g0174 a0001c0001t0004g0012 a0001c0001t0004g0244 others(15): Show |
18 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(15): Show |
intron_variant | MODIFIER | c.4559-94C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17611949 | |||||||
chr19:17612296 | G | A | 1 | a0001c0002t0028g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4559-441C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17612296 | |||||||
chr19:17612340 | C | T | 1 | a0001c0003t0001g0205 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.4559-485G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17612340 | |||||||
chr19:17612462 | C | T | 6 | a0001c0002t0011g0039 a0001c0002t0011g0064 a0001c0002t0011g0184 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.4559-607G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17612462 | |||||||
chr19:17612487 | T | G | 1 | a0001c0001t0004g0244 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.4559-632A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17612487 | |||||||
chr19:17612565 | C | T | 34 | a0001c0001t0004g0012 a0001c0002t0004g0139 a0001c0002t0004g0215 others(31): Show |
34 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(31): Show |
intron_variant | MODIFIER | c.4559-710G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17612565 | |||||||
chr19:17612739 | G | A | 1 | a0002c0006t0001g0281 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4559-884C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17612739 | |||||||
chr19:17612829 | A | G | 2 | a0001c0004t0021g0073 a0002c0039t0021g0026 |
2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4559-974T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17612829 | |||||||
chr19:17612870 | C | A | 63 | a0001c0002t0003g0068 a0001c0002t0003g0096 a0001c0002t0012g0017 others(60): Show |
63 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.4559-1015G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17612870 | |||||||
chr19:17613030 | A | G | 26 | a0001c0002t0012g0017 a0001c0002t0012g0077 a0001c0002t0012g0291 others(23): Show |
26 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(23): Show |
intron_variant | MODIFIER | c.4559-1175T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17613030 | |||||||
chr19:17613088 | C | T | 2 | a0002c0013t0002g0307 a0002c0033t0030g0141 |
2 | HG00733.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4559-1233G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17613088 | |||||||
chr19:17613114 | C | T | 15 | a0001c0002t0027g0295 a0001c0002t0031g0298 a0001c0008t0002g0075 others(12): Show |
15 | HG01123.hp1 HG01981.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.4559-1259G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17613114 | |||||||
chr19:17613282 | A | T | 41 | a0001c0002t0003g0068 a0001c0002t0003g0096 a0001c0002t0018g0103 others(38): Show |
41 | HG00735.hp1 HG01123.hp1 HG01361.hp1 others(38): Show |
intron_variant | MODIFIER | c.4559-1427T>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17613282 | |||||||
chr19:17613532 | C | T | 2 | a0001c0004t0021g0073 a0002c0039t0021g0026 |
2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4559-1677G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17613532 | |||||||
chr19:17613559 | C | T | 40 | a0001c0002t0003g0068 a0001c0002t0003g0096 a0001c0002t0018g0103 others(37): Show |
40 | HG00735.hp1 HG01123.hp1 HG01361.hp1 others(37): Show |
intron_variant | MODIFIER | c.4559-1704G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17613559 | |||||||
chr19:17613674 | T | C | 1 | a0001c0003t0001g0198 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.4559-1819A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17613674 | |||||||
chr19:17613701 | T | C | 23 | a0001c0002t0012g0017 a0001c0002t0012g0077 a0001c0002t0012g0291 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(20): Show |
intron_variant | MODIFIER | c.4559-1846A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17613701 | |||||||
chr19:17613702 | C | CT | 11 | a0001c0001t0001g0166 a0001c0001t0001g0195 a0001c0001t0001g0199 others(8): Show |
11 | HG00741.hp1 HG01175.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.4559-1848dupA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17613702 | |||||||
chr19:17613702 | CT | C | 13 | a0001c0001t0001g0245 a0001c0001t0003g0203 a0001c0001t0003g0271 others(10): Show |
13 | HG01516.hp2 HG01884.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.4559-1848delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17613702 | |||||||
chr19:17613702 | CTT | C | 10 | a0001c0002t0015g0054 a0001c0002t0029g0167 a0001c0007t0015g0041 others(7): Show |
10 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.4559-1849_4559-184 others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17613702 | |||||||
chr19:17613702 | CTTT | C | 60 | a0001c0002t0003g0068 a0001c0002t0003g0096 a0001c0002t0012g0017 others(57): Show |
60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.4559-1850_4559-184 others(7): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17613702 | |||||||
chr19:17613702 | CTTTTTTT | C | 22 | a0001c0001t0001g0011 a0001c0001t0007g0223 a0001c0001t0007g0232 others(19): Show |
22 | HG00099.hp1 HG00544.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.4559-1854_4559-184 others(11): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17613702 | |||||||
chr19:17613710 | T | C | 61 | a0001c0002t0003g0068 a0001c0002t0003g0096 a0001c0002t0012g0017 others(58): Show |
61 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.4559-1855A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17613710 | |||||||
chr19:17613711 | T | C | 2 | a0001c0002t0012g0077 a0001c0008t0026g0083 |
2 | HG02683.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.4559-1856A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17613711 | |||||||
chr19:17613747 | G | A | 40 | a0001c0002t0003g0068 a0001c0002t0003g0096 a0001c0002t0018g0103 others(37): Show |
40 | HG00735.hp1 HG01123.hp1 HG01361.hp1 others(37): Show |
intron_variant | MODIFIER | c.4559-1892C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17613747 | |||||||
chr19:17613755 | G | A | 8 | a0001c0002t0019g0092 a0001c0002t0020g0025 a0001c0011t0020g0035 others(5): Show |
8 | HG00733.hp2 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.4559-1900C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17613755 | |||||||
chr19:17613807 | C | T | 9 | a0001c0002t0003g0068 a0001c0002t0003g0096 a0001c0002t0018g0103 others(6): Show |
9 | HG00735.hp1 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.4559-1952G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17613807 | |||||||
chr19:17613957 | G | A | 1 | a0002c0059t0009g0121 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.4559-2102C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17613957 | |||||||
chr19:17614027 | G | A | 10 | a0001c0002t0015g0054 a0001c0002t0029g0167 a0001c0007t0015g0041 others(7): Show |
10 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.4559-2172C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17614027 | |||||||
chr19:17614043 | G | C | 2 | a0001c0053t0023g0053 a0002c0038t0023g0084 |
2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4559-2188C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17614043 | |||||||
chr19:17614092 | G | A | 1 | a0008c0035t0001g0002 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4559-2237C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17614092 | |||||||
chr19:17614116 | C | G | 6 | a0001c0011t0001g0089 a0001c0011t0001g0156 a0001c0011t0001g0300 others(3): Show |
6 | HG01361.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.4559-2261G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17614116 | |||||||
chr19:17614328 | A | T | 1 | a0001c0002t0028g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4559-2473T>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17614328 | |||||||
chr19:17614394 | G | C | 31 | a0001c0002t0003g0068 a0001c0002t0003g0096 a0001c0002t0012g0017 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.4559-2539C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17614394 | |||||||
chr19:17614552 | A | G | 37 | a0001c0001t0034g0304 a0001c0002t0001g0308 a0001c0002t0012g0017 others(34): Show |
37 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(34): Show |
intron_variant | MODIFIER | c.4559-2697T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17614552 | |||||||
chr19:17614579 | A | C | 8 | a0001c0001t0007g0223 a0001c0001t0007g0232 a0001c0002t0007g0018 others(5): Show |
8 | HG00544.hp2 HG00609.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.4559-2724T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17614579 | |||||||
chr19:17614586 | G | A | 2 | a0002c0005t0004g0118 a0002c0005t0004g0119 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.4559-2731C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17614586 | |||||||
chr19:17614796 | C | A | 1 | a0001c0001t0001g0262 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.4558+2906G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17614796 | |||||||
chr19:17614828 | C | T | 1 | a0001c0002t0003g0068 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4558+2874G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17614828 | |||||||
chr19:17614843 | C | T | 1 | a0001c0004t0007g0151 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4558+2859G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17614843 | |||||||
chr19:17614885 | C | T | 1 | a0002c0005t0020g0088 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4558+2817G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17614885 | |||||||
chr19:17614957 | G | C | 1 | a0004c0049t0006g0293 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.4558+2745C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17614957 | |||||||
chr19:17614958 | G | C | 3 | a0001c0002t0038g0037 a0001c0053t0023g0053 a0002c0038t0023g0084 |
3 | HG02257.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4558+2744C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17614958 | |||||||
chr19:17615030 | C | T | 3 | a0001c0002t0038g0037 a0001c0053t0023g0053 a0002c0038t0023g0084 |
3 | HG02257.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4558+2672G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17615030 | |||||||
chr19:17615055 | C | A | 18 | a0001c0002t0012g0017 a0001c0002t0012g0077 a0001c0002t0012g0291 others(15): Show |
18 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.4558+2647G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17615055 | |||||||
chr19:17615101 | G | A | 4 | a0001c0002t0038g0037 a0001c0022t0024g0061 a0001c0053t0023g0053 others(1): Show |
4 | HG02257.hp1 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.4558+2601C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17615101 | |||||||
chr19:17615113 | G | C | 1 | a0001c0001t0001g0252 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.4558+2589C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17615113 | |||||||
chr19:17615132 | G | C | 23 | a0001c0002t0008g0027 a0001c0002t0008g0046 a0001c0002t0008g0284 others(20): Show |
23 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.4558+2570C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17615132 | |||||||
chr19:17615177 | A | C | 4 | a0001c0002t0015g0054 a0001c0002t0029g0167 a0001c0007t0015g0041 others(1): Show |
4 | HG03209.hp2 NA18906.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.4558+2525T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17615177 | |||||||
chr19:17615219 | C | T | 1 | a0001c0002t0005g0120 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4558+2483G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17615219 | |||||||
chr19:17615281 | C | T | 39 | a0001c0001t0001g0080 a0001c0001t0001g0107 a0001c0001t0001g0165 others(36): Show |
39 | HG00544.hp1 HG00597.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.4558+2421G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17615281 | |||||||
chr19:17615322 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.4558+2380G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17615322 | |||||||
chr19:17615403 | G | A | 1 | a0001c0002t0003g0127 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4558+2299C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17615403 | |||||||
chr19:17615484 | G | T | 5 | a0001c0002t0003g0096 a0001c0002t0018g0103 a0001c0002t0018g0269 others(2): Show |
5 | HG00735.hp1 HG02886.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.4558+2218C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17615484 | |||||||
chr19:17615507 | C | T | 7 | a0001c0002t0010g0033 a0001c0002t0010g0069 a0001c0002t0010g0097 others(4): Show |
7 | HG01109.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.4558+2195G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17615507 | |||||||
chr19:17615842 | C | T | 1 | a0001c0003t0001g0040 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4558+1860G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17615842 | |||||||
chr19:17615843 | G | A | 1 | a0001c0002t0045g0164 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4558+1859C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17615843 | |||||||
chr19:17615867 | G | A | 2 | a0001c0001t0001g0253 a0002c0006t0016g0289 |
2 | HG00280.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.4558+1835C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17615867 | |||||||
chr19:17615871 | G | A | 10 | a0001c0002t0038g0037 a0001c0011t0001g0089 a0001c0011t0001g0156 others(7): Show |
10 | HG01123.hp2 HG01361.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.4558+1831C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17615871 | |||||||
chr19:17615973 | A | AAAT | 72 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(69): Show |
72 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.4558+1726_4558+172 others(7): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17615973 | |||||||
chr19:17616000 | T | G | 27 | a0001c0002t0008g0027 a0001c0002t0008g0046 a0001c0002t0008g0284 others(24): Show |
27 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.4558+1702A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17616000 | |||||||
chr19:17616128 | GACA | G | 5 | a0001c0002t0003g0096 a0001c0002t0018g0103 a0001c0002t0018g0269 others(2): Show |
5 | HG00735.hp1 HG02886.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.4558+1571_4558+157 others(7): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17616128 | |||||||
chr19:17616184 | A | G | 2 | a0001c0003t0001g0205 a0001c0003t0001g0292 |
2 | HG03710.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.4558+1518T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17616184 | |||||||
chr19:17616258 | C | T | 1 | a0001c0022t0024g0061 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4558+1444G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17616258 | |||||||
chr19:17616261 | G | T | 1 | a0001c0002t0004g0215 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.4558+1441C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17616261 | |||||||
chr19:17616374 | G | A | 1 | a0001c0002t0004g0224 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4558+1328C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17616374 | |||||||
chr19:17616493 | G | A | 1 | a0004c0049t0006g0293 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.4558+1209C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17616493 | |||||||
chr19:17616592 | G | A | 11 | a0001c0002t0038g0037 a0001c0011t0001g0089 a0001c0011t0001g0156 others(8): Show |
11 | HG01123.hp2 HG01361.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.4558+1110C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17616592 | |||||||
chr19:17616684 | G | A | 5 | a0001c0008t0002g0274 a0001c0021t0014g0318 a0001c0021t0014g0319 others(2): Show |
5 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.4558+1018C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17616684 | |||||||
chr19:17616775 | G | T | 2 | a0001c0056t0002g0155 a0001c0057t0024g0233 |
2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4558+927C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17616775 | |||||||
chr19:17616776 | G | T | 2 | a0001c0056t0002g0155 a0001c0057t0024g0233 |
2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4558+926C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17616776 | |||||||
chr19:17616847 | C | G | 2 | a0001c0003t0001g0015 a0002c0006t0001g0021 |
2 | HG01978.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.4558+855G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17616847 | |||||||
chr19:17616847 | C | T | 7 | a0001c0011t0001g0089 a0001c0011t0001g0156 a0001c0011t0001g0300 others(4): Show |
7 | HG01123.hp2 HG01361.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.4558+855G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17616847 | |||||||
chr19:17616915 | G | C | 1 | a0001c0023t0047g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4558+787C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17616915 | |||||||
chr19:17616989 | T | G | 313 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0080 others(310): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.4558+713A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17616989 | |||||||
chr19:17617055 | G | C | 2 | a0001c0004t0021g0073 a0002c0039t0021g0026 |
2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4558+647C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17617055 | |||||||
chr19:17617325 | G | A | 4 | a0001c0002t0012g0017 a0001c0002t0012g0077 a0001c0002t0012g0291 others(1): Show |
4 | HG01975.hp2 HG02004.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.4558+377C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17617325 | |||||||
chr19:17617377 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.4558+325C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17617377 | |||||||
chr19:17617481 | A | C | 2 | a0001c0023t0047g0275 a0001c0050t0033g0085 |
2 | HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.4558+221T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17617481 | |||||||
chr19:17617693 | T | C | 152 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(149): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.4558+9A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 41/43 | chr19 | 17617693 | |||||||
chr19:17617917 | C | A | 19 | a0001c0002t0003g0068 a0001c0002t0027g0295 a0001c0002t0028g0047 others(16): Show |
19 | HG01123.hp1 HG02145.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.4411-68G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 40/43 | chr19 | 17617917 | |||||||
chr19:17618239 | C | T | 3 | a0001c0011t0020g0035 a0001c0023t0001g0045 a0002c0005t0020g0088 |
3 | HG03098.hp1 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.4410+182G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 40/43 | chr19 | 17618239 | |||||||
chr19:17618280 | C | A | 1 | a0001c0002t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4410+141G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 40/43 | chr19 | 17618280 | |||||||
chr19:17618311 | C | T | 125 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(122): Show |
125 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.4410+110G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 40/43 | chr19 | 17618311 | |||||||
chr19:17618339 | C | T | 79 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(76): Show |
79 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.4410+82G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 40/43 | chr19 | 17618339 | |||||||
chr19:17618344 | C | T | 5 | a0001c0002t0003g0096 a0001c0002t0018g0103 a0001c0002t0018g0269 others(2): Show |
5 | HG00735.hp1 HG02886.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.4410+77G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 40/43 | chr19 | 17618344 | |||||||
chr19:17618345 | G | T | 4 | a0001c0002t0015g0054 a0001c0002t0029g0167 a0001c0007t0015g0041 others(1): Show |
4 | HG03209.hp2 NA18906.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.4410+76C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 40/43 | chr19 | 17618345 | |||||||
chr19:17618584 | A | G | 3 | a0001c0002t0038g0037 a0001c0053t0023g0053 a0002c0038t0023g0084 |
3 | HG02257.hp1 HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.4330-83T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 39/43 | chr19 | 17618584 | |||||||
chr19:17618636 | A | G | 8 | a0001c0004t0021g0073 a0001c0008t0002g0274 a0001c0021t0014g0318 others(5): Show |
8 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.4330-135T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 39/43 | chr19 | 17618636 | |||||||
chr19:17618757 | T | C | 18 | a0001c0002t0038g0037 a0001c0004t0021g0073 a0001c0008t0002g0274 others(15): Show |
18 | HG01123.hp2 HG01361.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.4329+149A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 39/43 | chr19 | 17618757 | |||||||
chr19:17618863 | T | TG | 74 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(71): Show |
74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.4329+42dupC | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 39/43 | chr19 | 17618863 | |||||||
chr19:17618881 | G | A | 7 | a0001c0004t0021g0073 a0001c0008t0002g0274 a0001c0021t0014g0318 others(4): Show |
7 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.4329+25C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 39/43 | chr19 | 17618881 | |||||||
chr19:17618894 | C | T | 10 | a0001c0002t0038g0037 a0001c0011t0001g0089 a0001c0011t0001g0156 others(7): Show |
10 | HG01123.hp2 HG01361.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.4329+12G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 39/43 | chr19 | 17618894 | |||||||
chr19:17618978 | T | G | 74 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(71): Show |
74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.4273-16A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17618978 | |||||||
chr19:17619033 | C | T | 10 | a0001c0002t0038g0037 a0001c0011t0001g0089 a0001c0011t0001g0156 others(7): Show |
10 | HG01123.hp2 HG01361.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.4273-71G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619033 | |||||||
chr19:17619122 | G | A | 1 | a0001c0002t0045g0164 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4273-160C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619122 | |||||||
chr19:17619164 | TC | T | 71 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(68): Show |
71 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.4273-203delG | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619164 | |||||||
chr19:17619225 | T | C | 1 | a0001c0014t0001g0125 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.4273-263A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619225 | |||||||
chr19:17619246 | G | A | 9 | a0001c0029t0006g0243 a0001c0064t0001g0048 a0002c0017t0013g0023 others(6): Show |
9 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.4273-284C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619246 | |||||||
chr19:17619247 | G | A | 113 | a0001c0001t0004g0012 a0001c0002t0001g0106 a0001c0002t0001g0113 others(110): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.4273-285C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619247 | |||||||
chr19:17619248 | A | G | 113 | a0001c0001t0004g0012 a0001c0002t0001g0106 a0001c0002t0001g0113 others(110): Show |
113 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.4273-286T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619248 | |||||||
chr19:17619328 | G | A | 2 | a0001c0053t0023g0053 a0002c0038t0023g0084 |
2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4273-366C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619328 | |||||||
chr19:17619332 | G | T | 72 | a0001c0001t0004g0012 a0001c0002t0001g0106 a0001c0002t0001g0113 others(69): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.4273-370C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619332 | |||||||
chr19:17619357 | T | C | 154 | a0001c0001t0004g0012 a0001c0002t0001g0106 a0001c0002t0001g0113 others(151): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.4273-395A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619357 | |||||||
chr19:17619357 | TTCC | T | 14 | a0001c0001t0034g0304 a0001c0002t0001g0001 a0001c0002t0003g0127 others(11): Show |
14 | HG00099.hp1 HG01346.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.4273-398_4273-396d others(5): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619357 | |||||||
chr19:17619370 | A | AG | 82 | a0001c0001t0004g0012 a0001c0002t0001g0106 a0001c0002t0001g0113 others(79): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.4273-409dupC | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619370 | |||||||
chr19:17619379 | C | T | 2 | a0002c0012t0001g0169 a0002c0012t0001g0175 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.4273-417G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619379 | |||||||
chr19:17619435 | TTTC | T | 70 | a0001c0001t0004g0012 a0001c0002t0001g0106 a0001c0002t0001g0113 others(67): Show |
70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.4273-476_4273-474d others(5): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619435 | |||||||
chr19:17619438 | C | CT | 14 | a0001c0002t0004g0139 a0001c0002t0004g0215 a0001c0002t0004g0227 others(11): Show |
14 | HG00558.hp1 HG00558.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.4273-477dupA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619438 | |||||||
chr19:17619438 | CT | C | 27 | a0001c0002t0008g0027 a0001c0002t0008g0046 a0001c0002t0008g0284 others(24): Show |
27 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.4273-477delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619438 | |||||||
chr19:17619438 | CTT | C | 43 | a0001c0002t0003g0068 a0001c0002t0003g0096 a0001c0002t0018g0103 others(40): Show |
43 | HG00642.hp1 HG00735.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.4273-478_4273-477d others(4): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619438 | |||||||
chr19:17619438 | CTTT | C | 8 | a0001c0004t0021g0073 a0001c0008t0002g0274 a0001c0021t0014g0318 others(5): Show |
8 | HG02258.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.4273-479_4273-477d others(5): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619438 | |||||||
chr19:17619472 | G | C | 72 | a0001c0001t0004g0012 a0001c0002t0001g0106 a0001c0002t0001g0113 others(69): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.4273-510C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619472 | |||||||
chr19:17619549 | C | T | 2 | a0001c0002t0009g0176 a0002c0005t0001g0285 |
2 | HG01175.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.4273-587G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619549 | |||||||
chr19:17619631 | T | C | 71 | a0001c0001t0004g0012 a0001c0002t0001g0106 a0001c0002t0001g0113 others(68): Show |
71 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.4273-669A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619631 | |||||||
chr19:17619712 | C | T | 3 | a0001c0011t0020g0035 a0001c0023t0001g0045 a0002c0005t0020g0088 |
3 | HG03098.hp1 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.4273-750G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619712 | |||||||
chr19:17619780 | T | C | 63 | a0001c0001t0004g0012 a0001c0002t0003g0068 a0001c0002t0015g0054 others(60): Show |
63 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.4273-818A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619780 | |||||||
chr19:17619784 | C | T | 3 | a0001c0011t0020g0035 a0001c0023t0001g0045 a0002c0005t0020g0088 |
3 | HG03098.hp1 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.4273-822G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619784 | |||||||
chr19:17619802 | C | A | 1 | a0001c0001t0001g0080 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.4273-840G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619802 | |||||||
chr19:17619899 | G | T | 4 | a0001c0011t0020g0035 a0001c0023t0001g0045 a0001c0023t0047g0275 others(1): Show |
4 | HG03098.hp1 HG03130.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.4272+794C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619899 | |||||||
chr19:17619964 | T | A | 1 | a0001c0001t0001g0011 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4272+729A>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17619964 | |||||||
chr19:17620026 | C | T | 3 | a0001c0002t0004g0139 a0001c0002t0004g0215 a0001c0004t0004g0188 |
3 | HG00558.hp1 HG02074.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.4272+667G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17620026 | |||||||
chr19:17620040 | G | A | 21 | a0001c0001t0004g0012 a0001c0002t0015g0054 a0001c0002t0029g0167 others(18): Show |
21 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.4272+653C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17620040 | |||||||
chr19:17620046 | G | A | 2 | a0001c0001t0001g0253 a0002c0006t0016g0289 |
2 | HG00280.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.4272+647C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17620046 | |||||||
chr19:17620072 | C | G | 1 | a0001c0001t0001g0011 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4272+621G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17620072 | |||||||
chr19:17620266 | G | A | 3 | a0001c0008t0002g0034 a0001c0008t0002g0071 a0001c0008t0002g0095 |
3 | HG01167.hp2 HG01169.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.4272+427C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17620266 | |||||||
chr19:17620283 | A | G | 79 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(76): Show |
79 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(76): Show |
intron_variant | MODIFIER | c.4272+410T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17620283 | |||||||
chr19:17620336 | A | T | 136 | a0001c0001t0004g0012 a0001c0002t0001g0106 a0001c0002t0001g0113 others(133): Show |
136 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.4272+357T>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17620336 | |||||||
chr19:17620452 | C | A | 5 | a0001c0002t0025g0315 a0002c0005t0001g0051 a0002c0005t0001g0067 others(2): Show |
5 | HG02055.hp2 HG02486.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.4272+241G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17620452 | |||||||
chr19:17620462 | C | T | 1 | a0002c0013t0002g0078 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4272+231G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 38/43 | chr19 | 17620462 | |||||||
chr19:17620863 | C | G | 1 | a0001c0002t0027g0295 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4243-141G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 37/43 | chr19 | 17620863 | |||||||
chr19:17620887 | G | T | 2 | a0001c0002t0003g0096 a0001c0072t0003g0312 |
2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4243-165C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 37/43 | chr19 | 17620887 | |||||||
chr19:17620907 | G | C | 19 | a0001c0002t0003g0068 a0001c0002t0028g0047 a0001c0002t0031g0298 others(16): Show |
19 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.4243-185C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 37/43 | chr19 | 17620907 | |||||||
chr19:17620910 | G | A | 1 | a0001c0002t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4243-188C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 37/43 | chr19 | 17620910 | |||||||
chr19:17620963 | A | T | 1 | a0009c0043t0001g0202 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.4243-241T>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 37/43 | chr19 | 17620963 | |||||||
chr19:17621160 | C | A | 1 | a0001c0004t0041g0111 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4243-438G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 37/43 | chr19 | 17621160 | |||||||
chr19:17621268 | G | T | 1 | a0002c0017t0001g0086 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4243-546C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 37/43 | chr19 | 17621268 | |||||||
chr19:17621764 | G | A | 1 | a0001c0002t0001g0193 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.4242+68C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 37/43 | chr19 | 17621764 | |||||||
chr19:17622042 | C | T | 7 | a0001c0011t0001g0089 a0001c0011t0001g0156 a0001c0011t0001g0300 others(4): Show |
7 | HG01123.hp2 HG01361.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.4204-172G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 36/43 | chr19 | 17622042 | |||||||
chr19:17622067 | C | G | 1 | a0002c0009t0005g0182 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4204-197G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 36/43 | chr19 | 17622067 | |||||||
chr19:17622075 | G | C | 5 | a0001c0002t0025g0315 a0002c0005t0001g0051 a0002c0005t0001g0067 others(2): Show |
5 | HG02055.hp2 HG02486.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.4204-205C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 36/43 | chr19 | 17622075 | |||||||
chr19:17622096 | AAGAG | A | 14 | a0001c0002t0004g0139 a0001c0002t0004g0215 a0001c0002t0004g0227 others(11): Show |
14 | HG00558.hp1 HG00558.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.4204-230_4204-227d others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 36/43 | chr19 | 17622096 | |||||||
chr19:17622306 | C | T | 2 | a0001c0056t0002g0155 a0001c0057t0024g0233 |
2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.4204-436G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 36/43 | chr19 | 17622306 | |||||||
chr19:17622329 | C | T | 3 | a0001c0002t0003g0096 a0001c0002t0027g0295 a0001c0072t0003g0312 |
3 | HG02559.hp1 HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4204-459G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 36/43 | chr19 | 17622329 | |||||||
chr19:17622396 | C | G | 1 | a0002c0019t0003g0074 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4204-526G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 36/43 | chr19 | 17622396 | |||||||
chr19:17622424 | G | C | 1 | a0001c0011t0001g0300 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4204-554C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 36/43 | chr19 | 17622424 | |||||||
chr19:17622604 | G | C | 1 | a0001c0002t0029g0167 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4204-734C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 36/43 | chr19 | 17622604 | |||||||
chr19:17622651 | T | TCAC | 4 | a0001c0002t0015g0054 a0001c0002t0029g0167 a0001c0007t0015g0041 others(1): Show |
4 | HG03209.hp2 NA18906.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.4204-784_4204-782d others(5): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 36/43 | chr19 | 17622651 | |||||||
chr19:17622651 | TCAC | T | 3 | a0001c0008t0002g0276 a0001c0008t0002g0277 a0001c0063t0002g0104 |
3 | HG02896.hp2 HG02897.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4204-784_4204-782d others(5): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 36/43 | chr19 | 17622651 | |||||||
chr19:17622651 | TCACCACC others(5): Show |
T | 2 | a0001c0002t0003g0096 a0001c0072t0003g0312 |
2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4204-793_4204-782d others(14): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 36/43 | chr19 | 17622651 | |||||||
chr19:17622803 | G | T | 1 | a0001c0002t0027g0295 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4203+739C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 36/43 | chr19 | 17622803 | |||||||
chr19:17622908 | C | T | 6 | a0001c0008t0002g0034 a0001c0008t0002g0071 a0001c0008t0002g0095 others(3): Show |
6 | HG01167.hp2 HG01169.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.4203+634G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 36/43 | chr19 | 17622908 | |||||||
chr19:17623109 | G | A | 1 | a0002c0039t0021g0026 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4203+433C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 36/43 | chr19 | 17623109 | |||||||
chr19:17623146 | A | C | 1 | a0001c0004t0041g0111 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4203+396T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 36/43 | chr19 | 17623146 | |||||||
chr19:17623147 | G | C | 1 | a0001c0004t0041g0111 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4203+395C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 36/43 | chr19 | 17623147 | |||||||
chr19:17623225 | G | A | 4 | a0001c0002t0015g0054 a0001c0002t0029g0167 a0001c0007t0015g0041 others(1): Show |
4 | HG03209.hp2 NA18906.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.4203+317C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 36/43 | chr19 | 17623225 | |||||||
chr19:17623387 | G | A | 4 | a0001c0002t0015g0054 a0001c0002t0029g0167 a0001c0007t0015g0041 others(1): Show |
4 | HG03209.hp2 NA18906.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.4203+155C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 36/43 | chr19 | 17623387 | |||||||
chr19:17623587 | G | A | 3 | a0001c0002t0003g0096 a0001c0002t0027g0295 a0001c0072t0003g0312 |
3 | HG02559.hp1 HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4198-40C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 35/43 | chr19 | 17623587 | |||||||
chr19:17623667 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.4198-120C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 35/43 | chr19 | 17623667 | |||||||
chr19:17623679 | A | G | 239 | a0001c0001t0001g0022 a0001c0001t0001g0137 a0001c0001t0001g0171 others(236): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.4198-132T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 35/43 | chr19 | 17623679 | |||||||
chr19:17623741 | T | G | 48 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(45): Show |
48 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.4198-194A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 35/43 | chr19 | 17623741 | |||||||
chr19:17623825 | C | T | 37 | a0001c0001t0004g0012 a0001c0002t0003g0068 a0001c0002t0028g0047 others(34): Show |
37 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.4198-278G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 35/43 | chr19 | 17623825 | |||||||
chr19:17624039 | C | T | 93 | a0001c0001t0004g0012 a0001c0002t0001g0106 a0001c0002t0001g0113 others(90): Show |
93 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.4198-492G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 35/43 | chr19 | 17624039 | |||||||
chr19:17624122 | C | CT | 17 | a0001c0002t0001g0178 a0001c0002t0008g0027 a0001c0002t0008g0046 others(14): Show |
17 | HG00735.hp1 HG01168.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.4198-576dupA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 35/43 | chr19 | 17624122 | |||||||
chr19:17624122 | C | CTT | 47 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(44): Show |
47 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.4198-577_4198-576d others(4): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 35/43 | chr19 | 17624122 | |||||||
chr19:17624134 | TG | T | 8 | a0001c0002t0045g0164 a0001c0008t0002g0095 a0001c0021t0014g0318 others(5): Show |
8 | HG01169.hp2 HG01516.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.4198-588delC | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 35/43 | chr19 | 17624134 | |||||||
chr19:17624135 | G | T | 137 | a0001c0001t0004g0012 a0001c0002t0001g0106 a0001c0002t0001g0113 others(134): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.4198-588C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 35/43 | chr19 | 17624135 | |||||||
chr19:17624273 | C | T | 6 | a0001c0001t0003g0126 a0001c0001t0003g0203 a0001c0001t0003g0271 others(3): Show |
6 | HG02080.hp2 NA18952.hp2 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.4197+556G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 35/43 | chr19 | 17624273 | |||||||
chr19:17624366 | G | A | 1 | a0001c0002t0042g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4197+463C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 35/43 | chr19 | 17624366 | |||||||
chr19:17624461 | A | G | 48 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(45): Show |
48 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.4197+368T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 35/43 | chr19 | 17624461 | |||||||
chr19:17624490 | G | A | 1 | a0001c0002t0038g0037 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4197+339C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 35/43 | chr19 | 17624490 | |||||||
chr19:17624629 | T | C | 48 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(45): Show |
48 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.4197+200A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 35/43 | chr19 | 17624629 | |||||||
chr19:17624630 | G | T | 1 | a0001c0002t0045g0164 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4197+199C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 35/43 | chr19 | 17624630 | |||||||
chr19:17624777 | T | C | 1 | a0001c0003t0001g0205 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.4197+52A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 35/43 | chr19 | 17624777 | |||||||
chr19:17624822 | G | A | 3 | a0001c0007t0005g0173 a0002c0009t0005g0182 a0002c0033t0030g0141 |
3 | HG00741.hp1 HG03831.hp2 HG06807.hp1 |
splice_region_variant&intron_variant | LOW | c.4197+7C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 35/43 | chr19 | 17624822 | |||||||
chr19:17624974 | G | A | 8 | a0001c0008t0002g0274 a0001c0011t0020g0035 a0001c0021t0014g0318 others(5): Show |
8 | HG02258.hp2 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.4074-22C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17624974 | |||||||
chr19:17625159 | T | C | 48 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(45): Show |
48 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.4074-207A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17625159 | |||||||
chr19:17625174 | A | G | 2 | a0001c0002t0009g0176 a0002c0005t0001g0285 |
2 | HG01175.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.4074-222T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17625174 | |||||||
chr19:17625191 | T | G | 16 | a0001c0001t0004g0012 a0001c0015t0006g0090 a0001c0015t0006g0303 others(13): Show |
16 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.4074-239A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17625191 | |||||||
chr19:17625215 | G | C | 1 | a0001c0002t0045g0164 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4074-263C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17625215 | |||||||
chr19:17625334 | C | T | 9 | a0001c0001t0001g0145 a0001c0001t0001g0235 a0001c0003t0001g0130 others(6): Show |
9 | HG00673.hp1 HG02165.hp2 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.4074-382G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17625334 | |||||||
chr19:17625374 | C | A | 2 | a0001c0055t0001g0102 a0002c0040t0014g0316 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4074-422G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17625374 | |||||||
chr19:17625449 | G | C | 2 | a0001c0002t0010g0033 a0001c0007t0001g0062 |
2 | HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.4074-497C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17625449 | |||||||
chr19:17625830 | C | T | 1 | a0001c0023t0047g0275 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4073+803G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17625830 | |||||||
chr19:17625842 | C | CATTT | 48 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(45): Show |
48 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.4073+790_4073+791i others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17625842 | |||||||
chr19:17625933 | TCATC | T | 48 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(45): Show |
48 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.4073+696_4073+699d others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17625933 | |||||||
chr19:17626135 | A | G | 48 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(45): Show |
48 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.4073+498T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17626135 | |||||||
chr19:17626150 | T | TATCC | 24 | a0001c0001t0001g0137 a0001c0001t0001g0190 a0001c0001t0001g0216 others(21): Show |
24 | HG00597.hp2 HG01081.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.4073+479_4073+482d others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17626150 | |||||||
chr19:17626150 | T | TATCCATC others(1): Show |
3 | a0001c0001t0001g0249 a0001c0056t0002g0155 a0001c0057t0024g0233 |
3 | HG02647.hp1 HG02809.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.4073+475_4073+482d others(10): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17626150 | |||||||
chr19:17626150 | TATCC | T | 88 | a0001c0001t0001g0115 a0001c0001t0001g0136 a0001c0001t0001g0143 others(85): Show |
88 | HG00423.hp2 HG00738.hp1 HG00741.hp1 others(85): Show |
intron_variant | MODIFIER | c.4073+479_4073+482d others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17626150 | |||||||
chr19:17626171 | A | ATCCG | 6 | a0001c0002t0038g0037 a0001c0027t0002g0044 a0001c0027t0014g0314 others(3): Show |
6 | HG02257.hp1 HG02572.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.4073+461_4073+462i others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17626171 | |||||||
chr19:17626230 | A | C | 13 | a0001c0002t0038g0037 a0001c0011t0001g0089 a0001c0011t0001g0156 others(10): Show |
13 | HG01123.hp2 HG01361.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.4073+403T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17626230 | |||||||
chr19:17626237 | C | T | 48 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(45): Show |
48 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.4073+396G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17626237 | |||||||
chr19:17626316 | C | T | 48 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(45): Show |
48 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.4073+317G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17626316 | |||||||
chr19:17626396 | CAT | C | 16 | a0001c0001t0004g0012 a0001c0015t0006g0090 a0001c0015t0006g0303 others(13): Show |
16 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(13): Show |
intron_variant | MODIFIER | c.4073+235_4073+236d others(4): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17626396 | |||||||
chr19:17626446 | C | G | 48 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(45): Show |
48 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.4073+187G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17626446 | |||||||
chr19:17626626 | A | G | 48 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(45): Show |
48 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(45): Show |
splice_region_variant&intron_variant | LOW | c.4073+7T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 34/43 | chr19 | 17626626 | |||||||
chr19:17626841 | G | A | 48 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(45): Show |
48 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.3921-56C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 33/43 | chr19 | 17626841 | |||||||
chr19:17626969 | G | A | 5 | a0001c0002t0011g0039 a0001c0002t0011g0064 a0001c0002t0011g0184 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.3921-184C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 33/43 | chr19 | 17626969 | |||||||
chr19:17627164 | C | CA | 14 | a0001c0001t0001g0194 a0001c0002t0003g0096 a0001c0002t0008g0027 others(11): Show |
14 | HG01433.hp2 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.3920+344dupT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 33/43 | chr19 | 17627164 | |||||||
chr19:17627164 | CA | C | 18 | a0001c0001t0001g0270 a0001c0001t0004g0012 a0001c0002t0042g0038 others(15): Show |
18 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.3920+344delT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 33/43 | chr19 | 17627164 | |||||||
chr19:17627437 | C | T | 2 | a0001c0024t0019g0100 a0001c0066t0019g0043 |
2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3920+72G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 33/43 | chr19 | 17627437 | |||||||
chr19:17627486 | C | T | 13 | a0001c0002t0038g0037 a0001c0011t0001g0089 a0001c0011t0001g0156 others(10): Show |
13 | HG01123.hp2 HG01361.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3920+23G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 33/43 | chr19 | 17627486 | |||||||
chr19:17627626 | G | A | 2 | a0001c0002t0003g0096 a0001c0072t0003g0312 |
2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3832-29C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 32/43 | chr19 | 17627626 | |||||||
chr19:17627657 | T | C | 48 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(45): Show |
48 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.3832-60A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 32/43 | chr19 | 17627657 | |||||||
chr19:17627707 | G | T | 8 | a0001c0008t0002g0274 a0001c0011t0020g0035 a0001c0021t0014g0318 others(5): Show |
8 | HG02258.hp2 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.3832-110C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 32/43 | chr19 | 17627707 | |||||||
chr19:17627718 | C | A | 38 | a0001c0002t0003g0096 a0001c0002t0008g0027 a0001c0002t0008g0046 others(35): Show |
38 | HG00735.hp1 HG01109.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.3832-121G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 32/43 | chr19 | 17627718 | |||||||
chr19:17627718 | C | G | 1 | a0001c0008t0002g0274 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3832-121G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 32/43 | chr19 | 17627718 | |||||||
chr19:17627849 | C | T | 7 | a0001c0044t0001g0301 a0001c0050t0033g0085 a0002c0012t0001g0124 others(4): Show |
7 | HG00642.hp1 HG00735.hp2 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.3831+14G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 32/43 | chr19 | 17627849 | |||||||
chr19:17627968 | A | C | 13 | a0001c0002t0038g0037 a0001c0011t0001g0089 a0001c0011t0001g0156 others(10): Show |
13 | HG01123.hp2 HG01361.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3754-28T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 31/43 | chr19 | 17627968 | |||||||
chr19:17627977 | G | A | 7 | a0001c0011t0001g0089 a0001c0011t0001g0156 a0001c0011t0001g0300 others(4): Show |
7 | HG01123.hp2 HG01361.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.3754-37C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 31/43 | chr19 | 17627977 | |||||||
chr19:17628041 | C | T | 144 | a0001c0001t0004g0012 a0001c0002t0001g0106 a0001c0002t0001g0113 others(141): Show |
144 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.3754-101G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 31/43 | chr19 | 17628041 | |||||||
chr19:17628108 | G | GGCGTGTT others(12): Show |
1 | a0001c0028t0002g0082 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3754-187_3754-169d others(21): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 31/43 | chr19 | 17628108 | |||||||
chr19:17628111 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3754-171C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 31/43 | chr19 | 17628111 | |||||||
chr19:17628257 | A | G | 1 | a0006c0025t0001g0087 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3754-317T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 31/43 | chr19 | 17628257 | |||||||
chr19:17628412 | C | T | 179 | a0001c0001t0004g0012 a0001c0002t0001g0001 a0001c0002t0001g0106 others(176): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.3754-472G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 31/43 | chr19 | 17628412 | |||||||
chr19:17628521 | C | T | 164 | a0001c0001t0004g0012 a0001c0002t0001g0001 a0001c0002t0001g0106 others(161): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.3754-581G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 31/43 | chr19 | 17628521 | |||||||
chr19:17628529 | C | T | 44 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(41): Show |
44 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.3754-589G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 31/43 | chr19 | 17628529 | |||||||
chr19:17628597 | C | A | 1 | a0003c0010t0001g0070 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3753+643G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 31/43 | chr19 | 17628597 | |||||||
chr19:17628729 | T | C | 1 | a0001c0002t0042g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3753+511A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 31/43 | chr19 | 17628729 | |||||||
chr19:17628762 | T | C | 4 | a0001c0002t0015g0054 a0001c0002t0029g0167 a0001c0007t0015g0041 others(1): Show |
4 | HG03209.hp2 NA18906.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.3753+478A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 31/43 | chr19 | 17628762 | |||||||
chr19:17629108 | C | T | 45 | a0001c0002t0003g0096 a0001c0002t0008g0027 a0001c0002t0008g0046 others(42): Show |
45 | HG00735.hp1 HG01109.hp2 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.3753+132G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 31/43 | chr19 | 17629108 | |||||||
chr19:17629167 | T | C | 86 | a0001c0002t0001g0001 a0001c0002t0003g0068 a0001c0002t0003g0096 others(83): Show |
86 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.3753+73A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 31/43 | chr19 | 17629167 | |||||||
chr19:17629225 | G | A | 1 | a0001c0022t0024g0061 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3753+15C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 31/43 | chr19 | 17629225 | |||||||
chr19:17629376 | G | A | 1 | a0001c0004t0041g0111 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3670-53C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 30/43 | chr19 | 17629376 | |||||||
chr19:17629408 | C | T | 13 | a0001c0002t0038g0037 a0001c0011t0001g0089 a0001c0011t0001g0156 others(10): Show |
13 | HG01123.hp2 HG01361.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3670-85G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 30/43 | chr19 | 17629408 | |||||||
chr19:17629447 | C | T | 13 | a0001c0002t0038g0037 a0001c0011t0001g0089 a0001c0011t0001g0156 others(10): Show |
13 | HG01123.hp2 HG01361.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3670-124G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 30/43 | chr19 | 17629447 | |||||||
chr19:17629475 | G | T | 4 | a0001c0002t0038g0037 a0001c0027t0002g0044 a0001c0027t0014g0314 others(1): Show |
4 | HG02572.hp2 HG03195.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.3670-152C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 30/43 | chr19 | 17629475 | |||||||
chr19:17629507 | C | T | 3 | a0001c0003t0001g0129 a0001c0053t0023g0053 a0002c0038t0023g0084 |
3 | HG02257.hp1 HG03471.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.3670-184G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 30/43 | chr19 | 17629507 | |||||||
chr19:17629592 | C | T | 13 | a0001c0002t0038g0037 a0001c0011t0001g0089 a0001c0011t0001g0156 others(10): Show |
13 | HG01123.hp2 HG01361.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3670-269G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 30/43 | chr19 | 17629592 | |||||||
chr19:17629660 | A | C | 3 | a0001c0002t0004g0139 a0001c0002t0004g0215 a0001c0004t0004g0188 |
3 | HG00558.hp1 HG02074.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.3670-337T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 30/43 | chr19 | 17629660 | |||||||
chr19:17629755 | C | T | 1 | a0001c0023t0001g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3669+390G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 30/43 | chr19 | 17629755 | |||||||
chr19:17629794 | A | G | 5 | a0001c0002t0015g0054 a0001c0002t0029g0167 a0001c0007t0015g0041 others(2): Show |
5 | HG02559.hp2 HG03209.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.3669+351T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 30/43 | chr19 | 17629794 | |||||||
chr19:17629892 | TCAACTCC others(23): Show |
T | 48 | a0001c0002t0001g0106 a0001c0002t0001g0113 a0001c0002t0001g0157 others(45): Show |
48 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.3669+223_3669+252d others(32): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 30/43 | chr19 | 17629892 | |||||||
chr19:17630083 | A | G | 9 | a0001c0011t0001g0089 a0001c0011t0001g0156 a0001c0011t0001g0300 others(6): Show |
9 | HG01123.hp2 HG01361.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.3669+62T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 30/43 | chr19 | 17630083 | |||||||
chr19:17630535 | T | C | 8 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0012g0017 others(5): Show |
8 | HG01975.hp2 HG02004.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.3525+119A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 29/43 | chr19 | 17630535 | |||||||
chr19:17630613 | G | A | 47 | a0001c0002t0001g0308 a0001c0002t0003g0096 a0001c0002t0008g0027 others(44): Show |
47 | HG00642.hp1 HG00735.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.3525+41C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 29/43 | chr19 | 17630613 | |||||||
chr19:17630869 | T | C | 2 | a0001c0023t0001g0045 a0001c0024t0001g0057 |
2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3429-119A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17630869 | |||||||
chr19:17630925 | A | T | 1 | a0001c0004t0049g0317 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3429-175T>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17630925 | |||||||
chr19:17631000 | G | GCTGCCCA others(106): Show |
3 | a0001c0002t0010g0097 a0001c0016t0002g0065 a0001c0016t0002g0091 |
3 | HG02451.hp2 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3429-363_3429-251d others(115): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631000 | |||||||
chr19:17631000 | GCTGCCCA others(106): Show |
G | 2 | a0001c0007t0003g0072 a0002c0019t0003g0074 |
2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.3429-363_3429-251d others(2): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631000 | |||||||
chr19:17631023 | TTCTCTGA others(4): Show |
T | 4 | a0001c0002t0018g0103 a0001c0022t0024g0061 a0001c0023t0001g0045 others(1): Show |
4 | HG00099.hp2 HG02886.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3429-284_3429-274d others(13): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631023 | |||||||
chr19:17631034 | C | CTCTCTGA others(95): Show |
1 | a0001c0002t0012g0017 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3429-285_3429-284i others(104): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631034 | |||||||
chr19:17631034 | C | CTCTCTGA others(95): Show |
1 | a0001c0011t0020g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3429-386_3429-285d others(104): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631034 | |||||||
chr19:17631049 | G | A | 8 | a0001c0001t0004g0012 a0001c0002t0012g0077 a0001c0002t0012g0291 others(5): Show |
8 | HG01975.hp2 HG02145.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.3429-299C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631049 | |||||||
chr19:17631061 | C | CTCCCTCC others(87): Show |
2 | a0001c0002t0003g0096 a0001c0053t0023g0053 |
2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3429-312_3429-311i others(96): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631061 | |||||||
chr19:17631073 | C | CTCCT | 17 | a0001c0001t0001g0132 a0001c0001t0001g0199 a0001c0001t0001g0231 others(14): Show |
17 | HG00099.hp1 HG00438.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.3429-327_3429-324d others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631073 | |||||||
chr19:17631073 | CTCCT | C | 60 | a0001c0001t0004g0012 a0001c0001t0034g0304 a0001c0002t0001g0113 others(57): Show |
60 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.3429-327_3429-324d others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631073 | |||||||
chr19:17631073 | CTCCTTCC others(5): Show |
C | 1 | a0002c0006t0016g0296 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3429-335_3429-324d others(14): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631073 | |||||||
chr19:17631077 | T | C | 1 | a0001c0004t0007g0151 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3429-327A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631077 | |||||||
chr19:17631077 | T | TTCCTTCC others(91): Show |
3 | a0001c0002t0012g0291 a0001c0022t0008g0185 a0002c0013t0002g0200 |
3 | HG01975.hp2 HG02630.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.3429-328_3429-327i others(100): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631077 | |||||||
chr19:17631077 | T | TTCCTTCC others(87): Show |
4 | a0001c0002t0003g0131 a0001c0002t0028g0047 a0001c0008t0002g0075 others(1): Show |
4 | HG01978.hp2 HG02630.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.3429-328_3429-327i others(96): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631077 | |||||||
chr19:17631077 | T | TTCCTTCC others(283): Show |
1 | a0002c0005t0006g0310 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3429-328_3429-327i others(292): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631077 | |||||||
chr19:17631081 | T | C | 7 | a0001c0011t0001g0089 a0001c0011t0001g0156 a0001c0011t0001g0300 others(4): Show |
7 | HG01123.hp2 HG01361.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.3429-331A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631081 | |||||||
chr19:17631081 | T | TTCCTTCC others(185): Show |
12 | a0001c0002t0010g0069 a0001c0002t0011g0039 a0001c0002t0011g0064 others(9): Show |
12 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.3429-332_3429-331i others(194): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631081 | |||||||
chr19:17631081 | T | TTCCTTCC others(83): Show |
1 | a0001c0008t0002g0034 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3429-332_3429-331i others(92): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631081 | |||||||
chr19:17631081 | T | TTCCTTCC others(177): Show |
2 | a0001c0008t0002g0071 a0001c0008t0002g0095 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3429-332_3429-331i others(186): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631081 | |||||||
chr19:17631085 | T | TTCCTTCC others(79): Show |
2 | a0001c0008t0026g0083 a0001c0072t0003g0312 |
2 | HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3429-336_3429-335i others(88): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631085 | |||||||
chr19:17631145 | C | T | 1 | a0001c0071t0002g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3429-395G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631145 | |||||||
chr19:17631146 | T | C | 1 | a0001c0071t0002g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3429-396A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631146 | |||||||
chr19:17631149 | T | C | 1 | a0001c0071t0002g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3429-399A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631149 | |||||||
chr19:17631150 | G | C | 1 | a0001c0071t0002g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3429-400C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631150 | |||||||
chr19:17631151 | T | G | 1 | a0001c0071t0002g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3429-401A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631151 | |||||||
chr19:17631153 | T | C | 1 | a0001c0071t0002g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3429-403A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631153 | |||||||
chr19:17631154 | T | C | 1 | a0001c0071t0002g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3429-404A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631154 | |||||||
chr19:17631154 | T | TCTCC | 5 | a0001c0002t0011g0064 a0001c0002t0011g0287 a0001c0002t0038g0037 others(2): Show |
5 | HG02280.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3429-408_3429-405d others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631154 | |||||||
chr19:17631154 | T | TCTCCCTC others(21): Show |
1 | a0001c0004t0001g0135 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3429-405_3429-404i others(30): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631154 | |||||||
chr19:17631155 | C | A | 1 | a0001c0071t0002g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3429-405G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631155 | |||||||
chr19:17631155 | C | CTCCCTCC others(37): Show |
1 | a0001c0002t0004g0224 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3429-406_3429-405i others(46): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631155 | |||||||
chr19:17631159 | C | T | 1 | a0001c0071t0002g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3429-409G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631159 | |||||||
chr19:17631175 | C | T | 6 | a0001c0002t0004g0215 a0001c0069t0001g0261 a0002c0005t0001g0051 others(3): Show |
6 | HG02055.hp2 HG02165.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3429-425G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631175 | |||||||
chr19:17631175 | CTCCTT | C | 6 | a0001c0002t0003g0068 a0001c0002t0027g0295 a0001c0002t0045g0164 others(3): Show |
6 | HG02258.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3429-430_3429-426d others(7): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631175 | |||||||
chr19:17631175 | CTCCTTTC others(2): Show |
C | 5 | a0001c0003t0001g0152 a0001c0053t0023g0053 a0001c0055t0001g0102 others(2): Show |
5 | HG02027.hp1 HG02257.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.3429-434_3429-426d others(11): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631175 | |||||||
chr19:17631177 | C | T | 6 | a0001c0002t0004g0215 a0001c0069t0001g0261 a0002c0005t0001g0051 others(3): Show |
6 | HG02055.hp2 HG02165.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3429-427G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631177 | |||||||
chr19:17631178 | CT | C | 10 | a0001c0004t0021g0073 a0001c0011t0001g0089 a0001c0011t0001g0156 others(7): Show |
10 | HG01123.hp2 HG01361.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.3429-429delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631178 | |||||||
chr19:17631179 | T | C | 47 | a0001c0001t0004g0012 a0001c0002t0003g0131 a0001c0002t0004g0215 others(44): Show |
47 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(44): Show |
intron_variant | MODIFIER | c.3429-429A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631179 | |||||||
chr19:17631180 | T | C | 10 | a0001c0004t0021g0073 a0001c0011t0001g0089 a0001c0011t0001g0156 others(7): Show |
10 | HG01123.hp2 HG01361.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.3429-430A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(158): Show |
1 | a0001c0007t0005g0173 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3429-431_3429-430i others(167): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(4): Show |
2 | a0001c0001t0001g0171 a0002c0013t0002g0307 |
2 | HG00733.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.3429-431_3429-430i others(13): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(8): Show |
1 | a0001c0022t0024g0061 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3429-431_3429-430i others(17): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(159): Show |
1 | a0001c0028t0002g0082 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3429-431_3429-430i others(168): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(97): Show |
1 | a0001c0003t0001g0117 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3429-431_3429-430i others(106): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(121): Show |
1 | a0001c0002t0005g0120 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3429-431_3429-430i others(130): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(117): Show |
1 | a0001c0001t0001g0022 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3429-431_3429-430i others(126): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(137): Show |
6 | a0001c0001t0001g0216 a0001c0001t0001g0262 a0001c0002t0017g0028 others(3): Show |
6 | HG00673.hp2 HG01192.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.3429-431_3429-430i others(146): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(348): Show |
1 | a0001c0003t0007g0206 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3429-431_3429-430i others(357): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(420): Show |
1 | a0001c0001t0001g0190 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3429-431_3429-430i others(429): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(222): Show |
1 | a0001c0001t0001g0107 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3429-431_3429-430i others(231): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(345): Show |
1 | a0001c0004t0001g0238 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3429-431_3429-430i others(354): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(149): Show |
1 | a0001c0015t0006g0090 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3429-431_3429-430i others(158): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(116): Show |
3 | a0001c0001t0001g0230 a0001c0001t0001g0249 a0005c0051t0001g0259 |
3 | HG00423.hp1 NA19004.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.3429-431_3429-430i others(125): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(49): Show |
1 | a0002c0005t0004g0220 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3429-431_3429-430i others(58): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(73): Show |
2 | a0002c0005t0004g0118 a0002c0005t0004g0119 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3429-431_3429-430i others(82): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(157): Show |
1 | a0001c0003t0001g0247 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.3429-431_3429-430i others(166): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(311): Show |
1 | a0001c0003t0001g0014 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3429-431_3429-430i others(320): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(149): Show |
1 | a0001c0002t0003g0127 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3429-431_3429-430i others(158): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(251): Show |
1 | a0001c0001t0001g0201 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3429-431_3429-430i others(260): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(157): Show |
1 | a0001c0001t0001g0080 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.3429-431_3429-430i others(166): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(326): Show |
1 | a0001c0014t0001g0254 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3429-431_3429-430i others(335): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(157): Show |
41 | a0001c0001t0001g0165 a0001c0001t0001g0179 a0001c0001t0001g0194 others(38): Show |
41 | HG00597.hp1 HG00642.hp1 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.3429-431_3429-430i others(166): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(201): Show |
1 | a0001c0001t0001g0174 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3429-431_3429-430i others(210): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(331): Show |
1 | a0001c0064t0001g0048 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3429-431_3429-430i others(340): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(327): Show |
1 | a0001c0001t0001g0253 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3429-431_3429-430i others(336): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(331): Show |
3 | a0001c0002t0009g0176 a0001c0003t0001g0288 a0002c0006t0016g0289 |
3 | HG00280.hp1 HG01109.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.3429-431_3429-430i others(340): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(262): Show |
1 | a0001c0003t0001g0129 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3429-431_3429-430i others(271): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(177): Show |
5 | a0001c0003t0001g0015 a0001c0003t0001g0066 a0001c0046t0001g0280 others(2): Show |
5 | HG01081.hp1 HG01496.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.3429-431_3429-430i others(186): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCCTCCC others(641): Show |
1 | a0001c0003t0001g0040 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3429-431_3429-430i others(650): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631180 | T | TCCTTCCT others(262): Show |
1 | a0001c0071t0002g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3429-431_3429-430i others(271): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631180 | |||||||
chr19:17631181 | T | C | 41 | a0001c0001t0004g0012 a0001c0002t0003g0131 a0001c0002t0008g0046 others(38): Show |
41 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(38): Show |
intron_variant | MODIFIER | c.3429-431A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631181 | |||||||
chr19:17631183 | C | T | 41 | a0001c0001t0004g0012 a0001c0002t0003g0131 a0001c0002t0008g0046 others(38): Show |
41 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(38): Show |
intron_variant | MODIFIER | c.3429-433G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631183 | |||||||
chr19:17631184 | T | A | 1 | a0001c0071t0002g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3429-434A>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631184 | |||||||
chr19:17631184 | T | C | 11 | a0001c0001t0001g0171 a0001c0001t0001g0253 a0001c0004t0021g0073 others(8): Show |
11 | HG00733.hp1 HG01123.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.3429-434A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631184 | |||||||
chr19:17631184 | T | TTCCTCCC | 5 | a0001c0002t0004g0215 a0001c0069t0001g0261 a0002c0005t0001g0051 others(2): Show |
5 | HG02055.hp2 HG02165.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.3429-435_3429-434i others(9): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631184 | |||||||
chr19:17631184 | T | TTCCTCCC others(20): Show |
1 | a0002c0005t0001g0273 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3429-435_3429-434i others(29): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631184 | |||||||
chr19:17631184 | T | TTCCTTCC others(5): Show |
1 | a0001c0003t0003g0109 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3429-446_3429-435d others(14): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631184 | |||||||
chr19:17631184 | T | TTCCTTCC others(33): Show |
1 | a0001c0004t0004g0272 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3429-435_3429-434i others(42): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631184 | |||||||
chr19:17631184 | T | TTCCTTCC others(4): Show |
68 | a0001c0001t0001g0011 a0001c0001t0001g0132 a0001c0001t0001g0145 others(65): Show |
68 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.3429-435_3429-434i others(13): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631184 | |||||||
chr19:17631184 | T | TTCCTTCC others(88): Show |
1 | a0001c0003t0040g0024 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3429-435_3429-434i others(97): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631184 | |||||||
chr19:17631186 | C | T | 1 | a0001c0022t0024g0061 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3429-436G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631186 | |||||||
chr19:17631187 | CT | C | 3 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0018g0103 |
3 | HG02723.hp2 HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3429-438delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631187 | |||||||
chr19:17631188 | T | C | 92 | a0001c0001t0001g0022 a0001c0001t0001g0080 a0001c0001t0001g0107 others(89): Show |
92 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.3429-438A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631188 | |||||||
chr19:17631188 | T | TTCC | 4 | a0001c0002t0011g0064 a0001c0002t0011g0287 a0001c0056t0002g0155 others(1): Show |
4 | HG02280.hp2 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.3429-441_3429-439d others(5): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631188 | |||||||
chr19:17631188 | T | TTCCTCCC others(8): Show |
1 | a0001c0002t0001g0178 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.3429-439_3429-438i others(17): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631188 | |||||||
chr19:17631189 | TC | T | 68 | a0001c0001t0004g0012 a0001c0002t0003g0131 a0001c0002t0008g0046 others(65): Show |
68 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.3429-440delG | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631189 | |||||||
chr19:17631190 | C | T | 8 | a0001c0004t0021g0073 a0001c0011t0001g0089 a0001c0011t0001g0156 others(5): Show |
8 | HG01123.hp2 HG01361.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.3429-440G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631190 | |||||||
chr19:17631192 | C | T | 1 | a0001c0028t0002g0196 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3429-442G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631192 | |||||||
chr19:17631194 | C | T | 47 | a0001c0001t0004g0012 a0001c0002t0003g0131 a0001c0002t0008g0046 others(44): Show |
47 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(44): Show |
intron_variant | MODIFIER | c.3429-444G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631194 | |||||||
chr19:17631196 | C | T | 2 | a0001c0002t0011g0064 a0001c0002t0011g0287 |
2 | HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3429-446G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631196 | |||||||
chr19:17631198 | C | T | 7 | a0001c0004t0021g0073 a0001c0011t0001g0089 a0001c0011t0001g0156 others(4): Show |
7 | HG01123.hp2 HG01361.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.3429-448G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631198 | |||||||
chr19:17631200 | C | A | 1 | a0001c0001t0001g0174 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3429-450G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631200 | |||||||
chr19:17631200 | C | T | 30 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0069 others(27): Show |
30 | HG00280.hp2 HG00733.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.3429-450G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631200 | |||||||
chr19:17631201 | TC | T | 40 | a0001c0001t0004g0012 a0001c0002t0003g0131 a0001c0002t0008g0046 others(37): Show |
40 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(37): Show |
intron_variant | MODIFIER | c.3429-452delG | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631201 | |||||||
chr19:17631202 | C | T | 13 | a0001c0002t0003g0068 a0001c0002t0020g0025 a0001c0002t0027g0295 others(10): Show |
13 | HG02258.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.3429-452G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631202 | |||||||
chr19:17631203 | C | CCTCCCTT others(16): Show |
2 | a0001c0056t0002g0155 a0001c0057t0024g0233 |
2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3429-454_3429-453i others(25): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631203 | |||||||
chr19:17631203 | CCTTCCTT others(12): Show |
C | 2 | a0001c0004t0001g0020 a0001c0004t0001g0123 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3429-472_3429-454d others(21): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631203 | |||||||
chr19:17631204 | C | T | 8 | a0001c0001t0001g0022 a0001c0002t0005g0120 a0001c0002t0017g0028 others(5): Show |
8 | HG01192.hp1 HG02886.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.3429-454G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631204 | |||||||
chr19:17631204 | CT | C | 11 | a0001c0004t0021g0073 a0001c0011t0001g0089 a0001c0011t0001g0156 others(8): Show |
11 | HG01123.hp2 HG01361.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.3429-455delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631204 | |||||||
chr19:17631206 | T | C | 42 | a0001c0001t0001g0022 a0001c0001t0001g0171 a0001c0001t0001g0253 others(39): Show |
42 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.3429-456A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631206 | |||||||
chr19:17631208 | C | T | 1 | a0001c0028t0002g0082 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3429-458G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631208 | |||||||
chr19:17631209 | T | C | 52 | a0001c0001t0004g0012 a0001c0002t0003g0068 a0001c0002t0003g0131 others(49): Show |
52 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.3429-459A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631209 | |||||||
chr19:17631210 | T | C | 38 | a0001c0001t0001g0022 a0001c0002t0005g0120 a0001c0002t0008g0027 others(35): Show |
38 | HG00280.hp2 HG00733.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.3429-460A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631210 | |||||||
chr19:17631213 | T | C | 137 | a0001c0001t0001g0080 a0001c0001t0001g0107 a0001c0001t0001g0165 others(134): Show |
137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.3429-463A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631213 | |||||||
chr19:17631214 | T | C | 38 | a0001c0001t0001g0022 a0001c0002t0005g0120 a0001c0002t0008g0027 others(35): Show |
38 | HG00280.hp2 HG00733.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.3429-464A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631214 | |||||||
chr19:17631215 | CCTTCCTT | C | 23 | a0001c0002t0010g0069 a0001c0002t0010g0097 a0001c0002t0011g0184 others(20): Show |
23 | HG00280.hp2 HG00733.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.3429-472_3429-466d others(9): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631215 | |||||||
chr19:17631217 | T | C | 141 | a0001c0001t0001g0080 a0001c0001t0001g0107 a0001c0001t0001g0165 others(138): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.3429-467A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631217 | |||||||
chr19:17631218 | T | C | 9 | a0001c0001t0001g0022 a0001c0002t0005g0120 a0001c0002t0017g0028 others(6): Show |
9 | HG01192.hp1 HG02886.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.3429-468A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631218 | |||||||
chr19:17631219 | CCTT | C | 6 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0018g0103 others(3): Show |
6 | HG02572.hp2 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3429-472_3429-470d others(5): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631219 | |||||||
chr19:17631220 | CTT | C | 51 | a0001c0001t0004g0012 a0001c0002t0003g0068 a0001c0002t0003g0131 others(48): Show |
51 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(48): Show |
intron_variant | MODIFIER | c.3429-472_3429-471d others(4): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631220 | |||||||
chr19:17631221 | T | C | 90 | a0001c0001t0001g0080 a0001c0001t0001g0107 a0001c0001t0001g0165 others(87): Show |
90 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.3429-471A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631221 | |||||||
chr19:17631221 | T | TC | 6 | a0001c0001t0001g0022 a0001c0002t0005g0120 a0001c0002t0017g0028 others(3): Show |
6 | HG01192.hp1 HG03017.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.3429-472_3429-471i others(3): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631221 | |||||||
chr19:17631222 | T | C | 7 | a0001c0001t0001g0022 a0001c0002t0005g0120 a0001c0002t0017g0028 others(4): Show |
7 | HG01192.hp1 HG03017.hp2 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.3429-472A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631222 | |||||||
chr19:17631222 | T | TCC | 87 | a0001c0001t0001g0080 a0001c0001t0001g0107 a0001c0001t0001g0165 others(84): Show |
87 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.3429-473_3429-472i others(4): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631222 | |||||||
chr19:17631222 | T | TCCCTCCC others(147): Show |
1 | a0001c0001t0001g0171 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3429-473_3429-472i others(156): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631222 | |||||||
chr19:17631222 | T | TCCTTCCT others(434): Show |
1 | a0001c0001t0034g0304 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3429-473_3429-472i others(443): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631222 | |||||||
chr19:17631222 | T | TCTTCAGA others(101): Show |
1 | a0001c0071t0002g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3429-473_3429-472i others(110): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631222 | |||||||
chr19:17631224 | T | C | 1 | a0001c0028t0002g0082 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3429-474A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631224 | |||||||
chr19:17631225 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3429-475A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631225 | |||||||
chr19:17631260 | G | A | 1 | a0001c0004t0041g0111 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3429-510C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631260 | |||||||
chr19:17631376 | A | G | 178 | a0001c0001t0001g0011 a0001c0001t0001g0080 a0001c0001t0001g0107 others(175): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.3429-626T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631376 | |||||||
chr19:17631382 | G | A | 2 | a0001c0008t0002g0276 a0001c0008t0002g0277 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3429-632C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631382 | |||||||
chr19:17631427 | G | A | 91 | a0001c0001t0001g0080 a0001c0001t0001g0107 a0001c0001t0001g0132 others(88): Show |
91 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.3429-677C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631427 | |||||||
chr19:17631434 | C | T | 1 | a0002c0006t0001g0302 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3429-684G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631434 | |||||||
chr19:17631660 | C | T | 73 | a0001c0001t0001g0011 a0001c0001t0001g0171 a0001c0001t0001g0174 others(70): Show |
73 | HG00140.hp1 HG00423.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.3429-910G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631660 | |||||||
chr19:17631681 | G | T | 3 | a0001c0002t0020g0025 a0001c0002t0027g0295 a0001c0002t0045g0164 |
3 | HG02280.hp1 HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.3429-931C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631681 | |||||||
chr19:17631739 | T | C | 66 | a0001c0001t0001g0170 a0001c0002t0001g0178 a0001c0002t0001g0229 others(63): Show |
66 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.3429-989A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631739 | |||||||
chr19:17631766 | A | G | 86 | a0001c0001t0001g0170 a0001c0002t0001g0178 a0001c0002t0001g0229 others(83): Show |
86 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.3428+1016T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631766 | |||||||
chr19:17631807 | C | T | 1 | a0001c0020t0001g0005 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.3428+975G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631807 | |||||||
chr19:17631929 | G | C | 1 | a0001c0004t0003g0030 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3428+853C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631929 | |||||||
chr19:17631976 | T | C | 1 | a0001c0002t0018g0103 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3428+806A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631976 | |||||||
chr19:17631978 | T | G | 2 | a0001c0001t0001g0209 a0001c0002t0004g0215 |
2 | NA18971.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.3428+804A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17631978 | |||||||
chr19:17632015 | A | T | 1 | a0001c0028t0002g0082 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.3428+767T>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17632015 | |||||||
chr19:17632118 | C | T | 1 | a0001c0067t0004g0265 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3428+664G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17632118 | |||||||
chr19:17632124 | C | T | 58 | a0001c0002t0001g0178 a0001c0002t0001g0229 a0001c0002t0003g0096 others(55): Show |
58 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.3428+658G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17632124 | |||||||
chr19:17632227 | T | C | 59 | a0001c0002t0001g0178 a0001c0002t0001g0229 a0001c0002t0003g0096 others(56): Show |
59 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.3428+555A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17632227 | |||||||
chr19:17632265 | G | A | 1 | a0001c0002t0028g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3428+517C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17632265 | |||||||
chr19:17632290 | C | T | 2 | a0001c0056t0002g0155 a0001c0057t0024g0233 |
2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3428+492G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17632290 | |||||||
chr19:17632507 | G | A | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3428+275C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17632507 | |||||||
chr19:17632511 | A | T | 1 | a0001c0003t0001g0292 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3428+271T>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17632511 | |||||||
chr19:17632597 | C | CTG | 242 | a0001c0001t0001g0011 a0001c0001t0001g0080 a0001c0001t0001g0107 others(239): Show |
242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.3428+183_3428+184d others(4): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17632597 | |||||||
chr19:17632651 | C | T | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3428+131G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17632651 | |||||||
chr19:17632763 | C | A | 1 | a0001c0002t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3428+19G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 28/43 | chr19 | 17632763 | |||||||
chr19:17632964 | G | A | 1 | a0001c0002t0038g0037 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3302-56C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 27/43 | chr19 | 17632964 | |||||||
chr19:17632973 | G | T | 1 | a0001c0028t0002g0196 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3302-65C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 27/43 | chr19 | 17632973 | |||||||
chr19:17633266 | G | GC | 71 | a0001c0001t0001g0011 a0001c0001t0001g0145 a0001c0001t0001g0171 others(68): Show |
71 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.3216-74dupG | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17633266 | |||||||
chr19:17633312 | T | C | 1 | a0001c0022t0008g0185 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3216-119A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17633312 | |||||||
chr19:17633632 | T | C | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3216-439A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17633632 | |||||||
chr19:17633706 | CATTCATT others(5): Show |
C | 1 | a0001c0002t0012g0291 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3216-525_3216-514d others(14): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17633706 | |||||||
chr19:17633723 | A | T | 22 | a0001c0001t0001g0253 a0001c0002t0003g0068 a0001c0015t0006g0090 others(19): Show |
22 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(19): Show |
intron_variant | MODIFIER | c.3216-530T>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17633723 | |||||||
chr19:17633957 | C | T | 4 | a0001c0008t0002g0034 a0001c0008t0002g0071 a0001c0008t0002g0095 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.3216-764G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17633957 | |||||||
chr19:17634111 | G | A | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3216-918C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17634111 | |||||||
chr19:17634437 | C | T | 1 | a0001c0032t0008g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3216-1244G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17634437 | |||||||
chr19:17634449 | G | A | 2 | a0001c0002t0012g0077 a0001c0002t0012g0299 |
2 | HG02683.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.3216-1256C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17634449 | |||||||
chr19:17634592 | G | A | 8 | a0001c0008t0002g0034 a0001c0008t0002g0071 a0001c0008t0002g0095 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.3216-1399C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17634592 | |||||||
chr19:17634631 | C | T | 1 | a0002c0013t0002g0307 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3215+1393G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17634631 | |||||||
chr19:17634645 | G | A | 1 | a0001c0003t0001g0130 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.3215+1379C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17634645 | |||||||
chr19:17634719 | G | A | 2 | a0001c0003t0001g0222 a0001c0004t0001g0238 |
2 | HG02027.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.3215+1305C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17634719 | |||||||
chr19:17634726 | G | A | 4 | a0001c0002t0009g0176 a0001c0002t0019g0092 a0001c0002t0025g0315 others(1): Show |
4 | HG01175.hp1 HG02145.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3215+1298C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17634726 | |||||||
chr19:17634756 | C | T | 1 | a0001c0001t0009g0160 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3215+1268G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17634756 | |||||||
chr19:17634757 | G | A | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3215+1267C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17634757 | |||||||
chr19:17634763 | T | C | 1 | a0002c0017t0001g0086 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3215+1261A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17634763 | |||||||
chr19:17634782 | G | A | 3 | a0001c0002t0020g0025 a0001c0002t0027g0295 a0001c0002t0045g0164 |
3 | HG02280.hp1 HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.3215+1242C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17634782 | |||||||
chr19:17634807 | T | C | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3215+1217A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17634807 | |||||||
chr19:17634888 | T | C | 2 | a0001c0002t0001g0157 a0001c0002t0028g0047 |
2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3215+1136A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17634888 | |||||||
chr19:17635015 | C | T | 1 | a0001c0022t0008g0185 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3215+1009G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17635015 | |||||||
chr19:17635016 | G | A | 1 | a0001c0001t0007g0223 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3215+1008C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17635016 | |||||||
chr19:17635026 | A | G | 1 | a0001c0002t0018g0103 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3215+998T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17635026 | |||||||
chr19:17635028 | T | G | 1 | a0001c0002t0018g0103 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3215+996A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17635028 | |||||||
chr19:17635102 | A | G | 2 | a0001c0002t0018g0103 a0001c0050t0033g0085 |
2 | HG03041.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3215+922T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17635102 | |||||||
chr19:17635109 | G | A | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3215+915C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17635109 | |||||||
chr19:17635156 | G | A | 2 | a0001c0002t0001g0157 a0001c0002t0028g0047 |
2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3215+868C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17635156 | |||||||
chr19:17635290 | T | C | 161 | a0001c0001t0001g0011 a0001c0001t0001g0145 a0001c0001t0001g0171 others(158): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.3215+734A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17635290 | |||||||
chr19:17635390 | G | A | 1 | a0001c0002t0038g0037 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3215+634C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17635390 | |||||||
chr19:17635497 | T | C | 1 | a0001c0002t0038g0037 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3215+527A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17635497 | |||||||
chr19:17635573 | T | C | 4 | a0001c0002t0001g0157 a0001c0002t0018g0103 a0001c0002t0028g0047 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.3215+451A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17635573 | |||||||
chr19:17635797 | A | G | 77 | a0001c0001t0001g0080 a0001c0001t0001g0107 a0001c0001t0001g0132 others(74): Show |
77 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.3215+227T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17635797 | |||||||
chr19:17635947 | T | C | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3215+77A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 26/43 | chr19 | 17635947 | |||||||
chr19:17636171 | T | C | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3082-14A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17636171 | |||||||
chr19:17636293 | T | C | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3082-136A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17636293 | |||||||
chr19:17636514 | A | G | 3 | a0001c0002t0001g0157 a0001c0002t0018g0103 a0001c0002t0028g0047 |
3 | HG03041.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3082-357T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17636514 | |||||||
chr19:17636594 | G | A | 3 | a0001c0002t0018g0103 a0001c0002t0028g0047 a0001c0050t0033g0085 |
3 | HG03041.hp1 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3082-437C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17636594 | |||||||
chr19:17636661 | C | T | 3 | a0001c0002t0020g0025 a0001c0002t0027g0295 a0001c0002t0045g0164 |
3 | HG02280.hp1 HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.3082-504G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17636661 | |||||||
chr19:17636690 | C | G | 5 | a0001c0011t0001g0089 a0001c0011t0001g0156 a0001c0011t0001g0300 others(2): Show |
5 | HG01123.hp2 HG01361.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.3082-533G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17636690 | |||||||
chr19:17636691 | C | A | 4 | a0001c0007t0003g0072 a0001c0023t0047g0275 a0002c0019t0003g0074 others(1): Show |
4 | HG02145.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.3082-534G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17636691 | |||||||
chr19:17636695 | T | C | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3082-538A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17636695 | |||||||
chr19:17636698 | G | C | 3 | a0001c0002t0001g0157 a0001c0002t0018g0103 a0001c0002t0028g0047 |
3 | HG03041.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3082-541C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17636698 | |||||||
chr19:17636729 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3082-572G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17636729 | |||||||
chr19:17636825 | A | G | 3 | a0001c0002t0001g0157 a0001c0002t0018g0103 a0001c0002t0028g0047 |
3 | HG03041.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3082-668T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17636825 | |||||||
chr19:17636973 | AT | A | 6 | a0001c0002t0001g0157 a0001c0002t0018g0103 a0001c0002t0028g0047 others(3): Show |
6 | HG01256.hp2 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.3082-817delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17636973 | |||||||
chr19:17637086 | T | C | 3 | a0001c0002t0001g0157 a0001c0002t0018g0103 a0001c0002t0028g0047 |
3 | HG03041.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3082-929A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17637086 | |||||||
chr19:17637178 | T | C | 36 | a0001c0001t0001g0253 a0001c0002t0003g0068 a0001c0002t0010g0069 others(33): Show |
36 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.3082-1021A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17637178 | |||||||
chr19:17637271 | A | G | 1 | a0002c0039t0021g0026 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3082-1114T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17637271 | |||||||
chr19:17637299 | AT | A | 119 | a0001c0001t0001g0011 a0001c0001t0001g0136 a0001c0001t0001g0145 others(116): Show |
119 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.3082-1143delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17637299 | |||||||
chr19:17637442 | T | C | 3 | a0001c0002t0001g0157 a0001c0002t0018g0103 a0001c0002t0028g0047 |
3 | HG03041.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3082-1285A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17637442 | |||||||
chr19:17637442 | T | G | 2 | a0001c0028t0002g0082 a0001c0060t0002g0192 |
2 | NA18970.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.3082-1285A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17637442 | |||||||
chr19:17637497 | A | C | 3 | a0001c0002t0001g0157 a0001c0002t0018g0103 a0001c0002t0028g0047 |
3 | HG03041.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3082-1340T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17637497 | |||||||
chr19:17637503 | T | C | 1 | a0001c0002t0018g0103 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3082-1346A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17637503 | |||||||
chr19:17637519 | C | T | 4 | a0001c0002t0020g0025 a0001c0002t0027g0295 a0001c0002t0045g0164 others(1): Show |
4 | HG02280.hp1 HG02559.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3082-1362G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17637519 | |||||||
chr19:17637564 | C | T | 3 | a0001c0002t0001g0157 a0001c0002t0018g0103 a0001c0002t0028g0047 |
3 | HG03041.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3082-1407G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17637564 | |||||||
chr19:17637587 | T | C | 3 | a0001c0002t0001g0157 a0001c0002t0018g0103 a0001c0002t0028g0047 |
3 | HG03041.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3082-1430A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17637587 | |||||||
chr19:17637630 | T | C | 36 | a0001c0001t0001g0253 a0001c0002t0003g0068 a0001c0002t0010g0069 others(33): Show |
36 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.3081+1453A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17637630 | |||||||
chr19:17637673 | TCTAATTT others(257): Show |
T | 259 | a0001c0001t0001g0011 a0001c0001t0001g0080 a0001c0001t0001g0107 others(256): Show |
259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.3081+1146_3081+140 others(4): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17637673 | |||||||
chr19:17637984 | C | A | 39 | a0001c0002t0001g0178 a0001c0002t0001g0229 a0001c0002t0003g0096 others(36): Show |
39 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.3081+1099G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17637984 | |||||||
chr19:17637993 | A | G | 3 | a0001c0002t0001g0157 a0001c0002t0018g0103 a0001c0002t0028g0047 |
3 | HG03041.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3081+1090T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17637993 | |||||||
chr19:17638003 | A | G | 3 | a0001c0002t0001g0157 a0001c0002t0018g0103 a0001c0002t0028g0047 |
3 | HG03041.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3081+1080T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17638003 | |||||||
chr19:17638055 | T | A | 8 | a0001c0008t0002g0034 a0001c0008t0002g0071 a0001c0008t0002g0095 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.3081+1028A>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17638055 | |||||||
chr19:17638316 | A | G | 14 | a0001c0002t0010g0069 a0001c0002t0011g0039 a0001c0002t0011g0184 others(11): Show |
14 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.3081+767T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17638316 | |||||||
chr19:17638487 | A | C | 5 | a0001c0011t0001g0089 a0001c0011t0001g0156 a0001c0011t0001g0300 others(2): Show |
5 | HG01123.hp2 HG01361.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.3081+596T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17638487 | |||||||
chr19:17638607 | A | C | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3081+476T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17638607 | |||||||
chr19:17638608 | C | T | 3 | a0001c0002t0001g0157 a0001c0002t0018g0103 a0001c0002t0028g0047 |
3 | HG03041.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3081+475G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17638608 | |||||||
chr19:17638623 | T | C | 8 | a0001c0008t0002g0034 a0001c0008t0002g0071 a0001c0008t0002g0095 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.3081+460A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17638623 | |||||||
chr19:17638646 | G | A | 3 | a0001c0002t0001g0157 a0001c0002t0018g0103 a0001c0002t0028g0047 |
3 | HG03041.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3081+437C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17638646 | |||||||
chr19:17638706 | G | A | 3 | a0001c0002t0020g0025 a0001c0002t0027g0295 a0001c0002t0045g0164 |
3 | HG02280.hp1 HG02559.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.3081+377C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17638706 | |||||||
chr19:17638733 | G | A | 69 | a0001c0001t0001g0011 a0001c0001t0001g0137 a0001c0001t0001g0145 others(66): Show |
69 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.3081+350C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17638733 | |||||||
chr19:17638753 | T | C | 3 | a0001c0002t0001g0157 a0001c0002t0018g0103 a0001c0002t0028g0047 |
3 | HG03041.hp1 HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.3081+330A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17638753 | |||||||
chr19:17638829 | CA | C | 8 | a0001c0008t0002g0034 a0001c0008t0002g0071 a0001c0008t0002g0095 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.3081+253delT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17638829 | |||||||
chr19:17638841 | A | T | 36 | a0001c0002t0001g0178 a0001c0002t0001g0229 a0001c0002t0003g0096 others(33): Show |
36 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.3081+242T>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17638841 | |||||||
chr19:17638878 | G | A | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3081+205C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17638878 | |||||||
chr19:17639006 | G | A | 1 | a0002c0038t0023g0084 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3081+77C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 25/43 | chr19 | 17639006 | |||||||
chr19:17639243 | C | T | 1 | a0001c0002t0010g0033 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2947-26G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 24/43 | chr19 | 17639243 | |||||||
chr19:17639263 | G | A | 3 | a0001c0024t0001g0057 a0001c0024t0019g0100 a0001c0066t0019g0043 |
3 | HG02451.hp1 HG03471.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2947-46C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 24/43 | chr19 | 17639263 | |||||||
chr19:17639306 | T | G | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2947-89A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 24/43 | chr19 | 17639306 | |||||||
chr19:17639374 | T | C | 39 | a0001c0002t0001g0178 a0001c0002t0001g0229 a0001c0002t0003g0096 others(36): Show |
39 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.2946+62A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 24/43 | chr19 | 17639374 | |||||||
chr19:17639398 | C | A | 39 | a0001c0002t0001g0178 a0001c0002t0001g0229 a0001c0002t0003g0096 others(36): Show |
39 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.2946+38G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 24/43 | chr19 | 17639398 | |||||||
chr19:17639594 | G | C | 2 | a0001c0002t0001g0157 a0001c0002t0028g0047 |
2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2857-69C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 23/43 | chr19 | 17639594 | |||||||
chr19:17639741 | G | A | 5 | a0001c0003t0003g0162 a0001c0004t0018g0060 a0001c0004t0021g0073 others(2): Show |
5 | HG02922.hp2 HG03041.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2856+99C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 23/43 | chr19 | 17639741 | |||||||
chr19:17639804 | G | A | 1 | a0001c0003t0001g0152 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2856+36C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 23/43 | chr19 | 17639804 | |||||||
chr19:17639916 | G | A | 4 | a0001c0002t0003g0096 a0001c0002t0029g0167 a0001c0008t0002g0274 others(1): Show |
4 | HG02559.hp2 HG03195.hp1 NA20300.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.2788-8C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 22/43 | chr19 | 17639916 | |||||||
chr19:17639985 | G | A | 2 | a0001c0056t0002g0155 a0001c0057t0024g0233 |
2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2788-77C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 22/43 | chr19 | 17639985 | |||||||
chr19:17640032 | T | C | 1 | a0001c0054t0009g0290 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2788-124A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 22/43 | chr19 | 17640032 | |||||||
chr19:17640044 | T | G | 1 | a0001c0002t0018g0103 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2788-136A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 22/43 | chr19 | 17640044 | |||||||
chr19:17640336 | A | G | 213 | a0001c0001t0001g0011 a0001c0001t0001g0080 a0001c0001t0001g0107 others(210): Show |
213 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.2787+175T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 22/43 | chr19 | 17640336 | |||||||
chr19:17640355 | C | T | 1 | a0002c0012t0006g0181 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2787+156G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 22/43 | chr19 | 17640355 | |||||||
chr19:17640880 | C | CT | 17 | a0001c0002t0001g0157 a0001c0002t0038g0037 a0001c0003t0003g0162 others(14): Show |
17 | HG01167.hp2 HG01169.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2637-220dupA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 21/43 | chr19 | 17640880 | |||||||
chr19:17640880 | CT | C | 7 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0002t0004g0227 others(4): Show |
7 | HG01167.hp1 HG01256.hp2 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.2637-220delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 21/43 | chr19 | 17640880 | |||||||
chr19:17640880 | CTTTT | C | 64 | a0001c0001t0001g0011 a0001c0001t0001g0137 a0001c0001t0001g0171 others(61): Show |
64 | HG00140.hp1 HG00423.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.2637-223_2637-220d others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 21/43 | chr19 | 17640880 | |||||||
chr19:17640883 | T | TC | 41 | a0001c0002t0001g0178 a0001c0002t0001g0229 a0001c0002t0003g0096 others(38): Show |
41 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.2637-223_2637-222i others(3): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 21/43 | chr19 | 17640883 | |||||||
chr19:17640884 | T | C | 2 | a0001c0003t0001g0117 a0002c0006t0001g0302 |
2 | HG04228.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2637-223A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 21/43 | chr19 | 17640884 | |||||||
chr19:17640964 | T | C | 1 | a0001c0002t0038g0037 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2637-303A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 21/43 | chr19 | 17640964 | |||||||
chr19:17640990 | C | T | 5 | a0001c0002t0018g0103 a0001c0027t0002g0044 a0001c0055t0001g0102 others(2): Show |
5 | HG02717.hp2 HG03041.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.2637-329G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 21/43 | chr19 | 17640990 | |||||||
chr19:17641022 | G | A | 9 | a0001c0002t0009g0176 a0001c0002t0019g0092 a0001c0002t0025g0315 others(6): Show |
9 | HG01123.hp2 HG01175.hp1 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.2637-361C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 21/43 | chr19 | 17641022 | |||||||
chr19:17641215 | G | C | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2636+178C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 21/43 | chr19 | 17641215 | |||||||
chr19:17641244 | C | G | 1 | a0002c0036t0002g0004 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2636+149G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 21/43 | chr19 | 17641244 | |||||||
chr19:17641583 | T | C | 4 | a0002c0005t0001g0051 a0002c0005t0001g0067 a0002c0005t0001g0273 others(1): Show |
4 | HG02055.hp2 HG02486.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2473-27A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 20/43 | chr19 | 17641583 | |||||||
chr19:17641615 | G | A | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2473-59C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 20/43 | chr19 | 17641615 | |||||||
chr19:17641671 | T | TTCATCTA others(314): Show |
3 | a0001c0002t0009g0176 a0001c0003t0001g0014 a0001c0003t0001g0288 |
3 | HG01109.hp1 HG01175.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2473-116_2473-115i others(323): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 20/43 | chr19 | 17641671 | |||||||
chr19:17641880 | A | C | 150 | a0001c0001t0001g0011 a0001c0001t0001g0080 a0001c0001t0001g0107 others(147): Show |
150 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.2473-324T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 20/43 | chr19 | 17641880 | |||||||
chr19:17641893 | C | T | 3 | a0001c0001t0004g0244 a0001c0003t0001g0031 a0001c0003t0001g0112 |
3 | NA18944.hp2 NA19056.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.2473-337G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 20/43 | chr19 | 17641893 | |||||||
chr19:17641958 | A | G | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2473-402T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 20/43 | chr19 | 17641958 | |||||||
chr19:17641997 | C | T | 1 | a0001c0002t0038g0037 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2473-441G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 20/43 | chr19 | 17641997 | |||||||
chr19:17642032 | A | ACATCCAT others(1): Show |
57 | a0001c0002t0001g0178 a0001c0002t0001g0229 a0001c0002t0003g0096 others(54): Show |
57 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.2473-484_2473-477d others(10): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 20/43 | chr19 | 17642032 | |||||||
chr19:17642032 | A | ACATCCAT others(5): Show |
7 | a0001c0002t0018g0103 a0001c0027t0002g0044 a0001c0055t0001g0102 others(4): Show |
7 | HG02647.hp1 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2473-488_2473-477d others(14): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 20/43 | chr19 | 17642032 | |||||||
chr19:17642032 | A | ACATCCAT others(9): Show |
68 | a0001c0001t0001g0011 a0001c0001t0001g0137 a0001c0001t0001g0171 others(65): Show |
68 | HG00140.hp1 HG00423.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.2473-492_2473-477d others(18): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 20/43 | chr19 | 17642032 | |||||||
chr19:17642077 | T | G | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2473-521A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 20/43 | chr19 | 17642077 | |||||||
chr19:17642351 | C | A | 38 | a0001c0001t0001g0253 a0001c0002t0003g0068 a0001c0002t0010g0069 others(35): Show |
38 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.2472+494G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 20/43 | chr19 | 17642351 | |||||||
chr19:17642430 | C | G | 69 | a0001c0001t0001g0011 a0001c0001t0001g0137 a0001c0001t0001g0171 others(66): Show |
69 | HG00140.hp1 HG00423.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.2472+415G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 20/43 | chr19 | 17642430 | |||||||
chr19:17642495 | C | T | 1 | a0001c0002t0028g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2472+350G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 20/43 | chr19 | 17642495 | |||||||
chr19:17642699 | G | A | 1 | a0001c0002t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2472+146C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 20/43 | chr19 | 17642699 | |||||||
chr19:17642770 | C | T | 2 | a0001c0002t0012g0077 a0001c0002t0012g0299 |
2 | HG02683.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.2472+75G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 20/43 | chr19 | 17642770 | |||||||
chr19:17642998 | C | T | 1 | a0001c0003t0007g0206 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2357-38G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17642998 | |||||||
chr19:17643036 | A | G | 1 | a0001c0001t0001g0011 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2357-76T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17643036 | |||||||
chr19:17643111 | A | T | 104 | a0001c0001t0001g0011 a0001c0001t0001g0137 a0001c0001t0001g0171 others(101): Show |
104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.2357-151T>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17643111 | |||||||
chr19:17643232 | G | A | 12 | a0001c0002t0010g0069 a0001c0002t0011g0039 a0001c0002t0011g0184 others(9): Show |
12 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2357-272C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17643232 | |||||||
chr19:17643302 | G | A | 38 | a0001c0001t0001g0253 a0001c0002t0003g0068 a0001c0002t0007g0018 others(35): Show |
38 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.2357-342C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17643302 | |||||||
chr19:17643369 | G | A | 1 | a0001c0002t0018g0103 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2357-409C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17643369 | |||||||
chr19:17643380 | C | T | 1 | a0001c0032t0008g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2357-420G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17643380 | |||||||
chr19:17643381 | G | A | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2357-421C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17643381 | |||||||
chr19:17643508 | G | A | 103 | a0001c0001t0001g0011 a0001c0001t0001g0137 a0001c0001t0001g0171 others(100): Show |
103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.2357-548C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17643508 | |||||||
chr19:17643995 | G | A | 1 | a0001c0003t0003g0109 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2357-1035C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17643995 | |||||||
chr19:17644050 | A | T | 27 | a0001c0002t0001g0157 a0001c0002t0001g0178 a0001c0002t0001g0229 others(24): Show |
27 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.2357-1090T>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17644050 | |||||||
chr19:17644228 | G | A | 3 | a0001c0008t0026g0083 a0001c0022t0024g0061 a0002c0038t0023g0084 |
3 | HG02886.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2357-1268C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17644228 | |||||||
chr19:17644330 | A | G | 203 | a0001c0001t0001g0011 a0001c0001t0001g0080 a0001c0001t0001g0107 others(200): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.2356+1344T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17644330 | |||||||
chr19:17644354 | A | T | 1 | a0001c0004t0001g0150 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2356+1320T>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17644354 | |||||||
chr19:17644354 | AT | A | 40 | a0001c0001t0001g0080 a0001c0002t0001g0178 a0001c0002t0001g0229 others(37): Show |
40 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.2356+1319delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17644354 | |||||||
chr19:17644372 | G | A | 1 | a0003c0010t0001g0070 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2356+1302C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17644372 | |||||||
chr19:17644501 | AT | A | 93 | a0001c0001t0001g0171 a0001c0001t0001g0174 a0001c0001t0001g0179 others(90): Show |
93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.2356+1172delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17644501 | |||||||
chr19:17644523 | G | GT | 12 | a0001c0001t0003g0203 a0001c0001t0003g0271 a0001c0002t0011g0039 others(9): Show |
12 | HG01884.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.2356+1150dupA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17644523 | |||||||
chr19:17644523 | G | T | 1 | a0001c0003t0001g0228 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2356+1151C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17644523 | |||||||
chr19:17644523 | GT | G | 82 | a0001c0001t0001g0011 a0001c0001t0001g0080 a0001c0001t0001g0132 others(79): Show |
82 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.2356+1150delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17644523 | |||||||
chr19:17644523 | GTT | G | 52 | a0001c0001t0001g0137 a0001c0001t0001g0236 a0001c0001t0001g0249 others(49): Show |
52 | HG00423.hp1 HG00597.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.2356+1149_2356+115 others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17644523 | |||||||
chr19:17644523 | GTTT | G | 86 | a0001c0001t0001g0171 a0001c0001t0001g0174 a0001c0001t0001g0179 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.2356+1148_2356+115 others(7): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17644523 | |||||||
chr19:17644547 | G | A | 2 | a0001c0002t0029g0167 a0001c0008t0002g0274 |
2 | HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2356+1127C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17644547 | |||||||
chr19:17644652 | G | A | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2356+1022C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17644652 | |||||||
chr19:17645009 | C | CT | 29 | a0001c0002t0003g0096 a0001c0002t0010g0033 a0001c0002t0011g0064 others(26): Show |
29 | HG00735.hp1 HG01256.hp2 HG01258.hp2 others(26): Show |
intron_variant | MODIFIER | c.2356+664dupA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17645009 | |||||||
chr19:17645009 | C | CTT | 158 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0165 others(155): Show |
158 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.2356+663_2356+664d others(4): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17645009 | |||||||
chr19:17645095 | G | A | 3 | a0001c0002t0018g0103 a0001c0002t0019g0092 a0001c0002t0025g0315 |
3 | HG02145.hp1 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2356+579C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17645095 | |||||||
chr19:17645172 | C | T | 11 | a0001c0002t0010g0069 a0001c0002t0011g0184 a0001c0002t0038g0037 others(8): Show |
11 | HG01109.hp2 HG02257.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2356+502G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17645172 | |||||||
chr19:17645220 | G | A | 46 | a0001c0001t0001g0171 a0001c0001t0001g0179 a0001c0001t0001g0190 others(43): Show |
46 | HG00140.hp2 HG00597.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.2356+454C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17645220 | |||||||
chr19:17645285 | A | G | 103 | a0001c0001t0001g0137 a0001c0001t0001g0171 a0001c0001t0001g0174 others(100): Show |
103 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.2356+389T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17645285 | |||||||
chr19:17645289 | G | A | 122 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0165 others(119): Show |
122 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.2356+385C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17645289 | |||||||
chr19:17645293 | G | C | 3 | a0001c0002t0018g0103 a0001c0002t0019g0092 a0001c0002t0025g0315 |
3 | HG02145.hp1 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2356+381C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17645293 | |||||||
chr19:17645355 | C | T | 2 | a0002c0005t0003g0168 a0002c0006t0001g0283 |
2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2356+319G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17645355 | |||||||
chr19:17645370 | T | C | 54 | a0001c0001t0001g0171 a0001c0001t0001g0179 a0001c0001t0001g0190 others(51): Show |
54 | HG00140.hp2 HG00597.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.2356+304A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17645370 | |||||||
chr19:17645399 | C | T | 5 | a0001c0002t0010g0097 a0001c0004t0021g0073 a0001c0016t0002g0065 others(2): Show |
5 | HG02451.hp2 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2356+275G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17645399 | |||||||
chr19:17645570 | C | A | 1 | a0001c0007t0008g0212 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2356+104G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 19/43 | chr19 | 17645570 | |||||||
chr19:17646145 | C | T | 1 | a0001c0053t0023g0053 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2045-34G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17646145 | |||||||
chr19:17646185 | G | A | 34 | a0001c0001t0001g0137 a0001c0001t0001g0174 a0001c0001t0001g0236 others(31): Show |
34 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.2045-74C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17646185 | |||||||
chr19:17646269 | G | GTGTT | 79 | a0001c0001t0001g0137 a0001c0001t0001g0171 a0001c0001t0001g0179 others(76): Show |
79 | HG00140.hp2 HG00423.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.2045-162_2045-159d others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17646269 | |||||||
chr19:17646269 | G | GTGTTTGT others(5): Show |
2 | a0001c0007t0001g0042 a0001c0007t0025g0320 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2045-159_2045-158i others(14): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17646269 | |||||||
chr19:17646269 | G | GTGTTTGT others(9): Show |
15 | a0001c0007t0001g0052 a0001c0007t0005g0173 a0001c0007t0008g0063 others(12): Show |
15 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.2045-159_2045-158i others(18): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17646269 | |||||||
chr19:17646269 | G | GTGTTTGT others(13): Show |
1 | a0001c0007t0003g0072 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2045-159_2045-158i others(22): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17646269 | |||||||
chr19:17646269 | G | GTGTTTGT others(1): Show |
11 | a0001c0001t0001g0174 a0001c0002t0003g0096 a0001c0002t0009g0176 others(8): Show |
11 | HG01175.hp1 HG01496.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.2045-166_2045-159d others(10): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17646269 | |||||||
chr19:17646269 | G | GTGTTTGT others(5): Show |
1 | a0001c0002t0001g0157 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2045-170_2045-159d others(14): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17646269 | |||||||
chr19:17646269 | GTGTT | G | 3 | a0001c0002t0010g0097 a0001c0016t0002g0065 a0001c0016t0002g0091 |
3 | HG02451.hp2 HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2045-162_2045-159d others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17646269 | |||||||
chr19:17646420 | A | G | 1 | a0002c0059t0009g0121 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2045-309T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17646420 | |||||||
chr19:17646426 | T | A | 2 | a0001c0004t0010g0056 a0001c0004t0011g0055 |
2 | HG02257.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2045-315A>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17646426 | |||||||
chr19:17646563 | G | A | 1 | a0001c0002t0003g0096 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2045-452C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17646563 | |||||||
chr19:17646620 | G | T | 2 | a0001c0004t0021g0073 a0001c0027t0014g0314 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2045-509C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17646620 | |||||||
chr19:17646650 | C | T | 40 | a0001c0001t0001g0137 a0001c0001t0001g0174 a0001c0001t0001g0236 others(37): Show |
40 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.2045-539G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17646650 | |||||||
chr19:17646893 | C | G | 112 | a0001c0001t0001g0137 a0001c0001t0001g0171 a0001c0001t0001g0174 others(109): Show |
112 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.2044+372G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17646893 | |||||||
chr19:17646905 | CAGCAT | C | 100 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0165 others(97): Show |
100 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.2044+355_2044+359d others(7): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17646905 | |||||||
chr19:17646911 | T | C | 100 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0165 others(97): Show |
100 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.2044+354A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17646911 | |||||||
chr19:17646913 | T | G | 53 | a0001c0001t0001g0171 a0001c0001t0001g0179 a0001c0001t0001g0190 others(50): Show |
53 | HG00140.hp2 HG00597.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.2044+352A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17646913 | |||||||
chr19:17646928 | C | A | 1 | a0001c0001t0001g0237 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2044+337G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17646928 | |||||||
chr19:17646944 | T | G | 139 | a0001c0001t0001g0137 a0001c0001t0001g0171 a0001c0001t0001g0174 others(136): Show |
139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.2044+321A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17646944 | |||||||
chr19:17646984 | C | T | 2 | a0001c0055t0001g0102 a0002c0040t0014g0316 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2044+281G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17646984 | |||||||
chr19:17647011 | C | A | 108 | a0001c0001t0001g0137 a0001c0001t0001g0171 a0001c0001t0001g0174 others(105): Show |
108 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.2044+254G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17647011 | |||||||
chr19:17647115 | A | T | 2 | a0001c0029t0006g0243 a0001c0029t0022g0148 |
2 | HG00140.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.2044+150T>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17647115 | |||||||
chr19:17647208 | A | C | 3 | a0001c0002t0018g0103 a0001c0002t0019g0092 a0001c0002t0025g0315 |
3 | HG02145.hp1 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2044+57T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 17/43 | chr19 | 17647208 | |||||||
chr19:17647502 | C | A | 65 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0165 others(62): Show |
65 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1817-10G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 16/43 | chr19 | 17647502 | |||||||
chr19:17647559 | A | G | 45 | a0001c0001t0001g0137 a0001c0001t0001g0174 a0001c0001t0001g0236 others(42): Show |
45 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.1817-67T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 16/43 | chr19 | 17647559 | |||||||
chr19:17647581 | C | G | 5 | a0001c0007t0001g0062 a0001c0007t0015g0041 a0001c0007t0015g0094 others(2): Show |
5 | HG02647.hp1 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1817-89G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 16/43 | chr19 | 17647581 | |||||||
chr19:17647745 | T | A | 49 | a0001c0001t0001g0137 a0001c0001t0001g0174 a0001c0001t0001g0236 others(46): Show |
49 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1817-253A>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 16/43 | chr19 | 17647745 | |||||||
chr19:17647788 | C | T | 12 | a0001c0002t0010g0033 a0001c0002t0010g0069 a0001c0002t0011g0184 others(9): Show |
12 | HG01109.hp2 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1817-296G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 16/43 | chr19 | 17647788 | |||||||
chr19:17647870 | C | G | 2 | a0001c0004t0021g0073 a0001c0027t0014g0314 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1817-378G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 16/43 | chr19 | 17647870 | |||||||
chr19:17647881 | T | C | 221 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0137 others(218): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.1817-389A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 16/43 | chr19 | 17647881 | |||||||
chr19:17647917 | A | C | 1 | a0001c0002t0018g0103 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1817-425T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 16/43 | chr19 | 17647917 | |||||||
chr19:17648044 | G | A | 10 | a0001c0002t0008g0027 a0001c0002t0011g0039 a0001c0002t0015g0054 others(7): Show |
10 | HG01884.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1816+387C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 16/43 | chr19 | 17648044 | |||||||
chr19:17648363 | T | TCCCCGCC others(7): Show |
1 | a0001c0001t0001g0179 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1816+54_1816+67dup others(14): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 16/43 | chr19 | 17648363 | |||||||
chr19:17648835 | C | G | 1 | a0002c0005t0003g0168 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1596+77G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 15/43 | chr19 | 17648835 | |||||||
chr19:17648852 | T | C | 1 | a0001c0003t0001g0292 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1596+60A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 15/43 | chr19 | 17648852 | |||||||
chr19:17649036 | C | G | 16 | a0001c0002t0010g0069 a0001c0002t0011g0064 a0001c0002t0011g0184 others(13): Show |
16 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1525-53G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 14/43 | chr19 | 17649036 | |||||||
chr19:17649139 | A | G | 1 | a0001c0004t0001g0150 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1525-156T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 14/43 | chr19 | 17649139 | |||||||
chr19:17649273 | G | T | 21 | a0001c0002t0010g0069 a0001c0002t0011g0064 a0001c0002t0011g0184 others(18): Show |
21 | HG01109.hp2 HG01123.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.1524+66C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 14/43 | chr19 | 17649273 | |||||||
chr19:17649371 | G | T | 2 | a0001c0004t0021g0073 a0001c0027t0014g0314 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1519-27C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 13/43 | chr19 | 17649371 | |||||||
chr19:17649423 | C | T | 42 | a0001c0001t0001g0137 a0001c0001t0001g0174 a0001c0001t0001g0189 others(39): Show |
42 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1519-79G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 13/43 | chr19 | 17649423 | |||||||
chr19:17649632 | C | T | 2 | a0001c0002t0019g0092 a0001c0002t0025g0315 |
2 | HG02145.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1440-45G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17649632 | |||||||
chr19:17649641 | A | C | 1 | a0001c0002t0001g0266 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1440-54T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17649641 | |||||||
chr19:17649699 | A | G | 12 | a0001c0001t0001g0137 a0001c0001t0001g0174 a0001c0001t0001g0236 others(9): Show |
12 | HG00423.hp1 HG00597.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.1440-112T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17649699 | |||||||
chr19:17649752 | C | T | 254 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0137 others(251): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.1440-165G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17649752 | |||||||
chr19:17650131 | C | A | 49 | a0001c0002t0003g0096 a0001c0002t0010g0069 a0001c0002t0011g0064 others(46): Show |
49 | HG00140.hp1 HG00741.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.1440-544G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17650131 | |||||||
chr19:17650214 | C | G | 2 | a0001c0004t0021g0073 a0001c0027t0014g0314 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1440-627G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17650214 | |||||||
chr19:17650248 | C | T | 5 | a0001c0002t0018g0103 a0001c0002t0018g0269 a0001c0002t0019g0092 others(2): Show |
5 | HG00735.hp1 HG02145.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440-661G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17650248 | |||||||
chr19:17650301 | G | A | 3 | a0001c0008t0002g0274 a0001c0053t0023g0053 a0001c0066t0019g0043 |
3 | HG02257.hp1 HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1440-714C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17650301 | |||||||
chr19:17650324 | A | G | 10 | a0001c0002t0010g0069 a0001c0002t0011g0184 a0001c0002t0042g0038 others(7): Show |
10 | HG01109.hp2 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1440-737T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17650324 | |||||||
chr19:17650432 | T | C | 3 | a0001c0008t0002g0276 a0001c0008t0002g0277 a0001c0021t0014g0318 |
3 | HG02896.hp2 HG02897.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1440-845A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17650432 | |||||||
chr19:17650450 | T | C | 1 | a0002c0006t0001g0281 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1440-863A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17650450 | |||||||
chr19:17650500 | G | A | 49 | a0001c0002t0003g0096 a0001c0002t0010g0069 a0001c0002t0011g0064 others(46): Show |
49 | HG00140.hp1 HG00741.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.1440-913C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17650500 | |||||||
chr19:17650609 | C | T | 1 | a0001c0002t0003g0096 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1440-1022G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17650609 | |||||||
chr19:17650645 | T | G | 228 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0137 others(225): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.1440-1058A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17650645 | |||||||
chr19:17650676 | C | T | 49 | a0001c0002t0003g0096 a0001c0002t0010g0069 a0001c0002t0011g0064 others(46): Show |
49 | HG00140.hp1 HG00741.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.1440-1089G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17650676 | |||||||
chr19:17650933 | A | AT | 19 | a0001c0001t0001g0115 a0001c0001t0001g0136 a0001c0001t0001g0143 others(16): Show |
19 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1440-1347dupA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17650933 | |||||||
chr19:17650933 | ATTT | A | 6 | a0001c0001t0003g0225 a0001c0002t0001g0178 a0001c0002t0004g0227 others(3): Show |
6 | HG02027.hp1 HG02523.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1440-1349_1440-134 others(7): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17650933 | |||||||
chr19:17650933 | ATTTT | A | 164 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0137 others(161): Show |
164 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1440-1350_1440-134 others(8): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17650933 | |||||||
chr19:17650933 | ATTTTT | A | 55 | a0001c0001t0001g0252 a0001c0002t0010g0069 a0001c0002t0011g0064 others(52): Show |
55 | HG00140.hp1 HG00741.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.1440-1351_1440-134 others(9): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17650933 | |||||||
chr19:17650976 | C | T | 5 | a0001c0011t0001g0089 a0001c0011t0001g0156 a0001c0011t0001g0300 others(2): Show |
5 | HG01123.hp2 HG01361.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440-1389G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17650976 | |||||||
chr19:17651068 | G | T | 1 | a0001c0022t0008g0185 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1440-1481C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651068 | |||||||
chr19:17651091 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1440-1504G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651091 | |||||||
chr19:17651173 | A | C | 16 | a0001c0002t0010g0069 a0001c0002t0011g0064 a0001c0002t0011g0184 others(13): Show |
16 | HG01109.hp2 HG02257.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1439+1458T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651173 | |||||||
chr19:17651189 | A | C | 226 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0137 others(223): Show |
226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.1439+1442T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651189 | |||||||
chr19:17651192 | C | T | 28 | a0001c0002t0003g0096 a0001c0007t0001g0042 a0001c0007t0001g0052 others(25): Show |
28 | HG00140.hp1 HG00741.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.1439+1439G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651192 | |||||||
chr19:17651250 | A | AT | 225 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0137 others(222): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.1439+1380dupA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651250 | |||||||
chr19:17651252 | T | TA | 47 | a0001c0001t0001g0022 a0001c0001t0001g0107 a0001c0001t0001g0115 others(44): Show |
47 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.1439+1378dupT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651252 | |||||||
chr19:17651253 | A | T | 1 | a0001c0067t0004g0265 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1439+1378T>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651253 | |||||||
chr19:17651272 | G | C | 5 | a0001c0007t0001g0062 a0001c0007t0015g0041 a0001c0007t0015g0094 others(2): Show |
5 | HG02647.hp1 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1439+1359C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651272 | |||||||
chr19:17651285 | C | T | 165 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0137 others(162): Show |
165 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.1439+1346G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651285 | |||||||
chr19:17651365 | A | C | 226 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0137 others(223): Show |
226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.1439+1266T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651365 | |||||||
chr19:17651373 | A | G | 3 | a0001c0014t0001g0081 a0001c0028t0002g0196 a0001c0061t0001g0239 |
3 | NA18962.hp1 NA19004.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1439+1258T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651373 | |||||||
chr19:17651380 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1439+1251G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651380 | |||||||
chr19:17651401 | AT | A | 3 | a0001c0044t0001g0301 a0002c0012t0001g0169 a0002c0012t0001g0175 |
3 | HG00735.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1439+1229delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651401 | |||||||
chr19:17651407 | G | T | 3 | a0001c0044t0001g0301 a0002c0012t0001g0169 a0002c0012t0001g0175 |
3 | HG00735.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1439+1224C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651407 | |||||||
chr19:17651408 | T | C | 3 | a0001c0044t0001g0301 a0002c0012t0001g0169 a0002c0012t0001g0175 |
3 | HG00735.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1439+1223A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651408 | |||||||
chr19:17651456 | C | T | 19 | a0001c0002t0010g0069 a0001c0002t0011g0064 a0001c0002t0011g0184 others(16): Show |
19 | HG01109.hp2 HG01123.hp2 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.1439+1175G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651456 | |||||||
chr19:17651517 | A | C | 226 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0137 others(223): Show |
226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.1439+1114T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651517 | |||||||
chr19:17651527 | C | G | 176 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0137 others(173): Show |
176 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.1439+1104G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651527 | |||||||
chr19:17651534 | G | A | 1 | a0002c0006t0003g0267 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1439+1097C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651534 | |||||||
chr19:17651619 | C | A | 2 | a0001c0002t0019g0092 a0001c0002t0025g0315 |
2 | HG02145.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1439+1012G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651619 | |||||||
chr19:17651635 | C | T | 1 | a0001c0024t0001g0057 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1439+996G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651635 | |||||||
chr19:17651665 | G | A | 1 | a0001c0004t0001g0114 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1439+966C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651665 | |||||||
chr19:17651735 | G | C | 226 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0137 others(223): Show |
226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.1439+896C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651735 | |||||||
chr19:17651745 | A | C | 226 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0137 others(223): Show |
226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.1439+886T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651745 | |||||||
chr19:17651805 | T | C | 227 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0137 others(224): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.1439+826A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651805 | |||||||
chr19:17651806 | G | A | 40 | a0001c0001t0001g0166 a0001c0001t0001g0194 a0001c0001t0001g0199 others(37): Show |
40 | HG00558.hp1 HG01256.hp2 HG01258.hp2 others(37): Show |
intron_variant | MODIFIER | c.1439+825C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651806 | |||||||
chr19:17651851 | G | A | 1 | a0001c0007t0005g0173 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1439+780C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651851 | |||||||
chr19:17651882 | T | A | 58 | a0001c0002t0003g0096 a0001c0002t0005g0120 a0001c0002t0010g0069 others(55): Show |
58 | HG00140.hp1 HG00735.hp1 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.1439+749A>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17651882 | |||||||
chr19:17652031 | G | A | 50 | a0001c0002t0003g0096 a0001c0002t0005g0120 a0001c0002t0010g0069 others(47): Show |
50 | HG00140.hp1 HG00741.hp1 HG01109.hp2 others(47): Show |
intron_variant | MODIFIER | c.1439+600C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17652031 | |||||||
chr19:17652081 | G | A | 227 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0137 others(224): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.1439+550C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17652081 | |||||||
chr19:17652100 | G | C | 227 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0137 others(224): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.1439+531C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17652100 | |||||||
chr19:17652115 | CATTT | C | 227 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0137 others(224): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.1439+512_1439+515d others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17652115 | |||||||
chr19:17652177 | G | A | 34 | a0001c0002t0003g0096 a0001c0002t0005g0120 a0001c0007t0001g0042 others(31): Show |
34 | HG00140.hp1 HG00741.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.1439+454C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17652177 | |||||||
chr19:17652421 | C | T | 5 | a0001c0007t0001g0062 a0001c0007t0015g0041 a0001c0007t0015g0094 others(2): Show |
5 | HG02647.hp1 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1439+210G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17652421 | |||||||
chr19:17652492 | C | T | 1 | a0001c0002t0005g0120 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1439+139G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17652492 | |||||||
chr19:17652583 | A | G | 250 | a0001c0001t0001g0080 a0001c0001t0001g0132 a0001c0001t0001g0165 others(247): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1439+48T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 12/43 | chr19 | 17652583 | |||||||
chr19:17652848 | C | T | 3 | a0001c0001t0001g0187 a0001c0001t0001g0207 a0001c0004t0001g0191 |
3 | HG01943.hp1 HG02004.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1393-171G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17652848 | |||||||
chr19:17652975 | C | T | 1 | a0001c0003t0017g0049 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1393-298G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17652975 | |||||||
chr19:17653034 | C | T | 2 | a0001c0004t0021g0073 a0001c0027t0014g0314 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1393-357G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17653034 | |||||||
chr19:17653249 | G | T | 1 | a0001c0004t0021g0073 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1393-572C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17653249 | |||||||
chr19:17653329 | A | AAT | 19 | a0001c0002t0001g0308 a0001c0002t0003g0096 a0001c0002t0008g0284 others(16): Show |
19 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1393-654_1393-653d others(4): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17653329 | |||||||
chr19:17653329 | A | AATAT | 139 | a0001c0001t0001g0080 a0001c0001t0001g0165 a0001c0001t0001g0174 others(136): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1393-656_1393-653d others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17653329 | |||||||
chr19:17653329 | A | AATATAT | 20 | a0001c0002t0012g0077 a0001c0002t0012g0299 a0001c0002t0038g0037 others(17): Show |
20 | HG00741.hp1 HG01175.hp2 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.1393-658_1393-653d others(8): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17653329 | |||||||
chr19:17653441 | G | A | 1 | a0001c0056t0002g0155 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1393-764C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17653441 | |||||||
chr19:17653496 | C | T | 5 | a0001c0002t0018g0103 a0001c0002t0018g0269 a0001c0007t0008g0063 others(2): Show |
5 | HG00735.hp1 HG02451.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1393-819G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17653496 | |||||||
chr19:17653520 | T | C | 4 | a0003c0010t0006g0306 a0003c0010t0013g0016 a0003c0010t0013g0019 others(1): Show |
4 | HG00738.hp1 HG01070.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1393-843A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17653520 | |||||||
chr19:17653610 | A | G | 1 | a0002c0005t0001g0285 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1393-933T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17653610 | |||||||
chr19:17653821 | CT | C | 174 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0165 others(171): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1393-1145delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17653821 | |||||||
chr19:17653821 | CTT | C | 61 | a0001c0001t0001g0022 a0001c0002t0001g0001 a0001c0002t0001g0193 others(58): Show |
61 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.1393-1146_1393-114 others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17653821 | |||||||
chr19:17653821 | CTTT | C | 12 | a0001c0002t0008g0027 a0001c0002t0010g0069 a0001c0002t0011g0287 others(9): Show |
12 | HG01109.hp2 HG01433.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1393-1147_1393-114 others(7): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17653821 | |||||||
chr19:17653861 | C | G | 2 | a0002c0005t0001g0285 a0002c0006t0001g0021 |
2 | HG01346.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1393-1184G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17653861 | |||||||
chr19:17653869 | C | G | 2 | a0002c0012t0001g0169 a0002c0012t0001g0175 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1393-1192G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17653869 | |||||||
chr19:17653888 | G | A | 4 | a0003c0010t0006g0306 a0003c0010t0013g0016 a0003c0010t0013g0019 others(1): Show |
4 | HG00738.hp1 HG01070.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.1393-1211C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17653888 | |||||||
chr19:17653920 | G | A | 7 | a0001c0002t0011g0039 a0001c0002t0020g0025 a0001c0002t0032g0098 others(4): Show |
7 | HG00738.hp1 HG01070.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1393-1243C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17653920 | |||||||
chr19:17653951 | C | T | 1 | a0001c0003t0001g0009 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1393-1274G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17653951 | |||||||
chr19:17653987 | C | T | 1 | a0001c0002t0001g0193 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1392+1287G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17653987 | |||||||
chr19:17654018 | G | A | 28 | a0001c0002t0001g0266 a0001c0002t0004g0224 a0001c0002t0008g0046 others(25): Show |
28 | HG00099.hp1 HG00738.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1392+1256C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17654018 | |||||||
chr19:17654127 | A | G | 7 | a0001c0002t0011g0039 a0001c0002t0020g0025 a0001c0002t0032g0098 others(4): Show |
7 | HG00738.hp1 HG01070.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1392+1147T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17654127 | |||||||
chr19:17654193 | T | C | 1 | a0001c0015t0006g0090 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1392+1081A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17654193 | |||||||
chr19:17654395 | A | C | 5 | a0001c0002t0003g0096 a0001c0004t0021g0073 a0001c0011t0001g0089 others(2): Show |
5 | HG01361.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1392+879T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17654395 | |||||||
chr19:17654594 | T | G | 5 | a0001c0002t0018g0269 a0001c0016t0002g0065 a0001c0016t0002g0091 others(2): Show |
5 | HG00735.hp1 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1392+680A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17654594 | |||||||
chr19:17654599 | G | A | 8 | a0001c0002t0009g0176 a0001c0003t0001g0014 a0001c0003t0003g0133 others(5): Show |
8 | HG00735.hp2 HG01175.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1392+675C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17654599 | |||||||
chr19:17654604 | G | A | 1 | a0001c0003t0007g0206 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1392+670C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17654604 | |||||||
chr19:17654893 | G | A | 31 | a0001c0002t0001g0157 a0001c0002t0001g0308 a0001c0002t0008g0284 others(28): Show |
31 | HG00735.hp2 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.1392+381C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17654893 | |||||||
chr19:17654937 | T | C | 36 | a0001c0001t0001g0231 a0001c0001t0001g0236 a0001c0001t0001g0249 others(33): Show |
36 | HG00438.hp2 HG00597.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1392+337A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17654937 | |||||||
chr19:17655257 | C | T | 10 | a0001c0002t0003g0096 a0001c0002t0018g0269 a0001c0004t0021g0073 others(7): Show |
10 | HG00735.hp1 HG01361.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1392+17G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17655257 | |||||||
chr19:17655263 | G | A | 1 | a0001c0071t0002g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1392+11C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 11/43 | chr19 | 17655263 | |||||||
chr19:17655548 | C | T | 1 | a0002c0034t0002g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1284-166G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 10/43 | chr19 | 17655548 | |||||||
chr19:17655682 | C | T | 21 | a0001c0001t0001g0022 a0001c0002t0001g0001 a0001c0002t0001g0193 others(18): Show |
21 | HG00558.hp1 HG00741.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.1283+201G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 10/43 | chr19 | 17655682 | |||||||
chr19:17655807 | C | T | 1 | a0002c0034t0002g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1283+76G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 10/43 | chr19 | 17655807 | |||||||
chr19:17655810 | T | G | 2 | a0002c0034t0002g0099 a0002c0039t0021g0026 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1283+73A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 10/43 | chr19 | 17655810 | |||||||
chr19:17656427 | T | TG | 9 | a0001c0001t0001g0297 a0001c0002t0001g0113 a0001c0002t0007g0018 others(6): Show |
9 | HG01109.hp1 HG01109.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.768-30dupC | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17656427 | |||||||
chr19:17656499 | G | T | 54 | a0001c0002t0003g0068 a0001c0002t0008g0027 a0001c0002t0008g0046 others(51): Show |
54 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.768-101C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17656499 | |||||||
chr19:17656526 | G | A | 1 | a0001c0002t0004g0139 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.768-128C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17656526 | |||||||
chr19:17656563 | C | T | 11 | a0001c0002t0009g0176 a0001c0003t0001g0014 a0001c0003t0003g0133 others(8): Show |
11 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.768-165G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17656563 | |||||||
chr19:17656573 | C | T | 11 | a0001c0002t0015g0054 a0001c0002t0042g0038 a0001c0003t0003g0162 others(8): Show |
11 | HG02257.hp2 HG02451.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.768-175G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17656573 | |||||||
chr19:17656587 | C | T | 3 | a0001c0003t0001g0154 a0001c0003t0001g0198 a0001c0003t0001g0210 |
3 | HG03834.hp2 NA18612.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.768-189G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17656587 | |||||||
chr19:17656664 | C | T | 9 | a0001c0002t0009g0176 a0001c0003t0001g0014 a0001c0003t0003g0133 others(6): Show |
9 | HG00280.hp2 HG00735.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.768-266G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17656664 | |||||||
chr19:17656725 | G | A | 1 | a0001c0007t0008g0212 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.768-327C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17656725 | |||||||
chr19:17656848 | G | A | 2 | a0002c0005t0004g0118 a0002c0005t0004g0119 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.768-450C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17656848 | |||||||
chr19:17656852 | C | CA | 17 | a0001c0001t0001g0115 a0001c0001t0001g0132 a0001c0001t0001g0143 others(14): Show |
17 | HG00438.hp2 HG00642.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.768-455dupT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17656852 | |||||||
chr19:17656852 | CA | C | 26 | a0001c0001t0001g0022 a0001c0001t0001g0252 a0001c0002t0001g0193 others(23): Show |
26 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.768-455delT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17656852 | |||||||
chr19:17656852 | CAA | C | 9 | a0001c0002t0001g0001 a0001c0002t0007g0018 a0001c0002t0007g0257 others(6): Show |
9 | HG00733.hp2 HG02155.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.768-456_768-455del others(2): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17656852 | |||||||
chr19:17656852 | CAAA | C | 17 | a0001c0002t0008g0027 a0001c0002t0010g0097 a0001c0002t0011g0287 others(14): Show |
17 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.768-457_768-455del others(3): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17656852 | |||||||
chr19:17656852 | CAAAA | C | 43 | a0001c0002t0001g0157 a0001c0002t0001g0308 a0001c0002t0003g0068 others(40): Show |
43 | HG00438.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.768-458_768-455del others(4): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17656852 | |||||||
chr19:17656852 | CAAAAA | C | 124 | a0001c0001t0001g0190 a0001c0001t0001g0216 a0001c0001t0001g0250 others(121): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.768-459_768-455del others(5): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17656852 | |||||||
chr19:17656852 | CAAAAAA | C | 15 | a0001c0001t0004g0012 a0001c0002t0011g0039 a0001c0003t0001g0217 others(12): Show |
15 | HG01070.hp1 HG01168.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.768-460_768-455del others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17656852 | |||||||
chr19:17656907 | G | A | 3 | a0001c0002t0003g0068 a0001c0008t0002g0075 a0001c0050t0033g0085 |
3 | HG02258.hp1 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.768-509C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17656907 | |||||||
chr19:17656911 | A | G | 54 | a0001c0002t0003g0068 a0001c0002t0008g0027 a0001c0002t0008g0046 others(51): Show |
54 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.768-513T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17656911 | |||||||
chr19:17656961 | C | A | 11 | a0001c0002t0015g0054 a0001c0002t0042g0038 a0001c0003t0003g0162 others(8): Show |
11 | HG02257.hp2 HG02451.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.768-563G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17656961 | |||||||
chr19:17656980 | T | G | 242 | a0001c0001t0001g0022 a0001c0001t0001g0190 a0001c0001t0001g0199 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.768-582A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17656980 | |||||||
chr19:17656994 | A | G | 3 | a0001c0007t0001g0042 a0001c0007t0001g0052 a0001c0007t0025g0320 |
3 | HG02970.hp1 HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.768-596T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17656994 | |||||||
chr19:17657028 | C | T | 85 | a0001c0002t0001g0157 a0001c0002t0001g0308 a0001c0002t0003g0096 others(82): Show |
85 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.768-630G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17657028 | |||||||
chr19:17657070 | C | T | 11 | a0001c0002t0015g0054 a0001c0002t0042g0038 a0001c0003t0003g0162 others(8): Show |
11 | HG02257.hp2 HG02451.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.768-672G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17657070 | |||||||
chr19:17657071 | T | C | 1 | a0001c0071t0002g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.768-673A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17657071 | |||||||
chr19:17657106 | G | A | 8 | a0001c0002t0011g0039 a0001c0008t0026g0083 a0001c0011t0001g0089 others(5): Show |
8 | HG01361.hp1 HG01884.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.768-708C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17657106 | |||||||
chr19:17657134 | C | T | 1 | a0004c0065t0005g0134 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.768-736G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17657134 | |||||||
chr19:17657278 | C | T | 1 | a0001c0004t0049g0317 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.767+784G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17657278 | |||||||
chr19:17657308 | A | T | 10 | a0001c0002t0015g0054 a0001c0003t0003g0162 a0001c0004t0010g0056 others(7): Show |
10 | HG02257.hp2 HG02451.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.767+754T>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17657308 | |||||||
chr19:17657371 | A | G | 1 | a0001c0002t0003g0096 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.767+691T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17657371 | |||||||
chr19:17657372 | C | T | 1 | a0001c0007t0008g0212 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.767+690G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17657372 | |||||||
chr19:17657404 | C | T | 10 | a0001c0002t0008g0046 a0001c0002t0018g0103 a0001c0002t0038g0037 others(7): Show |
10 | HG02572.hp2 HG02647.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.767+658G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17657404 | |||||||
chr19:17657423 | G | A | 32 | a0001c0002t0003g0068 a0001c0002t0008g0046 a0001c0002t0011g0039 others(29): Show |
32 | HG01361.hp1 HG01884.hp2 HG02257.hp2 others(29): Show |
intron_variant | MODIFIER | c.767+639C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17657423 | |||||||
chr19:17657435 | G | A | 32 | a0001c0002t0003g0068 a0001c0002t0008g0046 a0001c0002t0011g0039 others(29): Show |
32 | HG01361.hp1 HG01884.hp2 HG02257.hp2 others(29): Show |
intron_variant | MODIFIER | c.767+627C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17657435 | |||||||
chr19:17657468 | C | T | 1 | a0004c0049t0006g0293 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.767+594G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17657468 | |||||||
chr19:17657531 | C | T | 1 | a0002c0034t0002g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.767+531G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17657531 | |||||||
chr19:17657722 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.767+340T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17657722 | |||||||
chr19:17657845 | G | C | 1 | a0002c0006t0001g0302 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.767+217C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17657845 | |||||||
chr19:17657883 | GA | G | 45 | a0001c0002t0003g0068 a0001c0002t0008g0046 a0001c0002t0009g0176 others(42): Show |
45 | HG00280.hp2 HG00733.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.767+178delT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17657883 | |||||||
chr19:17658009 | A | G | 73 | a0001c0001t0001g0190 a0001c0001t0001g0216 a0001c0001t0001g0250 others(70): Show |
73 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.767+53T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17658009 | |||||||
chr19:17658050 | C | T | 1 | a0002c0006t0006g0278 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.767+12G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 9/43 | chr19 | 17658050 | |||||||
chr19:17658299 | G | A | 1 | a0002c0039t0021g0026 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.560-30C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17658299 | |||||||
chr19:17658303 | G | A | 10 | a0001c0002t0015g0054 a0001c0003t0003g0162 a0001c0004t0010g0056 others(7): Show |
10 | HG02257.hp2 HG02451.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.560-34C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17658303 | |||||||
chr19:17658325 | G | A | 1 | a0001c0003t0001g0014 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.560-56C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17658325 | |||||||
chr19:17658357 | C | T | 239 | a0001c0001t0001g0022 a0001c0001t0001g0190 a0001c0001t0001g0216 others(236): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.560-88G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17658357 | |||||||
chr19:17658479 | G | C | 1 | a0004c0048t0005g0177 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.560-210C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17658479 | |||||||
chr19:17658513 | A | G | 9 | a0001c0002t0009g0176 a0001c0003t0001g0014 a0001c0003t0003g0133 others(6): Show |
9 | HG00280.hp2 HG00735.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.560-244T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17658513 | |||||||
chr19:17658577 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.560-308A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17658577 | |||||||
chr19:17658629 | A | G | 2 | a0001c0008t0026g0083 a0001c0022t0008g0185 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.560-360T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17658629 | |||||||
chr19:17658699 | C | T | 128 | a0001c0002t0001g0113 a0001c0002t0001g0157 a0001c0002t0001g0308 others(125): Show |
128 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.560-430G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17658699 | |||||||
chr19:17658704 | C | T | 55 | a0001c0001t0001g0190 a0001c0001t0001g0216 a0001c0001t0001g0250 others(52): Show |
55 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.560-435G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17658704 | |||||||
chr19:17659074 | GAA | G | 63 | a0001c0002t0001g0113 a0001c0002t0012g0017 a0001c0003t0001g0128 others(60): Show |
63 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.560-807_560-806del others(2): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17659074 | |||||||
chr19:17659081 | A | G | 1 | a0001c0002t0001g0001 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.560-812T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17659081 | |||||||
chr19:17659361 | G | T | 236 | a0001c0001t0001g0022 a0001c0001t0001g0190 a0001c0001t0001g0216 others(233): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.560-1092C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17659361 | |||||||
chr19:17659386 | T | G | 4 | a0001c0002t0011g0039 a0001c0011t0001g0089 a0001c0011t0001g0300 others(1): Show |
4 | HG01361.hp1 HG01884.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-1117A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17659386 | |||||||
chr19:17659470 | T | G | 1 | a0002c0039t0021g0026 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.560-1201A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17659470 | |||||||
chr19:17659615 | A | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0235 |
2 | NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.560-1346T>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17659615 | |||||||
chr19:17659646 | G | A | 2 | a0001c0016t0002g0065 a0001c0016t0002g0091 |
2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.560-1377C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17659646 | |||||||
chr19:17659818 | A | G | 10 | a0001c0002t0015g0054 a0001c0003t0003g0162 a0001c0004t0010g0056 others(7): Show |
10 | HG02257.hp2 HG02451.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.560-1549T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17659818 | |||||||
chr19:17659842 | G | T | 2 | a0001c0004t0003g0030 a0004c0065t0005g0134 |
2 | HG00733.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.560-1573C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17659842 | |||||||
chr19:17659848 | A | G | 2 | a0001c0002t0003g0068 a0001c0008t0002g0075 |
2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.560-1579T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17659848 | |||||||
chr19:17659948 | C | T | 26 | a0001c0002t0001g0001 a0001c0002t0001g0193 a0001c0002t0001g0229 others(23): Show |
26 | HG00558.hp1 HG00741.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.560-1679G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17659948 | |||||||
chr19:17659949 | G | A | 1 | a0001c0002t0008g0046 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.560-1680C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17659949 | |||||||
chr19:17659958 | C | T | 6 | a0001c0002t0011g0039 a0001c0011t0001g0089 a0001c0011t0001g0300 others(3): Show |
6 | HG01361.hp1 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.560-1689G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17659958 | |||||||
chr19:17660068 | T | G | 16 | a0001c0002t0001g0157 a0001c0002t0027g0295 a0001c0002t0028g0047 others(13): Show |
16 | HG01167.hp2 HG01169.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.560-1799A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17660068 | |||||||
chr19:17660163 | C | A | 2 | a0001c0004t0003g0030 a0004c0065t0005g0134 |
2 | HG00733.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.560-1894G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17660163 | |||||||
chr19:17660191 | C | T | 7 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(4): Show |
7 | HG01884.hp1 HG02280.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.560-1922G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17660191 | |||||||
chr19:17660209 | T | C | 52 | a0001c0002t0001g0157 a0001c0002t0001g0266 a0001c0002t0001g0308 others(49): Show |
52 | HG00099.hp1 HG00738.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.560-1940A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17660209 | |||||||
chr19:17660213 | T | C | 52 | a0001c0002t0001g0157 a0001c0002t0001g0266 a0001c0002t0001g0308 others(49): Show |
52 | HG00099.hp1 HG00738.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.560-1944A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17660213 | |||||||
chr19:17660231 | G | T | 1 | a0001c0001t0007g0232 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.560-1962C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17660231 | |||||||
chr19:17660253 | T | C | 2 | a0001c0002t0003g0068 a0001c0003t0007g0206 |
2 | HG02258.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.560-1984A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17660253 | |||||||
chr19:17660282 | GT | G | 103 | a0001c0001t0001g0190 a0001c0001t0001g0216 a0001c0001t0001g0250 others(100): Show |
103 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.560-2014delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17660282 | |||||||
chr19:17660510 | G | T | 53 | a0001c0001t0001g0190 a0001c0001t0001g0216 a0001c0001t0001g0250 others(50): Show |
53 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.560-2241C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17660510 | |||||||
chr19:17660523 | G | T | 197 | a0001c0001t0001g0190 a0001c0001t0001g0216 a0001c0001t0001g0250 others(194): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.560-2254C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17660523 | |||||||
chr19:17660528 | T | C | 1 | a0001c0003t0001g0009 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.560-2259A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17660528 | |||||||
chr19:17660535 | G | GT | 193 | a0001c0001t0001g0011 a0001c0001t0001g0174 a0001c0001t0001g0190 others(190): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.560-2267dupA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17660535 | |||||||
chr19:17660535 | G | GTT | 17 | a0001c0002t0031g0298 a0001c0003t0001g0110 a0001c0003t0001g0138 others(14): Show |
17 | HG00597.hp1 HG01243.hp2 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.560-2268_560-2267d others(4): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17660535 | |||||||
chr19:17660583 | G | A | 2 | a0001c0004t0003g0030 a0004c0065t0005g0134 |
2 | HG00733.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.560-2314C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17660583 | |||||||
chr19:17660656 | C | T | 1 | a0001c0003t0001g0129 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.560-2387G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17660656 | |||||||
chr19:17660713 | G | A | 7 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(4): Show |
7 | HG01884.hp1 HG02280.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.560-2444C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17660713 | |||||||
chr19:17660766 | A | G | 6 | a0001c0001t0001g0166 a0001c0001t0001g0187 a0001c0001t0001g0207 others(3): Show |
6 | HG00423.hp1 HG01943.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.560-2497T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17660766 | |||||||
chr19:17660859 | T | C | 1 | a0001c0067t0004g0265 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.560-2590A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17660859 | |||||||
chr19:17660943 | CTATT | C | 23 | a0001c0002t0001g0001 a0001c0002t0001g0193 a0001c0002t0001g0229 others(20): Show |
23 | HG00558.hp1 HG00741.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.559+2585_559+2588d others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17660943 | |||||||
chr19:17660987 | A | G | 22 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(19): Show |
22 | HG00733.hp2 HG01884.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.559+2545T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17660987 | |||||||
chr19:17661003 | A | G | 6 | a0001c0002t0011g0039 a0001c0011t0001g0089 a0001c0011t0001g0300 others(3): Show |
6 | HG01361.hp1 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.559+2529T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17661003 | |||||||
chr19:17661099 | C | T | 8 | a0001c0003t0001g0014 a0001c0003t0003g0133 a0001c0020t0001g0005 others(5): Show |
8 | HG00280.hp2 HG00735.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.559+2433G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17661099 | |||||||
chr19:17661102 | C | A | 22 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(19): Show |
22 | HG00733.hp2 HG01884.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.559+2430G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17661102 | |||||||
chr19:17661104 | C | CTTTT | 16 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(13): Show |
16 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.559+2424_559+2427d others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17661104 | |||||||
chr19:17661104 | CT | C | 98 | a0001c0002t0001g0113 a0001c0002t0003g0068 a0001c0002t0008g0046 others(95): Show |
98 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.559+2427delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17661104 | |||||||
chr19:17661333 | C | T | 22 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(19): Show |
22 | HG00733.hp2 HG01884.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.559+2199G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17661333 | |||||||
chr19:17661344 | G | A | 22 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(19): Show |
22 | HG00733.hp2 HG01884.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.559+2188C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17661344 | |||||||
chr19:17661349 | A | C | 1 | a0001c0002t0001g0308 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.559+2183T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17661349 | |||||||
chr19:17661578 | C | T | 1 | a0001c0024t0001g0057 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.559+1954G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17661578 | |||||||
chr19:17661587 | G | A | 22 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(19): Show |
22 | HG00733.hp2 HG01884.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.559+1945C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17661587 | |||||||
chr19:17661607 | C | T | 238 | a0001c0001t0001g0190 a0001c0001t0001g0216 a0001c0001t0001g0250 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.559+1925G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17661607 | |||||||
chr19:17661608 | T | C | 22 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(19): Show |
22 | HG00733.hp2 HG01884.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.559+1924A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17661608 | |||||||
chr19:17661616 | C | A | 4 | a0001c0002t0011g0039 a0001c0011t0001g0089 a0001c0011t0001g0300 others(1): Show |
4 | HG01361.hp1 HG01884.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.559+1916G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17661616 | |||||||
chr19:17661751 | G | A | 2 | a0002c0005t0004g0144 a0002c0006t0001g0241 |
2 | HG02293.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.559+1781C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17661751 | |||||||
chr19:17661757 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.559+1775C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17661757 | |||||||
chr19:17661855 | A | G | 1 | a0001c0003t0003g0264 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.559+1677T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17661855 | |||||||
chr19:17661907 | C | T | 102 | a0001c0001t0001g0190 a0001c0001t0001g0216 a0001c0001t0001g0250 others(99): Show |
102 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.559+1625G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17661907 | |||||||
chr19:17661948 | A | G | 1 | a0001c0071t0002g0311 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.559+1584T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17661948 | |||||||
chr19:17661964 | G | A | 11 | a0001c0002t0015g0054 a0001c0003t0003g0162 a0001c0004t0010g0056 others(8): Show |
11 | HG02145.hp2 HG02257.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.559+1568C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17661964 | |||||||
chr19:17662004 | G | A | 23 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(20): Show |
23 | HG00733.hp2 HG01884.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.559+1528C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662004 | |||||||
chr19:17662062 | T | C | 3 | a0001c0002t0008g0284 a0001c0002t0020g0025 a0001c0002t0032g0098 |
3 | HG02280.hp1 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.559+1470A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662062 | |||||||
chr19:17662071 | A | G | 238 | a0001c0001t0001g0190 a0001c0001t0001g0216 a0001c0001t0001g0250 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.559+1461T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662071 | |||||||
chr19:17662132 | A | G | 23 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(20): Show |
23 | HG00733.hp2 HG01884.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.559+1400T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662132 | |||||||
chr19:17662144 | C | G | 23 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(20): Show |
23 | HG00733.hp2 HG01884.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.559+1388G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662144 | |||||||
chr19:17662150 | C | T | 3 | a0001c0002t0003g0068 a0001c0008t0002g0075 a0001c0050t0033g0085 |
3 | HG02258.hp1 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.559+1382G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662150 | |||||||
chr19:17662166 | T | C | 23 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(20): Show |
23 | HG00733.hp2 HG01884.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.559+1366A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662166 | |||||||
chr19:17662190 | C | T | 23 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(20): Show |
23 | HG00733.hp2 HG01884.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.559+1342G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662190 | |||||||
chr19:17662199 | G | A | 21 | a0001c0002t0001g0193 a0001c0002t0001g0229 a0001c0002t0004g0139 others(18): Show |
21 | HG00558.hp1 HG00741.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.559+1333C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662199 | |||||||
chr19:17662214 | C | T | 23 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(20): Show |
23 | HG00733.hp2 HG01884.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.559+1318G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662214 | |||||||
chr19:17662234 | A | G | 2 | a0001c0008t0026g0083 a0001c0022t0008g0185 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.559+1298T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662234 | |||||||
chr19:17662245 | C | A | 2 | a0001c0008t0026g0083 a0001c0022t0008g0185 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.559+1287G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662245 | |||||||
chr19:17662245 | C | CA | 24 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(21): Show |
24 | HG00733.hp2 HG01884.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.559+1286dupT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662245 | |||||||
chr19:17662267 | C | T | 9 | a0001c0003t0003g0162 a0001c0004t0010g0056 a0001c0004t0010g0242 others(6): Show |
9 | HG02257.hp2 HG02451.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.559+1265G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662267 | |||||||
chr19:17662350 | T | C | 1 | a0002c0026t0002g0263 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.559+1182A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662350 | |||||||
chr19:17662437 | G | C | 8 | a0001c0003t0001g0014 a0001c0003t0003g0133 a0001c0020t0001g0005 others(5): Show |
8 | HG00280.hp2 HG00735.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.559+1095C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662437 | |||||||
chr19:17662468 | GTAATAA | G | 23 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(20): Show |
23 | HG00733.hp2 HG01884.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.559+1058_559+1063d others(8): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662468 | |||||||
chr19:17662553 | T | C | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.559+979A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662553 | |||||||
chr19:17662585 | T | C | 23 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(20): Show |
23 | HG00733.hp2 HG01884.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.559+947A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662585 | |||||||
chr19:17662606 | C | T | 4 | a0001c0001t0001g0136 a0001c0004t0001g0211 a0001c0030t0001g0122 others(1): Show |
4 | HG01256.hp2 HG01258.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.559+926G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662606 | |||||||
chr19:17662624 | C | T | 112 | a0001c0002t0001g0001 a0001c0002t0001g0157 a0001c0002t0001g0308 others(109): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.559+908G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662624 | |||||||
chr19:17662716 | C | G | 6 | a0001c0002t0044g0093 a0001c0007t0008g0212 a0001c0008t0026g0083 others(3): Show |
6 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.559+816G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662716 | |||||||
chr19:17662737 | G | A | 13 | a0001c0002t0008g0046 a0001c0002t0008g0284 a0001c0002t0018g0103 others(10): Show |
13 | HG02280.hp1 HG02572.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.559+795C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662737 | |||||||
chr19:17662747 | C | T | 14 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(11): Show |
14 | HG00733.hp2 HG01884.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.559+785G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662747 | |||||||
chr19:17662780 | C | T | 1 | a0001c0015t0006g0303 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.559+752G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662780 | |||||||
chr19:17662789 | G | A | 8 | a0001c0004t0010g0056 a0001c0004t0010g0242 a0001c0004t0011g0055 others(5): Show |
8 | HG02257.hp2 HG02451.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.559+743C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662789 | |||||||
chr19:17662794 | C | A | 1 | a0001c0001t0001g0115 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.559+738G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662794 | |||||||
chr19:17662813 | G | A | 1 | a0002c0013t0002g0200 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.559+719C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662813 | |||||||
chr19:17662836 | C | T | 2 | a0001c0008t0026g0083 a0001c0022t0008g0185 |
2 | HG02630.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.559+696G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662836 | |||||||
chr19:17662843 | C | T | 1 | a0001c0007t0001g0042 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.559+689G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662843 | |||||||
chr19:17662861 | G | A | 1 | a0001c0002t0008g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.559+671C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662861 | |||||||
chr19:17662913 | C | T | 8 | a0001c0003t0001g0014 a0001c0003t0003g0133 a0001c0020t0001g0005 others(5): Show |
8 | HG00280.hp2 HG00735.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.559+619G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662913 | |||||||
chr19:17662919 | C | CA | 49 | a0001c0001t0007g0232 a0001c0002t0001g0193 a0001c0002t0001g0229 others(46): Show |
49 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.559+612dupT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662919 | |||||||
chr19:17662919 | CA | C | 6 | a0001c0001t0001g0136 a0001c0001t0001g0245 a0001c0001t0001g0270 others(3): Show |
6 | HG01167.hp2 HG01168.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.559+612delT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662919 | |||||||
chr19:17662953 | C | G | 54 | a0001c0002t0001g0193 a0001c0002t0001g0229 a0001c0002t0003g0096 others(51): Show |
54 | HG00140.hp2 HG00558.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.559+579G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17662953 | |||||||
chr19:17663040 | G | T | 3 | a0001c0001t0004g0244 a0001c0004t0001g0135 a0001c0028t0002g0082 |
3 | HG02155.hp1 NA19056.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.559+492C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17663040 | |||||||
chr19:17663212 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.559+320G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17663212 | |||||||
chr19:17663293 | C | A | 1 | a0001c0011t0010g0059 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.559+239G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17663293 | |||||||
chr19:17663298 | C | A | 1 | a0001c0001t0001g0143 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.559+234G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17663298 | |||||||
chr19:17663319 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.559+213G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17663319 | |||||||
chr19:17663455 | G | C | 1 | a0001c0067t0004g0265 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.559+77C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 8/43 | chr19 | 17663455 | |||||||
chr19:17663703 | C | T | 56 | a0001c0002t0001g0157 a0001c0002t0003g0068 a0001c0002t0003g0096 others(53): Show |
56 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.524-136G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17663703 | |||||||
chr19:17663708 | G | T | 1 | a0001c0002t0012g0291 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.524-141C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17663708 | |||||||
chr19:17663771 | A | G | 93 | a0001c0001t0004g0012 a0001c0002t0001g0106 a0001c0002t0001g0178 others(90): Show |
93 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.524-204T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17663771 | |||||||
chr19:17663788 | TTTTTC | T | 32 | a0001c0001t0004g0012 a0001c0002t0001g0106 a0001c0002t0003g0127 others(29): Show |
32 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.524-226_524-222del others(5): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17663788 | |||||||
chr19:17663804 | T | A | 1 | a0001c0002t0001g0178 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.524-237A>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17663804 | |||||||
chr19:17663864 | C | T | 1 | a0007c0068t0002g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.524-297G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17663864 | |||||||
chr19:17663901 | T | C | 64 | a0001c0002t0001g0157 a0001c0002t0003g0068 a0001c0002t0003g0096 others(61): Show |
64 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.524-334A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17663901 | |||||||
chr19:17663907 | C | T | 2 | a0001c0002t0018g0269 a0001c0024t0019g0100 |
2 | HG00735.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.524-340G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17663907 | |||||||
chr19:17663970 | GTTCTTGG others(49): Show |
G | 4 | a0001c0007t0001g0042 a0001c0007t0001g0052 a0001c0007t0025g0320 others(1): Show |
4 | HG02970.hp1 HG03139.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.524-459_524-404del others(56): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17663970 | |||||||
chr19:17663980 | G | GT | 64 | a0001c0002t0001g0157 a0001c0002t0003g0068 a0001c0002t0003g0096 others(61): Show |
64 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.524-414dupA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17663980 | |||||||
chr19:17664027 | C | A | 4 | a0001c0007t0001g0042 a0001c0007t0001g0052 a0001c0007t0025g0320 others(1): Show |
4 | HG02970.hp1 HG03139.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.524-460G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17664027 | |||||||
chr19:17664028 | A | C | 4 | a0001c0007t0001g0042 a0001c0007t0001g0052 a0001c0007t0025g0320 others(1): Show |
4 | HG02970.hp1 HG03139.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.524-461T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17664028 | |||||||
chr19:17664045 | G | A | 1 | a0001c0003t0001g0129 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.524-478C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17664045 | |||||||
chr19:17664100 | G | A | 2 | a0001c0002t0010g0033 a0001c0007t0003g0072 |
2 | HG02145.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.524-533C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17664100 | |||||||
chr19:17664226 | G | T | 1 | a0001c0056t0002g0155 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.524-659C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17664226 | |||||||
chr19:17664376 | G | A | 62 | a0001c0002t0001g0157 a0001c0002t0003g0068 a0001c0002t0003g0096 others(59): Show |
62 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.524-809C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17664376 | |||||||
chr19:17664377 | C | T | 2 | a0001c0002t0003g0068 a0001c0008t0002g0075 |
2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.524-810G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17664377 | |||||||
chr19:17664414 | G | A | 1 | a0001c0056t0002g0155 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.524-847C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17664414 | |||||||
chr19:17664576 | A | G | 236 | a0001c0001t0001g0174 a0001c0001t0004g0012 a0001c0002t0001g0001 others(233): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.524-1009T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17664576 | |||||||
chr19:17664658 | T | C | 2 | a0001c0002t0003g0068 a0001c0008t0002g0075 |
2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.524-1091A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17664658 | |||||||
chr19:17664815 | C | A | 4 | a0001c0002t0011g0287 a0001c0008t0002g0286 a0001c0011t0001g0156 others(1): Show |
4 | HG01884.hp1 HG02280.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.524-1248G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17664815 | |||||||
chr19:17664817 | G | A | 62 | a0001c0002t0001g0157 a0001c0002t0003g0068 a0001c0002t0003g0096 others(59): Show |
62 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.524-1250C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17664817 | |||||||
chr19:17664870 | G | A | 62 | a0001c0002t0001g0157 a0001c0002t0003g0068 a0001c0002t0003g0096 others(59): Show |
62 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.524-1303C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17664870 | |||||||
chr19:17664935 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.524-1368G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17664935 | |||||||
chr19:17664958 | G | A | 1 | a0001c0027t0002g0044 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.524-1391C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17664958 | |||||||
chr19:17664978 | T | A | 99 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(96): Show |
99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.524-1411A>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17664978 | |||||||
chr19:17664995 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.524-1428A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17664995 | |||||||
chr19:17665112 | A | G | 98 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(95): Show |
98 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.523+1538T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17665112 | |||||||
chr19:17665203 | G | GA | 123 | a0001c0002t0001g0157 a0001c0002t0001g0178 a0001c0002t0001g0266 others(120): Show |
123 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.523+1446dupT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17665203 | |||||||
chr19:17665203 | G | GAA | 96 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(93): Show |
96 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.523+1445_523+1446d others(4): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17665203 | |||||||
chr19:17665237 | T | C | 1 | a0001c0001t0001g0250 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.523+1413A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17665237 | |||||||
chr19:17665350 | A | C | 1 | a0009c0043t0001g0202 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.523+1300T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17665350 | |||||||
chr19:17665421 | A | G | 65 | a0001c0002t0001g0157 a0001c0002t0003g0068 a0001c0002t0003g0096 others(62): Show |
65 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.523+1229T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17665421 | |||||||
chr19:17665450 | A | G | 26 | a0001c0002t0001g0266 a0001c0002t0001g0308 a0001c0002t0004g0224 others(23): Show |
26 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.523+1200T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17665450 | |||||||
chr19:17665485 | A | G | 98 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(95): Show |
98 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.523+1165T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17665485 | |||||||
chr19:17665522 | G | T | 62 | a0001c0002t0001g0157 a0001c0002t0003g0068 a0001c0002t0003g0096 others(59): Show |
62 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.523+1128C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17665522 | |||||||
chr19:17665580 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.523+1070C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17665580 | |||||||
chr19:17665681 | C | T | 61 | a0001c0002t0001g0157 a0001c0002t0003g0068 a0001c0002t0003g0096 others(58): Show |
61 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.523+969G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17665681 | |||||||
chr19:17665682 | A | G | 61 | a0001c0002t0001g0157 a0001c0002t0003g0068 a0001c0002t0003g0096 others(58): Show |
61 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.523+968T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17665682 | |||||||
chr19:17665749 | G | T | 3 | a0001c0002t0011g0287 a0001c0008t0002g0286 a0001c0011t0001g0156 |
3 | HG01884.hp1 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.523+901C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17665749 | |||||||
chr19:17665903 | C | T | 1 | a0001c0002t0001g0229 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.523+747G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17665903 | |||||||
chr19:17665904 | G | A | 3 | a0001c0002t0027g0295 a0001c0022t0008g0185 a0001c0032t0008g0163 |
3 | HG02559.hp1 HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.523+746C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17665904 | |||||||
chr19:17665977 | AATCAAGC others(51): Show |
A | 220 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(217): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.523+615_523+672del others(58): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17665977 | |||||||
chr19:17666057 | T | C | 1 | a0001c0002t0019g0092 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.523+593A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666057 | |||||||
chr19:17666087 | T | C | 220 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(217): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.523+563A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666087 | |||||||
chr19:17666112 | TTC | T | 98 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(95): Show |
98 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.523+536_523+537del others(2): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666112 | |||||||
chr19:17666114 | C | CTTT | 4 | a0001c0007t0003g0072 a0001c0071t0002g0311 a0002c0017t0013g0023 others(1): Show |
4 | HG01243.hp1 HG01981.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+535_523+536ins others(3): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666114 | |||||||
chr19:17666116 | C | T | 118 | a0001c0002t0001g0157 a0001c0002t0001g0266 a0001c0002t0001g0308 others(115): Show |
118 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.523+534G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666116 | |||||||
chr19:17666119 | T | C | 118 | a0001c0002t0001g0157 a0001c0002t0001g0266 a0001c0002t0001g0308 others(115): Show |
118 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.523+531A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666119 | |||||||
chr19:17666121 | C | T | 97 | a0001c0002t0001g0157 a0001c0002t0001g0308 a0001c0002t0003g0068 others(94): Show |
97 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.523+529G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666121 | |||||||
chr19:17666121 | CTTTTCTT others(3): Show |
C | 8 | a0001c0004t0010g0056 a0001c0004t0010g0242 a0001c0004t0011g0055 others(5): Show |
8 | HG02257.hp2 HG02451.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.523+519_523+528del others(10): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666121 | |||||||
chr19:17666124 | T | C | 97 | a0001c0002t0001g0157 a0001c0002t0001g0308 a0001c0002t0003g0068 others(94): Show |
97 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.523+526A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666124 | |||||||
chr19:17666124 | T | TTC | 3 | a0001c0007t0003g0072 a0001c0071t0002g0311 a0002c0017t0013g0023 |
3 | HG01243.hp1 HG02145.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.523+524_523+525dup others(2): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666124 | |||||||
chr19:17666126 | CTT | C | 99 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(96): Show |
99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.523+522_523+523del others(2): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666126 | |||||||
chr19:17666126 | CTTTCT | C | 21 | a0001c0002t0001g0266 a0001c0002t0008g0027 a0001c0002t0010g0033 others(18): Show |
21 | HG00738.hp2 HG01109.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.523+519_523+523del others(5): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666126 | |||||||
chr19:17666130 | C | T | 100 | a0001c0002t0001g0157 a0001c0002t0001g0308 a0001c0002t0003g0068 others(97): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.523+520G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666130 | |||||||
chr19:17666131 | T | C | 100 | a0001c0002t0001g0157 a0001c0002t0001g0308 a0001c0002t0003g0068 others(97): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.523+519A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666131 | |||||||
chr19:17666135 | T | C | 99 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(96): Show |
99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.523+515A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666135 | |||||||
chr19:17666136 | C | T | 99 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(96): Show |
99 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.523+514G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666136 | |||||||
chr19:17666144 | C | A | 1 | a0002c0006t0017g0309 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.523+506G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666144 | |||||||
chr19:17666181 | C | CTCTCTCT others(1): Show |
8 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(5): Show |
8 | HG02280.hp1 HG02723.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.523+468_523+469ins others(8): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666181 | |||||||
chr19:17666191 | T | C | 9 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(6): Show |
9 | HG02280.hp1 HG02723.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.523+459A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666191 | |||||||
chr19:17666191 | T | TTCTCTCT others(3): Show |
15 | a0001c0001t0001g0174 a0001c0004t0003g0030 a0001c0004t0010g0056 others(12): Show |
15 | HG00733.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.523+458_523+459ins others(10): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666191 | |||||||
chr19:17666197 | C | CTCTCTCT others(17): Show |
1 | a0002c0005t0006g0310 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.523+452_523+453ins others(24): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666197 | |||||||
chr19:17666197 | C | CTCTCTCT others(11): Show |
2 | a0001c0002t0004g0215 a0001c0003t0001g0130 |
2 | NA18994.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.523+452_523+453ins others(18): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666197 | |||||||
chr19:17666197 | C | CTCTCTCT others(9): Show |
208 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(205): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.523+452_523+453ins others(16): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666197 | |||||||
chr19:17666197 | C | CTCTCTCT others(5): Show |
1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.523+452_523+453ins others(12): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666197 | |||||||
chr19:17666199 | T | C | 212 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(209): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.523+451A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666199 | |||||||
chr19:17666199 | T | TTCTTTC | 8 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0010g0097 others(5): Show |
8 | HG02280.hp1 HG02723.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.523+445_523+450dup others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666199 | |||||||
chr19:17666243 | T | C | 219 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.523+407A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666243 | |||||||
chr19:17666378 | A | AT | 57 | a0001c0002t0001g0157 a0001c0002t0003g0068 a0001c0002t0003g0096 others(54): Show |
57 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.523+271dupA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666378 | |||||||
chr19:17666430 | G | T | 1 | a0002c0041t0036g0279 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.523+220C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666430 | |||||||
chr19:17666546 | A | G | 1 | a0001c0023t0001g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.523+104T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666546 | |||||||
chr19:17666557 | C | T | 3 | a0001c0004t0021g0073 a0001c0027t0002g0044 a0001c0027t0014g0314 |
3 | HG02922.hp2 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.523+93G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666557 | |||||||
chr19:17666622 | A | G | 220 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(217): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.523+28T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 7/43 | chr19 | 17666622 | |||||||
chr19:17666747 | C | T | 1 | a0001c0055t0001g0102 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.469-43G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17666747 | |||||||
chr19:17666786 | C | A | 7 | a0001c0001t0001g0174 a0001c0001t0004g0012 a0001c0004t0003g0030 others(4): Show |
7 | HG00733.hp2 HG02738.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.469-82G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17666786 | |||||||
chr19:17666790 | C | A | 1 | a0007c0068t0002g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.469-86G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17666790 | |||||||
chr19:17666879 | CACGA | C | 40 | a0001c0002t0003g0068 a0001c0002t0003g0096 a0001c0002t0011g0039 others(37): Show |
40 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.469-179_469-176del others(4): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17666879 | |||||||
chr19:17666879 | CACGAGAG others(1): Show |
C | 18 | a0001c0002t0001g0157 a0001c0002t0008g0027 a0001c0002t0010g0097 others(15): Show |
18 | HG01167.hp2 HG01169.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.469-183_469-176del others(8): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17666879 | |||||||
chr19:17666879 | CACGAGAG others(5): Show |
C | 4 | a0001c0001t0001g0174 a0001c0001t0004g0012 a0001c0004t0003g0030 others(1): Show |
4 | HG00733.hp2 HG02738.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.469-187_469-176del others(12): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17666879 | |||||||
chr19:17666880 | A | G | 1 | a0001c0022t0024g0061 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.469-176T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17666880 | |||||||
chr19:17666881 | C | A | 1 | a0001c0022t0024g0061 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.469-177G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17666881 | |||||||
chr19:17666881 | CGA | C | 3 | a0001c0002t0011g0287 a0001c0008t0002g0286 a0001c0011t0001g0156 |
3 | HG01884.hp1 HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.469-179_469-178del others(2): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17666881 | |||||||
chr19:17666881 | CGAGA | C | 6 | a0001c0002t0010g0033 a0001c0002t0015g0054 a0001c0003t0003g0162 others(3): Show |
6 | HG02145.hp2 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.469-181_469-178del others(4): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17666881 | |||||||
chr19:17666881 | CGAGAGAG others(1): Show |
C | 3 | a0001c0001t0001g0137 a0001c0001t0001g0199 a0001c0001t0001g0235 |
3 | NA18942.hp2 NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.469-185_469-178del others(8): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17666881 | |||||||
chr19:17666906 | GAGAGAAA others(3): Show |
G | 150 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(147): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.469-212_469-203del others(10): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17666906 | |||||||
chr19:17666908 | GAGAAAGA others(1): Show |
G | 3 | a0001c0003t0001g0213 a0002c0039t0021g0026 a0003c0037t0001g0282 |
3 | HG00642.hp1 HG03453.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.469-212_469-205del others(8): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17666908 | |||||||
chr19:17666912 | AAGACAG | A | 66 | a0001c0002t0001g0157 a0001c0002t0003g0068 a0001c0002t0003g0096 others(63): Show |
66 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.469-214_469-209del others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17666912 | |||||||
chr19:17666918 | G | A | 153 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(150): Show |
153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.469-214C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17666918 | |||||||
chr19:17666969 | A | C | 101 | a0001c0001t0003g0271 a0001c0002t0001g0001 a0001c0002t0001g0106 others(98): Show |
101 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.469-265T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17666969 | |||||||
chr19:17666994 | C | T | 219 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.469-290G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17666994 | |||||||
chr19:17666996 | G | A | 219 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.469-292C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17666996 | |||||||
chr19:17667003 | C | T | 219 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.469-299G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667003 | |||||||
chr19:17667007 | A | G | 216 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.469-303T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667007 | |||||||
chr19:17667022 | A | G | 219 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.469-318T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667022 | |||||||
chr19:17667024 | C | A | 1 | a0001c0002t0007g0257 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.469-320G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667024 | |||||||
chr19:17667035 | C | T | 219 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.469-331G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667035 | |||||||
chr19:17667053 | A | G | 1 | a0001c0003t0007g0206 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.469-349T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667053 | |||||||
chr19:17667120 | G | A | 219 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.469-416C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667120 | |||||||
chr19:17667138 | T | C | 219 | a0001c0002t0001g0001 a0001c0002t0001g0106 a0001c0002t0001g0113 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.469-434A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667138 | |||||||
chr19:17667176 | G | A | 2 | a0001c0053t0023g0053 a0002c0034t0002g0099 |
2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.469-472C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667176 | |||||||
chr19:17667245 | G | A | 9 | a0001c0004t0010g0056 a0001c0004t0010g0242 a0001c0004t0011g0055 others(6): Show |
9 | HG02257.hp2 HG02451.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.469-541C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667245 | |||||||
chr19:17667256 | G | GA | 78 | a0001c0002t0001g0266 a0001c0002t0001g0308 a0001c0002t0003g0068 others(75): Show |
78 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.469-553dupT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667256 | |||||||
chr19:17667256 | G | GAA | 140 | a0001c0001t0001g0201 a0001c0002t0001g0001 a0001c0002t0001g0106 others(137): Show |
140 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.469-554_469-553dup others(2): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667256 | |||||||
chr19:17667310 | G | A | 4 | a0001c0002t0011g0287 a0001c0008t0002g0286 a0001c0011t0001g0156 others(1): Show |
4 | HG01884.hp1 HG02280.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-606C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667310 | |||||||
chr19:17667327 | A | G | 220 | a0001c0001t0001g0201 a0001c0002t0001g0001 a0001c0002t0001g0106 others(217): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.469-623T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667327 | |||||||
chr19:17667416 | A | G | 220 | a0001c0001t0001g0201 a0001c0002t0001g0001 a0001c0002t0001g0106 others(217): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.468+701T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667416 | |||||||
chr19:17667436 | C | T | 58 | a0001c0002t0001g0266 a0001c0002t0001g0308 a0001c0002t0004g0224 others(55): Show |
58 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.468+681G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667436 | |||||||
chr19:17667547 | C | T | 1 | a0001c0002t0044g0093 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.468+570G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667547 | |||||||
chr19:17667695 | G | C | 2 | a0001c0028t0002g0082 a0002c0026t0002g0263 |
2 | NA18998.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.468+422C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667695 | |||||||
chr19:17667706 | C | T | 1 | a0001c0003t0001g0205 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.468+411G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667706 | |||||||
chr19:17667776 | A | AT | 25 | a0001c0001t0001g0107 a0001c0001t0001g0199 a0001c0001t0001g0268 others(22): Show |
25 | HG00438.hp1 HG00544.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.468+340dupA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667776 | |||||||
chr19:17667776 | AT | A | 55 | a0001c0001t0001g0165 a0001c0002t0001g0266 a0001c0002t0001g0308 others(52): Show |
55 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.468+340delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667776 | |||||||
chr19:17667776 | ATT | A | 58 | a0001c0002t0001g0157 a0001c0002t0003g0068 a0001c0002t0003g0096 others(55): Show |
58 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.468+339_468+340del others(2): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667776 | |||||||
chr19:17667776 | ATTT | A | 6 | a0001c0007t0008g0212 a0001c0008t0002g0095 a0001c0021t0014g0319 others(3): Show |
6 | HG01169.hp2 HG01516.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.468+338_468+340del others(3): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667776 | |||||||
chr19:17667841 | G | T | 60 | a0001c0002t0001g0157 a0001c0002t0003g0068 a0001c0002t0003g0096 others(57): Show |
60 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.468+276C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667841 | |||||||
chr19:17667912 | C | T | 2 | a0001c0001t0001g0080 a0002c0026t0002g0251 |
2 | NA18951.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.468+205G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667912 | |||||||
chr19:17667964 | C | T | 1 | a0001c0003t0037g0147 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.468+153G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17667964 | |||||||
chr19:17668023 | A | G | 221 | a0001c0001t0001g0201 a0001c0002t0001g0001 a0001c0002t0001g0106 others(218): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.468+94T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 6/43 | chr19 | 17668023 | |||||||
chr19:17668232 | TGCCGCTC others(1): Show |
T | 40 | a0001c0002t0001g0157 a0001c0002t0003g0068 a0001c0002t0008g0027 others(37): Show |
40 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.395-50_395-43delTG others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 5/43 | chr19 | 17668232 | |||||||
chr19:17668273 | C | T | 1 | a0001c0007t0008g0212 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.395-83G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 5/43 | chr19 | 17668273 | |||||||
chr19:17668465 | A | C | 3 | a0001c0004t0021g0073 a0001c0027t0002g0044 a0001c0027t0014g0314 |
3 | HG02922.hp2 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.395-275T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 5/43 | chr19 | 17668465 | |||||||
chr19:17668550 | A | G | 235 | a0001c0001t0001g0132 a0001c0001t0001g0174 a0001c0001t0001g0201 others(232): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.395-360T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 5/43 | chr19 | 17668550 | |||||||
chr19:17668618 | C | A | 9 | a0001c0002t0011g0039 a0001c0002t0027g0295 a0001c0008t0002g0274 others(6): Show |
9 | HG01361.hp1 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.395-428G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 5/43 | chr19 | 17668618 | |||||||
chr19:17668681 | G | A | 1 | a0002c0006t0016g0289 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.395-491C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 5/43 | chr19 | 17668681 | |||||||
chr19:17668714 | C | T | 3 | a0001c0002t0044g0093 a0001c0056t0002g0155 a0007c0068t0002g0003 |
3 | HG02055.hp1 HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.395-524G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 5/43 | chr19 | 17668714 | |||||||
chr19:17668714 | CCTGACAT others(12): Show |
C | 1 | a0002c0026t0002g0263 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.395-543_395-525del others(19): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 5/43 | chr19 | 17668714 | |||||||
chr19:17668977 | A | G | 4 | a0001c0002t0003g0096 a0001c0004t0021g0073 a0001c0027t0002g0044 others(1): Show |
4 | HG02922.hp2 HG03195.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.394+576T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 5/43 | chr19 | 17668977 | |||||||
chr19:17669044 | C | G | 102 | a0001c0001t0001g0132 a0001c0001t0001g0201 a0001c0002t0001g0001 others(99): Show |
102 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.394+509G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 5/43 | chr19 | 17669044 | |||||||
chr19:17669060 | T | C | 102 | a0001c0001t0001g0132 a0001c0001t0001g0201 a0001c0002t0001g0001 others(99): Show |
102 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.394+493A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 5/43 | chr19 | 17669060 | |||||||
chr19:17669138 | G | A | 2 | a0001c0002t0031g0298 a0001c0002t0042g0038 |
2 | HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.394+415C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 5/43 | chr19 | 17669138 | |||||||
chr19:17669251 | T | C | 1 | a0002c0039t0021g0026 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.394+302A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 5/43 | chr19 | 17669251 | |||||||
chr19:17669728 | C | T | 1 | a0001c0002t0008g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.271-52G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17669728 | |||||||
chr19:17669793 | C | T | 239 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0174 others(236): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.271-117G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17669793 | |||||||
chr19:17669830 | T | G | 1 | a0001c0042t0001g0214 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.271-154A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17669830 | |||||||
chr19:17669874 | T | C | 105 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0209 others(102): Show |
105 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.271-198A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17669874 | |||||||
chr19:17669948 | CT | C | 7 | a0001c0001t0001g0237 a0001c0002t0010g0069 a0001c0002t0044g0093 others(4): Show |
7 | HG01109.hp2 HG01517.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-273delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17669948 | |||||||
chr19:17669948 | CTT | C | 161 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0209 others(158): Show |
161 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.271-274_271-273del others(2): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17669948 | |||||||
chr19:17669948 | CTTT | C | 66 | a0001c0002t0001g0157 a0001c0002t0003g0068 a0001c0002t0008g0027 others(63): Show |
66 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.271-275_271-273del others(3): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17669948 | |||||||
chr19:17669970 | A | G | 232 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0201 others(229): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.271-294T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17669970 | |||||||
chr19:17670047 | C | T | 3 | a0001c0002t0010g0069 a0001c0003t0003g0133 a0001c0023t0047g0275 |
3 | HG01109.hp2 HG03225.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.271-371G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17670047 | |||||||
chr19:17670090 | G | A | 4 | a0001c0001t0001g0174 a0001c0001t0004g0012 a0001c0004t0003g0030 others(1): Show |
4 | HG00733.hp2 HG02738.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-414C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17670090 | |||||||
chr19:17670092 | A | G | 126 | a0001c0002t0001g0113 a0001c0002t0001g0157 a0001c0002t0001g0308 others(123): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.271-416T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17670092 | |||||||
chr19:17670241 | C | T | 1 | a0001c0004t0001g0135 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.271-565G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17670241 | |||||||
chr19:17670259 | T | C | 106 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0201 others(103): Show |
106 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.271-583A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17670259 | |||||||
chr19:17670361 | C | T | 100 | a0001c0001t0001g0132 a0001c0001t0001g0201 a0001c0002t0001g0001 others(97): Show |
100 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.271-685G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17670361 | |||||||
chr19:17670398 | T | G | 230 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0201 others(227): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.271-722A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17670398 | |||||||
chr19:17670432 | G | A | 6 | a0001c0002t0029g0167 a0002c0005t0001g0051 a0002c0005t0001g0067 others(3): Show |
6 | HG02055.hp2 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-756C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17670432 | |||||||
chr19:17670470 | C | T | 126 | a0001c0002t0001g0113 a0001c0002t0001g0157 a0001c0002t0001g0308 others(123): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.271-794G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17670470 | |||||||
chr19:17670907 | G | GTAAAA | 95 | a0001c0001t0001g0080 a0001c0001t0001g0107 a0001c0001t0001g0115 others(92): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.271-1236_271-1232d others(7): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17670907 | |||||||
chr19:17670907 | G | GTAAAATA others(3): Show |
27 | a0001c0001t0007g0223 a0001c0002t0001g0229 a0001c0002t0007g0172 others(24): Show |
27 | HG00544.hp2 HG00741.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.271-1241_271-1232d others(12): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17670907 | |||||||
chr19:17670907 | G | GTAAAATA others(8): Show |
10 | a0001c0002t0032g0098 a0001c0003t0001g0228 a0001c0004t0004g0272 others(7): Show |
10 | HG00558.hp2 HG01123.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.271-1246_271-1232d others(17): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17670907 | |||||||
chr19:17670907 | G | GTAAAATA others(13): Show |
1 | a0001c0022t0024g0061 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.271-1251_271-1232d others(22): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17670907 | |||||||
chr19:17670907 | G | GTAAAATA others(18): Show |
9 | a0001c0002t0011g0039 a0001c0002t0027g0295 a0001c0008t0002g0274 others(6): Show |
9 | HG01361.hp1 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.271-1256_271-1232d others(27): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17670907 | |||||||
chr19:17670907 | GTAAAA | G | 19 | a0001c0002t0008g0027 a0001c0002t0008g0284 a0001c0002t0011g0064 others(16): Show |
19 | HG02055.hp1 HG02257.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.271-1236_271-1232d others(7): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17670907 | |||||||
chr19:17670907 | GTAAAATA others(3): Show |
G | 13 | a0001c0001t0001g0179 a0001c0002t0003g0131 a0001c0002t0010g0033 others(10): Show |
13 | HG00642.hp1 HG01109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.271-1241_271-1232d others(12): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17670907 | |||||||
chr19:17670907 | GTAAAATA others(8): Show |
G | 48 | a0001c0001t0001g0231 a0001c0001t0001g0236 a0001c0001t0001g0249 others(45): Show |
48 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.271-1246_271-1232d others(17): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17670907 | |||||||
chr19:17670942 | A | ATAAAATA others(4): Show |
2 | a0001c0001t0004g0012 a0004c0065t0005g0134 |
2 | HG00733.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.271-1277_271-1267d others(13): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17670942 | |||||||
chr19:17670942 | A | ATAAAATA others(9): Show |
2 | a0001c0001t0001g0174 a0001c0004t0003g0030 |
2 | HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.271-1282_271-1267d others(18): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17670942 | |||||||
chr19:17671081 | A | G | 1 | a0001c0002t0027g0295 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.270+1297T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17671081 | |||||||
chr19:17671359 | A | C | 1 | a0001c0002t0001g0193 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.270+1019T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17671359 | |||||||
chr19:17671408 | G | A | 120 | a0001c0002t0001g0113 a0001c0002t0001g0157 a0001c0002t0001g0308 others(117): Show |
120 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.270+970C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17671408 | |||||||
chr19:17671531 | G | T | 1 | a0001c0027t0002g0044 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.270+847C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17671531 | |||||||
chr19:17671684 | G | A | 1 | a0001c0050t0033g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.270+694C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17671684 | |||||||
chr19:17671807 | C | T | 2 | a0001c0003t0001g0210 a0001c0003t0007g0248 |
2 | HG00609.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.270+571G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17671807 | |||||||
chr19:17671832 | A | G | 3 | a0001c0002t0044g0093 a0001c0056t0002g0155 a0007c0068t0002g0003 |
3 | HG02055.hp1 HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.270+546T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17671832 | |||||||
chr19:17671998 | A | G | 1 | a0001c0056t0002g0155 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.270+380T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17671998 | |||||||
chr19:17672009 | T | C | 1 | a0001c0056t0002g0155 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.270+369A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17672009 | |||||||
chr19:17672011 | G | C | 5 | a0001c0001t0001g0174 a0001c0001t0004g0012 a0001c0004t0003g0030 others(2): Show |
5 | HG00733.hp2 HG02738.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.270+367C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17672011 | |||||||
chr19:17672045 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.270+333C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17672045 | |||||||
chr19:17672076 | G | C | 1 | a0001c0002t0003g0131 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.270+302C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17672076 | |||||||
chr19:17672096 | C | G | 2 | a0001c0002t0004g0224 a0001c0003t0001g0294 |
2 | HG00099.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.270+282G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17672096 | |||||||
chr19:17672114 | C | T | 17 | a0001c0002t0001g0157 a0001c0002t0008g0027 a0001c0002t0020g0025 others(14): Show |
17 | HG01167.hp2 HG01169.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.270+264G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17672114 | |||||||
chr19:17672210 | G | A | 62 | a0001c0001t0001g0022 a0001c0001t0001g0249 a0001c0001t0046g0197 others(59): Show |
62 | HG00558.hp1 HG00639.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.270+168C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17672210 | |||||||
chr19:17672282 | G | C | 1 | a0007c0068t0002g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.270+96C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17672282 | |||||||
chr19:17672333 | G | A | 1 | a0001c0007t0008g0212 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.270+45C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 4/43 | chr19 | 17672333 | |||||||
chr19:17672520 | C | T | 2 | a0001c0002t0018g0103 a0001c0007t0008g0063 |
2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.153-25G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17672520 | |||||||
chr19:17672737 | C | T | 1 | a0001c0004t0001g0150 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.153-242G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17672737 | |||||||
chr19:17672784 | C | T | 40 | a0001c0002t0003g0096 a0001c0002t0005g0120 a0001c0002t0011g0184 others(37): Show |
40 | HG00733.hp1 HG00735.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.153-289G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17672784 | |||||||
chr19:17672795 | C | T | 15 | a0001c0002t0008g0027 a0001c0002t0020g0025 a0001c0002t0031g0298 others(12): Show |
15 | HG02280.hp1 HG02647.hp1 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.153-300G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17672795 | |||||||
chr19:17672804 | A | C | 22 | a0001c0001t0001g0174 a0001c0002t0008g0027 a0001c0002t0011g0039 others(19): Show |
22 | HG00733.hp2 HG01361.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.153-309T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17672804 | |||||||
chr19:17672910 | C | T | 19 | a0001c0002t0003g0096 a0001c0002t0011g0184 a0001c0002t0011g0287 others(16): Show |
19 | HG01123.hp2 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.153-415G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17672910 | |||||||
chr19:17673018 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.153-523T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17673018 | |||||||
chr19:17673213 | C | T | 25 | a0001c0002t0005g0120 a0001c0002t0011g0287 a0001c0002t0017g0028 others(22): Show |
25 | HG00733.hp1 HG00735.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.153-718G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17673213 | |||||||
chr19:17673217 | C | T | 3 | a0001c0008t0002g0274 a0001c0008t0002g0276 a0001c0008t0002g0277 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.153-722G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17673217 | |||||||
chr19:17673226 | G | A | 2 | a0001c0016t0002g0091 a0001c0024t0001g0057 |
2 | HG02451.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.153-731C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17673226 | |||||||
chr19:17673249 | C | T | 1 | a0001c0004t0001g0219 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.153-754G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17673249 | |||||||
chr19:17673270 | T | C | 2 | a0001c0002t0003g0068 a0001c0008t0002g0075 |
2 | HG02258.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.153-775A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17673270 | |||||||
chr19:17673313 | C | T | 1 | a0001c0007t0003g0072 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.153-818G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17673313 | |||||||
chr19:17673352 | A | G | 1 | a0001c0002t0012g0291 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.153-857T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17673352 | |||||||
chr19:17673357 | C | CA | 158 | a0001c0001t0001g0011 a0001c0001t0001g0080 a0001c0001t0001g0115 others(155): Show |
158 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.153-863dupT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17673357 | |||||||
chr19:17673357 | C | CAA | 13 | a0001c0001t0001g0174 a0001c0001t0034g0304 a0001c0002t0001g0308 others(10): Show |
13 | HG00733.hp2 HG01123.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.153-864_153-863dup others(2): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17673357 | |||||||
chr19:17673412 | T | G | 44 | a0001c0002t0001g0308 a0001c0002t0003g0096 a0001c0002t0008g0027 others(41): Show |
44 | HG01123.hp2 HG02055.hp1 HG02145.hp2 others(41): Show |
intron_variant | MODIFIER | c.153-917A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17673412 | |||||||
chr19:17673414 | G | A | 2 | a0001c0016t0002g0091 a0001c0024t0001g0057 |
2 | HG02451.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.153-919C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17673414 | |||||||
chr19:17673435 | A | G | 2 | a0001c0022t0008g0185 a0001c0071t0002g0311 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.153-940T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17673435 | |||||||
chr19:17673538 | C | T | 110 | a0001c0001t0001g0011 a0001c0001t0001g0080 a0001c0001t0001g0115 others(107): Show |
110 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.153-1043G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17673538 | |||||||
chr19:17673554 | A | T | 2 | a0001c0002t0008g0284 a0001c0002t0028g0047 |
2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.153-1059T>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17673554 | |||||||
chr19:17673655 | T | C | 1 | a0001c0002t0020g0025 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.152+1002A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17673655 | |||||||
chr19:17673909 | G | A | 3 | a0001c0008t0002g0274 a0001c0008t0002g0276 a0001c0008t0002g0277 |
3 | HG02559.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.152+748C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17673909 | |||||||
chr19:17674018 | A | G | 253 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0080 others(250): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.152+639T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17674018 | |||||||
chr19:17674044 | A | C | 47 | a0001c0002t0001g0157 a0001c0002t0003g0068 a0001c0002t0009g0176 others(44): Show |
47 | HG01081.hp1 HG01167.hp2 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.152+613T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17674044 | |||||||
chr19:17674181 | T | TG | 72 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0001t0001g0174 others(69): Show |
72 | HG00099.hp1 HG00423.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.152+475dupC | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17674181 | |||||||
chr19:17674203 | G | A | 10 | a0001c0003t0001g0009 a0001c0029t0006g0243 a0001c0029t0022g0148 others(7): Show |
10 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(7): Show |
intron_variant | MODIFIER | c.152+454C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17674203 | |||||||
chr19:17674250 | A | C | 1 | a0001c0003t0001g0117 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.152+407T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17674250 | |||||||
chr19:17674443 | G | A | 1 | a0001c0004t0001g0219 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.152+214C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17674443 | |||||||
chr19:17674522 | A | G | 9 | a0001c0002t0011g0184 a0001c0002t0042g0038 a0001c0002t0045g0164 others(6): Show |
9 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.152+135T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17674522 | |||||||
chr19:17674618 | T | G | 1 | a0002c0005t0004g0220 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.152+39A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17674618 | |||||||
chr19:17674626 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.152+31T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 3/43 | chr19 | 17674626 | |||||||
chr19:17674809 | C | G | 1 | a0001c0056t0002g0155 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.53-53G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17674809 | |||||||
chr19:17675078 | A | G | 1 | a0001c0003t0003g0162 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.53-322T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675078 | |||||||
chr19:17675086 | G | C | 1 | a0001c0003t0001g0040 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.53-330C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675086 | |||||||
chr19:17675096 | G | A | 5 | a0001c0004t0010g0242 a0001c0004t0018g0060 a0001c0004t0049g0317 others(2): Show |
5 | HG02630.hp2 HG03130.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-340C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675096 | |||||||
chr19:17675306 | C | A | 3 | a0001c0001t0001g0268 a0001c0002t0029g0167 a0001c0011t0001g0156 |
3 | HG00642.hp2 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.53-550G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675306 | |||||||
chr19:17675344 | T | A | 84 | a0001c0001t0001g0297 a0001c0001t0004g0012 a0001c0001t0034g0304 others(81): Show |
84 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.53-588A>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675344 | |||||||
chr19:17675402 | C | T | 2 | a0001c0003t0040g0024 a0002c0039t0021g0026 |
2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.52+610G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675402 | |||||||
chr19:17675468 | C | G | 1 | a0001c0001t0001g0187 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.52+544G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675468 | |||||||
chr19:17675488 | C | T | 3 | a0001c0001t0001g0268 a0001c0002t0029g0167 a0001c0011t0001g0156 |
3 | HG00642.hp2 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.52+524G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675488 | |||||||
chr19:17675516 | C | G | 2 | a0001c0003t0040g0024 a0002c0039t0021g0026 |
2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.52+496G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675516 | |||||||
chr19:17675580 | G | A | 1 | a0005c0051t0001g0259 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.52+432C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675580 | |||||||
chr19:17675588 | G | A | 3 | a0001c0003t0001g0305 a0002c0012t0001g0169 a0002c0012t0001g0175 |
3 | HG01258.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.52+424C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675588 | |||||||
chr19:17675596 | A | T | 1 | a0001c0002t0001g0193 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.52+416T>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675596 | |||||||
chr19:17675630 | C | CA | 18 | a0001c0001t0001g0270 a0001c0002t0010g0033 a0001c0002t0038g0037 others(15): Show |
18 | HG00140.hp2 HG01358.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.52+381dupT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675630 | |||||||
chr19:17675630 | C | CAAA | 13 | a0001c0002t0008g0027 a0001c0002t0011g0184 a0001c0002t0029g0167 others(10): Show |
13 | HG01123.hp2 HG02257.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.52+379_52+381dupTT others(1): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675630 | |||||||
chr19:17675630 | CA | C | 53 | a0001c0001t0001g0080 a0001c0001t0001g0297 a0001c0001t0004g0012 others(50): Show |
53 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.52+381delT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675630 | |||||||
chr19:17675644 | A | AAG | 14 | a0001c0002t0011g0039 a0001c0002t0027g0295 a0001c0002t0028g0047 others(11): Show |
14 | HG00639.hp1 HG00738.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.52+367_52+368insCT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675644 | |||||||
chr19:17675644 | A | AG | 11 | a0001c0002t0003g0068 a0001c0002t0008g0046 a0001c0002t0011g0064 others(8): Show |
11 | HG02258.hp1 HG02486.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.52+367_52+368insC | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675644 | |||||||
chr19:17675644 | A | G | 59 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0165 others(56): Show |
59 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.52+368T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675644 | |||||||
chr19:17675647 | G | A | 29 | a0001c0002t0008g0027 a0001c0002t0010g0033 a0001c0002t0011g0184 others(26): Show |
29 | HG00140.hp2 HG01123.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.52+365C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675647 | |||||||
chr19:17675828 | C | A | 1 | a0001c0003t0016g0149 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.52+184G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675828 | |||||||
chr19:17675843 | C | G | 15 | a0001c0002t0010g0033 a0001c0002t0019g0092 a0001c0002t0038g0037 others(12): Show |
15 | HG00140.hp2 HG01496.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.52+169G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675843 | |||||||
chr19:17675885 | C | G | 4 | a0001c0004t0021g0073 a0001c0007t0003g0072 a0001c0072t0003g0312 others(1): Show |
4 | HG02145.hp2 HG02886.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+127G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675885 | |||||||
chr19:17675939 | C | T | 56 | a0001c0001t0001g0022 a0001c0001t0001g0165 a0001c0001t0001g0171 others(53): Show |
56 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.52+73G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675939 | |||||||
chr19:17675957 | GAGAC | G | 25 | a0001c0002t0003g0068 a0001c0002t0008g0046 a0001c0002t0011g0039 others(22): Show |
25 | HG00639.hp1 HG00738.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.52+51_52+54delGTCT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675957 | |||||||
chr19:17675983 | G | A | 27 | a0001c0001t0001g0297 a0001c0001t0004g0012 a0001c0001t0034g0304 others(24): Show |
27 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.52+29C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 2/43 | chr19 | 17675983 | |||||||
chr19:17676109 | G | A | 4 | a0001c0002t0020g0025 a0001c0021t0014g0318 a0001c0021t0014g0319 others(1): Show |
4 | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-68C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17676109 | |||||||
chr19:17676186 | A | G | 2 | a0001c0001t0001g0199 a0001c0003t0001g0198 |
2 | NA18990.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.23-145T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17676186 | |||||||
chr19:17676294 | C | T | 1 | a0001c0002t0032g0098 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.23-253G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17676294 | |||||||
chr19:17676521 | G | A | 14 | a0001c0002t0019g0092 a0001c0002t0038g0037 a0001c0004t0021g0073 others(11): Show |
14 | HG00140.hp2 HG01496.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.23-480C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17676521 | |||||||
chr19:17676589 | G | A | 4 | a0001c0001t0001g0268 a0001c0003t0040g0024 a0001c0011t0001g0156 others(1): Show |
4 | HG00642.hp2 HG03453.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.23-548C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17676589 | |||||||
chr19:17676633 | C | T | 22 | a0001c0001t0001g0080 a0001c0002t0003g0096 a0001c0002t0010g0097 others(19): Show |
22 | HG00099.hp2 HG02055.hp2 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.23-592G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17676633 | |||||||
chr19:17676733 | G | A | 1 | a0001c0004t0001g0238 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.23-692C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17676733 | |||||||
chr19:17676787 | G | T | 1 | a0001c0001t0001g0235 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.23-746C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17676787 | |||||||
chr19:17676811 | C | T | 3 | a0001c0046t0001g0280 a0002c0006t0006g0278 a0002c0041t0036g0279 |
3 | HG00140.hp2 HG01496.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.23-770G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17676811 | |||||||
chr19:17676812 | A | G | 174 | a0001c0001t0001g0022 a0001c0001t0001g0080 a0001c0001t0001g0165 others(171): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.23-771T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17676812 | |||||||
chr19:17677054 | C | A | 3 | a0001c0004t0010g0242 a0001c0004t0049g0317 a0002c0040t0014g0316 |
3 | HG03130.hp2 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.23-1013G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17677054 | |||||||
chr19:17677350 | T | G | 3 | a0001c0001t0001g0221 a0001c0004t0001g0150 a0002c0006t0001g0241 |
3 | NA18983.hp2 NA18993.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.23-1309A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17677350 | |||||||
chr19:17677352 | C | CTTTTCTT others(5): Show |
1 | a0001c0001t0001g0011 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.23-1323_23-1312dup others(12): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17677352 | |||||||
chr19:17677352 | CTTTTCTT others(5): Show |
C | 127 | a0001c0001t0001g0022 a0001c0001t0001g0080 a0001c0001t0001g0165 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.23-1323_23-1312del others(12): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17677352 | |||||||
chr19:17677357 | CTTTTTTT others(6): Show |
C | 2 | a0001c0011t0001g0089 a0001c0070t0001g0313 |
2 | HG01361.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.23-1329_23-1317del others(13): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17677357 | |||||||
chr19:17677441 | G | A | 44 | a0001c0001t0001g0165 a0001c0001t0001g0171 a0001c0001t0001g0174 others(41): Show |
44 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.23-1400C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17677441 | |||||||
chr19:17677513 | G | A | 129 | a0001c0001t0001g0022 a0001c0001t0001g0080 a0001c0001t0001g0297 others(126): Show |
129 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.23-1472C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17677513 | |||||||
chr19:17677546 | G | A | 98 | a0001c0001t0001g0022 a0001c0001t0001g0080 a0001c0002t0001g0193 others(95): Show |
98 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(95): Show |
intron_variant | MODIFIER | c.23-1505C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17677546 | |||||||
chr19:17677613 | C | T | 2 | a0001c0008t0002g0071 a0001c0008t0002g0095 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.23-1572G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17677613 | |||||||
chr19:17677839 | T | C | 27 | a0001c0001t0001g0297 a0001c0001t0004g0012 a0001c0001t0034g0304 others(24): Show |
27 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.23-1798A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17677839 | |||||||
chr19:17677980 | G | A | 23 | a0001c0001t0001g0080 a0001c0002t0003g0096 a0001c0002t0010g0033 others(20): Show |
23 | HG00099.hp2 HG01934.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.23-1939C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17677980 | |||||||
chr19:17677995 | T | C | 98 | a0001c0001t0001g0022 a0001c0001t0001g0080 a0001c0002t0001g0193 others(95): Show |
98 | HG00099.hp2 HG00639.hp1 HG00738.hp1 others(95): Show |
intron_variant | MODIFIER | c.23-1954A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17677995 | |||||||
chr19:17678131 | G | C | 36 | a0001c0002t0003g0068 a0001c0002t0008g0027 a0001c0002t0008g0046 others(33): Show |
36 | HG00639.hp1 HG00738.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.23-2090C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17678131 | |||||||
chr19:17678205 | G | A | 2 | a0001c0001t0001g0022 a0002c0006t0001g0021 |
2 | HG01978.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.23-2164C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17678205 | |||||||
chr19:17678226 | C | A | 1 | a0001c0003t0001g0079 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.23-2185G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17678226 | |||||||
chr19:17678356 | C | G | 129 | a0001c0001t0001g0022 a0001c0001t0001g0080 a0001c0001t0001g0297 others(126): Show |
129 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.23-2315G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17678356 | |||||||
chr19:17678506 | T | A | 44 | a0001c0001t0001g0297 a0001c0001t0004g0012 a0001c0001t0034g0304 others(41): Show |
44 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.23-2465A>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17678506 | |||||||
chr19:17678600 | G | T | 130 | a0001c0001t0001g0022 a0001c0001t0001g0080 a0001c0001t0001g0297 others(127): Show |
130 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.23-2559C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17678600 | |||||||
chr19:17678666 | G | A | 1 | a0001c0067t0004g0265 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.23-2625C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17678666 | |||||||
chr19:17678745 | C | T | 26 | a0001c0001t0001g0297 a0001c0001t0004g0012 a0001c0001t0034g0304 others(23): Show |
26 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.23-2704G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17678745 | |||||||
chr19:17678787 | A | AGAGGTAG others(15): Show |
1 | a0001c0001t0001g0170 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.23-2768_23-2747dup others(22): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17678787 | |||||||
chr19:17678802 | C | T | 1 | a0001c0028t0002g0196 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.23-2761G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17678802 | |||||||
chr19:17678904 | A | T | 1 | a0001c0003t0040g0024 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.23-2863T>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17678904 | |||||||
chr19:17678967 | A | G | 129 | a0001c0001t0001g0022 a0001c0001t0001g0080 a0001c0001t0001g0297 others(126): Show |
129 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.23-2926T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17678967 | |||||||
chr19:17679082 | G | A | 5 | a0001c0004t0010g0242 a0001c0004t0049g0317 a0001c0008t0002g0034 others(2): Show |
5 | HG02896.hp1 HG03130.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.23-3041C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17679082 | |||||||
chr19:17679089 | T | C | 104 | a0001c0001t0001g0022 a0001c0001t0001g0080 a0001c0002t0001g0193 others(101): Show |
104 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(101): Show |
intron_variant | MODIFIER | c.23-3048A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17679089 | |||||||
chr19:17679150 | C | A | 46 | a0001c0001t0001g0022 a0001c0001t0001g0080 a0001c0002t0001g0193 others(43): Show |
46 | HG00639.hp2 HG00738.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.23-3109G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17679150 | |||||||
chr19:17679219 | G | T | 26 | a0001c0001t0001g0297 a0001c0001t0004g0012 a0001c0001t0034g0304 others(23): Show |
26 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.23-3178C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17679219 | |||||||
chr19:17679225 | C | A | 35 | a0001c0002t0003g0068 a0001c0002t0008g0046 a0001c0002t0010g0069 others(32): Show |
35 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.23-3184G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17679225 | |||||||
chr19:17679256 | C | T | 2 | a0001c0002t0020g0025 a0001c0003t0040g0024 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.23-3215G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17679256 | |||||||
chr19:17679408 | T | TATA | 12 | a0001c0002t0029g0167 a0001c0002t0032g0098 a0001c0002t0045g0164 others(9): Show |
12 | HG01361.hp1 HG02145.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.23-3370_23-3368dup others(3): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17679408 | |||||||
chr19:17679525 | C | G | 1 | a0001c0002t0018g0269 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.23-3484G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17679525 | |||||||
chr19:17679595 | G | T | 1 | a0001c0002t0032g0098 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.23-3554C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17679595 | |||||||
chr19:17679617 | A | G | 1 | a0001c0029t0006g0243 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.23-3576T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17679617 | |||||||
chr19:17679682 | TTCTC | T | 7 | a0001c0002t0019g0092 a0001c0011t0001g0089 a0001c0015t0006g0090 others(4): Show |
7 | HG01361.hp1 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-3645_23-3642del others(4): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17679682 | |||||||
chr19:17679842 | C | A | 9 | a0001c0002t0029g0167 a0001c0002t0045g0164 a0001c0003t0003g0162 others(6): Show |
9 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.23-3801G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17679842 | |||||||
chr19:17679949 | C | T | 1 | a0001c0004t0003g0030 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.23-3908G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17679949 | |||||||
chr19:17680005 | T | C | 1 | a0003c0010t0013g0161 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.23-3964A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680005 | |||||||
chr19:17680049 | G | A | 1 | a0001c0031t0001g0116 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.23-4008C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680049 | |||||||
chr19:17680410 | C | A | 3 | a0001c0046t0001g0280 a0002c0006t0006g0278 a0002c0041t0036g0279 |
3 | HG00140.hp2 HG01496.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.23-4369G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680410 | |||||||
chr19:17680466 | G | C | 2 | a0002c0017t0001g0086 a0006c0025t0001g0087 |
2 | HG00099.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.23-4425C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680466 | |||||||
chr19:17680537 | G | A | 6 | a0001c0004t0049g0317 a0001c0007t0025g0320 a0001c0021t0014g0318 others(3): Show |
6 | HG02895.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.23-4496C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680537 | |||||||
chr19:17680540 | G | C | 25 | a0001c0001t0001g0022 a0001c0001t0004g0012 a0001c0002t0007g0018 others(22): Show |
25 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.23-4499C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680540 | |||||||
chr19:17680565 | C | T | 6 | a0001c0004t0049g0317 a0001c0007t0025g0320 a0001c0021t0014g0318 others(3): Show |
6 | HG02895.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.23-4524G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680565 | |||||||
chr19:17680611 | C | A | 2 | a0001c0002t0001g0266 a0002c0006t0003g0267 |
2 | HG02148.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.23-4570G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680611 | |||||||
chr19:17680723 | T | C | 1 | a0001c0002t0027g0295 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.23-4682A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680723 | |||||||
chr19:17680749 | T | C | 1 | a0001c0002t0019g0092 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.23-4708A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680749 | |||||||
chr19:17680869 | C | CT | 54 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0297 others(51): Show |
54 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.23-4829dupA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680869 | |||||||
chr19:17680876 | T | C | 1 | a0001c0001t0001g0245 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.23-4835A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680876 | |||||||
chr19:17680888 | TC | T | 3 | a0001c0046t0001g0280 a0002c0006t0006g0278 a0002c0041t0036g0279 |
3 | HG00140.hp2 HG01496.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.23-4848delG | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680888 | |||||||
chr19:17680889 | C | CT | 27 | a0001c0001t0001g0107 a0001c0001t0001g0145 a0001c0001t0001g0209 others(24): Show |
27 | HG00544.hp1 HG00673.hp1 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.23-4849dupA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680889 | |||||||
chr19:17680889 | C | CTT | 39 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0174 others(36): Show |
39 | HG00280.hp1 HG00642.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.23-4850_23-4849dup others(2): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680889 | |||||||
chr19:17680889 | C | CTTT | 10 | a0001c0001t0001g0297 a0001c0002t0003g0096 a0001c0002t0009g0176 others(7): Show |
10 | HG00280.hp2 HG01123.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.23-4851_23-4849dup others(3): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680889 | |||||||
chr19:17680889 | C | CTTTTT | 13 | a0001c0002t0003g0068 a0001c0002t0008g0046 a0001c0002t0010g0069 others(10): Show |
13 | HG01109.hp2 HG01928.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.23-4853_23-4849dup others(5): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680889 | |||||||
chr19:17680889 | C | CTTTTTT | 19 | a0001c0002t0011g0064 a0001c0002t0011g0184 a0001c0002t0015g0054 others(16): Show |
19 | HG00738.hp2 HG02257.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.23-4854_23-4849dup others(6): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680889 | |||||||
chr19:17680889 | C | CTTTTTTT | 16 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0002t0008g0027 others(13): Show |
16 | HG00639.hp1 HG01070.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.23-4855_23-4849dup others(7): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680889 | |||||||
chr19:17680889 | C | CTTTTTTT others(1): Show |
7 | a0001c0001t0004g0012 a0001c0002t0007g0018 a0001c0003t0001g0014 others(4): Show |
7 | HG00639.hp2 HG00738.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-4856_23-4849dup others(8): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680889 | |||||||
chr19:17680889 | C | CTTTTTTT others(3): Show |
1 | a0001c0008t0002g0277 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.23-4858_23-4849dup others(10): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680889 | |||||||
chr19:17680889 | C | CTTTTTTT others(4): Show |
3 | a0001c0008t0002g0274 a0001c0008t0002g0276 a0001c0023t0047g0275 |
3 | HG02559.hp2 HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.23-4859_23-4849dup others(11): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680889 | |||||||
chr19:17680889 | C | CTTTTTTT others(6): Show |
1 | a0006c0025t0001g0029 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.23-4861_23-4849dup others(13): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680889 | |||||||
chr19:17680889 | C | CTTTTTTT others(7): Show |
1 | a0002c0005t0001g0273 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.23-4862_23-4849dup others(14): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680889 | |||||||
chr19:17680889 | C | T | 1 | a0001c0002t0028g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.23-4848G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680889 | |||||||
chr19:17680889 | CT | C | 14 | a0001c0001t0001g0166 a0001c0001t0001g0231 a0001c0001t0001g0270 others(11): Show |
14 | HG00438.hp2 HG01081.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.23-4849delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680889 | |||||||
chr19:17680889 | CTT | C | 20 | a0001c0001t0001g0080 a0001c0002t0018g0103 a0001c0003t0001g0079 others(17): Show |
20 | HG00099.hp2 HG02055.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.23-4850_23-4849del others(2): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680889 | |||||||
chr19:17680895 | T | C | 7 | a0001c0003t0001g0009 a0001c0004t0049g0317 a0001c0007t0025g0320 others(4): Show |
7 | HG01081.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-4854A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680895 | |||||||
chr19:17680948 | G | A | 6 | a0001c0004t0049g0317 a0001c0007t0025g0320 a0001c0021t0014g0318 others(3): Show |
6 | HG02895.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.23-4907C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17680948 | |||||||
chr19:17681037 | C | G | 31 | a0001c0001t0001g0080 a0001c0002t0012g0077 a0001c0002t0018g0103 others(28): Show |
31 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.23-4996G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17681037 | |||||||
chr19:17681069 | C | CT | 26 | a0001c0001t0001g0080 a0001c0001t0001g0115 a0001c0001t0001g0194 others(23): Show |
26 | HG00423.hp2 HG01361.hp2 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.23-5029dupA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17681069 | |||||||
chr19:17681069 | C | CTT | 28 | a0001c0001t0007g0232 a0001c0002t0012g0077 a0001c0002t0018g0103 others(25): Show |
28 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.23-5030_23-5029dup others(2): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17681069 | |||||||
chr19:17681069 | CT | C | 72 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0174 others(69): Show |
72 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.23-5029delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17681069 | |||||||
chr19:17681069 | CTTTTTTT others(4): Show |
C | 3 | a0001c0046t0001g0280 a0002c0006t0006g0278 a0002c0041t0036g0279 |
3 | HG00140.hp2 HG01496.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.23-5039_23-5029del others(11): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17681069 | |||||||
chr19:17681173 | C | A | 5 | a0001c0008t0026g0083 a0001c0050t0033g0085 a0002c0017t0001g0086 others(2): Show |
5 | HG00099.hp2 HG02922.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.23-5132G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17681173 | |||||||
chr19:17681268 | G | A | 1 | a0001c0002t0025g0315 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.23-5227C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17681268 | |||||||
chr19:17681279 | G | C | 2 | a0001c0001t0009g0160 a0001c0002t0001g0229 |
2 | HG02074.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.23-5238C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17681279 | |||||||
chr19:17681284 | T | C | 3 | a0001c0046t0001g0280 a0002c0006t0006g0278 a0002c0041t0036g0279 |
3 | HG00140.hp2 HG01496.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.23-5243A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17681284 | |||||||
chr19:17681336 | T | C | 1 | a0003c0010t0013g0161 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.23-5295A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17681336 | |||||||
chr19:17681353 | G | A | 1 | a0001c0002t0009g0176 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.23-5312C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17681353 | |||||||
chr19:17681543 | C | G | 31 | a0001c0001t0001g0080 a0001c0002t0012g0077 a0001c0002t0018g0103 others(28): Show |
31 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.23-5502G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17681543 | |||||||
chr19:17681584 | G | A | 4 | a0001c0002t0019g0092 a0001c0011t0001g0089 a0001c0015t0006g0090 others(1): Show |
4 | HG01361.hp1 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-5543C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17681584 | |||||||
chr19:17681849 | G | T | 5 | a0001c0008t0002g0274 a0001c0008t0002g0276 a0001c0008t0002g0277 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-5808C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17681849 | |||||||
chr19:17681895 | C | T | 3 | a0001c0046t0001g0280 a0002c0006t0006g0278 a0002c0041t0036g0279 |
3 | HG00140.hp2 HG01496.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.23-5854G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17681895 | |||||||
chr19:17681951 | AT | A | 134 | a0001c0001t0001g0115 a0001c0001t0001g0132 a0001c0001t0001g0136 others(131): Show |
134 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.23-5911delA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17681951 | |||||||
chr19:17681951 | ATT | A | 14 | a0001c0002t0018g0269 a0001c0002t0025g0315 a0001c0002t0029g0167 others(11): Show |
14 | HG00140.hp2 HG00735.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.23-5912_23-5911del others(2): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17681951 | |||||||
chr19:17681951 | ATTT | A | 11 | a0001c0002t0045g0164 a0001c0003t0001g0040 a0001c0004t0001g0010 others(8): Show |
11 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.23-5913_23-5911del others(3): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17681951 | |||||||
chr19:17681951 | ATTTT | A | 84 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0080 others(81): Show |
84 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.23-5914_23-5911del others(4): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17681951 | |||||||
chr19:17681951 | ATTTTT | A | 53 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0174 others(50): Show |
53 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.23-5915_23-5911del others(5): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17681951 | |||||||
chr19:17681978 | A | C | 5 | a0001c0002t0008g0027 a0001c0002t0011g0039 a0001c0002t0020g0025 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.23-5937T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17681978 | |||||||
chr19:17682239 | C | A | 5 | a0001c0002t0008g0027 a0001c0002t0011g0039 a0001c0002t0020g0025 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.22+5939G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17682239 | |||||||
chr19:17682245 | G | C | 160 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0080 others(157): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.22+5933C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17682245 | |||||||
chr19:17682263 | T | C | 5 | a0001c0008t0002g0274 a0001c0008t0002g0276 a0001c0008t0002g0277 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+5915A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17682263 | |||||||
chr19:17682347 | T | A | 6 | a0001c0004t0049g0317 a0001c0007t0025g0320 a0001c0021t0014g0318 others(3): Show |
6 | HG02895.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.22+5831A>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17682347 | |||||||
chr19:17682431 | G | T | 1 | a0001c0001t0001g0165 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.22+5747C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17682431 | |||||||
chr19:17682625 | G | A | 5 | a0001c0004t0021g0073 a0001c0007t0003g0072 a0001c0008t0002g0071 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+5553C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17682625 | |||||||
chr19:17682671 | C | T | 1 | a0001c0004t0009g0186 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.22+5507G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17682671 | |||||||
chr19:17682990 | G | A | 11 | a0001c0001t0001g0080 a0001c0002t0012g0077 a0001c0003t0001g0079 others(8): Show |
11 | HG01496.hp2 HG01934.hp1 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.22+5188C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17682990 | |||||||
chr19:17683055 | ACT | A | 5 | a0001c0001t0001g0080 a0001c0003t0001g0079 a0001c0014t0001g0081 others(2): Show |
5 | HG04228.hp1 NA18951.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.22+5121_22+5122del others(2): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17683055 | |||||||
chr19:17683109 | A | T | 160 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0080 others(157): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.22+5069T>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17683109 | |||||||
chr19:17683157 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.22+5021C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17683157 | |||||||
chr19:17683173 | T | G | 4 | a0001c0001t0001g0166 a0001c0001t0001g0230 a0001c0001t0001g0231 others(1): Show |
4 | HG00438.hp2 NA19004.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+5005A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17683173 | |||||||
chr19:17683182 | C | G | 1 | a0001c0063t0002g0104 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.22+4996G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17683182 | |||||||
chr19:17683360 | G | A | 1 | a0001c0002t0025g0315 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.22+4818C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17683360 | |||||||
chr19:17683398 | G | A | 1 | a0001c0002t0010g0069 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.22+4780C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17683398 | |||||||
chr19:17683430 | A | G | 154 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0080 others(151): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.22+4748T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17683430 | |||||||
chr19:17683517 | G | A | 3 | a0001c0002t0003g0096 a0001c0002t0010g0097 a0001c0024t0019g0100 |
3 | HG02965.hp1 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.22+4661C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17683517 | |||||||
chr19:17683568 | A | G | 160 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0080 others(157): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.22+4610T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17683568 | |||||||
chr19:17683632 | C | T | 154 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0080 others(151): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.22+4546G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17683632 | |||||||
chr19:17683660 | A | AAAAC | 26 | a0001c0001t0001g0080 a0001c0002t0012g0077 a0001c0002t0018g0103 others(23): Show |
26 | HG00099.hp2 HG01496.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.22+4514_22+4517dup others(4): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17683660 | |||||||
chr19:17683660 | A | AAAACAAA others(5): Show |
5 | a0001c0004t0021g0073 a0001c0007t0003g0072 a0001c0008t0002g0071 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+4506_22+4517dup others(12): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17683660 | |||||||
chr19:17683733 | C | T | 6 | a0001c0004t0049g0317 a0001c0007t0025g0320 a0001c0021t0014g0318 others(3): Show |
6 | HG02895.hp2 HG02897.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.22+4445G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17683733 | |||||||
chr19:17683778 | T | C | 2 | a0001c0001t0003g0271 a0001c0004t0004g0272 |
2 | HG00558.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.22+4400A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17683778 | |||||||
chr19:17683814 | C | T | 1 | a0001c0055t0001g0102 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.22+4364G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17683814 | |||||||
chr19:17683842 | A | G | 29 | a0001c0001t0001g0297 a0001c0001t0034g0304 a0001c0002t0001g0308 others(26): Show |
29 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+4336T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17683842 | |||||||
chr19:17683906 | G | C | 1 | a0004c0048t0005g0177 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.22+4272C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17683906 | |||||||
chr19:17683993 | G | A | 1 | a0001c0001t0007g0232 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.22+4185C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17683993 | |||||||
chr19:17684233 | G | A | 1 | a0001c0002t0029g0167 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.22+3945C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17684233 | |||||||
chr19:17684401 | G | A | 4 | a0001c0007t0025g0320 a0001c0021t0014g0318 a0001c0021t0014g0319 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+3777C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17684401 | |||||||
chr19:17684426 | G | T | 4 | a0001c0002t0019g0092 a0001c0011t0001g0089 a0001c0015t0006g0090 others(1): Show |
4 | HG01361.hp1 HG02145.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+3752C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17684426 | |||||||
chr19:17684439 | G | A | 1 | a0003c0010t0001g0070 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.22+3739C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17684439 | |||||||
chr19:17684506 | G | C | 55 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0174 others(52): Show |
55 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.22+3672C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17684506 | |||||||
chr19:17684551 | C | G | 154 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0080 others(151): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.22+3627G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17684551 | |||||||
chr19:17684606 | C | G | 160 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0080 others(157): Show |
160 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.22+3572G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17684606 | |||||||
chr19:17684616 | T | C | 36 | a0001c0002t0003g0068 a0001c0002t0008g0046 a0001c0002t0010g0069 others(33): Show |
36 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.22+3562A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17684616 | |||||||
chr19:17684805 | G | A | 1 | a0001c0002t0017g0028 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.22+3373C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17684805 | |||||||
chr19:17685004 | C | G | 4 | a0001c0003t0001g0009 a0002c0009t0005g0006 a0002c0009t0005g0007 others(1): Show |
4 | HG01070.hp1 HG01081.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+3174G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17685004 | |||||||
chr19:17685075 | G | A | 18 | a0001c0001t0001g0080 a0001c0002t0012g0077 a0001c0003t0001g0079 others(15): Show |
18 | HG00099.hp2 HG01496.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.22+3103C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17685075 | |||||||
chr19:17685117 | T | C | 28 | a0001c0001t0001g0080 a0001c0002t0012g0077 a0001c0003t0001g0079 others(25): Show |
28 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.22+3061A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17685117 | |||||||
chr19:17685167 | G | A | 26 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0004g0012 others(23): Show |
26 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.22+3011C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17685167 | |||||||
chr19:17685199 | C | CT | 30 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0004g0012 others(27): Show |
30 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.22+2978dupA | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17685199 | |||||||
chr19:17685245 | C | A | 1 | a0001c0008t0002g0095 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.22+2933G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17685245 | |||||||
chr19:17685364 | T | G | 151 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0080 others(148): Show |
151 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.22+2814A>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17685364 | |||||||
chr19:17685462 | G | C | 2 | a0001c0001t0001g0179 a0001c0002t0001g0178 |
2 | NA18964.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.22+2716C>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17685462 | |||||||
chr19:17685524 | A | G | 4 | a0001c0007t0025g0320 a0001c0021t0014g0318 a0001c0021t0014g0319 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+2654T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17685524 | |||||||
chr19:17685588 | A | G | 67 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0004g0012 others(64): Show |
67 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.22+2590T>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17685588 | |||||||
chr19:17685623 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.22+2555C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17685623 | |||||||
chr19:17685645 | C | T | 1 | a0001c0002t0008g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.22+2533G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17685645 | |||||||
chr19:17685852 | T | C | 9 | a0001c0002t0025g0315 a0001c0008t0002g0274 a0001c0008t0002g0276 others(6): Show |
9 | HG00140.hp2 HG01496.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+2326A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17685852 | |||||||
chr19:17685868 | G | T | 71 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0004g0012 others(68): Show |
71 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.22+2310C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17685868 | |||||||
chr19:17685923 | T | C | 3 | a0001c0070t0001g0313 a0001c0071t0002g0311 a0001c0072t0003g0312 |
3 | HG02717.hp1 HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.22+2255A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17685923 | |||||||
chr19:17686014 | C | A | 105 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0080 others(102): Show |
105 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.22+2164G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17686014 | |||||||
chr19:17686035 | C | T | 1 | a0001c0003t0001g0101 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.22+2143G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17686035 | |||||||
chr19:17686098 | CTTCCCCA others(5): Show |
C | 5 | a0001c0008t0026g0083 a0001c0050t0033g0085 a0002c0017t0001g0086 others(2): Show |
5 | HG00099.hp2 HG02922.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.22+2068_22+2079del others(12): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17686098 | |||||||
chr19:17686131 | T | C | 1 | a0001c0001t0007g0232 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.22+2047A>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17686131 | |||||||
chr19:17686231 | G | GC | 76 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0004g0012 others(73): Show |
76 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.22+1946dupG | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17686231 | |||||||
chr19:17686298 | G | GC | 51 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0001g0190 others(48): Show |
51 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.22+1879dupG | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17686298 | |||||||
chr19:17686298 | G | GCC | 42 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(39): Show |
42 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.22+1878_22+1879dup others(2): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17686298 | |||||||
chr19:17686298 | GCCCC | G | 17 | a0001c0001t0001g0297 a0001c0001t0034g0304 a0001c0002t0010g0033 others(14): Show |
17 | HG00735.hp2 HG01258.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.22+1876_22+1879del others(4): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17686298 | |||||||
chr19:17686298 | GCCCCC | G | 17 | a0001c0002t0003g0096 a0001c0002t0008g0284 a0001c0002t0010g0097 others(14): Show |
17 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.22+1875_22+1879del others(5): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17686298 | |||||||
chr19:17686298 | GCCCCCCC others(2): Show |
G | 53 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0080 others(50): Show |
53 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.22+1871_22+1879del others(9): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17686298 | |||||||
chr19:17686298 | GCCCCCCC others(3): Show |
G | 45 | a0001c0002t0003g0068 a0001c0002t0008g0046 a0001c0002t0010g0069 others(42): Show |
45 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.22+1870_22+1879del others(10): Show |
UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17686298 | |||||||
chr19:17686301 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.22+1877G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17686301 | |||||||
chr19:17686313 | C | G | 4 | a0001c0002t0010g0033 a0001c0008t0002g0034 a0001c0011t0020g0035 others(1): Show |
4 | HG02723.hp2 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+1865G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17686313 | |||||||
chr19:17686911 | G | A | 8 | a0001c0008t0002g0274 a0001c0008t0002g0276 a0001c0008t0002g0277 others(5): Show |
8 | HG00140.hp2 HG01496.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.22+1267C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17686911 | |||||||
chr19:17686927 | C | G | 1 | a0001c0003t0001g0031 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.22+1251G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17686927 | |||||||
chr19:17686951 | C | T | 7 | a0001c0002t0025g0315 a0001c0004t0049g0317 a0001c0007t0025g0320 others(4): Show |
7 | HG02895.hp2 HG02897.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.22+1227G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17686951 | |||||||
chr19:17687245 | G | A | 3 | a0001c0046t0001g0280 a0002c0006t0006g0278 a0002c0041t0036g0279 |
3 | HG00140.hp2 HG01496.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.22+933C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17687245 | |||||||
chr19:17687288 | G | A | 4 | a0001c0007t0025g0320 a0001c0021t0014g0318 a0001c0021t0014g0319 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+890C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17687288 | |||||||
chr19:17687302 | C | A | 28 | a0001c0001t0001g0297 a0001c0001t0034g0304 a0001c0002t0001g0308 others(25): Show |
28 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.22+876G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17687302 | |||||||
chr19:17687303 | C | T | 26 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0004g0012 others(23): Show |
26 | HG00639.hp2 HG00738.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.22+875G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17687303 | |||||||
chr19:17687307 | C | A | 1 | a0002c0006t0001g0281 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.22+871G>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17687307 | |||||||
chr19:17687337 | C | T | 29 | a0001c0001t0001g0297 a0001c0001t0034g0304 a0001c0002t0001g0308 others(26): Show |
29 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+841G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17687337 | |||||||
chr19:17687647 | G | T | 1 | a0001c0020t0001g0005 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.22+531C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17687647 | |||||||
chr19:17687704 | C | T | 3 | a0001c0070t0001g0313 a0001c0071t0002g0311 a0001c0072t0003g0312 |
3 | HG02717.hp1 HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.22+474G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17687704 | |||||||
chr19:17687805 | G | T | 1 | a0001c0027t0014g0314 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.22+373C>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17687805 | |||||||
chr19:17687940 | C | CA | 29 | a0001c0001t0001g0297 a0001c0001t0034g0304 a0001c0002t0001g0308 others(26): Show |
29 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.22+237dupT | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17687940 | |||||||
chr19:17687955 | G | A | 1 | a0002c0005t0006g0310 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.22+223C>T | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17687955 | |||||||
chr19:17688002 | C | T | 1 | a0002c0036t0002g0004 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.22+176G>A | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17688002 | |||||||
chr19:17688013 | A | C | 1 | a0007c0068t0002g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.22+165T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17688013 | |||||||
chr19:17688059 | A | C | 1 | a0008c0035t0001g0002 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.22+119T>G | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17688059 | |||||||
chr19:17688162 | C | G | 1 | a0001c0002t0001g0001 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.22+16G>C | UNC13A | ENSG00000130477.16 | transcript | ENST00000519716.7 | protein_coding | 1/43 | chr19 | 17688162 |