geneid | 4254 |
---|---|
ensemblid | ENSG00000049130.16 |
hgncid | 6343 |
symbol | KITLG |
name | KIT ligand |
refseq_nuc | NM_000899.5 |
refseq_prot | NP_000890.1 |
ensembl_nuc | ENST00000644744.1 |
ensembl_prot | ENSP00000495951.1 |
mane_status | MANE Select |
chr | chr12 |
start | 88492793 |
end | 88580471 |
strand | - |
ver | v1.2 |
region | chr12:88492793-88580471 |
region5000 | chr12:88487793-88585471 |
regionname0 | KITLG_chr12_88492793_88580471 |
regionname5000 | KITLG_chr12_88487793_88585471 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 273 | 239 | 84 | 24 | 107 | 6 | 16 | 89 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0002 | 0/0 | 273 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 822 | 235 | 80 | 24 | 107 | 6 | 16 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
c0002 | 0/0 | 822 | 4 | 4 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
c0003 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 4620 | 65 | 9 | 9 | 39 | 2 | 5 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0002 | 1/0 | 4620 | 57 | 26 | 4 | 20 | 1 | 5 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0003 | 0/0 | 4620 | 44 | 6 | 1 | 36 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0004 | 0/0 | 4620 | 15 | 3 | 5 | 5 | 1 | 1 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0005 | 0/0 | 4620 | 9 | 9 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0006 | 0/0 | 4620 | 6 | 0 | 0 | 6 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0007 | 0/0 | 4620 | 6 | 5 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0008 | 0/0 | 4620 | 4 | 0 | 2 | 0 | 1 | 1 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0009 | 0/0 | 4620 | 4 | 4 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0010 | 0/0 | 4620 | 4 | 4 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0011 | 0/0 | 4620 | 2 | 1 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0012 | 0/0 | 4620 | 2 | 2 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0013 | 0/0 | 4620 | 2 | 2 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0014 | 0/0 | 4620 | 2 | 2 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0015 | 0/0 | 4620 | 2 | 2 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0016 | 0/0 | 4620 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0017 | 0/0 | 4620 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0018 | 0/0 | 4620 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0019 | 0/0 | 4620 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0020 | 0/0 | 4620 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0021 | 0/0 | 4620 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0022 | 0/0 | 4620 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0023 | 0/0 | 4620 | 1 | 0 | 0 | 0 | 1 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0024 | 0/0 | 4620 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0025 | 0/0 | 4620 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0026 | 0/0 | 4620 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0027 | 0/0 | 4620 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0028 | 0/0 | 4620 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0029 | 0/0 | 4620 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0030 | 0/0 | 4620 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
t0031 | 0/0 | 4620 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0003 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 822 | 235 | 80 | 24 | 107 | 6 | 16 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0002 | 0/0 | 822 | 4 | 4 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0002c0003 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5441 | 64 | 9 | 9 | 38 | 2 | 5 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0002 | 1/0 | 5441 | 53 | 22 | 4 | 20 | 1 | 5 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0003 | 0/0 | 5441 | 44 | 6 | 1 | 36 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0004 | 0/0 | 5441 | 15 | 3 | 5 | 5 | 1 | 1 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0005 | 0/0 | 5441 | 9 | 9 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0006 | 0/0 | 5441 | 6 | 0 | 0 | 6 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0007 | 0/0 | 5441 | 6 | 5 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0008 | 0/0 | 5441 | 4 | 0 | 2 | 0 | 1 | 1 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0009 | 0/0 | 5441 | 4 | 4 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0010 | 0/0 | 5441 | 4 | 4 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0011 | 0/0 | 5441 | 2 | 1 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0012 | 0/0 | 5441 | 2 | 2 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0013 | 0/0 | 5441 | 2 | 2 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0014 | 0/0 | 5441 | 2 | 2 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0015 | 0/0 | 5441 | 2 | 2 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0016 | 0/0 | 5441 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0017 | 0/0 | 5441 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0018 | 0/0 | 5441 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0019 | 0/0 | 5441 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0020 | 0/0 | 5441 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0021 | 0/0 | 5441 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0022 | 0/0 | 5441 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0023 | 0/0 | 5441 | 1 | 0 | 0 | 0 | 1 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0024 | 0/0 | 5441 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0025 | 0/0 | 5441 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0026 | 0/0 | 5441 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0027 | 0/0 | 5441 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0028 | 0/0 | 5441 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0029 | 0/0 | 5441 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0030 | 0/0 | 5441 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0001t0031 | 0/0 | 5441 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0001c0002t0002 | 0/0 | 5441 | 4 | 4 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
a0002c0003t0001 | 0/0 | 5441 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | copy fasta | chr12 | 88487793 | 88585471 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0006g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0006g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0006g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0006g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0006g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0007g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0007g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0007g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0008g0003 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0008g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0009g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0009g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0010g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0010g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0010g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0011g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0011g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0012g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0012g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0013g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0013g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0014g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0015g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0015g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0016g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0017g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0018g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0019g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0020g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0021g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0022g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0023g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0024g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0025g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0026g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0027g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0028g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0029g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0030g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0031g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0002c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0008 | g0192 | EUR | GBR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0050 | EUR | GBR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | FIN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | FIN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | CHS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | CHS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00738 | hp2 | a0001 | c0001 | t0008 | g0003 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0129 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0053 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0044 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0047 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01192 | hp2 | a0001 | c0001 | t0011 | g0039 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01346 | hp1 | a0001 | c0001 | t0018 | g0183 | AMR | CLM | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0043 | AMR | CLM | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01496 | hp1 | a0001 | c0001 | t0008 | g0003 | AMR | CLM | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0049 | AMR | CLM | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | IBS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01517 | hp2 | a0001 | c0001 | t0023 | g0046 | EUR | IBS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01891 | hp2 | a0001 | c0001 | t0031 | g0221 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PEL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02055 | hp1 | a0001 | c0001 | t0015 | g0218 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | KHV | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02083 | hp1 | a0001 | c0001 | t0021 | g0208 | EAS | KHV | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02145 | hp1 | a0001 | c0001 | t0013 | g0114 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CDX | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CDX | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02257 | hp1 | a0001 | c0001 | t0007 | g0201 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02257 | hp2 | a0001 | c0001 | t0015 | g0219 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02280 | hp1 | a0001 | c0001 | t0011 | g0128 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0078 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02300 | hp2 | a0001 | c0001 | t0019 | g0024 | AMR | PEL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02451 | hp2 | a0001 | c0001 | t0014 | g0010 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02615 | hp1 | a0001 | c0001 | t0013 | g0070 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02622 | hp1 | a0001 | c0001 | t0022 | g0028 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02622 | hp2 | a0001 | c0001 | t0009 | g0052 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0205 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0135 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02647 | hp2 | a0001 | c0002 | t0002 | g0065 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02809 | hp1 | a0001 | c0001 | t0025 | g0144 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0133 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02896 | hp2 | a0001 | c0001 | t0007 | g0203 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02922 | hp1 | a0001 | c0001 | t0014 | g0010 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02965 | hp1 | a0001 | c0002 | t0002 | g0150 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02965 | hp2 | a0001 | c0002 | t0002 | g0041 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02970 | hp2 | a0001 | c0001 | t0009 | g0042 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03098 | hp1 | a0001 | c0001 | t0016 | g0019 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03098 | hp2 | a0001 | c0001 | t0009 | g0051 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03130 | hp1 | a0001 | c0001 | t0029 | g0146 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03130 | hp2 | a0001 | c0001 | t0010 | g0007 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03139 | hp2 | a0001 | c0001 | t0009 | g0061 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0204 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03209 | hp1 | a0001 | c0001 | t0026 | g0040 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0142 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0156 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03453 | hp1 | a0001 | c0001 | t0010 | g0116 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03453 | hp2 | a0001 | c0001 | t0028 | g0153 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03516 | hp1 | a0001 | c0001 | t0010 | g0007 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0120 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0143 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03579 | hp2 | a0001 | c0001 | t0005 | g0057 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03688 | hp1 | a0001 | c0001 | t0017 | g0045 | SAS | STU | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | STU | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03704 | hp1 | a0001 | c0001 | t0004 | g0048 | SAS | PJL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | BEB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03834 | hp2 | a0001 | c0001 | t0008 | g0003 | SAS | BEB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0131 | SAS | STU | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | STU | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG04184 | hp1 | a0001 | c0001 | t0007 | g0200 | SAS | BEB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0062 | SAS | BEB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | STU | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG04228 | hp2 | a0001 | c0001 | t0024 | g0054 | SAS | STU | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | CHB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18906 | hp1 | a0001 | c0001 | t0012 | g0075 | AFR | YRI | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0145 | AFR | YRI | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18939 | hp2 | a0002 | c0003 | t0001 | g0193 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18949 | hp2 | a0001 | c0001 | t0004 | g0217 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18973 | hp2 | a0001 | c0001 | t0006 | g0015 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18975 | hp1 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18982 | hp1 | a0001 | c0001 | t0020 | g0195 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18990 | hp1 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19002 | hp2 | a0001 | c0001 | t0006 | g0018 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19005 | hp2 | a0001 | c0001 | t0006 | g0017 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0063 | AFR | LWK | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | LWK | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | LWK | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | LWK | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19058 | hp2 | a0001 | c0001 | t0004 | g0214 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19083 | hp2 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0220 | AFR | YRI | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19240 | hp2 | a0001 | c0001 | t0027 | g0148 | AFR | YRI | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ASW | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA20129 | hp2 | a0001 | c0001 | t0030 | g0124 | AFR | ASW | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02486 | hp2 | a0001 | c0001 | t0010 | g0123 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02559 | hp2 | a0001 | c0001 | t0012 | g0056 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0147 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0105 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0212 | AFR | USA | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | USA | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18955 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | USA | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | USA | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | LWK | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA21309 | hp2 | a0001 | c0001 | t0007 | g0036 | AFR | LWK | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0161 | REF | REF | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0104 | REF | REF | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:88532473
|
T | C | 1 | a0002 | 1 | NA18939.hp2 | missense_variant | MODERATE | c.160A>G | p.Thr54Ala | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/10 | 353/5441 | 160/822 | 54/273 | chr12 | 88532473 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:88518847
|
G | A | 1 | a0001c0002 | 4 | HG02647.hp2 HG02965.hp1 HG02965.hp2 others(1): Show |
synonymous_variant | LOW | c.213C>T | p.Ser71Ser | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/10 | 406/5441 | 213/822 | 71/273 | chr12 | 88518847 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:88492845
|
T | C | 1 | a0001c0001t0020 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4374A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 12351 | chr12 | 88492845 | |||||
chr12:88493147
|
A | G | 1 | a0001c0001t0015 | 2 | HG02055.hp1 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4072T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 12049 | chr12 | 88493147 | |||||
chr12:88493176
|
T | A | 1 | a0001c0001t0013 | 2 | HG02145.hp1 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4043A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 12020 | chr12 | 88493176 | |||||
chr12:88493186
|
T | C | 6 | a0001c0001t0004a0001c0001t0009a0001c0001t0017others(3): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*4033A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 12010 | chr12 | 88493186 | |||||
chr12:88493300
|
T | C | 1 | a0001c0001t0024 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3919A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 11896 | chr12 | 88493300 | |||||
chr12:88493509
|
A | T | 1 | a0001c0001t0026 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3710T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 11687 | chr12 | 88493509 | |||||
chr12:88493512
|
T | C | 8 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(5): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*3707A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 11684 | chr12 | 88493512 | |||||
chr12:88493594
|
T | G | 1 | a0001c0001t0027 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3625A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 11602 | chr12 | 88493594 | |||||
chr12:88493624
|
C | A | 1 | a0001c0001t0028 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3595G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 11572 | chr12 | 88493624 | |||||
chr12:88493947
|
G | T | 6 | a0001c0001t0004a0001c0001t0009a0001c0001t0017others(3): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3272C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 11249 | chr12 | 88493947 | |||||
chr12:88494114
|
T | C | 3 | a0001c0001t0003a0001c0001t0014a0001c0001t0028 | 47 | HG00741.hp2 HG02451.hp2 HG02615.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3105A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 11082 | chr12 | 88494114 | |||||
chr12:88494242
|
C | A | 1 | a0001c0001t0014 | 2 | HG02451.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2977G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 10954 | chr12 | 88494242 | |||||
chr12:88494438
|
T | C | 6 | a0001c0001t0004a0001c0001t0009a0001c0001t0017others(3): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2781A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 10758 | chr12 | 88494438 | |||||
chr12:88494470
|
T | C | 7 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(4): Show | 78 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*2749A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 10726 | chr12 | 88494470 | |||||
chr12:88494674
|
T | G | 1 | a0001c0001t0025 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2545A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 10522 | chr12 | 88494674 | |||||
chr12:88494693
|
A | C | 1 | a0001c0001t0012 | 2 | HG02559.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2526T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 10503 | chr12 | 88494693 | |||||
chr12:88494714
|
T | C | 1 | a0001c0001t0008 | 4 | HG00099.hp1 HG00738.hp2 HG01496.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2505A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 10482 | chr12 | 88494714 | |||||
chr12:88494904
|
C | A | 1 | a0001c0001t0021 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2315G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 10292 | chr12 | 88494904 | |||||
chr12:88494976
|
T | C | 1 | a0001c0001t0015 | 2 | HG02055.hp1 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2243A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 10220 | chr12 | 88494976 | |||||
chr12:88495184
|
T | C | 1 | a0001c0001t0011 | 2 | HG01192.hp2 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2035A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 10012 | chr12 | 88495184 | |||||
chr12:88495246
|
A | G | 1 | a0001c0001t0010 | 4 | HG02486.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1973T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 9950 | chr12 | 88495246 | |||||
chr12:88495593
|
C | T | 1 | a0001c0001t0029 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1626G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 9603 | chr12 | 88495593 | |||||
chr12:88495960
|
C | T | 1 | a0001c0001t0019 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1259G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 9236 | chr12 | 88495960 | |||||
chr12:88496121
|
A | C | 1 | a0001c0001t0009 | 4 | HG02622.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1098T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 9075 | chr12 | 88496121 | |||||
chr12:88496200
|
A | T | 8 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(5): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1019T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 8996 | chr12 | 88496200 | |||||
chr12:88496206
|
A | T | 1 | a0001c0001t0023 | 1 | HG01517.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1013T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 8990 | chr12 | 88496206 | |||||
chr12:88496214
|
G | A | 1 | a0001c0001t0022 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1005C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 8982 | chr12 | 88496214 | |||||
chr12:88496381
|
G | A | 2 | a0001c0001t0005a0001c0001t0029 | 10 | HG02280.hp2 HG02647.hp1 HG02895.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*838C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 8815 | chr12 | 88496381 | |||||
chr12:88496584
|
G | T | 1 | a0001c0001t0018 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*635C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 8612 | chr12 | 88496584 | |||||
chr12:88496744
|
C | T | 20 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(17): Show | 114 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*475G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 8452 | chr12 | 88496744 | |||||
chr12:88496804
|
C | G | 6 | a0001c0001t0004a0001c0001t0009a0001c0001t0017others(3): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*415G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 8392 | chr12 | 88496804 | |||||
chr12:88496894
|
A | G | 11 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(8): Show | 87 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*325T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 8302 | chr12 | 88496894 | |||||
chr12:88496912
|
G | A | 1 | a0001c0001t0030 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*307C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 8284 | chr12 | 88496912 | |||||
chr12:88497126
|
A | T | 1 | a0001c0001t0017 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*93T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 8070 | chr12 | 88497126 | |||||
chr12:88580422
|
C | T | 1 | a0001c0001t0016 | 1 | HG03098.hp1 | 5_prime_UTR_variant | MODIFIER | c.-144G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/10 | 144 | chr12 | 88580422 | |||||
chr12:88580425
|
T | C | 1 | a0001c0001t0031 | 1 | HG01891.hp2 | 5_prime_UTR_variant | MODIFIER | c.-147A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/10 | 147 | chr12 | 88580425 | |||||
chr12:88580435
|
A | G | 1 | a0001c0001t0006 | 6 | NA18955.hp2 NA18973.hp2 NA18975.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-157T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/10 | 157 | chr12 | 88580435 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:88497297
|
G | A | 5 | a0001c0001t0002g0008a0001c0001t0002g0125a0001c0001t0002g0126others(2): Show | 6 | NA18944.hp2 NA18964.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.*38-116C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88497297 | ||||||
chr12:88497327
|
T | C | 1 | a0001c0001t0005g0147 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.*38-146A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88497327 | ||||||
chr12:88497396
|
A | G | 1 | a0001c0001t0002g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.*38-215T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88497396 | ||||||
chr12:88497451
|
G | T | 17 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(14): Show | 17 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.*38-270C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88497451 | ||||||
chr12:88497671
|
A | G | 1 | a0001c0001t0004g0044 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.*38-490T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88497671 | ||||||
chr12:88497676
|
C | T | 23 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(20): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.*38-495G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88497676 | ||||||
chr12:88497885
|
C | T | 2 | a0001c0001t0026g0040a0001c0001t0027g0148 | 2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.*38-704G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88497885 | ||||||
chr12:88497931
|
C | T | 1 | a0001c0001t0007g0201 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.*38-750G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88497931 | ||||||
chr12:88497940
|
A | G | 4 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0113others(1): Show | 4 | NA18974.hp1 NA18981.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.*38-759T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88497940 | ||||||
chr12:88497999
|
T | A | 23 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(20): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.*38-818A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88497999 | ||||||
chr12:88498543
|
A | G | 2 | a0001c0001t0026g0040a0001c0001t0027g0148 | 2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.*38-1362T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88498543 | ||||||
chr12:88498579
|
G | C | 2 | a0001c0001t0011g0039a0001c0001t0011g0128 | 2 | HG01192.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.*38-1398C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88498579 | ||||||
chr12:88498838
|
C | CA | 29 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0059others(26): Show | 32 | HG00741.hp2 NA18747.hp1 NA18943.hp1 others(29): Show |
intron_variant | MODIFIER | c.*38-1658dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88498838 | ||||||
chr12:88498855
|
C | A | 6 | a0001c0001t0002g0077a0001c0001t0002g0100a0001c0001t0002g0101others(3): Show | 6 | HG02071.hp1 HG02559.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.*38-1674G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88498855 | ||||||
chr12:88498903
|
G | C | 1 | a0001c0001t0013g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.*38-1722C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88498903 | ||||||
chr12:88498956
|
C | T | 1 | a0001c0001t0009g0042 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*38-1775G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88498956 | ||||||
chr12:88499344
|
C | T | 1 | a0001c0001t0001g0211 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.*38-2163G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88499344 | ||||||
chr12:88499359
|
T | C | 1 | a0001c0001t0012g0056 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.*38-2178A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88499359 | ||||||
chr12:88499482
|
G | A | 23 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(20): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.*38-2301C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88499482 | ||||||
chr12:88499684
|
G | A | 2 | a0001c0001t0005g0057a0001c0001t0005g0078 | 2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.*38-2503C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88499684 | ||||||
chr12:88500111
|
A | C | 2 | a0001c0001t0011g0039a0001c0001t0011g0128 | 2 | HG01192.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.*38-2930T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88500111 | ||||||
chr12:88500215
|
C | T | 3 | a0001c0001t0010g0007a0001c0001t0010g0116a0001c0001t0010g0123 | 4 | HG02486.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.*38-3034G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88500215 | ||||||
chr12:88500309
|
T | C | 2 | a0001c0001t0002g0035a0001c0001t0002g0072 | 2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.*38-3128A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88500309 | ||||||
chr12:88500391
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.*38-3210C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88500391 | ||||||
chr12:88500445
|
T | A | 1 | a0001c0001t0022g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.*38-3264A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88500445 | ||||||
chr12:88500718
|
A | G | 23 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(20): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.*38-3537T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88500718 | ||||||
chr12:88501000
|
G | A | 1 | a0001c0001t0005g0220 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.*38-3819C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88501000 | ||||||
chr12:88501107
|
G | T | 1 | a0001c0001t0002g0100 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.*38-3926C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88501107 | ||||||
chr12:88501316
|
C | T | 2 | a0001c0001t0008g0003a0001c0001t0008g0192 | 4 | HG00099.hp1 HG00738.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.*37+3843G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88501316 | ||||||
chr12:88501529
|
C | T | 3 | a0001c0001t0010g0007a0001c0001t0010g0116a0001c0001t0010g0123 | 4 | HG02486.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.*37+3630G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88501529 | ||||||
chr12:88501934
|
C | T | 1 | a0001c0002t0002g0041 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.*37+3225G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88501934 | ||||||
chr12:88502333
|
T | C | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.*37+2826A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88502333 | ||||||
chr12:88502344
|
C | A | 1 | a0001c0001t0002g0101 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.*37+2815G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88502344 | ||||||
chr12:88502716
|
T | C | 1 | a0001c0001t0011g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.*37+2443A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88502716 | ||||||
chr12:88502817
|
A | G | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.*37+2342T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88502817 | ||||||
chr12:88502907
|
G | GA | 202 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(199): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.*37+2251dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88502907 | ||||||
chr12:88503415
|
T | C | 6 | a0001c0001t0005g0057a0001c0001t0005g0078a0001c0001t0005g0120others(3): Show | 6 | HG02280.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.*37+1744A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88503415 | ||||||
chr12:88503446
|
A | G | 3 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0103 | 3 | HG02145.hp2 HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.*37+1713T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88503446 | ||||||
chr12:88503556
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.*37+1603T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88503556 | ||||||
chr12:88504448
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.*37+711G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88504448 | ||||||
chr12:88504449
|
G | A | 1 | a0001c0001t0002g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.*37+710C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88504449 | ||||||
chr12:88504470
|
C | A | 10 | a0001c0001t0005g0057a0001c0001t0005g0078a0001c0001t0005g0120others(7): Show | 10 | HG02280.hp2 HG02647.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.*37+689G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88504470 | ||||||
chr12:88504685
|
C | A | 1 | a0001c0001t0004g0048 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.*37+474G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88504685 | ||||||
chr12:88504863
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.*37+296G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88504863 | ||||||
chr12:88504864
|
G | T | 23 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(20): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.*37+295C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88504864 | ||||||
chr12:88504993
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.*37+166T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88504993 | ||||||
chr12:88506199
|
A | T | 1 | a0001c0001t0006g0018 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.782+112T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 8/9 | chr12 | 88506199 | ||||||
chr12:88506260
|
G | A | 1 | a0001c0001t0002g0126 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.782+51C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 8/9 | chr12 | 88506260 | ||||||
chr12:88506469
|
G | T | 23 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(20): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.715-91C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 7/9 | chr12 | 88506469 | ||||||
chr12:88506757
|
A | C | 1 | a0001c0001t0010g0123 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.714+271T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 7/9 | chr12 | 88506757 | ||||||
chr12:88507270
|
A | G | 1 | a0001c0001t0002g0101 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.605-133T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88507270 | ||||||
chr12:88507877
|
A | C | 1 | a0001c0001t0003g0076 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.605-740T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88507877 | ||||||
chr12:88507916
|
G | A | 1 | a0001c0001t0022g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.605-779C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88507916 | ||||||
chr12:88508025
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.605-888T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508025 | ||||||
chr12:88508223
|
A | G | 3 | a0001c0001t0007g0203a0001c0001t0007g0204a0001c0001t0007g0205 | 3 | HG02630.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.605-1086T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508223 | ||||||
chr12:88508264
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0189 | 2 | HG00639.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.605-1127C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508264 | ||||||
chr12:88508556
|
C | CGT | 61 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0166others(58): Show | 65 | HG00099.hp2 HG00323.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.605-1421_605-1420d others(4): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508556 | ||||||
chr12:88508556
|
C | CGTGT | 22 | a0001c0001t0002g0055a0001c0001t0002g0058a0001c0001t0002g0064others(19): Show | 22 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.605-1423_605-1420d others(6): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508556 | ||||||
chr12:88508556
|
C | CGTGTGT | 3 | a0001c0001t0002g0138a0001c0001t0002g0140a0001c0001t0002g0141 | 3 | HG01243.hp1 HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.605-1425_605-1420d others(8): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508556 | ||||||
chr12:88508556
|
CGT | C | 3 | a0001c0001t0001g0173a0001c0001t0001g0175a0001c0001t0014g0010 | 4 | HG01975.hp1 HG02451.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.605-1421_605-1420d others(4): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508556 | ||||||
chr12:88508595
|
G | C | 10 | a0001c0001t0005g0057a0001c0001t0005g0078a0001c0001t0005g0120others(7): Show | 10 | HG02280.hp2 HG02647.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.605-1458C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508595 | ||||||
chr12:88508632
|
C | T | 1 | a0001c0001t0026g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.605-1495G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508632 | ||||||
chr12:88508677
|
T | C | 1 | a0001c0001t0005g0078 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.605-1540A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508677 | ||||||
chr12:88508963
|
A | G | 1 | a0001c0001t0022g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.605-1826T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508963 | ||||||
chr12:88508984
|
T | A | 1 | a0001c0001t0004g0048 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.605-1847A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508984 | ||||||
chr12:88509202
|
A | G | 1 | a0001c0001t0003g0091 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.605-2065T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88509202 | ||||||
chr12:88509711
|
T | C | 2 | a0001c0001t0001g0169a0001c0001t0001g0191 | 2 | HG02083.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.605-2574A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88509711 | ||||||
chr12:88509825
|
T | C | 8 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0031others(5): Show | 8 | HG00639.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.605-2688A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88509825 | ||||||
chr12:88510154
|
C | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(204): Show | 224 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.605-3017G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88510154 | ||||||
chr12:88510512
|
A | G | 4 | a0001c0001t0009g0042a0001c0001t0009g0051a0001c0001t0009g0052others(1): Show | 4 | HG02622.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.605-3375T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88510512 | ||||||
chr12:88510779
|
T | C | 1 | a0001c0001t0002g0011 | 2 | HG00323.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.605-3642A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88510779 | ||||||
chr12:88510987
|
C | T | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.605-3850G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88510987 | ||||||
chr12:88511906
|
C | T | 1 | a0001c0001t0016g0019 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.604+3628G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88511906 | ||||||
chr12:88512071
|
T | A | 1 | a0001c0001t0001g0037 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.604+3463A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88512071 | ||||||
chr12:88512127
|
A | G | 2 | a0001c0001t0003g0006a0001c0001t0003g0122 | 3 | NA18975.hp2 NA19068.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.604+3407T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88512127 | ||||||
chr12:88512192
|
G | A | 1 | a0001c0001t0001g0014 | 2 | NA18961.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.604+3342C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88512192 | ||||||
chr12:88512982
|
C | T | 1 | a0001c0001t0002g0073 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.604+2552G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88512982 | ||||||
chr12:88513012
|
C | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.604+2522G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88513012 | ||||||
chr12:88513051
|
T | C | 1 | a0001c0001t0002g0138 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.604+2483A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88513051 | ||||||
chr12:88513525
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(215): Show | 237 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.604+2009A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88513525 | ||||||
chr12:88513628
|
A | G | 1 | a0001c0001t0026g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.604+1906T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88513628 | ||||||
chr12:88513786
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(74): Show | 88 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.604+1748T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88513786 | ||||||
chr12:88513987
|
A | C | 3 | a0001c0001t0002g0055a0001c0001t0012g0056a0001c0001t0012g0075 | 3 | HG02559.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.604+1547T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88513987 | ||||||
chr12:88514028
|
C | A | 1 | a0001c0001t0022g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.604+1506G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88514028 | ||||||
chr12:88514092
|
T | C | 1 | a0001c0001t0002g0138 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.604+1442A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88514092 | ||||||
chr12:88515008
|
A | C | 1 | a0001c0001t0001g0164 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.604+526T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88515008 | ||||||
chr12:88515072
|
T | C | 6 | a0001c0001t0002g0035a0001c0001t0002g0072a0001c0001t0002g0138others(3): Show | 6 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.604+462A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88515072 | ||||||
chr12:88515213
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.604+321G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88515213 | ||||||
chr12:88516530
|
C | T | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.364-40G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/9 | chr12 | 88516530 | ||||||
chr12:88516693
|
G | T | 1 | a0001c0001t0001g0179 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.364-203C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/9 | chr12 | 88516693 | ||||||
chr12:88516840
|
G | GA | 26 | a0001c0001t0001g0014a0001c0001t0003g0087a0001c0001t0003g0097others(23): Show | 27 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.364-351dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/9 | chr12 | 88516840 | ||||||
chr12:88516857
|
C | A | 1 | a0001c0001t0001g0211 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.364-367G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/9 | chr12 | 88516857 | ||||||
chr12:88517009
|
A | C | 1 | a0001c0001t0026g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.364-519T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/9 | chr12 | 88517009 | ||||||
chr12:88517043
|
AC | A | 23 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(20): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.364-554delG | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/9 | chr12 | 88517043 | ||||||
chr12:88517181
|
A | C | 1 | a0001c0001t0007g0201 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.364-691T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/9 | chr12 | 88517181 | ||||||
chr12:88517245
|
G | C | 23 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(20): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.364-755C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/9 | chr12 | 88517245 | ||||||
chr12:88517985
|
C | A | 1 | a0001c0001t0002g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.363+712G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/9 | chr12 | 88517985 | ||||||
chr12:88518681
|
A | T | 7 | a0001c0001t0003g0009a0001c0001t0003g0021a0001c0001t0003g0152others(4): Show | 9 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.363+16T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/9 | chr12 | 88518681 | ||||||
chr12:88519123
|
A | G | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.193-256T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88519123 | ||||||
chr12:88519409
|
C | G | 1 | a0001c0001t0001g0184 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.193-542G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88519409 | ||||||
chr12:88519640
|
A | G | 23 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(20): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-773T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88519640 | ||||||
chr12:88519714
|
C | G | 26 | a0001c0001t0002g0035a0001c0001t0002g0058a0001c0001t0002g0064others(23): Show | 26 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.193-847G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88519714 | ||||||
chr12:88519827
|
C | T | 23 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(20): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-960G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88519827 | ||||||
chr12:88519844
|
G | A | 1 | a0001c0001t0003g0098 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.193-977C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88519844 | ||||||
chr12:88519863
|
A | G | 1 | a0001c0001t0016g0019 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.193-996T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88519863 | ||||||
chr12:88519890
|
C | T | 3 | a0001c0001t0010g0007a0001c0001t0010g0116a0001c0001t0010g0123 | 4 | HG02486.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-1023G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88519890 | ||||||
chr12:88520296
|
G | T | 1 | a0001c0001t0001g0178 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.193-1429C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88520296 | ||||||
chr12:88520533
|
T | C | 1 | a0001c0001t0007g0036 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.193-1666A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88520533 | ||||||
chr12:88520670
|
G | T | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.193-1803C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88520670 | ||||||
chr12:88520809
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.193-1942A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88520809 | ||||||
chr12:88520972
|
G | A | 1 | a0001c0001t0005g0220 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.193-2105C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88520972 | ||||||
chr12:88521023
|
G | A | 5 | a0001c0001t0002g0008a0001c0001t0002g0125a0001c0001t0002g0126others(2): Show | 6 | NA18944.hp2 NA18964.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-2156C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88521023 | ||||||
chr12:88521381
|
G | T | 1 | a0001c0001t0001g0211 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.193-2514C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88521381 | ||||||
chr12:88521386
|
G | A | 65 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(62): Show | 76 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.193-2519C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88521386 | ||||||
chr12:88521466
|
C | T | 1 | a0001c0001t0011g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.193-2599G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88521466 | ||||||
chr12:88521467
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.193-2600C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88521467 | ||||||
chr12:88521686
|
T | C | 3 | a0001c0001t0002g0055a0001c0001t0012g0056a0001c0001t0012g0075 | 3 | HG02559.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.193-2819A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88521686 | ||||||
chr12:88521785
|
C | T | 3 | a0001c0001t0004g0142a0001c0001t0004g0143a0001c0001t0025g0144 | 3 | HG02809.hp1 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.193-2918G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88521785 | ||||||
chr12:88521810
|
C | A | 1 | a0001c0001t0002g0138 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.193-2943G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88521810 | ||||||
chr12:88522058
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(113): Show | 127 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.193-3191C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522058 | ||||||
chr12:88522269
|
C | T | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.193-3402G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522269 | ||||||
chr12:88522426
|
CT | C | 111 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0002g0029others(108): Show | 118 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.193-3560delA | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522426 | ||||||
chr12:88522426
|
CTT | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(89): Show | 102 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.193-3561_193-3560d others(4): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522426 | ||||||
chr12:88522455
|
C | T | 1 | a0001c0001t0003g0154 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.193-3588G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522455 | ||||||
chr12:88522473
|
G | T | 1 | a0001c0001t0022g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.193-3606C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522473 | ||||||
chr12:88522531
|
G | C | 27 | a0001c0001t0002g0035a0001c0001t0002g0058a0001c0001t0002g0064others(24): Show | 28 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.193-3664C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522531 | ||||||
chr12:88522569
|
G | A | 1 | a0001c0001t0002g0069 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.193-3702C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522569 | ||||||
chr12:88522577
|
G | A | 1 | a0001c0001t0022g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.193-3710C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522577 | ||||||
chr12:88522734
|
C | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0202 | 2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.193-3867G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522734 | ||||||
chr12:88522838
|
A | G | 2 | a0001c0001t0013g0070a0001c0001t0013g0114 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.193-3971T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522838 | ||||||
chr12:88522907
|
T | A | 1 | a0001c0001t0002g0077 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.193-4040A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522907 | ||||||
chr12:88523770
|
C | T | 1 | a0001c0001t0027g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.193-4903G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88523770 | ||||||
chr12:88523807
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.193-4940A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88523807 | ||||||
chr12:88523903
|
T | C | 3 | a0001c0001t0002g0055a0001c0001t0012g0056a0001c0001t0012g0075 | 3 | HG02559.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.193-5036A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88523903 | ||||||
chr12:88524191
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.193-5324A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88524191 | ||||||
chr12:88524426
|
G | A | 2 | a0001c0001t0002g0134a0001c0001t0002g0137 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.193-5559C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88524426 | ||||||
chr12:88524628
|
A | T | 1 | a0001c0001t0003g0062 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.193-5761T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88524628 | ||||||
chr12:88524663
|
G | C | 23 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(20): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-5796C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88524663 | ||||||
chr12:88524806
|
T | C | 23 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(20): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-5939A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88524806 | ||||||
chr12:88524850
|
C | T | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.193-5983G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88524850 | ||||||
chr12:88524956
|
C | T | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.193-6089G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88524956 | ||||||
chr12:88524966
|
T | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.193-6099A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88524966 | ||||||
chr12:88525042
|
T | C | 1 | a0001c0001t0022g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.193-6175A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88525042 | ||||||
chr12:88525072
|
A | G | 23 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(20): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-6205T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88525072 | ||||||
chr12:88525128
|
C | T | 3 | a0001c0001t0010g0007a0001c0001t0010g0116a0001c0001t0010g0123 | 4 | HG02486.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-6261G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88525128 | ||||||
chr12:88525255
|
G | A | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.193-6388C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88525255 | ||||||
chr12:88525277
|
T | C | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.193-6410A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88525277 | ||||||
chr12:88525542
|
A | G | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.193-6675T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88525542 | ||||||
chr12:88525572
|
GTTA | G | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.193-6708_193-6706d others(5): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88525572 | ||||||
chr12:88525678
|
C | A | 1 | a0001c0001t0001g0014 | 2 | NA18961.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.192+6763G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88525678 | ||||||
chr12:88525706
|
T | C | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+6735A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88525706 | ||||||
chr12:88525819
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.192+6622G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88525819 | ||||||
chr12:88526159
|
G | T | 2 | a0001c0001t0011g0039a0001c0001t0011g0128 | 2 | HG01192.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.192+6282C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526159 | ||||||
chr12:88526242
|
A | G | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+6199T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526242 | ||||||
chr12:88526446
|
T | C | 2 | a0001c0001t0026g0040a0001c0001t0027g0148 | 2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+5995A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526446 | ||||||
chr12:88526659
|
A | C | 1 | a0001c0001t0001g0197 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.192+5782T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526659 | ||||||
chr12:88526863
|
C | CT | 10 | a0001c0001t0002g0055a0001c0001t0002g0067a0001c0001t0002g0103others(7): Show | 10 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.192+5577dupA | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526863 | ||||||
chr12:88526863
|
CT | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(79): Show | 93 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.192+5577delA | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526863 | ||||||
chr12:88526863
|
CTTTTT | C | 23 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(20): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+5573_192+5577d others(7): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526863 | ||||||
chr12:88526914
|
C | G | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+5527G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526914 | ||||||
chr12:88526982
|
T | C | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+5459A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526982 | ||||||
chr12:88526995
|
A | G | 1 | a0001c0002t0002g0150 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.192+5446T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526995 | ||||||
chr12:88526998
|
AGCTGGGA others(12): Show |
A | 1 | a0001c0001t0002g0138 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.192+5424_192+5442d others(21): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526998 | ||||||
chr12:88527087
|
C | A | 23 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(20): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+5354G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527087 | ||||||
chr12:88527105
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.192+5336A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527105 | ||||||
chr12:88527177
|
C | T | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+5264G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527177 | ||||||
chr12:88527184
|
G | T | 1 | a0001c0001t0001g0037 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.192+5257C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527184 | ||||||
chr12:88527340
|
C | G | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+5101G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527340 | ||||||
chr12:88527439
|
A | G | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+5002T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527439 | ||||||
chr12:88527452
|
G | A | 1 | a0001c0001t0030g0124 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.192+4989C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527452 | ||||||
chr12:88527540
|
C | T | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+4901G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527540 | ||||||
chr12:88527609
|
G | T | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+4832C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527609 | ||||||
chr12:88527617
|
G | A | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+4824C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527617 | ||||||
chr12:88527640
|
T | C | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+4801A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527640 | ||||||
chr12:88527783
|
A | G | 2 | a0001c0001t0026g0040a0001c0001t0027g0148 | 2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+4658T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527783 | ||||||
chr12:88528184
|
C | T | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+4257G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88528184 | ||||||
chr12:88528314
|
T | A | 1 | a0001c0001t0003g0062 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.192+4127A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88528314 | ||||||
chr12:88528829
|
T | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0194a0001c0001t0001g0198 | 3 | HG00597.hp1 NA18944.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.192+3612A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88528829 | ||||||
chr12:88528837
|
T | A | 4 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(1): Show | 4 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+3604A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88528837 | ||||||
chr12:88528878
|
G | A | 1 | a0001c0001t0003g0093 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.192+3563C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88528878 | ||||||
chr12:88528947
|
T | C | 1 | a0001c0001t0012g0075 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.192+3494A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88528947 | ||||||
chr12:88529012
|
T | C | 3 | a0001c0001t0007g0203a0001c0001t0007g0204a0001c0001t0007g0205 | 3 | HG02630.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.192+3429A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88529012 | ||||||
chr12:88529089
|
C | T | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+3352G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88529089 | ||||||
chr12:88529160
|
A | T | 1 | a0001c0001t0003g0085 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.192+3281T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88529160 | ||||||
chr12:88529197
|
A | T | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+3244T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88529197 | ||||||
chr12:88529446
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.192+2995C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88529446 | ||||||
chr12:88529860
|
T | C | 1 | a0001c0001t0022g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.192+2581A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88529860 | ||||||
chr12:88529934
|
A | C | 1 | a0001c0001t0007g0201 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.192+2507T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88529934 | ||||||
chr12:88530243
|
A | T | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+2198T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88530243 | ||||||
chr12:88530290
|
C | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(114): Show | 128 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.192+2151G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88530290 | ||||||
chr12:88530351
|
C | A | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+2090G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88530351 | ||||||
chr12:88530538
|
A | G | 2 | a0001c0001t0011g0039a0001c0001t0011g0128 | 2 | HG01192.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.192+1903T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88530538 | ||||||
chr12:88530559
|
G | GT | 3 | a0001c0001t0002g0077a0001c0001t0002g0100a0001c0001t0002g0101 | 3 | HG02071.hp1 HG02683.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.192+1881dupA | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88530559 | ||||||
chr12:88530676
|
C | T | 3 | a0001c0001t0002g0058a0001c0001t0002g0066a0001c0001t0002g0109 | 3 | HG00423.hp1 HG00597.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.192+1765G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88530676 | ||||||
chr12:88530714
|
A | G | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+1727T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88530714 | ||||||
chr12:88530887
|
C | A | 1 | a0001c0001t0001g0180 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.192+1554G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88530887 | ||||||
chr12:88530975
|
T | A | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+1466A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88530975 | ||||||
chr12:88531013
|
T | C | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+1428A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88531013 | ||||||
chr12:88531295
|
A | C | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+1146T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88531295 | ||||||
chr12:88531377
|
A | T | 1 | a0001c0001t0001g0167 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.192+1064T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88531377 | ||||||
chr12:88531436
|
T | C | 23 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(20): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+1005A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88531436 | ||||||
chr12:88531600
|
CTTG | C | 4 | a0001c0001t0003g0009a0001c0001t0003g0154a0001c0001t0003g0155others(1): Show | 5 | HG02615.hp2 HG02630.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+838_192+840del others(3): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88531600 | ||||||
chr12:88531660
|
T | C | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+781A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88531660 | ||||||
chr12:88531718
|
CT | C | 23 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(20): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+722delA | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88531718 | ||||||
chr12:88531819
|
C | T | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+622G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88531819 | ||||||
chr12:88531895
|
C | T | 4 | a0001c0001t0005g0145a0001c0001t0005g0147a0001c0001t0005g0156others(1): Show | 4 | HG03130.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+546G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88531895 | ||||||
chr12:88531906
|
G | A | 2 | a0001c0001t0015g0218a0001c0001t0015g0219 | 2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.192+535C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88531906 | ||||||
chr12:88532102
|
T | C | 3 | a0001c0001t0002g0055a0001c0001t0012g0056a0001c0001t0012g0075 | 3 | HG02559.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.192+339A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88532102 | ||||||
chr12:88532174
|
G | T | 1 | a0001c0001t0001g0186 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.192+267C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88532174 | ||||||
chr12:88532196
|
T | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(114): Show | 128 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.192+245A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88532196 | ||||||
chr12:88532213
|
A | C | 2 | a0001c0001t0003g0089a0001c0001t0003g0149 | 2 | NA18969.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.192+228T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88532213 | ||||||
chr12:88532295
|
C | T | 24 | a0001c0001t0002g0073a0001c0001t0004g0043a0001c0001t0004g0044others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+146G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88532295 | ||||||
chr12:88532513
|
C | CA | 25 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(22): Show | 25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-11dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88532513 | ||||||
chr12:88532663
|
C | A | 2 | a0001c0001t0026g0040a0001c0001t0027g0148 | 2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.130-160G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88532663 | ||||||
chr12:88532688
|
A | T | 3 | a0001c0001t0004g0213a0001c0001t0004g0214a0001c0001t0004g0217 | 3 | NA18949.hp2 NA19058.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.130-185T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88532688 | ||||||
chr12:88532828
|
T | C | 1 | a0001c0001t0031g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.130-325A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88532828 | ||||||
chr12:88532945
|
T | A | 6 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(3): Show | 6 | HG06807.hp1 NA18949.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-442A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88532945 | ||||||
chr12:88533010
|
C | T | 25 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(22): Show | 25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-507G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533010 | ||||||
chr12:88533052
|
C | T | 2 | a0001c0001t0011g0039a0001c0001t0011g0128 | 2 | HG01192.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.130-549G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533052 | ||||||
chr12:88533070
|
AC | A | 6 | a0001c0001t0002g0117a0001c0001t0010g0007a0001c0001t0010g0116others(3): Show | 7 | HG02486.hp2 HG02970.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.130-568delG | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533070 | ||||||
chr12:88533224
|
T | G | 1 | a0001c0001t0001g0209 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.130-721A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533224 | ||||||
chr12:88533258
|
G | C | 2 | a0001c0001t0021g0208a0001c0001t0022g0028 | 2 | HG02083.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.130-755C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533258 | ||||||
chr12:88533469
|
G | A | 2 | a0001c0001t0011g0039a0001c0001t0011g0128 | 2 | HG01192.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.130-966C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533469 | ||||||
chr12:88533538
|
T | C | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.130-1035A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533538 | ||||||
chr12:88533579
|
C | T | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.130-1076G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533579 | ||||||
chr12:88533592
|
T | C | 3 | a0001c0001t0004g0142a0001c0001t0004g0143a0001c0001t0025g0144 | 3 | HG02809.hp1 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.130-1089A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533592 | ||||||
chr12:88533635
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.130-1132A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533635 | ||||||
chr12:88533733
|
C | T | 1 | a0001c0001t0015g0218 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.130-1230G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533733 | ||||||
chr12:88533926
|
G | T | 1 | a0001c0001t0026g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130-1423C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533926 | ||||||
chr12:88534071
|
G | T | 1 | a0001c0001t0001g0160 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.130-1568C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88534071 | ||||||
chr12:88534232
|
G | A | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.130-1729C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88534232 | ||||||
chr12:88534342
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.130-1839G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88534342 | ||||||
chr12:88534605
|
G | A | 2 | a0001c0001t0021g0208a0001c0001t0022g0028 | 2 | HG02083.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.130-2102C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88534605 | ||||||
chr12:88534736
|
G | A | 1 | a0001c0001t0001g0163 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.130-2233C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88534736 | ||||||
chr12:88534976
|
T | C | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.130-2473A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88534976 | ||||||
chr12:88534984
|
C | T | 2 | a0001c0001t0021g0208a0001c0001t0022g0028 | 2 | HG02083.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.130-2481G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88534984 | ||||||
chr12:88535009
|
G | A | 1 | a0001c0001t0002g0035 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.130-2506C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88535009 | ||||||
chr12:88535079
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.130-2576G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88535079 | ||||||
chr12:88535249
|
T | C | 25 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(22): Show | 25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-2746A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88535249 | ||||||
chr12:88535489
|
C | T | 4 | a0001c0001t0002g0029a0001c0001t0002g0033a0001c0001t0002g0118others(1): Show | 4 | HG00639.hp2 HG02055.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-2986G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88535489 | ||||||
chr12:88535490
|
G | A | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.130-2987C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88535490 | ||||||
chr12:88535571
|
A | C | 25 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(22): Show | 25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-3068T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88535571 | ||||||
chr12:88535847
|
T | C | 8 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0031others(5): Show | 8 | HG00639.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-3344A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88535847 | ||||||
chr12:88535971
|
C | A | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.130-3468G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88535971 | ||||||
chr12:88536157
|
C | T | 1 | a0001c0001t0022g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.130-3654G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88536157 | ||||||
chr12:88536301
|
T | C | 25 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(22): Show | 25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-3798A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88536301 | ||||||
chr12:88536427
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0001g0182 | 2 | HG02155.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.130-3924G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88536427 | ||||||
chr12:88536838
|
T | C | 3 | a0001c0001t0004g0142a0001c0001t0004g0143a0001c0001t0025g0144 | 3 | HG02809.hp1 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.130-4335A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88536838 | ||||||
chr12:88536846
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.130-4343G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88536846 | ||||||
chr12:88536851
|
C | T | 1 | a0001c0001t0005g0220 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.130-4348G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88536851 | ||||||
chr12:88536949
|
T | C | 25 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(22): Show | 25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-4446A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88536949 | ||||||
chr12:88536961
|
A | G | 1 | a0001c0001t0007g0200 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.130-4458T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88536961 | ||||||
chr12:88537020
|
C | T | 1 | a0001c0001t0002g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130-4517G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88537020 | ||||||
chr12:88537198
|
G | A | 1 | a0001c0001t0004g0215 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.130-4695C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88537198 | ||||||
chr12:88537218
|
C | T | 4 | a0001c0001t0007g0200a0001c0001t0007g0203a0001c0001t0007g0204others(1): Show | 4 | HG02630.hp1 HG02896.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-4715G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88537218 | ||||||
chr12:88537229
|
C | T | 1 | a0001c0001t0011g0128 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.130-4726G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88537229 | ||||||
chr12:88537303
|
A | C | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.130-4800T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88537303 | ||||||
chr12:88537421
|
A | T | 1 | a0001c0001t0022g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.130-4918T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88537421 | ||||||
chr12:88537654
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.130-5151T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88537654 | ||||||
chr12:88537655
|
C | A | 4 | a0001c0001t0001g0165a0001c0001t0001g0171a0001c0001t0001g0172others(1): Show | 4 | HG00408.hp1 HG02071.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-5152G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88537655 | ||||||
chr12:88537675
|
G | GA | 7 | a0001c0001t0002g0033a0001c0001t0002g0077a0001c0001t0002g0100others(4): Show | 7 | HG02071.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.130-5173dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88537675 | ||||||
chr12:88537755
|
T | C | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.130-5252A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88537755 | ||||||
chr12:88538105
|
T | G | 25 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(22): Show | 25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-5602A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88538105 | ||||||
chr12:88538258
|
C | A | 25 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(22): Show | 25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-5755G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88538258 | ||||||
chr12:88538469
|
C | T | 25 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(22): Show | 25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-5966G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88538469 | ||||||
chr12:88538587
|
T | C | 25 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(22): Show | 25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-6084A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88538587 | ||||||
chr12:88538606
|
T | C | 1 | a0001c0001t0022g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.130-6103A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88538606 | ||||||
chr12:88538762
|
T | C | 1 | a0001c0001t0002g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.130-6259A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88538762 | ||||||
chr12:88538895
|
T | A | 1 | a0001c0001t0002g0131 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.130-6392A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88538895 | ||||||
chr12:88538947
|
T | C | 25 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(22): Show | 25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-6444A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88538947 | ||||||
chr12:88539027
|
C | G | 24 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(21): Show | 24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.130-6524G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88539027 | ||||||
chr12:88539227
|
G | A | 2 | a0001c0001t0015g0218a0001c0001t0015g0219 | 2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.129+6525C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88539227 | ||||||
chr12:88539564
|
G | A | 23 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(20): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.129+6188C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88539564 | ||||||
chr12:88539602
|
T | C | 1 | a0001c0001t0001g0181 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.129+6150A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88539602 | ||||||
chr12:88539692
|
T | C | 25 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(22): Show | 25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.129+6060A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88539692 | ||||||
chr12:88539774
|
A | T | 1 | a0001c0001t0002g0069 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.129+5978T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88539774 | ||||||
chr12:88539866
|
A | G | 1 | a0001c0001t0002g0138 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.129+5886T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88539866 | ||||||
chr12:88539873
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.129+5879G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88539873 | ||||||
chr12:88539936
|
T | C | 1 | a0001c0001t0007g0201 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.129+5816A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88539936 | ||||||
chr12:88539967
|
G | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(117): Show | 131 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.129+5785C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88539967 | ||||||
chr12:88540099
|
C | T | 1 | a0001c0001t0002g0069 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.129+5653G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88540099 | ||||||
chr12:88540252
|
A | T | 1 | a0001c0001t0002g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.129+5500T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88540252 | ||||||
chr12:88540334
|
A | G | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.129+5418T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88540334 | ||||||
chr12:88540430
|
T | A | 1 | a0001c0001t0022g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.129+5322A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88540430 | ||||||
chr12:88540594
|
G | A | 1 | a0001c0001t0002g0073 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.129+5158C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88540594 | ||||||
chr12:88540936
|
C | T | 3 | a0001c0001t0002g0026a0001c0001t0002g0027a0001c0001t0002g0103 | 3 | HG02145.hp2 HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.129+4816G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88540936 | ||||||
chr12:88541112
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.129+4640T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88541112 | ||||||
chr12:88541274
|
C | T | 1 | a0001c0001t0003g0084 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.129+4478G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88541274 | ||||||
chr12:88541359
|
T | A | 1 | a0001c0001t0001g0191 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.129+4393A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88541359 | ||||||
chr12:88541460
|
A | G | 35 | a0001c0001t0002g0159a0001c0001t0003g0002a0001c0001t0003g0006others(32): Show | 38 | HG00741.hp2 HG04184.hp2 NA18747.hp1 others(35): Show |
intron_variant | MODIFIER | c.129+4292T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88541460 | ||||||
chr12:88541794
|
T | C | 3 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0175 | 3 | HG01243.hp2 HG01975.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.129+3958A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88541794 | ||||||
chr12:88541815
|
T | G | 1 | a0001c0001t0002g0101 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.129+3937A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88541815 | ||||||
chr12:88541816
|
T | TA | 29 | a0001c0001t0002g0138a0001c0001t0002g0140a0001c0001t0002g0141others(26): Show | 29 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.129+3935dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88541816 | ||||||
chr12:88541817
|
A | T | 1 | a0001c0001t0027g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.129+3935T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88541817 | ||||||
chr12:88541852
|
G | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(111): Show | 125 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.129+3900C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88541852 | ||||||
chr12:88541866
|
G | A | 2 | a0001c0001t0002g0134a0001c0001t0002g0137 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.129+3886C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88541866 | ||||||
chr12:88542035
|
A | G | 2 | a0001c0001t0002g0068a0001c0001t0002g0074 | 2 | HG00438.hp2 HG00544.hp1 |
intron_variant | MODIFIER | c.129+3717T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88542035 | ||||||
chr12:88542300
|
C | A | 23 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(20): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.129+3452G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88542300 | ||||||
chr12:88542766
|
T | A | 1 | a0001c0001t0001g0191 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.129+2986A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88542766 | ||||||
chr12:88542871
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(214): Show | 236 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.129+2881C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88542871 | ||||||
chr12:88543160
|
G | C | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.129+2592C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88543160 | ||||||
chr12:88543927
|
T | G | 3 | a0001c0001t0001g0025a0001c0001t0001g0176a0001c0001t0019g0024 | 3 | HG01099.hp1 HG02300.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.129+1825A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88543927 | ||||||
chr12:88543947
|
C | T | 3 | a0001c0001t0021g0208a0001c0001t0026g0040a0001c0001t0027g0148 | 3 | HG02083.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.129+1805G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88543947 | ||||||
chr12:88544017
|
G | A | 3 | a0001c0001t0021g0208a0001c0001t0026g0040a0001c0001t0027g0148 | 3 | HG02083.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.129+1735C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544017 | ||||||
chr12:88544053
|
C | T | 7 | a0001c0001t0003g0009a0001c0001t0003g0021a0001c0001t0003g0152others(4): Show | 9 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.129+1699G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544053 | ||||||
chr12:88544200
|
G | A | 3 | a0001c0001t0021g0208a0001c0001t0026g0040a0001c0001t0027g0148 | 3 | HG02083.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.129+1552C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544200 | ||||||
chr12:88544487
|
A | C | 1 | a0001c0001t0001g0162 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.129+1265T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544487 | ||||||
chr12:88544511
|
T | TA | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.129+1240dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544511 | ||||||
chr12:88544512
|
A | T | 1 | a0001c0001t0004g0212 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.129+1240T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544512 | ||||||
chr12:88544517
|
A | C | 1 | a0001c0001t0027g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.129+1235T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544517 | ||||||
chr12:88544527
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0198 | 2 | NA18944.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.129+1225G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544527 | ||||||
chr12:88544741
|
A | G | 6 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(3): Show | 6 | HG06807.hp1 NA18949.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+1011T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544741 | ||||||
chr12:88544785
|
A | G | 63 | a0001c0001t0002g0035a0001c0001t0002g0058a0001c0001t0002g0064others(60): Show | 66 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.129+967T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544785 | ||||||
chr12:88544883
|
A | C | 2 | a0001c0001t0015g0218a0001c0001t0015g0219 | 2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.129+869T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544883 | ||||||
chr12:88545100
|
A | T | 26 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(23): Show | 26 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.129+652T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88545100 | ||||||
chr12:88545242
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.129+510C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88545242 | ||||||
chr12:88545266
|
C | G | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.129+486G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88545266 | ||||||
chr12:88545298
|
C | T | 23 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(20): Show | 23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.129+454G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88545298 | ||||||
chr12:88545356
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(117): Show | 131 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.129+396T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88545356 | ||||||
chr12:88545570
|
A | G | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.129+182T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88545570 | ||||||
chr12:88545714
|
T | C | 3 | a0001c0001t0002g0055a0001c0001t0012g0056a0001c0001t0012g0075 | 3 | HG02559.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.129+38A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88545714 | ||||||
chr12:88545934
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.16-69A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88545934 | ||||||
chr12:88545984
|
A | T | 1 | a0001c0001t0002g0115 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.16-119T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88545984 | ||||||
chr12:88546002
|
C | T | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-137G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546002 | ||||||
chr12:88546013
|
T | C | 3 | a0001c0001t0002g0058a0001c0001t0002g0066a0001c0001t0002g0109 | 3 | HG00423.hp1 HG00597.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.16-148A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546013 | ||||||
chr12:88546152
|
T | A | 1 | a0001c0001t0001g0164 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.16-287A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546152 | ||||||
chr12:88546380
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0189 | 2 | HG00639.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.16-515C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546380 | ||||||
chr12:88546496
|
T | G | 1 | a0001c0001t0022g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.16-631A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546496 | ||||||
chr12:88546551
|
T | C | 2 | a0001c0001t0026g0040a0001c0001t0027g0148 | 2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.16-686A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546551 | ||||||
chr12:88546574
|
T | A | 1 | a0001c0001t0001g0079 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.16-709A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546574 | ||||||
chr12:88546729
|
T | A | 1 | a0001c0001t0003g0129 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.16-864A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546729 | ||||||
chr12:88546735
|
T | C | 2 | a0001c0001t0026g0040a0001c0001t0027g0148 | 2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.16-870A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546735 | ||||||
chr12:88546928
|
C | A | 3 | a0001c0001t0007g0203a0001c0001t0007g0204a0001c0001t0007g0205 | 3 | HG02630.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.16-1063G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546928 | ||||||
chr12:88546944
|
A | G | 1 | a0001c0001t0011g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.16-1079T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546944 | ||||||
chr12:88547234
|
T | C | 17 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(14): Show | 17 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.16-1369A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88547234 | ||||||
chr12:88547365
|
C | A | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-1500G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88547365 | ||||||
chr12:88547437
|
C | T | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-1572G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88547437 | ||||||
chr12:88547781
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.16-1916G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88547781 | ||||||
chr12:88547827
|
G | A | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-1962C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88547827 | ||||||
chr12:88547846
|
A | C | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-1981T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88547846 | ||||||
chr12:88547873
|
C | T | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-2008G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88547873 | ||||||
chr12:88548026
|
T | C | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-2161A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88548026 | ||||||
chr12:88548182
|
G | A | 1 | a0001c0001t0001g0038 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.16-2317C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88548182 | ||||||
chr12:88548379
|
G | A | 74 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(71): Show | 85 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.16-2514C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88548379 | ||||||
chr12:88548385
|
C | T | 1 | a0001c0001t0016g0019 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.16-2520G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88548385 | ||||||
chr12:88548411
|
G | A | 10 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(7): Show | 10 | HG02965.hp2 HG03209.hp1 HG06807.hp1 others(7): Show |
intron_variant | MODIFIER | c.16-2546C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88548411 | ||||||
chr12:88548454
|
CAA | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(74): Show | 88 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.16-2591_16-2590del others(2): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88548454 | ||||||
chr12:88548577
|
G | A | 4 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0113others(1): Show | 4 | NA18974.hp1 NA18981.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-2712C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88548577 | ||||||
chr12:88548605
|
T | C | 2 | a0001c0001t0001g0190a0001c0001t0020g0195 | 2 | NA18982.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.16-2740A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88548605 | ||||||
chr12:88548964
|
A | T | 22 | a0001c0001t0002g0035a0001c0001t0002g0058a0001c0001t0002g0064others(19): Show | 22 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.16-3099T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88548964 | ||||||
chr12:88549076
|
G | A | 7 | a0001c0001t0003g0009a0001c0001t0003g0021a0001c0001t0003g0152others(4): Show | 9 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.16-3211C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549076 | ||||||
chr12:88549203
|
G | A | 28 | a0001c0001t0003g0002a0001c0001t0003g0006a0001c0001t0003g0059others(25): Show | 31 | HG00741.hp2 NA18747.hp1 NA18943.hp1 others(28): Show |
intron_variant | MODIFIER | c.16-3338C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549203 | ||||||
chr12:88549226
|
C | T | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-3361G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549226 | ||||||
chr12:88549372
|
A | C | 10 | a0001c0001t0002g0008a0001c0001t0002g0011a0001c0001t0002g0026others(7): Show | 12 | HG00323.hp1 HG00738.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.16-3507T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549372 | ||||||
chr12:88549546
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(74): Show | 88 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.16-3681C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549546 | ||||||
chr12:88549758
|
C | A | 2 | a0001c0001t0011g0039a0001c0001t0011g0128 | 2 | HG01192.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.16-3893G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549758 | ||||||
chr12:88549777
|
A | G | 1 | a0001c0001t0004g0212 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.16-3912T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549777 | ||||||
chr12:88549819
|
C | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(74): Show | 88 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.16-3954G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549819 | ||||||
chr12:88549820
|
G | T | 5 | a0001c0001t0003g0084a0001c0001t0003g0085a0001c0001t0003g0086others(2): Show | 5 | NA18951.hp1 NA18953.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-3955C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549820 | ||||||
chr12:88549982
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(74): Show | 88 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.16-4117C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549982 | ||||||
chr12:88549990
|
T | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(74): Show | 88 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.16-4125A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549990 | ||||||
chr12:88550016
|
T | C | 17 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(14): Show | 17 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.16-4151A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88550016 | ||||||
chr12:88550022
|
C | T | 10 | a0001c0001t0002g0008a0001c0001t0002g0011a0001c0001t0002g0026others(7): Show | 12 | HG00323.hp1 HG00738.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.16-4157G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88550022 | ||||||
chr12:88550113
|
T | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(74): Show | 88 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.16-4248A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88550113 | ||||||
chr12:88550232
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(74): Show | 88 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.16-4367T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88550232 | ||||||
chr12:88550426
|
TAGG | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(74): Show | 88 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.16-4564_16-4562del others(3): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88550426 | ||||||
chr12:88550445
|
A | G | 1 | a0001c0001t0002g0136 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.16-4580T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88550445 | ||||||
chr12:88550741
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(74): Show | 88 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.16-4876C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88550741 | ||||||
chr12:88550986
|
T | A | 4 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0113others(1): Show | 4 | NA18974.hp1 NA18981.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-5121A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88550986 | ||||||
chr12:88551359
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(74): Show | 88 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.16-5494G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88551359 | ||||||
chr12:88551691
|
C | G | 4 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(1): Show | 4 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-5826G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88551691 | ||||||
chr12:88551709
|
A | G | 1 | a0001c0002t0002g0063 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.16-5844T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88551709 | ||||||
chr12:88551742
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.16-5877C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88551742 | ||||||
chr12:88551948
|
T | C | 2 | a0001c0001t0003g0096a0001c0001t0003g0102 | 2 | NA18967.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.16-6083A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88551948 | ||||||
chr12:88552002
|
G | C | 1 | a0001c0001t0003g0154 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.16-6137C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552002 | ||||||
chr12:88552176
|
A | AT | 19 | a0001c0001t0001g0178a0001c0001t0001g0185a0001c0001t0001g0210others(16): Show | 19 | HG01192.hp2 HG01243.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.16-6312dupA | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552176 | ||||||
chr12:88552176
|
AT | A | 9 | a0001c0001t0001g0160a0001c0001t0002g0055a0001c0001t0002g0132others(6): Show | 9 | HG02280.hp1 HG02809.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-6312delA | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552176 | ||||||
chr12:88552350
|
C | CT | 5 | a0001c0001t0003g0009a0001c0001t0003g0152a0001c0001t0003g0154others(2): Show | 6 | HG02615.hp2 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.16-6486dupA | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552350 | ||||||
chr12:88552350
|
CT | C | 7 | a0001c0001t0002g0117a0001c0001t0010g0007a0001c0001t0010g0116others(4): Show | 8 | HG02083.hp1 HG02486.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.16-6486delA | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552350 | ||||||
chr12:88552416
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.16-6551G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552416 | ||||||
chr12:88552549
|
T | C | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-6684A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552549 | ||||||
chr12:88552560
|
T | C | 2 | a0001c0001t0003g0098a0001c0001t0003g0099 | 2 | NA18984.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.16-6695A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552560 | ||||||
chr12:88552592
|
T | C | 6 | a0001c0001t0005g0057a0001c0001t0005g0078a0001c0001t0005g0120others(3): Show | 6 | HG02280.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-6727A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552592 | ||||||
chr12:88552685
|
T | C | 22 | a0001c0001t0002g0035a0001c0001t0002g0058a0001c0001t0002g0064others(19): Show | 22 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.16-6820A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552685 | ||||||
chr12:88552763
|
A | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(74): Show | 88 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.16-6898T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552763 | ||||||
chr12:88552881
|
C | A | 1 | a0001c0001t0002g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.16-7016G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552881 | ||||||
chr12:88553000
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(74): Show | 88 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.16-7135C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88553000 | ||||||
chr12:88553010
|
C | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(204): Show | 224 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.16-7145G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88553010 | ||||||
chr12:88553094
|
A | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(90): Show | 104 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.16-7229T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88553094 | ||||||
chr12:88553346
|
A | G | 10 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(7): Show | 10 | HG02965.hp2 HG03209.hp1 HG06807.hp1 others(7): Show |
intron_variant | MODIFIER | c.16-7481T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88553346 | ||||||
chr12:88553620
|
C | T | 200 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(197): Show | 217 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.16-7755G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88553620 | ||||||
chr12:88553659
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(74): Show | 88 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.16-7794T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88553659 | ||||||
chr12:88553792
|
T | G | 2 | a0001c0001t0011g0039a0001c0001t0011g0128 | 2 | HG01192.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.16-7927A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88553792 | ||||||
chr12:88553821
|
T | C | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-7956A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88553821 | ||||||
chr12:88553970
|
T | C | 2 | a0001c0001t0002g0029a0001c0001t0002g0033 | 2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.16-8105A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88553970 | ||||||
chr12:88554201
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(197): Show | 217 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.16-8336A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88554201 | ||||||
chr12:88554348
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.16-8483A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88554348 | ||||||
chr12:88554355
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.16-8490G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88554355 | ||||||
chr12:88554874
|
G | C | 1 | a0001c0001t0002g0026 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.16-9009C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88554874 | ||||||
chr12:88554926
|
T | C | 16 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(13): Show | 16 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.16-9061A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88554926 | ||||||
chr12:88554990
|
T | C | 1 | a0001c0001t0003g0076 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.16-9125A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88554990 | ||||||
chr12:88555084
|
A | C | 1 | a0001c0001t0002g0115 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.16-9219T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88555084 | ||||||
chr12:88555095
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(72): Show | 86 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.16-9230C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88555095 | ||||||
chr12:88555149
|
C | T | 2 | a0001c0001t0026g0040a0001c0002t0002g0041 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.16-9284G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88555149 | ||||||
chr12:88555347
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(72): Show | 86 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.16-9482C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88555347 | ||||||
chr12:88555738
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(72): Show | 86 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.16-9873C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88555738 | ||||||
chr12:88555767
|
G | A | 4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 4 | HG01517.hp1 HG02683.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-9902C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88555767 | ||||||
chr12:88555849
|
A | T | 1 | a0001c0001t0011g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.16-9984T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88555849 | ||||||
chr12:88555997
|
G | T | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-10132C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88555997 | ||||||
chr12:88556218
|
C | CA | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(84): Show | 98 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.16-10354dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88556218 | ||||||
chr12:88556218
|
CA | C | 11 | a0001c0001t0002g0067a0001c0001t0005g0057a0001c0001t0005g0078others(8): Show | 11 | HG02280.hp2 HG02647.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.16-10354delT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88556218 | ||||||
chr12:88556250
|
T | C | 16 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(13): Show | 16 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.16-10385A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88556250 | ||||||
chr12:88556296
|
G | T | 10 | a0001c0001t0002g0008a0001c0001t0002g0011a0001c0001t0002g0026others(7): Show | 12 | HG00323.hp1 HG00738.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.16-10431C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88556296 | ||||||
chr12:88556401
|
G | A | 1 | a0001c0001t0003g0152 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.16-10536C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88556401 | ||||||
chr12:88556540
|
C | T | 5 | a0001c0001t0002g0008a0001c0001t0002g0125a0001c0001t0002g0126others(2): Show | 6 | NA18944.hp2 NA18964.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-10675G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88556540 | ||||||
chr12:88556683
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.16-10818C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88556683 | ||||||
chr12:88556802
|
G | T | 2 | a0001c0001t0015g0218a0001c0001t0015g0219 | 2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.16-10937C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88556802 | ||||||
chr12:88556874
|
C | A | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-11009G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88556874 | ||||||
chr12:88557098
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.16-11233C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88557098 | ||||||
chr12:88557102
|
T | C | 1 | a0001c0001t0001g0184 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.16-11237A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88557102 | ||||||
chr12:88557610
|
A | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(196): Show | 216 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.16-11745T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88557610 | ||||||
chr12:88557708
|
C | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(69): Show | 83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.16-11843G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88557708 | ||||||
chr12:88557769
|
G | A | 1 | a0001c0001t0018g0183 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.16-11904C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88557769 | ||||||
chr12:88557799
|
G | T | 5 | a0001c0001t0002g0118a0001c0001t0002g0119a0001c0001t0005g0120others(2): Show | 5 | HG00639.hp2 HG02055.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.16-11934C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88557799 | ||||||
chr12:88557856
|
T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(83): Show | 97 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.16-11991A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88557856 | ||||||
chr12:88557970
|
C | T | 2 | a0001c0001t0002g0055a0001c0001t0012g0056 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.16-12105G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88557970 | ||||||
chr12:88558072
|
A | G | 1 | a0001c0001t0002g0105 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.16-12207T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88558072 | ||||||
chr12:88558245
|
TTAAATAA others(1): Show |
T | 13 | a0001c0001t0002g0118a0001c0001t0002g0119a0001c0001t0005g0057others(10): Show | 13 | HG00639.hp2 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.16-12388_16-12381d others(10): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88558245 | ||||||
chr12:88558373
|
T | A | 1 | a0001c0001t0001g0184 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.16-12508A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88558373 | ||||||
chr12:88558485
|
C | G | 7 | a0001c0001t0003g0009a0001c0001t0003g0021a0001c0001t0003g0152others(4): Show | 9 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.16-12620G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88558485 | ||||||
chr12:88558552
|
T | C | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-12687A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88558552 | ||||||
chr12:88558650
|
T | A | 4 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(1): Show | 4 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-12785A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88558650 | ||||||
chr12:88558752
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.16-12887C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88558752 | ||||||
chr12:88558812
|
G | C | 7 | a0001c0001t0003g0009a0001c0001t0003g0021a0001c0001t0003g0152others(4): Show | 9 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.16-12947C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88558812 | ||||||
chr12:88558838
|
A | C | 7 | a0001c0001t0003g0009a0001c0001t0003g0021a0001c0001t0003g0152others(4): Show | 9 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.16-12973T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88558838 | ||||||
chr12:88559066
|
G | A | 1 | a0001c0001t0011g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.16-13201C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88559066 | ||||||
chr12:88559171
|
C | T | 4 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(1): Show | 4 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-13306G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88559171 | ||||||
chr12:88559315
|
G | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.16-13450C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88559315 | ||||||
chr12:88559489
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.16-13624C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88559489 | ||||||
chr12:88559547
|
A | G | 3 | a0001c0001t0005g0145a0001c0001t0005g0147a0001c0001t0029g0146 | 3 | HG03130.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.16-13682T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88559547 | ||||||
chr12:88559549
|
C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.16-13684G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88559549 | ||||||
chr12:88559622
|
C | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.16-13757G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88559622 | ||||||
chr12:88559784
|
C | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(69): Show | 83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.16-13919G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88559784 | ||||||
chr12:88559882
|
A | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(71): Show | 85 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.16-14017T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88559882 | ||||||
chr12:88560182
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.16-14317C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88560182 | ||||||
chr12:88560497
|
G | A | 13 | a0001c0001t0002g0118a0001c0001t0002g0119a0001c0001t0005g0057others(10): Show | 13 | HG00639.hp2 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.16-14632C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88560497 | ||||||
chr12:88560518
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.16-14653C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88560518 | ||||||
chr12:88560917
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.16-15052C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88560917 | ||||||
chr12:88560964
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.16-15099A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88560964 | ||||||
chr12:88560967
|
C | CA | 19 | a0001c0001t0002g0034a0001c0001t0002g0074a0001c0001t0002g0117others(16): Show | 19 | HG00438.hp2 HG02280.hp2 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.16-15103dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88560967 | ||||||
chr12:88560967
|
CA | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(74): Show | 88 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.16-15103delT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88560967 | ||||||
chr12:88560989
|
A | G | 3 | a0001c0001t0001g0037a0001c0001t0002g0130a0001c0001t0011g0128 | 3 | HG02280.hp1 HG02896.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.16-15124T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88560989 | ||||||
chr12:88560990
|
A | G | 1 | a0001c0001t0003g0099 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.16-15125T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88560990 | ||||||
chr12:88561052
|
G | T | 1 | a0001c0001t0003g0099 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.16-15187C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88561052 | ||||||
chr12:88561535
|
T | C | 4 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(1): Show | 4 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-15670A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88561535 | ||||||
chr12:88561672
|
C | A | 1 | a0001c0001t0011g0128 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-15807G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88561672 | ||||||
chr12:88561692
|
G | A | 65 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(62): Show | 76 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.16-15827C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88561692 | ||||||
chr12:88561783
|
G | T | 2 | a0001c0001t0001g0079a0001c0001t0003g0080 | 2 | HG00438.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.16-15918C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88561783 | ||||||
chr12:88561865
|
C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.16-16000G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88561865 | ||||||
chr12:88561898
|
A | G | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-16033T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88561898 | ||||||
chr12:88561952
|
TATCAC | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(215): Show | 237 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.16-16092_16-16088d others(7): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88561952 | ||||||
chr12:88562562
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.16-16697C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88562562 | ||||||
chr12:88562623
|
T | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.16-16758A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88562623 | ||||||
chr12:88562775
|
C | A | 1 | a0001c0001t0004g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.16-16910G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88562775 | ||||||
chr12:88562833
|
G | A | 6 | a0001c0001t0002g0077a0001c0001t0002g0100a0001c0001t0002g0101others(3): Show | 6 | HG02071.hp1 HG02559.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-16968C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88562833 | ||||||
chr12:88562848
|
T | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(204): Show | 224 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.16-16983A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88562848 | ||||||
chr12:88562970
|
A | G | 2 | a0001c0001t0005g0133a0001c0001t0005g0135 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.16-17105T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88562970 | ||||||
chr12:88562979
|
C | T | 4 | a0001c0001t0002g0110a0001c0001t0002g0111a0001c0001t0002g0113others(1): Show | 4 | NA18974.hp1 NA18981.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-17114G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88562979 | ||||||
chr12:88563089
|
A | C | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.15+17175T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88563089 | ||||||
chr12:88563381
|
C | A | 2 | a0001c0001t0003g0098a0001c0001t0003g0099 | 2 | NA18984.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.15+16883G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88563381 | ||||||
chr12:88563575
|
A | C | 98 | a0001c0001t0001g0079a0001c0001t0002g0035a0001c0001t0002g0055others(95): Show | 104 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.15+16689T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88563575 | ||||||
chr12:88563591
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.15+16673C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88563591 | ||||||
chr12:88563671
|
G | C | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.15+16593C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88563671 | ||||||
chr12:88563699
|
A | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.15+16565T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88563699 | ||||||
chr12:88563962
|
C | CA | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.15+16301dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88563962 | ||||||
chr12:88564085
|
T | G | 2 | a0001c0001t0002g0134a0001c0001t0002g0137 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.15+16179A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88564085 | ||||||
chr12:88564103
|
G | A | 7 | a0001c0001t0003g0009a0001c0001t0003g0021a0001c0001t0003g0152others(4): Show | 9 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+16161C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88564103 | ||||||
chr12:88564333
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.15+15931C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88564333 | ||||||
chr12:88564390
|
C | CTGTT | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.15+15873_15+15874i others(6): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88564390 | ||||||
chr12:88564432
|
G | A | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.15+15832C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88564432 | ||||||
chr12:88564573
|
C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.15+15691G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88564573 | ||||||
chr12:88564742
|
T | TA | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.15+15521dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88564742 | ||||||
chr12:88565004
|
C | T | 1 | a0001c0001t0004g0213 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.15+15260G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88565004 | ||||||
chr12:88565119
|
T | C | 1 | a0001c0001t0003g0099 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.15+15145A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88565119 | ||||||
chr12:88565223
|
T | C | 1 | a0001c0001t0004g0050 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.15+15041A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88565223 | ||||||
chr12:88565355
|
GGTGGCTC others(6): Show |
G | 1 | a0001c0001t0001g0191 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.15+14896_15+14908d others(15): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88565355 | ||||||
chr12:88565622
|
TAAAC | T | 9 | a0001c0001t0002g0055a0001c0001t0003g0009a0001c0001t0003g0021others(6): Show | 11 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.15+14638_15+14641d others(6): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88565622 | ||||||
chr12:88565660
|
G | A | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.15+14604C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88565660 | ||||||
chr12:88565733
|
G | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.15+14531C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88565733 | ||||||
chr12:88565991
|
G | C | 1 | a0001c0001t0008g0192 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.15+14273C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88565991 | ||||||
chr12:88566072
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(70): Show | 84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.15+14192A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88566072 | ||||||
chr12:88566083
|
A | G | 1 | a0001c0001t0028g0153 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.15+14181T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88566083 | ||||||
chr12:88566115
|
C | T | 14 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(11): Show | 14 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.15+14149G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88566115 | ||||||
chr12:88566580
|
G | A | 2 | a0001c0001t0015g0218a0001c0001t0015g0219 | 2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.15+13684C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88566580 | ||||||
chr12:88566615
|
T | C | 1 | a0001c0001t0012g0056 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.15+13649A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88566615 | ||||||
chr12:88566668
|
C | T | 1 | a0001c0001t0002g0030 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.15+13596G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88566668 | ||||||
chr12:88566931
|
T | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(84): Show | 99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.15+13333A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88566931 | ||||||
chr12:88566950
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(71): Show | 86 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.15+13314G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88566950 | ||||||
chr12:88567259
|
C | T | 14 | a0001c0001t0002g0118a0001c0001t0002g0119a0001c0001t0005g0057others(11): Show | 14 | HG00639.hp2 HG01891.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.15+13005G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88567259 | ||||||
chr12:88567672
|
A | G | 1 | a0001c0001t0007g0036 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.15+12592T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88567672 | ||||||
chr12:88567688
|
T | C | 1 | a0001c0001t0022g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.15+12576A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88567688 | ||||||
chr12:88567936
|
A | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(84): Show | 99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.15+12328T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88567936 | ||||||
chr12:88567972
|
A | C | 1 | a0001c0001t0001g0164 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.15+12292T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88567972 | ||||||
chr12:88567975
|
C | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(84): Show | 99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.15+12289G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88567975 | ||||||
chr12:88568075
|
T | C | 2 | a0001c0001t0015g0218a0001c0001t0015g0219 | 2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.15+12189A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568075 | ||||||
chr12:88568102
|
TA | T | 217 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(214): Show | 236 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.15+12161delT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568102 | ||||||
chr12:88568134
|
G | A | 6 | a0001c0001t0002g0077a0001c0001t0002g0100a0001c0001t0002g0101others(3): Show | 6 | HG02071.hp1 HG02559.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+12130C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568134 | ||||||
chr12:88568234
|
T | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(84): Show | 99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.15+12030A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568234 | ||||||
chr12:88568280
|
C | CATTT | 69 | a0001c0001t0001g0079a0001c0001t0002g0027a0001c0001t0002g0055others(66): Show | 73 | HG00408.hp2 HG00438.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.15+11980_15+11983d others(6): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568280 | ||||||
chr12:88568280
|
C | CATTTATT others(1): Show |
9 | a0001c0001t0002g0077a0001c0001t0002g0117a0001c0001t0002g0138others(6): Show | 9 | HG02071.hp1 HG02257.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.15+11976_15+11983d others(10): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568280 | ||||||
chr12:88568280
|
C | CATTTATT others(5): Show |
1 | a0001c0001t0004g0212 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.15+11972_15+11983d others(14): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568280 | ||||||
chr12:88568280
|
CATTT | C | 7 | a0001c0001t0003g0009a0001c0001t0003g0106a0001c0001t0003g0152others(4): Show | 9 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+11980_15+11983d others(6): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568280 | ||||||
chr12:88568280
|
CATTTATT others(1): Show |
C | 3 | a0001c0001t0005g0220a0001c0001t0012g0075a0001c0002t0002g0150 | 3 | HG02965.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.15+11976_15+11983d others(10): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568280 | ||||||
chr12:88568280
|
CATTTATT others(9): Show |
C | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(84): Show | 99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.15+11968_15+11983d others(18): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568280 | ||||||
chr12:88568284
|
T | C | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.15+11980A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568284 | ||||||
chr12:88568562
|
A | C | 10 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(7): Show | 10 | HG02965.hp2 HG03209.hp1 HG06807.hp1 others(7): Show |
intron_variant | MODIFIER | c.15+11702T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568562 | ||||||
chr12:88568588
|
C | T | 1 | a0001c0001t0002g0115 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.15+11676G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568588 | ||||||
chr12:88568765
|
A | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(84): Show | 99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.15+11499T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568765 | ||||||
chr12:88568904
|
A | C | 13 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(10): Show | 13 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.15+11360T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568904 | ||||||
chr12:88568982
|
T | A | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.15+11282A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568982 | ||||||
chr12:88569176
|
G | A | 1 | a0001c0001t0004g0217 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.15+11088C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88569176 | ||||||
chr12:88569186
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.15+11078G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88569186 | ||||||
chr12:88569666
|
C | T | 1 | a0001c0001t0002g0159 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.15+10598G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88569666 | ||||||
chr12:88569830
|
A | G | 1 | a0001c0001t0002g0109 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.15+10434T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88569830 | ||||||
chr12:88569942
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.15+10322G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88569942 | ||||||
chr12:88569969
|
G | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(84): Show | 99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.15+10295C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88569969 | ||||||
chr12:88569999
|
A | G | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(84): Show | 99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.15+10265T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88569999 | ||||||
chr12:88570058
|
T | C | 2 | a0001c0001t0009g0051a0001c0001t0009g0052 | 2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.15+10206A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570058 | ||||||
chr12:88570522
|
A | C | 1 | a0001c0001t0027g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.15+9742T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570522 | ||||||
chr12:88570533
|
A | G | 2 | a0001c0001t0026g0040a0001c0002t0002g0041 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.15+9731T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570533 | ||||||
chr12:88570537
|
C | CA | 87 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(84): Show | 99 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.15+9726dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570537 | ||||||
chr12:88570540
|
A | C | 1 | a0001c0001t0011g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.15+9724T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570540 | ||||||
chr12:88570598
|
T | C | 4 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(1): Show | 4 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+9666A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570598 | ||||||
chr12:88570603
|
G | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0198 | 2 | NA18944.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.15+9661C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570603 | ||||||
chr12:88570627
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.15+9637C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570627 | ||||||
chr12:88570683
|
C | G | 21 | a0001c0001t0002g0035a0001c0001t0002g0058a0001c0001t0002g0064others(18): Show | 21 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.15+9581G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570683 | ||||||
chr12:88570805
|
A | G | 4 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140others(1): Show | 4 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+9459T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570805 | ||||||
chr12:88570809
|
G | A | 1 | a0001c0001t0003g0108 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.15+9455C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570809 | ||||||
chr12:88570868
|
A | G | 1 | a0001c0001t0026g0040 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.15+9396T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570868 | ||||||
chr12:88571060
|
G | A | 1 | a0001c0001t0031g0221 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.15+9204C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88571060 | ||||||
chr12:88571195
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.15+9069G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88571195 | ||||||
chr12:88571347
|
T | G | 3 | a0001c0001t0005g0145a0001c0001t0005g0147a0001c0001t0029g0146 | 3 | HG03130.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.15+8917A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88571347 | ||||||
chr12:88571763
|
C | T | 2 | a0001c0001t0002g0055a0001c0001t0012g0056 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.15+8501G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88571763 | ||||||
chr12:88572338
|
A | T | 1 | a0001c0001t0022g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.15+7926T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572338 | ||||||
chr12:88572424
|
C | A | 1 | a0002c0003t0001g0193 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.15+7840G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572424 | ||||||
chr12:88572594
|
A | ATT | 6 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(3): Show | 6 | HG06807.hp1 NA18949.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+7668_15+7669dup others(2): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572594 | ||||||
chr12:88572595
|
T | A | 1 | a0001c0001t0003g0155 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.15+7669A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572595 | ||||||
chr12:88572595
|
T | TTA | 100 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(97): Show | 114 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.15+7667_15+7668dup others(2): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572595 | ||||||
chr12:88572595
|
T | TTATA | 15 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0037others(12): Show | 16 | HG00597.hp1 HG01099.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.15+7665_15+7668dup others(4): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572595 | ||||||
chr12:88572595
|
T | TTATATA | 8 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0002g0138others(5): Show | 8 | HG00544.hp2 HG01243.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+7663_15+7668dup others(6): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572595 | ||||||
chr12:88572595
|
T | TTATATAT others(1): Show |
6 | a0001c0001t0001g0198a0001c0001t0002g0027a0001c0001t0004g0142others(3): Show | 6 | HG02630.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+7661_15+7668dup others(8): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572595 | ||||||
chr12:88572595
|
TTA | T | 9 | a0001c0001t0002g0029a0001c0001t0002g0058a0001c0001t0003g0059others(6): Show | 9 | HG00423.hp1 HG01192.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+7667_15+7668del others(2): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572595 | ||||||
chr12:88572595
|
TTATA | T | 2 | a0001c0001t0002g0159a0001c0001t0005g0057 | 2 | HG03579.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.15+7665_15+7668del others(4): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572595 | ||||||
chr12:88572595
|
TTATATA | T | 2 | a0001c0001t0002g0055a0001c0001t0012g0056 | 2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.15+7663_15+7668del others(6): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572595 | ||||||
chr12:88572597
|
A | T | 1 | a0001c0001t0027g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.15+7667T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572597 | ||||||
chr12:88572599
|
A | T | 3 | a0001c0001t0011g0039a0001c0001t0026g0040a0001c0002t0002g0041 | 3 | HG01192.hp2 HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.15+7665T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572599 | ||||||
chr12:88572624
|
G | A | 7 | a0001c0001t0003g0009a0001c0001t0003g0021a0001c0001t0003g0152others(4): Show | 9 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+7640C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572624 | ||||||
chr12:88572636
|
T | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(72): Show | 87 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.15+7628A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572636 | ||||||
chr12:88573011
|
A | G | 1 | a0001c0001t0001g0037 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.15+7253T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88573011 | ||||||
chr12:88573230
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(63): Show | 78 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.15+7034G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88573230 | ||||||
chr12:88573504
|
C | G | 1 | a0001c0001t0011g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.15+6760G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88573504 | ||||||
chr12:88573520
|
ATT | A | 4 | a0001c0001t0005g0145a0001c0001t0005g0147a0001c0001t0005g0156others(1): Show | 4 | HG03130.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+6742_15+6743del others(2): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88573520 | ||||||
chr12:88573599
|
G | C | 1 | a0001c0001t0027g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.15+6665C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88573599 | ||||||
chr12:88573829
|
C | A | 1 | a0001c0001t0001g0014 | 2 | NA18961.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.15+6435G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88573829 | ||||||
chr12:88573931
|
C | A | 6 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0031others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+6333G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88573931 | ||||||
chr12:88574065
|
CT | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(74): Show | 89 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.15+6198delA | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88574065 | ||||||
chr12:88574080
|
A | T | 16 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0047others(13): Show | 16 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.15+6184T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88574080 | ||||||
chr12:88574114
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.15+6150A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88574114 | ||||||
chr12:88574180
|
G | A | 2 | a0001c0001t0003g0021a0001c0001t0014g0010 | 3 | HG02451.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.15+6084C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88574180 | ||||||
chr12:88574285
|
TAAAAGAA others(7): Show |
T | 1 | a0001c0001t0001g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.15+5965_15+5978del others(14): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88574285 | ||||||
chr12:88574290
|
GA | G | 72 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(69): Show | 84 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.15+5973delT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88574290 | ||||||
chr12:88574299
|
A | G | 1 | a0001c0001t0007g0036 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.15+5965T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88574299 | ||||||
chr12:88575902
|
T | C | 1 | a0001c0001t0021g0208 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.15+4362A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88575902 | ||||||
chr12:88575965
|
C | T | 1 | a0001c0001t0002g0035 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.15+4299G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88575965 | ||||||
chr12:88576131
|
G | A | 7 | a0001c0001t0003g0009a0001c0001t0003g0021a0001c0001t0003g0152others(4): Show | 9 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+4133C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88576131 | ||||||
chr12:88576275
|
T | C | 1 | a0001c0001t0022g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.15+3989A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88576275 | ||||||
chr12:88577277
|
T | C | 1 | a0001c0001t0005g0156 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.15+2987A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88577277 | ||||||
chr12:88577528
|
A | C | 1 | a0001c0001t0001g0157 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.15+2736T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88577528 | ||||||
chr12:88577641
|
CAG | C | 71 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(68): Show | 82 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.15+2621_15+2622del others(2): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88577641 | ||||||
chr12:88578622
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.15+1642A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88578622 | ||||||
chr12:88578955
|
T | C | 1 | a0001c0001t0001g0210 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.15+1309A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88578955 | ||||||
chr12:88578992
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.15+1272C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88578992 | ||||||
chr12:88579003
|
C | G | 6 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0031others(3): Show | 6 | HG02258.hp1 HG02572.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+1261G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88579003 | ||||||
chr12:88579445
|
C | T | 1 | a0001c0001t0022g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.15+819G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88579445 | ||||||
chr12:88579525
|
C | T | 2 | a0001c0001t0002g0026a0001c0001t0002g0027 | 2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.15+739G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88579525 | ||||||
chr12:88579955
|
A | G | 9 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(6): Show | 10 | HG01099.hp1 HG02300.hp2 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.15+309T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88579955 | ||||||
chr12:88580079
|
C | T | 1 | a0001c0001t0003g0021 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.15+185G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88580079 | ||||||
chr12:88580084
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.15+180G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88580084 | ||||||
chr12:88580091
|
G | A | 6 | a0001c0001t0004g0212a0001c0001t0004g0213a0001c0001t0004g0214others(3): Show | 6 | HG06807.hp1 NA18949.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+173C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88580091 | ||||||
chr12:88580174
|
C | A | 2 | a0001c0001t0015g0218a0001c0001t0015g0219 | 2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.15+90G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88580174 | ||||||
chr12:88580212
|
G | C | 1 | a0001c0001t0005g0220 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.15+52C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88580212 |