geneid | 3815 |
---|---|
ensemblid | ENSG00000157404.17 |
hgncid | 6342 |
symbol | KIT |
name | KIT proto-oncogene, receptor tyrosine kinase |
refseq_nuc | NM_000222.3 |
refseq_prot | NP_000213.1 |
ensembl_nuc | ENST00000288135.6 |
ensembl_prot | ENSP00000288135.6 |
mane_status | MANE Select |
chr | chr4 |
start | 54657957 |
end | 54740715 |
strand | + |
ver | v1.2 |
region | chr4:54657957-54740715 |
region5000 | chr4:54652957-54745715 |
regionname0 | KIT_chr4_54657957_54740715 |
regionname5000 | KIT_chr4_54652957_54745715 |
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 | 976 | 243 | 68 | 55 | 84 | 5 | 29 | 59 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0002 | 0/0 | 976 | 20 | 3 | 5 | 8 | 1 | 3 | 7 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0003 | 0/0 | 976 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0004 | 0/0 | 976 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0005 | 0/0 | 976 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0006 | 0/0 | 976 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
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 | 2931 | 199 | 40 | 47 | 79 | 5 | 26 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
c0002 | 0/0 | 2931 | 20 | 3 | 5 | 8 | 1 | 3 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
c0003 | 0/0 | 2931 | 18 | 16 | 0 | 0 | 0 | 2 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
c0004 | 0/0 | 2931 | 9 | 0 | 4 | 5 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
c0005 | 0/0 | 2931 | 4 | 3 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
c0006 | 0/0 | 2931 | 3 | 3 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
c0007 | 0/0 | 2931 | 3 | 0 | 2 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
c0008 | 0/0 | 2931 | 2 | 2 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
c0009 | 0/0 | 2931 | 2 | 2 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
c0010 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
c0011 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
c0012 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
c0013 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
c0014 | 0/0 | 2931 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
c0015 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
c0016 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
c0017 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
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 | 1/0 | 2217 | 178 | 35 | 48 | 73 | 3 | 18 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
t0002 | 0/1 | 2217 | 34 | 9 | 6 | 10 | 1 | 7 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
t0003 | 0/0 | 2217 | 27 | 10 | 5 | 8 | 1 | 3 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
t0004 | 0/0 | 2217 | 11 | 9 | 1 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
t0005 | 0/0 | 2216 | 3 | 3 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
t0006 | 0/0 | 2217 | 3 | 3 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
t0007 | 0/0 | 2217 | 2 | 2 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
t0008 | 0/0 | 2217 | 2 | 2 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
t0009 | 0/0 | 2217 | 2 | 0 | 0 | 0 | 1 | 1 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
t0010 | 0/0 | 2217 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
t0011 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
t0012 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
t0013 | 0/0 | 2217 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
t0014 | 0/0 | 2217 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
t0015 | 0/0 | 2217 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
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 | 2 | 2 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0023 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0201 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
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 | 2931 | 199 | 40 | 47 | 79 | 5 | 26 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0003 | 0/0 | 2931 | 18 | 16 | 0 | 0 | 0 | 2 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0004 | 0/0 | 2931 | 9 | 0 | 4 | 5 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0005 | 0/0 | 2931 | 4 | 3 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0006 | 0/0 | 2931 | 3 | 3 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0007 | 0/0 | 2931 | 3 | 0 | 2 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0009 | 0/0 | 2931 | 2 | 2 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0012 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0013 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0014 | 0/0 | 2931 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0015 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0016 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0002c0002 | 0/0 | 2931 | 20 | 3 | 5 | 8 | 1 | 3 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0003c0008 | 0/0 | 2931 | 2 | 2 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0004c0010 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0005c0011 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0006c0017 | 0/0 | 2931 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5147 | 155 | 25 | 41 | 68 | 3 | 17 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0001t0002 | 0/1 | 5147 | 32 | 7 | 6 | 10 | 1 | 7 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0001t0005 | 0/0 | 5146 | 3 | 3 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0001t0007 | 0/0 | 5147 | 2 | 2 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0001t0008 | 0/0 | 5147 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0001t0009 | 0/0 | 5147 | 2 | 0 | 0 | 0 | 1 | 1 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0001t0012 | 0/0 | 5147 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0001t0013 | 0/0 | 5147 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0001t0014 | 0/0 | 5147 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0001t0015 | 0/0 | 5147 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0003t0001 | 0/0 | 5147 | 4 | 4 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0003t0003 | 0/0 | 5147 | 7 | 5 | 0 | 0 | 0 | 2 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0003t0004 | 0/0 | 5147 | 7 | 7 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0004t0001 | 0/0 | 5147 | 9 | 0 | 4 | 5 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0005t0003 | 0/0 | 5147 | 2 | 2 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0005t0004 | 0/0 | 5147 | 2 | 1 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0006t0006 | 0/0 | 5147 | 3 | 3 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0007t0001 | 0/0 | 5147 | 3 | 0 | 2 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0009t0001 | 0/0 | 5147 | 2 | 2 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0012t0002 | 0/0 | 5147 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0013t0001 | 0/0 | 5147 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0014t0001 | 0/0 | 5147 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0015t0002 | 0/0 | 5147 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0001c0016t0001 | 0/0 | 5147 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0002c0002t0003 | 0/0 | 5147 | 18 | 3 | 5 | 8 | 1 | 1 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0002c0002t0004 | 0/0 | 5147 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0002c0002t0010 | 0/0 | 5147 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0003c0008t0001 | 0/0 | 5147 | 2 | 2 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0004c0010t0008 | 0/0 | 5147 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0005c0011t0011 | 0/0 | 5147 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
a0006c0017t0004 | 0/0 | 5147 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | copy fasta | chr4 | 54652957 | 54745715 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0201 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0023 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0007g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0008g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0009g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0009g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0012g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0013g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0014g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0001t0015g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0003t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0003t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0003t0003g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0003t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0003t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0003t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0003t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0003t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0003t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0003t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0003t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0003t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0003t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0003t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0003t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0003t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0004t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0004t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0004t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0004t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0004t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0004t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0004t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0004t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0005t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0005t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0005t0004g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0005t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0006t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0006t0006g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0006t0006g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0007t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0007t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0007t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0009t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0009t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0012t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0013t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0014t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0015t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0001c0016t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0002c0002t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0002c0002t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0002c0002t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0002c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0002c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0002c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0002c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0002c0002t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0002c0002t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0002c0002t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0002c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0002c0002t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0002c0002t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0002c0002t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0002c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0002c0002t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0002c0002t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0002c0002t0010g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0003c0008t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0003c0008t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0004c0010t0008g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0005c0011t0011g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
a0006c0017t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | GBR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | FIN | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG00280 | hp2 | a0002 | c0002 | t0003 | g0166 | EUR | FIN | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01070 | hp2 | a0002 | c0002 | t0003 | g0017 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01071 | hp2 | a0001 | c0014 | t0001 | g0184 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01074 | hp1 | a0002 | c0002 | t0003 | g0189 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01081 | hp2 | a0001 | c0004 | t0001 | g0114 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01168 | hp1 | a0001 | c0004 | t0001 | g0053 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01175 | hp2 | a0001 | c0004 | t0001 | g0087 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01243 | hp1 | a0002 | c0002 | t0003 | g0245 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01255 | hp1 | a0001 | c0007 | t0001 | g0115 | AMR | CLM | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01255 | hp2 | a0001 | c0005 | t0004 | g0140 | AMR | CLM | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01256 | hp1 | a0001 | c0004 | t0001 | g0052 | AMR | CLM | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01433 | hp1 | a0002 | c0002 | t0003 | g0192 | AMR | CLM | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01516 | hp1 | a0001 | c0001 | t0009 | g0092 | EUR | IBS | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | IBS | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01884 | hp1 | a0003 | c0008 | t0001 | g0011 | AFR | ACB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01884 | hp2 | a0006 | c0017 | t0004 | g0139 | AFR | ACB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01891 | hp1 | a0001 | c0003 | t0003 | g0049 | AFR | ACB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01891 | hp2 | a0001 | c0003 | t0004 | g0248 | AFR | ACB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PEL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | KHV | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02055 | hp1 | a0002 | c0002 | t0003 | g0129 | AFR | ACB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02055 | hp2 | a0001 | c0003 | t0003 | g0080 | AFR | ACB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02074 | hp2 | a0002 | c0002 | t0003 | g0004 | EAS | KHV | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02132 | hp1 | a0001 | c0004 | t0001 | g0227 | EAS | KHV | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | KHV | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02135 | hp2 | a0001 | c0004 | t0001 | g0177 | EAS | KHV | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02145 | hp1 | a0001 | c0003 | t0003 | g0149 | AFR | ACB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CDX | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CDX | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02257 | hp1 | a0001 | c0015 | t0002 | g0001 | AFR | ACB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02258 | hp1 | a0001 | c0003 | t0003 | g0044 | AFR | ACB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02258 | hp2 | a0002 | c0002 | t0003 | g0148 | AFR | ACB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02300 | hp1 | a0002 | c0002 | t0003 | g0224 | AMR | PEL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02572 | hp1 | a0001 | c0006 | t0006 | g0255 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02615 | hp2 | a0001 | c0003 | t0004 | g0259 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02622 | hp1 | a0001 | c0016 | t0001 | g0137 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02622 | hp2 | a0001 | c0003 | t0004 | g0220 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02630 | hp1 | a0001 | c0003 | t0004 | g0261 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02630 | hp2 | a0001 | c0001 | t0014 | g0144 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0074 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02723 | hp1 | a0001 | c0005 | t0003 | g0141 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02723 | hp2 | a0001 | c0006 | t0006 | g0262 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02809 | hp1 | a0001 | c0003 | t0004 | g0260 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02818 | hp2 | a0001 | c0006 | t0006 | g0256 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02886 | hp2 | a0001 | c0001 | t0007 | g0246 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02896 | hp2 | a0001 | c0005 | t0003 | g0136 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02970 | hp1 | a0001 | c0003 | t0003 | g0066 | AFR | ESN | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02976 | hp1 | a0003 | c0008 | t0001 | g0013 | AFR | ESN | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0197 | SAS | PJL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03017 | hp2 | a0001 | c0007 | t0001 | g0172 | SAS | PJL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03041 | hp2 | a0001 | c0003 | t0004 | g0118 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0135 | AFR | ESN | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0078 | AFR | ESN | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | MSL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | MSL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03225 | hp2 | a0001 | c0005 | t0004 | g0142 | AFR | MSL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03239 | hp2 | a0001 | c0001 | t0009 | g0120 | SAS | PJL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03453 | hp1 | a0001 | c0001 | t0008 | g0252 | AFR | MSL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03486 | hp2 | a0001 | c0013 | t0001 | g0257 | AFR | MSL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03492 | hp2 | a0002 | c0002 | t0003 | g0230 | SAS | PJL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03516 | hp1 | a0001 | c0012 | t0002 | g0250 | AFR | ESN | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03516 | hp2 | a0001 | c0009 | t0001 | g0145 | AFR | ESN | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03540 | hp1 | a0004 | c0010 | t0008 | g0253 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03669 | hp1 | a0001 | c0001 | t0013 | g0185 | SAS | PJL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03669 | hp2 | a0002 | c0002 | t0010 | g0088 | SAS | PJL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | STU | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | STU | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | BEB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03831 | hp2 | a0001 | c0003 | t0003 | g0054 | SAS | BEB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | BEB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | STU | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG04204 | hp1 | a0002 | c0002 | t0004 | g0057 | SAS | STU | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | STU | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | CHB | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18944 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18947 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18952 | hp1 | a0002 | c0002 | t0003 | g0100 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18983 | hp1 | a0002 | c0002 | t0003 | g0124 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18991 | hp2 | a0001 | c0004 | t0001 | g0199 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18993 | hp1 | a0002 | c0002 | t0003 | g0117 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19004 | hp1 | a0001 | c0004 | t0001 | g0223 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19007 | hp1 | a0002 | c0002 | t0003 | g0004 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19043 | hp1 | a0001 | c0009 | t0001 | g0015 | AFR | LWK | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0156 | AFR | LWK | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19056 | hp2 | a0001 | c0001 | t0015 | g0028 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19060 | hp1 | a0001 | c0004 | t0001 | g0045 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA19240 | hp2 | a0005 | c0011 | t0011 | g0050 | AFR | YRI | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0157 | AFR | ASW | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA20129 | hp2 | a0001 | c0003 | t0001 | g0258 | AFR | ASW | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA20905 | hp1 | a0001 | c0003 | t0003 | g0018 | SAS | GIH | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | GIH | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG01123 | hp2 | a0001 | c0007 | t0001 | g0101 | AMR | CLM | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | USA | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
HG06807 | hp2 | a0002 | c0002 | t0003 | g0146 | AFR | USA | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA18955 | hp2 | a0002 | c0002 | t0003 | g0125 | EAS | JPT | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | USA | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA20300 | hp2 | a0001 | c0003 | t0004 | g0076 | AFR | USA | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | LWK | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
NA21309 | hp2 | a0001 | c0001 | t0012 | g0014 | AFR | LWK | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0023 | REF | REF | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0201 | REF | REF | KIT_chr4_54652957_54745715 | KIT | chr4 | 54652957 | 54745715 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:54695590
|
G | A | 1 | a0004 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.146G>A | p.Arg49His | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 2/21 | 204/5147 | 146/2931 | 49/976 | chr4 | 54695590 | ||
chr4:54698478
|
G | A | 1 | a0003 | 2 | HG01884.hp1 HG02976.hp1 |
missense_variant | MODERATE | c.532G>A | p.Ala178Thr | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 3/21 | 590/5147 | 532/2931 | 178/976 | chr4 | 54698478 | ||
chr4:54709428
|
G | A | 1 | a0005 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.1120G>A | p.Val374Ile | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/21 | 1178/5147 | 1120/2931 | 374/976 | chr4 | 54709428 | ||
chr4:54709507
|
A | G | 1 | a0006 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.1199A>G | p.Asn400Ser | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/21 | 1257/5147 | 1199/2931 | 400/976 | chr4 | 54709507 | ||
chr4:54727298
|
A | C | 1 | a0002 | 20 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(17): Show |
missense_variant | MODERATE | c.1621A>C | p.Met541Leu | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 10/21 | 1679/5147 | 1621/2931 | 541/976 | chr4 | 54727298 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:54695696
|
G | T | 3 | a0001c0005a0001c0016a0006c0017 | 6 | HG01255.hp2 HG01884.hp2 HG02622.hp1 others(3): Show |
synonymous_variant | LOW | c.252G>T | p.Thr84Thr | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 2/21 | 310/5147 | 252/2931 | 84/976 | chr4 | 54695696 | ||
chr4:54698336
|
C | T | 1 | a0001c0015 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.390C>T | p.Asn130Asn | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 3/21 | 448/5147 | 390/2931 | 130/976 | chr4 | 54698336 | ||
chr4:54709427
|
C | T | 1 | a0001c0009 | 2 | HG03516.hp2 NA19043.hp1 |
synonymous_variant | LOW | c.1119C>T | p.Tyr373Tyr | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/21 | 1177/5147 | 1119/2931 | 373/976 | chr4 | 54709427 | ||
chr4:54709538
|
T | C | 1 | a0001c0012 | 1 | HG03516.hp1 | splice_region_variant&synonymous_variant | LOW | c.1230T>C | p.Asn410Asn | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/21 | 1288/5147 | 1230/2931 | 410/976 | chr4 | 54709538 | ||
chr4:54727264
|
C | T | 1 | a0001c0014 | 1 | HG01071.hp2 | synonymous_variant | LOW | c.1587C>T | p.Phe529Phe | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 10/21 | 1645/5147 | 1587/2931 | 529/976 | chr4 | 54727264 | ||
chr4:54727315
|
A | G | 1 | a0001c0004 | 9 | HG01081.hp2 HG01168.hp1 HG01175.hp2 others(6): Show |
synonymous_variant | LOW | c.1638A>G | p.Lys546Lys | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 10/21 | 1696/5147 | 1638/2931 | 546/976 | chr4 | 54727315 | ||
chr4:54731998
|
T | C | 1 | a0001c0006 | 3 | HG02572.hp1 HG02723.hp2 HG02818.hp2 |
splice_region_variant&synonymous_variant | LOW | c.2361T>C | p.Asn787Asn | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 16/21 | 2419/5147 | 2361/2931 | 787/976 | chr4 | 54731998 | ||
chr4:54733102
|
C | T | 1 | a0001c0007 | 3 | HG01123.hp2 HG01255.hp1 HG03017.hp2 |
synonymous_variant | LOW | c.2394C>T | p.Ile798Ile | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/21 | 2452/5147 | 2394/2931 | 798/976 | chr4 | 54733102 | ||
chr4:54736599
|
G | C | 5 | a0001c0003a0001c0005a0001c0006others(2): Show | 46 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(43): Show |
synonymous_variant | LOW | c.2586G>C | p.Leu862Leu | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 18/21 | 2644/5147 | 2586/2931 | 862/976 | chr4 | 54736599 | ||
chr4:54738473
|
C | T | 2 | a0001c0009a0001c0013 | 3 | HG03486.hp2 HG03516.hp2 NA19043.hp1 |
synonymous_variant | LOW | c.2847C>T | p.Pro949Pro | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 21/21 | 2905/5147 | 2847/2931 | 949/976 | chr4 | 54738473 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:54657994
|
G | T | 1 | a0001c0001t0015 | 1 | NA19056.hp2 | 5_prime_UTR_variant | MODIFIER | c.-21G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/21 | 21 | chr4 | 54657994 | |||||
chr4:54738623
|
T | G | 1 | a0001c0001t0007 | 2 | HG02886.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*66T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 21/21 | 66 | chr4 | 54738623 | |||||
chr4:54738706
|
C | T | 4 | a0001c0001t0002a0001c0001t0014a0001c0012t0002others(1): Show | 35 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*149C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 21/21 | 149 | chr4 | 54738706 | |||||
chr4:54738774
|
G | A | 4 | a0001c0003t0003a0001c0005t0003a0002c0002t0003others(1): Show | 28 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*217G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 21/21 | 217 | chr4 | 54738774 | |||||
chr4:54738870
|
GC | G | 1 | a0001c0001t0005 | 3 | HG02647.hp1 NA19043.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*316delC | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 21/21 | 316 | INFO_REALIGN_3_PRIME | chr4 | 54738870 | ||||
chr4:54738909
|
A | G | 1 | a0001c0001t0013 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*352A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 21/21 | 352 | chr4 | 54738909 | |||||
chr4:54739390
|
A | G | 1 | a0001c0006t0006 | 3 | HG02572.hp1 HG02723.hp2 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*833A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 21/21 | 833 | chr4 | 54739390 | |||||
chr4:54739468
|
C | G | 1 | a0001c0001t0014 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*911C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 21/21 | 911 | chr4 | 54739468 | |||||
chr4:54739643
|
C | T | 1 | a0002c0002t0010 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1086C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 21/21 | 1086 | chr4 | 54739643 | |||||
chr4:54739777
|
C | T | 1 | a0001c0001t0012 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1220C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 21/21 | 1220 | chr4 | 54739777 | |||||
chr4:54740003
|
C | A | 2 | a0001c0001t0008a0004c0010t0008 | 2 | HG03453.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1446C>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 21/21 | 1446 | chr4 | 54740003 | |||||
chr4:54740081
|
A | G | 1 | a0005c0011t0011 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1524A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 21/21 | 1524 | chr4 | 54740081 | |||||
chr4:54740261
|
G | T | 8 | a0001c0003t0003a0001c0003t0004a0001c0005t0003others(5): Show | 39 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1704G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 21/21 | 1704 | chr4 | 54740261 | |||||
chr4:54740574
|
T | C | 1 | a0001c0001t0009 | 2 | HG01516.hp1 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2017T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 21/21 | 2017 | chr4 | 54740574 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:54658085
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02735.hp2 HG03834.hp1 |
splice_region_variant&intron_variant | LOW | c.67+4G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54658085 | ||||||
chr4:54658137
|
T | C | 147 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(144): Show | 150 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.67+56T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54658137 | ||||||
chr4:54658171
|
A | G | 8 | a0001c0001t0001g0143a0001c0001t0001g0147a0001c0001t0001g0150others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+90A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54658171 | ||||||
chr4:54658297
|
A | G | 8 | a0001c0001t0002g0138a0001c0003t0001g0135a0001c0005t0003g0136others(5): Show | 8 | HG01255.hp2 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+216A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54658297 | ||||||
chr4:54658366
|
C | G | 151 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(148): Show | 154 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.67+285C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54658366 | ||||||
chr4:54658409
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(2): Show | 5 | HG01884.hp1 HG02809.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+328G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54658409 | ||||||
chr4:54658566
|
G | A | 8 | a0001c0001t0001g0143a0001c0001t0001g0147a0001c0001t0001g0150others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+485G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54658566 | ||||||
chr4:54658566
|
G | T | 57 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(54): Show | 59 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.67+485G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54658566 | ||||||
chr4:54658719
|
G | T | 1 | a0001c0001t0001g0079 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.67+638G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54658719 | ||||||
chr4:54658768
|
G | A | 4 | a0001c0003t0004g0259a0001c0003t0004g0260a0001c0003t0004g0261others(1): Show | 4 | HG02615.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+687G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54658768 | ||||||
chr4:54658783
|
C | T | 1 | a0001c0001t0002g0002 | 2 | HG00140.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.67+702C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54658783 | ||||||
chr4:54658806
|
C | A | 1 | a0001c0003t0003g0080 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.67+725C>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54658806 | ||||||
chr4:54658913
|
C | T | 58 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(55): Show | 60 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.67+832C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54658913 | ||||||
chr4:54658986
|
A | G | 167 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(164): Show | 171 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.67+905A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54658986 | ||||||
chr4:54658994
|
A | G | 3 | a0001c0001t0001g0012a0003c0008t0001g0011a0003c0008t0001g0013 | 3 | HG01884.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.67+913A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54658994 | ||||||
chr4:54659018
|
C | T | 1 | a0001c0005t0004g0142 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67+937C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54659018 | ||||||
chr4:54659137
|
C | A | 1 | a0001c0001t0001g0151 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.67+1056C>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54659137 | ||||||
chr4:54659160
|
G | C | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.67+1079G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54659160 | ||||||
chr4:54659234
|
A | G | 1 | a0001c0001t0001g0243 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.67+1153A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54659234 | ||||||
chr4:54659271
|
A | G | 5 | a0001c0001t0001g0075a0001c0001t0002g0001a0001c0001t0002g0077others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+1190A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54659271 | ||||||
chr4:54659365
|
C | T | 5 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(2): Show | 5 | HG02080.hp2 NA18946.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+1284C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54659365 | ||||||
chr4:54659488
|
C | G | 1 | a0001c0001t0001g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.67+1407C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54659488 | ||||||
chr4:54659493
|
T | G | 10 | a0001c0001t0001g0016a0001c0001t0001g0143a0001c0001t0001g0147others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+1412T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54659493 | ||||||
chr4:54659666
|
T | C | 148 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(145): Show | 151 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.67+1585T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54659666 | ||||||
chr4:54659763
|
A | C | 148 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(145): Show | 151 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.67+1682A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54659763 | ||||||
chr4:54659765
|
C | G | 10 | a0001c0001t0001g0016a0001c0001t0001g0143a0001c0001t0001g0147others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+1684C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54659765 | ||||||
chr4:54659843
|
A | G | 1 | a0001c0001t0007g0078 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.67+1762A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54659843 | ||||||
chr4:54660008
|
G | C | 148 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(145): Show | 151 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.67+1927G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54660008 | ||||||
chr4:54660085
|
G | T | 58 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(55): Show | 60 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.67+2004G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54660085 | ||||||
chr4:54660130
|
C | G | 1 | a0001c0001t0007g0078 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.67+2049C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54660130 | ||||||
chr4:54660449
|
C | T | 148 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(145): Show | 151 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.67+2368C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54660449 | ||||||
chr4:54660528
|
G | A | 58 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(55): Show | 60 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.67+2447G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54660528 | ||||||
chr4:54660536
|
A | G | 148 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(145): Show | 151 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.67+2455A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54660536 | ||||||
chr4:54660616
|
G | A | 1 | a0002c0002t0003g0017 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.67+2535G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54660616 | ||||||
chr4:54660622
|
G | A | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(76): Show | 80 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.67+2541G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54660622 | ||||||
chr4:54660754
|
G | T | 57 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(54): Show | 59 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.67+2673G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54660754 | ||||||
chr4:54660796
|
G | T | 148 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(145): Show | 151 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.67+2715G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54660796 | ||||||
chr4:54660854
|
T | G | 11 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0001g0249others(8): Show | 12 | HG01243.hp1 HG01891.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.67+2773T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54660854 | ||||||
chr4:54660899
|
A | G | 58 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(55): Show | 60 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.67+2818A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54660899 | ||||||
chr4:54661069
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.67+2988G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54661069 | ||||||
chr4:54661070
|
T | G | 1 | a0001c0001t0001g0143 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.67+2989T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54661070 | ||||||
chr4:54661208
|
T | C | 148 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(145): Show | 151 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.67+3127T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54661208 | ||||||
chr4:54661281
|
A | G | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.67+3200A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54661281 | ||||||
chr4:54661461
|
G | A | 22 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(19): Show | 22 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.67+3380G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54661461 | ||||||
chr4:54661619
|
C | G | 1 | a0001c0001t0001g0242 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67+3538C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54661619 | ||||||
chr4:54661795
|
T | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0143a0001c0001t0001g0147others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+3714T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54661795 | ||||||
chr4:54661820
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.67+3739A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54661820 | ||||||
chr4:54661913
|
C | T | 8 | a0001c0001t0002g0138a0001c0003t0001g0135a0001c0005t0003g0136others(5): Show | 8 | HG01255.hp2 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+3832C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54661913 | ||||||
chr4:54662125
|
T | A | 3 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0002g0153 | 3 | HG02040.hp2 HG02129.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.67+4044T>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54662125 | ||||||
chr4:54662141
|
G | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(2): Show | 5 | HG01070.hp2 HG01109.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+4060G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54662141 | ||||||
chr4:54662198
|
G | T | 1 | a0002c0002t0003g0129 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.67+4117G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54662198 | ||||||
chr4:54662421
|
C | T | 1 | a0001c0001t0005g0074 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.67+4340C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54662421 | ||||||
chr4:54662487
|
G | T | 52 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(49): Show | 52 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.67+4406G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54662487 | ||||||
chr4:54662697
|
T | C | 1 | a0001c0001t0007g0078 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.67+4616T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54662697 | ||||||
chr4:54662995
|
A | G | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(76): Show | 80 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.67+4914A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54662995 | ||||||
chr4:54662997
|
A | AG | 10 | a0001c0001t0001g0016a0001c0001t0001g0143a0001c0001t0001g0147others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+4916_67+4917ins others(1): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54662997 | ||||||
chr4:54663033
|
T | TA | 148 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(145): Show | 151 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.67+4954dupA | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54663033 | |||||
chr4:54663104
|
A | C | 71 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(68): Show | 72 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.67+5023A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54663104 | ||||||
chr4:54663218
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.67+5137C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54663218 | ||||||
chr4:54663243
|
G | C | 148 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(145): Show | 151 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.67+5162G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54663243 | ||||||
chr4:54663534
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.67+5453G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54663534 | ||||||
chr4:54663600
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.67+5519A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54663600 | ||||||
chr4:54663778
|
A | G | 4 | a0001c0003t0001g0258a0001c0006t0006g0255a0001c0006t0006g0256others(1): Show | 4 | HG02572.hp1 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+5697A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54663778 | ||||||
chr4:54663971
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.67+5890G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54663971 | ||||||
chr4:54664203
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.67+6122C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54664203 | ||||||
chr4:54664582
|
A | ATTAT | 31 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0001g0056others(28): Show | 32 | HG00280.hp1 HG01106.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.67+6542_67+6545dup others(4): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54664582 | |||||
chr4:54664582
|
A | ATTATTTA others(1): Show |
3 | a0001c0001t0001g0239a0001c0001t0001g0240a0004c0010t0008g0253 | 3 | HG03540.hp1 NA18988.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.67+6538_67+6545dup others(8): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54664582 | |||||
chr4:54664582
|
ATTAT | A | 36 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(33): Show | 37 | HG00741.hp2 HG01175.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.67+6542_67+6545del others(4): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54664582 | |||||
chr4:54664582
|
ATTATTTA others(1): Show |
A | 96 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(93): Show | 97 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.67+6538_67+6545del others(8): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54664582 | |||||
chr4:54664582
|
ATTATTTA others(5): Show |
A | 4 | a0001c0001t0001g0158a0001c0001t0005g0156a0001c0001t0005g0157others(1): Show | 4 | HG02630.hp2 HG02976.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+6534_67+6545del others(12): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54664582 | |||||
chr4:54664582
|
ATTATTTA others(9): Show |
A | 3 | a0001c0006t0006g0255a0001c0006t0006g0256a0001c0013t0001g0257 | 3 | HG02572.hp1 HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.67+6530_67+6545del others(16): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54664582 | |||||
chr4:54664715
|
C | T | 58 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(55): Show | 60 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.67+6634C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54664715 | ||||||
chr4:54664881
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.67+6800C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54664881 | ||||||
chr4:54664889
|
G | GT | 6 | a0001c0001t0001g0037a0001c0001t0001g0069a0001c0003t0004g0259others(3): Show | 6 | HG02451.hp1 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.67+6822dupT | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54664889 | |||||
chr4:54664889
|
GT | G | 61 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(58): Show | 63 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.67+6822delT | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54664889 | |||||
chr4:54664950
|
T | C | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(76): Show | 80 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.67+6869T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54664950 | ||||||
chr4:54664955
|
G | A | 10 | a0001c0001t0001g0016a0001c0001t0001g0143a0001c0001t0001g0147others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+6874G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54664955 | ||||||
chr4:54665039
|
G | C | 1 | a0001c0001t0014g0144 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.67+6958G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54665039 | ||||||
chr4:54665173
|
C | T | 1 | a0001c0001t0001g0219 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.67+7092C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54665173 | ||||||
chr4:54665292
|
A | G | 4 | a0001c0003t0004g0259a0001c0003t0004g0260a0001c0003t0004g0261others(1): Show | 4 | HG02615.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+7211A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54665292 | ||||||
chr4:54665369
|
A | G | 1 | a0002c0002t0003g0017 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.67+7288A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54665369 | ||||||
chr4:54665514
|
C | T | 58 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(55): Show | 60 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.67+7433C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54665514 | ||||||
chr4:54665548
|
G | A | 1 | a0001c0001t0007g0078 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.67+7467G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54665548 | ||||||
chr4:54665709
|
T | C | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(76): Show | 80 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.67+7628T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54665709 | ||||||
chr4:54665884
|
T | C | 1 | a0001c0003t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.67+7803T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54665884 | ||||||
chr4:54666279
|
T | G | 1 | a0001c0001t0001g0162 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.67+8198T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54666279 | ||||||
chr4:54666282
|
T | A | 58 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(55): Show | 60 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.67+8201T>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54666282 | ||||||
chr4:54666310
|
T | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0055 | 2 | NA19072.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.67+8229T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54666310 | ||||||
chr4:54666382
|
T | A | 138 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(135): Show | 141 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.67+8301T>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54666382 | ||||||
chr4:54666675
|
A | C | 1 | a0001c0001t0001g0242 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.67+8594A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54666675 | ||||||
chr4:54666709
|
A | G | 3 | a0001c0006t0006g0255a0001c0006t0006g0256a0001c0013t0001g0257 | 3 | HG02572.hp1 HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.67+8628A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54666709 | ||||||
chr4:54666891
|
G | T | 4 | a0001c0003t0001g0258a0001c0006t0006g0255a0001c0006t0006g0256others(1): Show | 4 | HG02572.hp1 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+8810G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54666891 | ||||||
chr4:54666892
|
A | T | 4 | a0001c0003t0001g0258a0001c0006t0006g0255a0001c0006t0006g0256others(1): Show | 4 | HG02572.hp1 HG02818.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+8811A>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54666892 | ||||||
chr4:54666950
|
C | T | 58 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(55): Show | 60 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.67+8869C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54666950 | ||||||
chr4:54667123
|
C | T | 1 | a0001c0004t0001g0114 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.67+9042C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54667123 | ||||||
chr4:54667385
|
T | G | 58 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(55): Show | 60 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.67+9304T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54667385 | ||||||
chr4:54667417
|
G | A | 58 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(55): Show | 60 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.67+9336G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54667417 | ||||||
chr4:54667421
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.67+9340A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54667421 | ||||||
chr4:54667455
|
A | T | 58 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(55): Show | 60 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.67+9374A>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54667455 | ||||||
chr4:54667488
|
G | A | 9 | a0001c0001t0001g0254a0001c0003t0001g0258a0001c0003t0004g0259others(6): Show | 9 | HG01123.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.67+9407G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54667488 | ||||||
chr4:54667558
|
T | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0163 | 2 | HG01168.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.67+9477T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54667558 | ||||||
chr4:54667627
|
C | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(11): Show | 14 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.67+9546C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54667627 | ||||||
chr4:54667654
|
C | T | 10 | a0001c0001t0001g0016a0001c0001t0001g0143a0001c0001t0001g0147others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.67+9573C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54667654 | ||||||
chr4:54667655
|
G | C | 1 | a0001c0001t0001g0164 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.67+9574G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54667655 | ||||||
chr4:54667717
|
TTCCTGCA others(18): Show |
T | 1 | a0001c0001t0001g0163 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.67+9638_67+9662del others(25): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54667717 | |||||
chr4:54667823
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.67+9742T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54667823 | ||||||
chr4:54667940
|
C | A | 1 | a0001c0009t0001g0015 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.67+9859C>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54667940 | ||||||
chr4:54667984
|
C | T | 3 | a0001c0001t0001g0113a0001c0001t0002g0111a0001c0001t0002g0112 | 3 | HG00735.hp1 HG00738.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.67+9903C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54667984 | ||||||
chr4:54668367
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.67+10286C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54668367 | ||||||
chr4:54668368
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.67+10287G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54668368 | ||||||
chr4:54668452
|
A | T | 1 | a0001c0003t0003g0054 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.67+10371A>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54668452 | ||||||
chr4:54668733
|
T | C | 16 | a0001c0001t0001g0016a0001c0001t0001g0143a0001c0001t0001g0147others(13): Show | 16 | HG01123.hp1 HG02145.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.67+10652T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54668733 | ||||||
chr4:54668767
|
A | G | 57 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(54): Show | 59 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.67+10686A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54668767 | ||||||
chr4:54669150
|
A | T | 81 | a0001c0001t0001g0016a0001c0001t0001g0081a0001c0001t0001g0082others(78): Show | 83 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.67+11069A>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54669150 | ||||||
chr4:54669170
|
G | A | 174 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(171): Show | 179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.67+11089G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54669170 | ||||||
chr4:54669180
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.67+11099G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54669180 | ||||||
chr4:54669184
|
C | G | 1 | a0001c0001t0002g0218 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.67+11103C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54669184 | ||||||
chr4:54669211
|
A | AC | 14 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0037others(11): Show | 14 | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+11140dupC | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54669211 | |||||
chr4:54669211
|
AC | A | 74 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0041others(71): Show | 76 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.67+11140delC | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54669211 | |||||
chr4:54669219
|
C | G | 8 | a0001c0001t0002g0138a0001c0003t0001g0135a0001c0005t0003g0136others(5): Show | 8 | HG01255.hp2 HG01884.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.67+11138C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54669219 | ||||||
chr4:54669291
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0001g0226 | 2 | NA18962.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.67+11210G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54669291 | ||||||
chr4:54669419
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.67+11338C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54669419 | ||||||
chr4:54669480
|
G | T | 1 | a0001c0003t0004g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.67+11399G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54669480 | ||||||
chr4:54669705
|
GAA | G | 104 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(101): Show | 106 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.67+11638_67+11639d others(4): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54669705 | |||||
chr4:54669837
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.67+11756G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54669837 | ||||||
chr4:54670109
|
A | G | 4 | a0001c0003t0004g0259a0001c0003t0004g0260a0001c0003t0004g0261others(1): Show | 4 | HG02615.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.67+12028A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54670109 | ||||||
chr4:54670209
|
T | G | 104 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(101): Show | 106 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.67+12128T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54670209 | ||||||
chr4:54670259
|
C | T | 1 | a0002c0002t0003g0129 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.67+12178C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54670259 | ||||||
chr4:54670441
|
A | G | 1 | a0001c0001t0001g0240 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.67+12360A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54670441 | ||||||
chr4:54670848
|
T | C | 113 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(110): Show | 115 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.67+12767T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54670848 | ||||||
chr4:54670975
|
ATAATAAC others(5): Show |
A | 56 | a0001c0001t0001g0016a0001c0001t0001g0083a0001c0001t0001g0084others(53): Show | 58 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.67+12905_67+12916d others(14): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54670975 | |||||
chr4:54671107
|
C | T | 7 | a0001c0001t0001g0254a0001c0003t0004g0259a0001c0003t0004g0260others(4): Show | 7 | HG01123.hp1 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+13026C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54671107 | ||||||
chr4:54671123
|
G | A | 1 | a0002c0002t0003g0146 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.67+13042G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54671123 | ||||||
chr4:54671262
|
A | G | 1 | a0002c0002t0003g0017 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.67+13181A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54671262 | ||||||
chr4:54671315
|
C | G | 56 | a0001c0001t0001g0016a0001c0001t0001g0083a0001c0001t0001g0084others(53): Show | 58 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.67+13234C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54671315 | ||||||
chr4:54671470
|
A | C | 4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(1): Show | 4 | HG02165.hp1 HG04204.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+13389A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54671470 | ||||||
chr4:54671481
|
A | C | 49 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(46): Show | 49 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.67+13400A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54671481 | ||||||
chr4:54671664
|
G | A | 1 | a0001c0003t0004g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.67+13583G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54671664 | ||||||
chr4:54671900
|
T | C | 14 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(11): Show | 14 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.67+13819T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54671900 | ||||||
chr4:54672070
|
A | G | 1 | a0001c0003t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.67+13989A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54672070 | ||||||
chr4:54672181
|
G | C | 56 | a0001c0001t0001g0016a0001c0001t0001g0083a0001c0001t0001g0084others(53): Show | 58 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.67+14100G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54672181 | ||||||
chr4:54672245
|
G | A | 1 | a0001c0003t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.67+14164G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54672245 | ||||||
chr4:54672305
|
A | ATT | 49 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(46): Show | 49 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.67+14233_67+14234d others(4): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54672305 | |||||
chr4:54672314
|
T | TTTC | 56 | a0001c0001t0001g0016a0001c0001t0001g0083a0001c0001t0001g0084others(53): Show | 58 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.67+14234_67+14235i others(5): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54672314 | |||||
chr4:54672339
|
G | T | 1 | a0001c0001t0002g0218 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.67+14258G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54672339 | ||||||
chr4:54672360
|
T | C | 5 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0009g0120others(2): Show | 5 | HG00639.hp1 HG01175.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.67+14279T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54672360 | ||||||
chr4:54672406
|
C | T | 9 | a0001c0001t0002g0138a0001c0001t0007g0078a0001c0003t0001g0135others(6): Show | 9 | HG01255.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+14325C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54672406 | ||||||
chr4:54672548
|
C | G | 1 | a0001c0003t0003g0080 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.67+14467C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54672548 | ||||||
chr4:54672714
|
T | C | 104 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(101): Show | 106 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.67+14633T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54672714 | ||||||
chr4:54672745
|
C | G | 40 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(37): Show | 40 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.67+14664C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54672745 | ||||||
chr4:54673087
|
A | G | 97 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(94): Show | 99 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.67+15006A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54673087 | ||||||
chr4:54673098
|
C | T | 106 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(103): Show | 108 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.67+15017C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54673098 | ||||||
chr4:54673452
|
T | G | 1 | a0001c0001t0007g0078 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.67+15371T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54673452 | ||||||
chr4:54673456
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.67+15375T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54673456 | ||||||
chr4:54673514
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.67+15433A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54673514 | ||||||
chr4:54673707
|
G | A | 1 | a0001c0003t0001g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.67+15626G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54673707 | ||||||
chr4:54673747
|
C | G | 2 | a0001c0001t0002g0216a0001c0001t0002g0217 | 2 | NA18950.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.67+15666C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54673747 | ||||||
chr4:54673816
|
C | CATTTT | 4 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0173others(1): Show | 4 | HG00639.hp2 HG01081.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.67+15751_67+15755d others(7): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54673816 | |||||
chr4:54673895
|
G | A | 8 | a0001c0001t0001g0016a0001c0001t0001g0143a0001c0001t0001g0147others(5): Show | 8 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.67+15814G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54673895 | ||||||
chr4:54673982
|
A | T | 46 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(43): Show | 46 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.67+15901A>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54673982 | ||||||
chr4:54674125
|
C | G | 1 | a0001c0001t0001g0215 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.67+16044C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54674125 | ||||||
chr4:54674334
|
G | A | 1 | a0002c0002t0003g0146 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.67+16253G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54674334 | ||||||
chr4:54674410
|
G | C | 1 | a0001c0003t0001g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.67+16329G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54674410 | ||||||
chr4:54674452
|
T | G | 1 | a0001c0003t0001g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.67+16371T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54674452 | ||||||
chr4:54674489
|
CTG | C | 5 | a0001c0003t0004g0118a0001c0003t0004g0259a0001c0003t0004g0260others(2): Show | 5 | HG02615.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+16410_67+16411d others(4): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54674489 | |||||
chr4:54674635
|
A | G | 39 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(36): Show | 39 | HG00423.hp1 HG00544.hp1 HG01257.hp2 others(36): Show |
intron_variant | MODIFIER | c.67+16554A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54674635 | ||||||
chr4:54674794
|
C | T | 7 | a0001c0001t0002g0138a0001c0005t0003g0136a0001c0005t0003g0141others(4): Show | 7 | HG01255.hp2 HG01884.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.67+16713C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54674794 | ||||||
chr4:54674795
|
G | A | 1 | a0001c0001t0014g0144 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.67+16714G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54674795 | ||||||
chr4:54674807
|
A | G | 10 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0001g0249others(7): Show | 11 | HG01891.hp2 HG02572.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.67+16726A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54674807 | ||||||
chr4:54674975
|
G | A | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.67+16894G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54674975 | ||||||
chr4:54674999
|
C | T | 39 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(36): Show | 39 | HG00423.hp1 HG00544.hp1 HG01257.hp2 others(36): Show |
intron_variant | MODIFIER | c.67+16918C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54674999 | ||||||
chr4:54675005
|
A | AT | 13 | a0001c0001t0001g0035a0001c0001t0001g0244a0001c0001t0001g0247others(10): Show | 14 | HG01891.hp2 HG02572.hp2 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.67+16930dupT | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54675005 | |||||
chr4:54675012
|
C | A | 5 | a0001c0003t0004g0118a0001c0003t0004g0259a0001c0003t0004g0260others(2): Show | 5 | HG02615.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.67+16931C>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54675012 | ||||||
chr4:54675242
|
G | A | 108 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(105): Show | 110 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.67+17161G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54675242 | ||||||
chr4:54675388
|
G | A | 1 | a0001c0003t0003g0049 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.67+17307G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54675388 | ||||||
chr4:54675713
|
T | C | 154 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.67+17632T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54675713 | ||||||
chr4:54675746
|
G | A | 40 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(37): Show | 40 | HG00423.hp1 HG00544.hp1 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.67+17665G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54675746 | ||||||
chr4:54676156
|
G | C | 40 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(37): Show | 40 | HG00423.hp1 HG00544.hp1 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.67+18075G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54676156 | ||||||
chr4:54676265
|
ACT | A | 40 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(37): Show | 40 | HG00423.hp1 HG00544.hp1 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.67+18187_67+18188d others(4): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54676265 | |||||
chr4:54676424
|
C | T | 2 | a0001c0004t0001g0052a0001c0004t0001g0053 | 2 | HG01168.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.67+18343C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54676424 | ||||||
chr4:54676429
|
A | G | 9 | a0001c0001t0001g0085a0001c0001t0001g0103a0001c0001t0001g0104others(6): Show | 9 | HG01099.hp2 HG01433.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.67+18348A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54676429 | ||||||
chr4:54676642
|
T | TCCTA | 40 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(37): Show | 40 | HG00423.hp1 HG00544.hp1 HG01257.hp2 others(37): Show |
intron_variant | MODIFIER | c.67+18564_67+18567d others(6): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54676642 | |||||
chr4:54676662
|
G | T | 45 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(42): Show | 45 | HG00423.hp1 HG00544.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.67+18581G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54676662 | ||||||
chr4:54676703
|
G | A | 45 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(42): Show | 45 | HG00423.hp1 HG00544.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.67+18622G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54676703 | ||||||
chr4:54676732
|
C | G | 45 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(42): Show | 45 | HG00423.hp1 HG00544.hp1 HG01257.hp2 others(42): Show |
intron_variant | MODIFIER | c.67+18651C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54676732 | ||||||
chr4:54676899
|
C | T | 46 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(43): Show | 46 | HG00423.hp1 HG00544.hp1 HG01257.hp2 others(43): Show |
intron_variant | MODIFIER | c.68-18613C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54676899 | ||||||
chr4:54676911
|
G | A | 1 | a0001c0009t0001g0145 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.68-18601G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54676911 | ||||||
chr4:54677035
|
T | C | 2 | a0001c0001t0001g0171a0001c0007t0001g0172 | 2 | HG01081.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.68-18477T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54677035 | ||||||
chr4:54677072
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG02080.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.68-18440G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54677072 | ||||||
chr4:54677249
|
C | T | 36 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0025others(33): Show | 36 | HG00423.hp1 HG00544.hp1 HG01257.hp2 others(33): Show |
intron_variant | MODIFIER | c.68-18263C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54677249 | ||||||
chr4:54677349
|
C | T | 3 | a0001c0006t0006g0255a0001c0006t0006g0256a0001c0013t0001g0257 | 3 | HG02572.hp1 HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.68-18163C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54677349 | ||||||
chr4:54677502
|
A | T | 9 | a0001c0001t0001g0016a0001c0001t0001g0143a0001c0001t0001g0147others(6): Show | 9 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-18010A>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54677502 | ||||||
chr4:54677535
|
G | A | 38 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0025others(35): Show | 38 | HG00423.hp1 HG00544.hp1 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.68-17977G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54677535 | ||||||
chr4:54677655
|
T | C | 1 | a0002c0002t0003g0129 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.68-17857T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54677655 | ||||||
chr4:54677668
|
C | T | 38 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0025others(35): Show | 38 | HG00423.hp1 HG00544.hp1 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.68-17844C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54677668 | ||||||
chr4:54677763
|
T | G | 38 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0025others(35): Show | 38 | HG00423.hp1 HG00544.hp1 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.68-17749T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54677763 | ||||||
chr4:54677987
|
T | C | 2 | a0001c0001t0001g0056a0005c0011t0011g0050 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.68-17525T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54677987 | ||||||
chr4:54678152
|
G | A | 12 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0075others(9): Show | 12 | HG02129.hp1 HG02145.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.68-17360G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54678152 | ||||||
chr4:54678224
|
T | A | 1 | a0001c0001t0002g0180 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.68-17288T>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54678224 | ||||||
chr4:54678229
|
C | G | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG02080.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.68-17283C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54678229 | ||||||
chr4:54678255
|
T | TCTTCATA others(9): Show |
31 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0025others(28): Show | 31 | HG00544.hp1 HG01257.hp2 HG02080.hp1 others(28): Show |
intron_variant | MODIFIER | c.68-17244_68-17243i others(18): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678255 | |||||
chr4:54678290
|
C | CTCCT | 9 | a0001c0001t0001g0007a0001c0001t0001g0163a0001c0001t0001g0226others(6): Show | 9 | HG01168.hp2 HG02004.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-17162_68-17159d others(6): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678290 | |||||
chr4:54678290
|
CTCCT | C | 30 | a0001c0001t0001g0005a0001c0001t0001g0062a0001c0001t0001g0064others(27): Show | 32 | HG00280.hp2 HG00735.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.68-17162_68-17159d others(6): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678290 | |||||
chr4:54678290
|
CTCCTTCC others(1): Show |
C | 19 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0059others(16): Show | 19 | HG00423.hp1 HG00597.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.68-17166_68-17159d others(10): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678290 | |||||
chr4:54678290
|
CTCCTTCC others(5): Show |
C | 8 | a0001c0001t0001g0061a0001c0001t0001g0169a0001c0001t0001g0243others(5): Show | 8 | HG00140.hp1 HG01496.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-17170_68-17159d others(14): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678290 | |||||
chr4:54678290
|
CTCCTTCC others(9): Show |
C | 6 | a0001c0001t0001g0056a0001c0001t0001g0239a0001c0001t0001g0240others(3): Show | 6 | HG01099.hp1 HG01891.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-17174_68-17159d others(18): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678290 | |||||
chr4:54678290
|
CTCCTTCC others(13): Show |
C | 4 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0229others(1): Show | 4 | HG03209.hp2 HG03579.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-17178_68-17159d others(22): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678290 | |||||
chr4:54678290
|
CTCCTTCC others(17): Show |
C | 12 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(9): Show | 12 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.68-17182_68-17159d others(26): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678290 | |||||
chr4:54678290
|
CTCCTTCC others(21): Show |
C | 1 | a0001c0003t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.68-17186_68-17159d others(30): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678290 | |||||
chr4:54678318
|
TTCCTTCC others(29): Show |
T | 30 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0025others(27): Show | 30 | HG00544.hp1 HG00639.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.68-17190_68-17155d others(38): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678318 | |||||
chr4:54678326
|
TTCCTTCC others(21): Show |
T | 1 | a0001c0001t0001g0016 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.68-17182_68-17155d others(30): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678326 | |||||
chr4:54678330
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.68-17182T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54678330 | ||||||
chr4:54678330
|
TTCCTTCC others(17): Show |
T | 7 | a0001c0001t0001g0143a0001c0001t0001g0147a0001c0001t0001g0150others(4): Show | 7 | HG01243.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.68-17178_68-17155d others(26): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678330 | |||||
chr4:54678334
|
TTCCTTCC others(13): Show |
T | 1 | a0001c0001t0007g0246 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.68-17174_68-17155d others(22): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678334 | |||||
chr4:54678338
|
T | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0121a0001c0001t0002g0181 | 3 | HG02698.hp2 HG03831.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.68-17174T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54678338 | ||||||
chr4:54678338
|
TTCCTTCC others(9): Show |
T | 2 | a0001c0003t0003g0149a0001c0009t0001g0015 | 2 | HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.68-17170_68-17155d others(18): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678338 | |||||
chr4:54678342
|
T | C | 11 | a0001c0001t0001g0021a0001c0001t0001g0042a0001c0001t0001g0048others(8): Show | 12 | HG00140.hp2 HG01109.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.68-17170T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54678342 | ||||||
chr4:54678342
|
TTCCTTCC others(5): Show |
T | 2 | a0001c0001t0001g0043a0001c0001t0002g0181 | 2 | HG03831.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.68-17166_68-17155d others(14): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678342 | |||||
chr4:54678342
|
TTCCTTCC others(9): Show |
T | 2 | a0001c0006t0006g0255a0001c0006t0006g0256 | 2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.68-17166_68-17151d others(18): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678342 | |||||
chr4:54678342
|
TTCCTTCC others(13): Show |
T | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.68-17166_68-17147d others(22): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678342 | |||||
chr4:54678343
|
T | C | 2 | a0001c0001t0002g0111a0001c0001t0002g0112 | 2 | HG00735.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.68-17169T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54678343 | ||||||
chr4:54678346
|
T | C | 22 | a0001c0001t0001g0022a0001c0001t0001g0040a0001c0001t0001g0041others(19): Show | 22 | HG00741.hp2 HG01099.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.68-17166T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54678346 | ||||||
chr4:54678346
|
TTCCTTCC others(1): Show |
T | 14 | a0001c0001t0001g0021a0001c0001t0001g0042a0001c0001t0001g0048others(11): Show | 15 | HG00140.hp2 HG01109.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.68-17162_68-17155d others(10): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678346 | |||||
chr4:54678350
|
T | C | 41 | a0001c0001t0001g0058a0001c0001t0001g0072a0001c0001t0001g0083others(38): Show | 43 | HG00280.hp1 HG01070.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.68-17162T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54678350 | ||||||
chr4:54678350
|
T | TTCCTTCC others(1): Show |
2 | a0001c0001t0001g0102a0001c0007t0001g0101 | 2 | HG01123.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.68-17159_68-17158i others(10): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678350 | |||||
chr4:54678350
|
TTCCC | T | 22 | a0001c0001t0001g0022a0001c0001t0001g0040a0001c0001t0001g0041others(19): Show | 22 | HG00741.hp2 HG01099.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.68-17137_68-17134d others(6): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678350 | |||||
chr4:54678354
|
C | CTCCT | 11 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0126others(8): Show | 12 | HG00735.hp1 HG00738.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.68-17155_68-17154i others(6): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678354 | |||||
chr4:54678354
|
C | T | 31 | a0001c0001t0001g0058a0001c0001t0001g0072a0001c0001t0001g0083others(28): Show | 32 | HG00280.hp1 HG01070.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.68-17158C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54678354 | ||||||
chr4:54678406
|
TCCTTCAC others(4): Show |
T | 33 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0025others(30): Show | 33 | HG00544.hp1 HG00639.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.68-17101_68-17091d others(13): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54678406 | |||||
chr4:54678414
|
G | A | 14 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0090others(11): Show | 14 | HG01070.hp1 HG01071.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-17098G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54678414 | ||||||
chr4:54678891
|
T | C | 1 | a0001c0001t0002g0180 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.68-16621T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54678891 | ||||||
chr4:54678981
|
G | T | 1 | a0001c0001t0001g0225 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.68-16531G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54678981 | ||||||
chr4:54679254
|
C | T | 2 | a0001c0001t0005g0074a0001c0003t0003g0049 | 2 | HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.68-16258C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54679254 | ||||||
chr4:54679353
|
G | A | 1 | a0001c0001t0002g0182 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.68-16159G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54679353 | ||||||
chr4:54679357
|
A | G | 1 | a0001c0001t0001g0239 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.68-16155A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54679357 | ||||||
chr4:54679549
|
G | A | 1 | a0001c0007t0001g0101 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.68-15963G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54679549 | ||||||
chr4:54679860
|
A | G | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.68-15652A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54679860 | ||||||
chr4:54680039
|
T | G | 1 | a0001c0001t0001g0231 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.68-15473T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54680039 | ||||||
chr4:54680120
|
A | G | 1 | a0001c0001t0002g0179 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.68-15392A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54680120 | ||||||
chr4:54680292
|
G | GT | 20 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0001g0096others(17): Show | 22 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.68-15217dupT | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54680292 | |||||
chr4:54680334
|
C | T | 1 | a0001c0001t0002g0068 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.68-15178C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54680334 | ||||||
chr4:54680385
|
C | CT | 30 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0025others(27): Show | 30 | HG00423.hp2 HG01243.hp1 HG01516.hp2 others(27): Show |
intron_variant | MODIFIER | c.68-15107dupT | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54680385 | |||||
chr4:54680385
|
C | CTT | 46 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(43): Show | 46 | HG00544.hp1 HG01257.hp2 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.68-15108_68-15107d others(4): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54680385 | |||||
chr4:54680385
|
CT | C | 10 | a0001c0001t0001g0089a0001c0001t0001g0096a0001c0001t0001g0161others(7): Show | 10 | HG01070.hp1 HG01070.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.68-15107delT | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54680385 | |||||
chr4:54680406
|
A | T | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(76): Show | 80 | HG00544.hp1 HG01243.hp1 HG01257.hp2 others(77): Show |
intron_variant | MODIFIER | c.68-15106A>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54680406 | ||||||
chr4:54680518
|
A | G | 8 | a0001c0001t0001g0016a0001c0001t0001g0143a0001c0001t0001g0147others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-14994A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54680518 | ||||||
chr4:54680549
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.68-14963G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54680549 | ||||||
chr4:54680552
|
C | T | 2 | a0001c0003t0001g0006a0001c0012t0002g0250 | 3 | HG02896.hp1 HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.68-14960C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54680552 | ||||||
chr4:54680567
|
A | G | 14 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0075others(11): Show | 14 | HG02129.hp1 HG02145.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.68-14945A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54680567 | ||||||
chr4:54680645
|
G | A | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.68-14867G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54680645 | ||||||
chr4:54680683
|
G | A | 2 | a0001c0001t0005g0074a0001c0003t0003g0049 | 2 | HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.68-14829G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54680683 | ||||||
chr4:54680758
|
C | T | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.68-14754C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54680758 | ||||||
chr4:54680793
|
G | C | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.68-14719G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54680793 | ||||||
chr4:54680806
|
C | T | 2 | a0001c0001t0001g0164a0001c0001t0002g0159 | 2 | HG04199.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.68-14706C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54680806 | ||||||
chr4:54680824
|
C | T | 3 | a0001c0006t0006g0255a0001c0006t0006g0256a0001c0013t0001g0257 | 3 | HG02572.hp1 HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.68-14688C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54680824 | ||||||
chr4:54680832
|
A | G | 167 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(164): Show | 171 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.68-14680A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54680832 | ||||||
chr4:54680957
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.68-14555C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54680957 | ||||||
chr4:54681006
|
G | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0038 | 2 | HG00423.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.68-14506G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54681006 | ||||||
chr4:54681124
|
A | G | 1 | a0001c0016t0001g0137 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.68-14388A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54681124 | ||||||
chr4:54681135
|
C | T | 1 | a0002c0002t0003g0017 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.68-14377C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54681135 | ||||||
chr4:54681214
|
T | C | 165 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(162): Show | 169 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(166): Show |
intron_variant | MODIFIER | c.68-14298T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54681214 | ||||||
chr4:54681251
|
A | C | 1 | a0001c0001t0001g0168 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.68-14261A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54681251 | ||||||
chr4:54681356
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.68-14156T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54681356 | ||||||
chr4:54681357
|
T | A | 1 | a0001c0001t0001g0188 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.68-14155T>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54681357 | ||||||
chr4:54681359
|
T | G | 1 | a0001c0001t0001g0188 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.68-14153T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54681359 | ||||||
chr4:54681360
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.68-14152G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54681360 | ||||||
chr4:54681362
|
T | A | 1 | a0001c0001t0001g0188 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.68-14150T>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54681362 | ||||||
chr4:54681364
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.68-14148A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54681364 | ||||||
chr4:54681365
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.68-14147G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54681365 | ||||||
chr4:54681366
|
G | C | 1 | a0001c0001t0001g0188 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.68-14146G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54681366 | ||||||
chr4:54681367
|
G | A | 68 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(65): Show | 69 | HG00544.hp1 HG01257.hp2 HG01884.hp1 others(66): Show |
intron_variant | MODIFIER | c.68-14145G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54681367 | ||||||
chr4:54681371
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.68-14141G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54681371 | ||||||
chr4:54681372
|
A | T | 1 | a0001c0001t0001g0188 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.68-14140A>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54681372 | ||||||
chr4:54681811
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.68-13701G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54681811 | ||||||
chr4:54681849
|
GGC | G | 3 | a0001c0001t0001g0164a0001c0001t0002g0159a0001c0001t0002g0197 | 3 | HG03017.hp1 HG04199.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.68-13662_68-13661d others(4): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54681849 | ||||||
chr4:54682090
|
C | CT | 10 | a0001c0001t0001g0027a0001c0001t0001g0048a0001c0001t0001g0210others(7): Show | 11 | HG00544.hp2 HG02055.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.68-13405dupT | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54682090 | |||||
chr4:54682090
|
C | CTT | 41 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0025others(38): Show | 41 | HG00544.hp1 HG01257.hp2 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.68-13406_68-13405d others(4): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54682090 | |||||
chr4:54682090
|
CT | C | 5 | a0001c0001t0001g0089a0001c0001t0001g0097a0001c0001t0001g0183others(2): Show | 5 | HG00423.hp2 HG01074.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-13405delT | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54682090 | |||||
chr4:54682092
|
T | TTC | 18 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(15): Show | 18 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.68-13419_68-13418i others(4): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54682092 | |||||
chr4:54682250
|
T | C | 167 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(164): Show | 171 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.68-13262T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54682250 | ||||||
chr4:54682251
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.68-13261G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54682251 | ||||||
chr4:54682309
|
T | C | 70 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(67): Show | 71 | HG00544.hp1 HG01257.hp2 HG01884.hp1 others(68): Show |
intron_variant | MODIFIER | c.68-13203T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54682309 | ||||||
chr4:54682419
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.68-13093T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54682419 | ||||||
chr4:54682586
|
C | T | 70 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(67): Show | 71 | HG00544.hp1 HG01257.hp2 HG01884.hp1 others(68): Show |
intron_variant | MODIFIER | c.68-12926C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54682586 | ||||||
chr4:54682681
|
C | T | 11 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0001g0249others(8): Show | 12 | HG01255.hp1 HG01891.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.68-12831C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54682681 | ||||||
chr4:54682718
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.68-12794C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54682718 | ||||||
chr4:54682750
|
G | GT | 32 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0071others(29): Show | 32 | HG00544.hp2 HG00597.hp1 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.68-12745dupT | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54682750 | |||||
chr4:54682750
|
GT | G | 71 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(68): Show | 72 | HG00544.hp1 HG01074.hp2 HG01257.hp2 others(69): Show |
intron_variant | MODIFIER | c.68-12745delT | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54682750 | |||||
chr4:54682756
|
T | G | 1 | a0001c0001t0001g0212 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.68-12756T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54682756 | ||||||
chr4:54682757
|
T | G | 69 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(66): Show | 70 | HG00544.hp1 HG01257.hp2 HG01884.hp1 others(67): Show |
intron_variant | MODIFIER | c.68-12755T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54682757 | ||||||
chr4:54682769
|
G | A | 70 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(67): Show | 71 | HG00544.hp1 HG01257.hp2 HG01884.hp1 others(68): Show |
intron_variant | MODIFIER | c.68-12743G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54682769 | ||||||
chr4:54682958
|
A | G | 167 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(164): Show | 171 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.68-12554A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54682958 | ||||||
chr4:54683068
|
TGG | T | 70 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(67): Show | 71 | HG00544.hp1 HG01257.hp2 HG01884.hp1 others(68): Show |
intron_variant | MODIFIER | c.68-12441_68-12440d others(4): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54683068 | |||||
chr4:54683186
|
T | C | 70 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(67): Show | 71 | HG00544.hp1 HG01257.hp2 HG01884.hp1 others(68): Show |
intron_variant | MODIFIER | c.68-12326T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54683186 | ||||||
chr4:54683191
|
A | C | 1 | a0001c0001t0001g0165 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.68-12321A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54683191 | ||||||
chr4:54683305
|
T | C | 1 | a0001c0003t0003g0049 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.68-12207T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54683305 | ||||||
chr4:54683343
|
G | T | 22 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0029others(19): Show | 22 | HG00544.hp1 HG01257.hp2 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.68-12169G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54683343 | ||||||
chr4:54683372
|
C | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0079a0001c0001t0001g0233 | 3 | NA18942.hp1 NA18973.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.68-12140C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54683372 | ||||||
chr4:54683418
|
C | G | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.68-12094C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54683418 | ||||||
chr4:54683564
|
A | G | 6 | a0001c0003t0001g0135a0001c0003t0004g0118a0001c0003t0004g0259others(3): Show | 6 | HG02615.hp2 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-11948A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54683564 | ||||||
chr4:54683815
|
G | A | 5 | a0001c0001t0001g0190a0001c0001t0001g0198a0001c0001t0001g0219others(2): Show | 5 | NA18944.hp1 NA18973.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-11697G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54683815 | ||||||
chr4:54684091
|
G | C | 4 | a0001c0001t0001g0061a0001c0001t0001g0070a0001c0001t0001g0113others(1): Show | 4 | HG00140.hp1 HG01099.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.68-11421G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54684091 | ||||||
chr4:54684128
|
C | A | 1 | a0001c0001t0001g0188 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.68-11384C>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54684128 | ||||||
chr4:54684130
|
A | G | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.68-11382A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54684130 | ||||||
chr4:54684172
|
TGGGTG | T | 69 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(66): Show | 70 | HG00544.hp1 HG01257.hp2 HG01884.hp1 others(67): Show |
intron_variant | MODIFIER | c.68-11318_68-11314d others(7): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54684172 | |||||
chr4:54684513
|
A | G | 57 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(54): Show | 57 | HG00544.hp1 HG01257.hp2 HG01884.hp1 others(54): Show |
intron_variant | MODIFIER | c.68-10999A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54684513 | ||||||
chr4:54684527
|
A | C | 70 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(67): Show | 71 | HG00544.hp1 HG01257.hp2 HG01884.hp1 others(68): Show |
intron_variant | MODIFIER | c.68-10985A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54684527 | ||||||
chr4:54684875
|
A | G | 1 | a0001c0003t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.68-10637A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54684875 | ||||||
chr4:54684958
|
A | G | 1 | a0001c0001t0014g0144 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.68-10554A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54684958 | ||||||
chr4:54685245
|
C | A | 1 | a0002c0002t0003g0129 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.68-10267C>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54685245 | ||||||
chr4:54685593
|
C | G | 1 | a0001c0001t0002g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.68-9919C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54685593 | ||||||
chr4:54685612
|
A | T | 9 | a0001c0001t0001g0016a0001c0001t0001g0143a0001c0001t0001g0147others(6): Show | 9 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.68-9900A>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54685612 | ||||||
chr4:54685692
|
C | T | 6 | a0001c0001t0001g0075a0001c0001t0002g0001a0001c0001t0002g0077others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-9820C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54685692 | ||||||
chr4:54685749
|
G | A | 1 | a0001c0001t0013g0185 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.68-9763G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54685749 | ||||||
chr4:54685811
|
C | T | 2 | a0001c0001t0001g0251a0001c0001t0008g0252 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.68-9701C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54685811 | ||||||
chr4:54686051
|
A | G | 1 | a0002c0002t0003g0003 | 2 | NA18944.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.68-9461A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54686051 | ||||||
chr4:54686091
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.68-9421G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54686091 | ||||||
chr4:54686164
|
T | C | 49 | a0001c0001t0001g0048a0001c0001t0001g0072a0001c0001t0001g0083others(46): Show | 51 | HG00280.hp1 HG00639.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.68-9348T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54686164 | ||||||
chr4:54686219
|
T | TA | 7 | a0001c0001t0001g0170a0001c0001t0001g0178a0001c0001t0001g0228others(4): Show | 8 | HG01106.hp1 HG02451.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-9282dupA | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54686219 | |||||
chr4:54686228
|
A | AC | 8 | a0001c0001t0001g0056a0001c0001t0001g0244a0001c0001t0001g0247others(5): Show | 8 | HG01891.hp2 HG02572.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.68-9284_68-9283ins others(1): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54686228 | ||||||
chr4:54686434
|
G | C | 12 | a0001c0001t0001g0056a0001c0001t0001g0244a0001c0001t0001g0247others(9): Show | 13 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.68-9078G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54686434 | ||||||
chr4:54686670
|
G | C | 6 | a0001c0003t0001g0135a0001c0003t0004g0118a0001c0003t0004g0259others(3): Show | 6 | HG02615.hp2 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-8842G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54686670 | ||||||
chr4:54686695
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.68-8817C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54686695 | ||||||
chr4:54686719
|
AT | A | 3 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0071 | 3 | HG02165.hp1 NA18991.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.68-8787delT | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54686719 | |||||
chr4:54686880
|
A | G | 6 | a0001c0003t0001g0135a0001c0003t0004g0118a0001c0003t0004g0259others(3): Show | 6 | HG02615.hp2 HG02630.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.68-8632A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54686880 | ||||||
chr4:54686943
|
G | A | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.68-8569G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54686943 | ||||||
chr4:54687204
|
G | A | 4 | a0001c0001t0012g0014a0001c0003t0001g0006a0001c0003t0001g0258others(1): Show | 5 | HG02896.hp1 HG02897.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-8308G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54687204 | ||||||
chr4:54687305
|
A | T | 1 | a0001c0003t0003g0018 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.68-8207A>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54687305 | ||||||
chr4:54687469
|
A | G | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.68-8043A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54687469 | ||||||
chr4:54687496
|
G | A | 11 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0001g0249others(8): Show | 12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.68-8016G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54687496 | ||||||
chr4:54687635
|
T | C | 57 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(54): Show | 57 | HG00544.hp1 HG01257.hp2 HG01884.hp1 others(54): Show |
intron_variant | MODIFIER | c.68-7877T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54687635 | ||||||
chr4:54687712
|
G | A | 19 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(16): Show | 19 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.68-7800G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54687712 | ||||||
chr4:54687857
|
G | A | 12 | a0001c0001t0001g0051a0001c0001t0001g0055a0001c0001t0001g0058others(9): Show | 13 | HG00140.hp2 HG01106.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.68-7655G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54687857 | ||||||
chr4:54687989
|
G | A | 110 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0022others(107): Show | 114 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.68-7523G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54687989 | ||||||
chr4:54688043
|
A | C | 1 | a0001c0001t0007g0078 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.68-7469A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54688043 | ||||||
chr4:54688089
|
C | T | 6 | a0001c0005t0003g0136a0001c0005t0003g0141a0001c0005t0004g0140others(3): Show | 6 | HG01255.hp2 HG01884.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-7423C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54688089 | ||||||
chr4:54688165
|
T | C | 110 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0022others(107): Show | 114 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(111): Show |
intron_variant | MODIFIER | c.68-7347T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54688165 | ||||||
chr4:54688193
|
G | A | 6 | a0001c0005t0003g0136a0001c0005t0003g0141a0001c0005t0004g0140others(3): Show | 6 | HG01255.hp2 HG01884.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-7319G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54688193 | ||||||
chr4:54688323
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0208 | 2 | NA19080.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.68-7189C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54688323 | ||||||
chr4:54688355
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.68-7157A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54688355 | ||||||
chr4:54688589
|
G | A | 2 | a0001c0001t0005g0074a0001c0003t0003g0049 | 2 | HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.68-6923G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54688589 | ||||||
chr4:54688667
|
G | A | 18 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0001g0249others(15): Show | 19 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.68-6845G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54688667 | ||||||
chr4:54688816
|
G | T | 1 | a0001c0001t0001g0151 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.68-6696G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54688816 | ||||||
chr4:54688895
|
T | G | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.68-6617T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54688895 | ||||||
chr4:54689029
|
C | T | 2 | a0001c0001t0005g0074a0001c0003t0003g0049 | 2 | HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.68-6483C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54689029 | ||||||
chr4:54689118
|
C | T | 1 | a0001c0003t0001g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.68-6394C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54689118 | ||||||
chr4:54689250
|
A | G | 2 | a0001c0009t0001g0015a0001c0009t0001g0145 | 2 | HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.68-6262A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54689250 | ||||||
chr4:54689401
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.68-6111A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54689401 | ||||||
chr4:54689615
|
G | T | 1 | a0001c0001t0001g0069 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.68-5897G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54689615 | ||||||
chr4:54689628
|
A | G | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.68-5884A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54689628 | ||||||
chr4:54689712
|
A | G | 2 | a0001c0001t0001g0254a0002c0002t0003g0166 | 2 | HG00280.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.68-5800A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54689712 | ||||||
chr4:54689874
|
A | C | 167 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(164): Show | 171 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.68-5638A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54689874 | ||||||
chr4:54690034
|
G | A | 2 | a0001c0001t0002g0036a0001c0001t0002g0216 | 2 | NA18950.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.68-5478G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54690034 | ||||||
chr4:54690056
|
T | TG | 14 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(11): Show | 14 | HG02083.hp2 HG02165.hp2 HG04204.hp2 others(11): Show |
intron_variant | MODIFIER | c.68-5455dupG | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54690056 | |||||
chr4:54690057
|
G | GGT | 5 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0032others(2): Show | 5 | HG00544.hp1 HG02080.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.68-5455_68-5454ins others(2): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54690057 | ||||||
chr4:54690057
|
G | T | 1 | a0001c0001t0001g0056 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.68-5455G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54690057 | ||||||
chr4:54690058
|
T | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0032others(3): Show | 6 | HG00544.hp1 HG02080.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-5454T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54690058 | ||||||
chr4:54690058
|
T | TG | 22 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0025others(19): Show | 22 | HG00544.hp2 HG01099.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.68-5442dupG | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54690058 | |||||
chr4:54690058
|
TG | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0222a0001c0001t0001g0238others(11): Show | 16 | HG01255.hp2 HG01884.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.68-5442delG | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54690058 | |||||
chr4:54690059
|
G | T | 7 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0001g0249others(4): Show | 7 | HG01891.hp2 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-5453G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54690059 | ||||||
chr4:54690060
|
G | T | 3 | a0001c0003t0001g0006a0001c0009t0001g0145a0001c0012t0002g0250 | 4 | HG02896.hp1 HG02897.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-5452G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54690060 | ||||||
chr4:54690062
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.68-5450G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54690062 | ||||||
chr4:54690069
|
G | GT | 51 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0040others(48): Show | 53 | HG00280.hp1 HG00639.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.68-5443_68-5442ins others(1): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54690069 | ||||||
chr4:54690069
|
G | T | 17 | a0001c0001t0001g0051a0001c0001t0001g0055a0001c0001t0001g0058others(14): Show | 18 | HG00140.hp2 HG01070.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.68-5443G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54690069 | ||||||
chr4:54690091
|
T | A | 2 | a0001c0001t0005g0074a0001c0003t0003g0049 | 2 | HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.68-5421T>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54690091 | ||||||
chr4:54690339
|
C | G | 1 | a0001c0003t0003g0080 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.68-5173C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54690339 | ||||||
chr4:54690403
|
C | T | 6 | a0001c0005t0003g0136a0001c0005t0003g0141a0001c0005t0004g0140others(3): Show | 6 | HG01255.hp2 HG01884.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.68-5109C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54690403 | ||||||
chr4:54690582
|
G | C | 1 | a0001c0001t0001g0243 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.68-4930G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54690582 | ||||||
chr4:54690716
|
C | T | 1 | a0002c0002t0003g0017 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.68-4796C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54690716 | ||||||
chr4:54690779
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.68-4733G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54690779 | ||||||
chr4:54691168
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.68-4344A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54691168 | ||||||
chr4:54691265
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.68-4247C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54691265 | ||||||
chr4:54691443
|
C | A | 1 | a0001c0001t0001g0215 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.68-4069C>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54691443 | ||||||
chr4:54691472
|
G | A | 4 | a0001c0005t0004g0140a0001c0005t0004g0142a0001c0016t0001g0137others(1): Show | 4 | HG01255.hp2 HG01884.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-4040G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54691472 | ||||||
chr4:54691478
|
C | T | 8 | a0001c0001t0001g0016a0001c0001t0001g0143a0001c0001t0001g0147others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-4034C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54691478 | ||||||
chr4:54691649
|
G | C | 8 | a0001c0001t0001g0016a0001c0001t0001g0143a0001c0001t0001g0147others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.68-3863G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54691649 | ||||||
chr4:54691747
|
G | T | 1 | a0001c0001t0002g0047 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.68-3765G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54691747 | ||||||
chr4:54691818
|
A | G | 167 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(164): Show | 171 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.68-3694A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54691818 | ||||||
chr4:54692020
|
G | T | 7 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0001g0249others(4): Show | 7 | HG01891.hp2 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.68-3492G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54692020 | ||||||
chr4:54692060
|
G | C | 11 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0001g0249others(8): Show | 12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.68-3452G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54692060 | ||||||
chr4:54692200
|
A | G | 2 | a0001c0001t0005g0074a0001c0003t0003g0049 | 2 | HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.68-3312A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54692200 | ||||||
chr4:54692596
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.68-2916A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54692596 | ||||||
chr4:54692614
|
G | T | 1 | a0001c0001t0001g0254 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.68-2898G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54692614 | ||||||
chr4:54692727
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.68-2785G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54692727 | ||||||
chr4:54692738
|
C | G | 3 | a0001c0001t0001g0086a0001c0001t0009g0120a0002c0002t0010g0088 | 3 | HG00639.hp1 HG03239.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.68-2774C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54692738 | ||||||
chr4:54692745
|
C | T | 11 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0001g0249others(8): Show | 12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.68-2767C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54692745 | ||||||
chr4:54692768
|
C | T | 11 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0001g0249others(8): Show | 12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.68-2744C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54692768 | ||||||
chr4:54692811
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.68-2701G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54692811 | ||||||
chr4:54693148
|
T | C | 167 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(164): Show | 171 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.68-2364T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54693148 | ||||||
chr4:54693168
|
A | G | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.68-2344A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54693168 | ||||||
chr4:54693198
|
A | G | 2 | a0001c0001t0001g0056a0001c0001t0007g0246 | 2 | HG02886.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.68-2314A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54693198 | ||||||
chr4:54693255
|
A | G | 1 | a0001c0001t0002g0180 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.68-2257A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54693255 | ||||||
chr4:54693397
|
G | C | 167 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(164): Show | 171 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.68-2115G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54693397 | ||||||
chr4:54693580
|
A | T | 2 | a0001c0009t0001g0015a0001c0009t0001g0145 | 2 | HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.68-1932A>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54693580 | ||||||
chr4:54693682
|
C | T | 11 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0001g0249others(8): Show | 12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.68-1830C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54693682 | ||||||
chr4:54693687
|
C | CAT | 75 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0040others(72): Show | 78 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.68-1822_68-1821dup others(2): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr4 | 54693687 | |||||
chr4:54693878
|
T | C | 1 | a0001c0003t0001g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.68-1634T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54693878 | ||||||
chr4:54693974
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.68-1538C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54693974 | ||||||
chr4:54694057
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.68-1455G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54694057 | ||||||
chr4:54694154
|
G | A | 1 | a0001c0003t0003g0049 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.68-1358G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54694154 | ||||||
chr4:54694232
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.68-1280G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54694232 | ||||||
chr4:54694390
|
C | T | 17 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0001g0249others(14): Show | 18 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.68-1122C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54694390 | ||||||
chr4:54694563
|
G | A | 1 | a0001c0001t0007g0078 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.68-949G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54694563 | ||||||
chr4:54694774
|
A | G | 3 | a0001c0001t0001g0005a0001c0001t0001g0222a0001c0001t0001g0238 | 4 | HG02615.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-738A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54694774 | ||||||
chr4:54694901
|
T | C | 70 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0040others(67): Show | 73 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.68-611T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54694901 | ||||||
chr4:54694909
|
T | C | 1 | a0001c0001t0002g0099 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.68-603T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54694909 | ||||||
chr4:54694937
|
G | A | 1 | a0002c0002t0003g0124 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.68-575G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54694937 | ||||||
chr4:54695031
|
C | T | 17 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0001g0249others(14): Show | 18 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.68-481C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54695031 | ||||||
chr4:54695050
|
A | G | 1 | a0001c0003t0003g0149 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.68-462A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54695050 | ||||||
chr4:54695069
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.68-443A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54695069 | ||||||
chr4:54695091
|
A | T | 1 | a0001c0001t0001g0007 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.68-421A>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54695091 | ||||||
chr4:54695206
|
G | A | 2 | a0001c0001t0002g0179a0001c0003t0003g0054 | 2 | HG03239.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.68-306G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54695206 | ||||||
chr4:54695382
|
T | C | 7 | a0001c0001t0001g0075a0001c0003t0001g0135a0001c0003t0004g0118others(4): Show | 7 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.68-130T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 1/20 | chr4 | 54695382 | ||||||
chr4:54695966
|
A | G | 11 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0001g0249others(8): Show | 12 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.337+185A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 2/20 | chr4 | 54695966 | ||||||
chr4:54696146
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0073 | 2 | NA18947.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.337+365G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 2/20 | chr4 | 54696146 | ||||||
chr4:54696177
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.337+396A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 2/20 | chr4 | 54696177 | ||||||
chr4:54696280
|
A | G | 1 | a0001c0001t0002g0112 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.337+499A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 2/20 | chr4 | 54696280 | ||||||
chr4:54696482
|
C | T | 1 | a0001c0003t0001g0006 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.337+701C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 2/20 | chr4 | 54696482 | ||||||
chr4:54696503
|
A | G | 3 | a0001c0001t0001g0056a0001c0001t0007g0078a0001c0001t0007g0246 | 3 | HG02886.hp1 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.337+722A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 2/20 | chr4 | 54696503 | ||||||
chr4:54697188
|
C | A | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.338-1096C>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 2/20 | chr4 | 54697188 | ||||||
chr4:54697296
|
A | G | 108 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0022others(105): Show | 112 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.338-988A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 2/20 | chr4 | 54697296 | ||||||
chr4:54697311
|
A | G | 2 | a0001c0001t0005g0074a0001c0003t0003g0049 | 2 | HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.338-973A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 2/20 | chr4 | 54697311 | ||||||
chr4:54697456
|
C | T | 3 | a0002c0002t0003g0004a0002c0002t0003g0117a0002c0002t0003g0125 | 4 | HG02074.hp2 NA18955.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.338-828C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 2/20 | chr4 | 54697456 | ||||||
chr4:54697489
|
C | T | 1 | a0001c0005t0004g0142 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.338-795C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 2/20 | chr4 | 54697489 | ||||||
chr4:54697517
|
T | G | 108 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0022others(105): Show | 112 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.338-767T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 2/20 | chr4 | 54697517 | ||||||
chr4:54697755
|
C | T | 1 | a0001c0003t0004g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.338-529C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 2/20 | chr4 | 54697755 | ||||||
chr4:54697848
|
T | C | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.338-436T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 2/20 | chr4 | 54697848 | ||||||
chr4:54697883
|
C | T | 70 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0040others(67): Show | 73 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.338-401C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 2/20 | chr4 | 54697883 | ||||||
chr4:54698018
|
A | G | 245 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(242): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.338-266A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 2/20 | chr4 | 54698018 | ||||||
chr4:54698733
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.619+168C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 3/20 | chr4 | 54698733 | ||||||
chr4:54698809
|
G | C | 15 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0090others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.619+244G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 3/20 | chr4 | 54698809 | ||||||
chr4:54698826
|
C | T | 1 | a0001c0001t0007g0246 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.619+261C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 3/20 | chr4 | 54698826 | ||||||
chr4:54698846
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.619+281C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 3/20 | chr4 | 54698846 | ||||||
chr4:54698970
|
T | G | 4 | a0001c0001t0005g0074a0001c0003t0003g0049a0001c0009t0001g0015others(1): Show | 4 | HG01891.hp1 HG02647.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.619+405T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 3/20 | chr4 | 54698970 | ||||||
chr4:54699102
|
G | A | 6 | a0001c0005t0003g0136a0001c0005t0003g0141a0001c0005t0004g0140others(3): Show | 6 | HG01255.hp2 HG01884.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-528G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 3/20 | chr4 | 54699102 | ||||||
chr4:54699242
|
A | G | 161 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(158): Show | 162 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.620-388A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 3/20 | chr4 | 54699242 | ||||||
chr4:54699279
|
A | G | 13 | a0001c0001t0001g0051a0001c0001t0001g0055a0001c0001t0001g0058others(10): Show | 14 | HG00140.hp2 HG01081.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.620-351A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 3/20 | chr4 | 54699279 | ||||||
chr4:54699292
|
G | T | 1 | a0001c0001t0001g0056 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.620-338G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 3/20 | chr4 | 54699292 | ||||||
chr4:54699358
|
G | T | 2 | a0001c0001t0001g0084a0001c0001t0002g0116 | 2 | HG01074.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.620-272G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 3/20 | chr4 | 54699358 | ||||||
chr4:54699564
|
A | G | 6 | a0001c0005t0003g0136a0001c0005t0003g0141a0001c0005t0004g0140others(3): Show | 6 | HG01255.hp2 HG01884.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-66A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 3/20 | chr4 | 54699564 | ||||||
chr4:54699909
|
A | G | 77 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(74): Show | 77 | HG00544.hp1 HG00735.hp2 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.756+143A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54699909 | ||||||
chr4:54700100
|
G | A | 161 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(158): Show | 162 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.756+334G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54700100 | ||||||
chr4:54700455
|
T | C | 2 | a0001c0001t0001g0174a0001c0001t0001g0175 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.756+689T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54700455 | ||||||
chr4:54700477
|
A | C | 259 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(256): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.756+711A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54700477 | ||||||
chr4:54701034
|
C | T | 260 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(257): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.756+1268C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54701034 | ||||||
chr4:54701048
|
A | G | 153 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(150): Show | 154 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.756+1282A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54701048 | ||||||
chr4:54701196
|
G | T | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.756+1430G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54701196 | ||||||
chr4:54701226
|
T | C | 6 | a0001c0001t0001g0075a0001c0003t0004g0118a0001c0003t0004g0259others(3): Show | 6 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.756+1460T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54701226 | ||||||
chr4:54701404
|
AC | A | 10 | a0001c0001t0001g0072a0001c0001t0001g0083a0001c0001t0001g0094others(7): Show | 10 | HG00280.hp1 HG00741.hp2 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.756+1641delC | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 54701404 | |||||
chr4:54701505
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.756+1739A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54701505 | ||||||
chr4:54701640
|
A | ACT | 7 | a0001c0001t0001g0075a0001c0003t0001g0135a0001c0003t0004g0118others(4): Show | 7 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.756+1875_756+1876d others(4): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr4 | 54701640 | |||||
chr4:54701722
|
A | C | 76 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(73): Show | 77 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.756+1956A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54701722 | ||||||
chr4:54701796
|
G | C | 1 | a0001c0001t0001g0240 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.757-1928G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54701796 | ||||||
chr4:54701806
|
G | C | 6 | a0001c0005t0003g0136a0001c0005t0003g0141a0001c0005t0004g0140others(3): Show | 6 | HG01255.hp2 HG01884.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.757-1918G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54701806 | ||||||
chr4:54702063
|
A | G | 153 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(150): Show | 154 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.757-1661A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54702063 | ||||||
chr4:54702071
|
A | C | 8 | a0001c0001t0001g0016a0001c0001t0001g0143a0001c0001t0001g0147others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.757-1653A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54702071 | ||||||
chr4:54702192
|
C | T | 1 | a0002c0002t0003g0017 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.757-1532C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54702192 | ||||||
chr4:54702373
|
G | T | 70 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0040others(67): Show | 73 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.757-1351G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54702373 | ||||||
chr4:54702546
|
C | T | 77 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(74): Show | 77 | HG00544.hp1 HG00735.hp2 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.757-1178C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54702546 | ||||||
chr4:54702709
|
G | A | 2 | a0001c0009t0001g0015a0001c0009t0001g0145 | 2 | HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.757-1015G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54702709 | ||||||
chr4:54702876
|
C | A | 259 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(256): Show | 263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.757-848C>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54702876 | ||||||
chr4:54702907
|
T | G | 3 | a0001c0001t0001g0005a0001c0001t0001g0222a0001c0001t0001g0238 | 4 | HG02615.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.757-817T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54702907 | ||||||
chr4:54702980
|
T | C | 76 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(73): Show | 77 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.757-744T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54702980 | ||||||
chr4:54703166
|
G | A | 4 | a0001c0001t0001g0081a0001c0001t0001g0082a0003c0008t0001g0011others(1): Show | 4 | HG01884.hp1 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.757-558G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54703166 | ||||||
chr4:54703215
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.757-509G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54703215 | ||||||
chr4:54703385
|
C | T | 1 | a0001c0004t0001g0052 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.757-339C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54703385 | ||||||
chr4:54703444
|
C | T | 2 | a0001c0004t0001g0052a0001c0004t0001g0053 | 2 | HG01168.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.757-280C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54703444 | ||||||
chr4:54703460
|
G | A | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.757-264G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54703460 | ||||||
chr4:54703494
|
C | T | 6 | a0001c0001t0001g0091a0001c0001t0001g0096a0001c0001t0009g0092others(3): Show | 6 | HG01081.hp2 HG01123.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.757-230C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54703494 | ||||||
chr4:54703545
|
T | A | 1 | a0001c0003t0001g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.757-179T>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54703545 | ||||||
chr4:54703702
|
T | C | 1 | a0001c0003t0001g0006 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.757-22T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 4/20 | chr4 | 54703702 | ||||||
chr4:54704037
|
C | T | 6 | a0001c0005t0003g0136a0001c0005t0003g0141a0001c0005t0004g0140others(3): Show | 6 | HG01255.hp2 HG01884.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.925+145C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54704037 | ||||||
chr4:54704295
|
G | A | 38 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0029others(35): Show | 38 | HG00544.hp1 HG00735.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.925+403G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54704295 | ||||||
chr4:54704399
|
TTCTC | T | 6 | a0001c0001t0001g0143a0001c0001t0001g0147a0001c0001t0001g0150others(3): Show | 6 | HG01243.hp1 HG02257.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+509_925+512del others(4): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr4 | 54704399 | |||||
chr4:54704461
|
A | G | 2 | a0001c0001t0005g0156a0001c0001t0005g0157 | 2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.925+569A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54704461 | ||||||
chr4:54704468
|
C | T | 9 | a0001c0001t0001g0016a0001c0001t0001g0143a0001c0001t0001g0147others(6): Show | 9 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.925+576C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54704468 | ||||||
chr4:54704498
|
T | A | 1 | a0001c0003t0003g0066 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.925+606T>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54704498 | ||||||
chr4:54704617
|
G | T | 1 | a0001c0001t0002g0217 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.925+725G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54704617 | ||||||
chr4:54704683
|
T | G | 84 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0022others(81): Show | 87 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.925+791T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54704683 | ||||||
chr4:54704820
|
C | T | 250 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(247): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.925+928C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54704820 | ||||||
chr4:54704910
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.925+1018A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54704910 | ||||||
chr4:54705266
|
G | A | 1 | a0001c0004t0001g0052 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.925+1374G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54705266 | ||||||
chr4:54705275
|
C | T | 74 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(71): Show | 75 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.925+1383C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54705275 | ||||||
chr4:54705622
|
C | T | 2 | a0001c0001t0005g0074a0001c0003t0003g0049 | 2 | HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.926-1476C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54705622 | ||||||
chr4:54705792
|
G | C | 8 | a0001c0001t0001g0016a0001c0001t0001g0143a0001c0001t0001g0147others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-1306G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54705792 | ||||||
chr4:54705793
|
G | A | 8 | a0001c0001t0001g0016a0001c0001t0001g0143a0001c0001t0001g0147others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.926-1305G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54705793 | ||||||
chr4:54705858
|
G | A | 6 | a0001c0005t0003g0136a0001c0005t0003g0141a0001c0005t0004g0140others(3): Show | 6 | HG01255.hp2 HG01884.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.926-1240G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54705858 | ||||||
chr4:54706084
|
C | T | 4 | a0001c0001t0005g0074a0001c0003t0003g0049a0001c0009t0001g0015others(1): Show | 4 | HG01891.hp1 HG02647.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.926-1014C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54706084 | ||||||
chr4:54706227
|
TA | T | 69 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0040others(66): Show | 72 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.926-862delA | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr4 | 54706227 | |||||
chr4:54706406
|
T | C | 1 | a0001c0001t0002g0067 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.926-692T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54706406 | ||||||
chr4:54706455
|
A | G | 1 | a0006c0017t0004g0139 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.926-643A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54706455 | ||||||
chr4:54706458
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.926-640T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54706458 | ||||||
chr4:54706706
|
C | T | 251 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(248): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.926-392C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54706706 | ||||||
chr4:54706778
|
A | G | 19 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(16): Show | 19 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.926-320A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54706778 | ||||||
chr4:54706804
|
T | A | 251 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(248): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.926-294T>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54706804 | ||||||
chr4:54706949
|
A | C | 1 | a0001c0001t0001g0238 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.926-149A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 5/20 | chr4 | 54706949 | ||||||
chr4:54707367
|
C | T | 2 | a0001c0009t0001g0015a0001c0009t0001g0145 | 2 | HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1115+80C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54707367 | ||||||
chr4:54707477
|
C | A | 1 | a0001c0001t0001g0247 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1115+190C>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54707477 | ||||||
chr4:54707527
|
G | A | 72 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0040others(69): Show | 75 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1115+240G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54707527 | ||||||
chr4:54707653
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1115+366A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54707653 | ||||||
chr4:54707685
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1115+398G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54707685 | ||||||
chr4:54707769
|
G | A | 70 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0040others(67): Show | 73 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1115+482G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54707769 | ||||||
chr4:54707845
|
A | C | 44 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0029others(41): Show | 44 | HG00544.hp1 HG00735.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.1115+558A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54707845 | ||||||
chr4:54707899
|
CAG | C | 74 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(71): Show | 75 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1115+615_1115+616d others(4): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr4 | 54707899 | |||||
chr4:54708016
|
C | T | 155 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(152): Show | 156 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.1115+729C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54708016 | ||||||
chr4:54708062
|
G | A | 2 | a0001c0009t0001g0015a0001c0009t0001g0145 | 2 | HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1115+775G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54708062 | ||||||
chr4:54708132
|
C | G | 1 | a0001c0009t0001g0145 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1115+845C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54708132 | ||||||
chr4:54708183
|
G | A | 3 | a0001c0001t0005g0074a0001c0003t0001g0135a0001c0003t0003g0049 | 3 | HG01891.hp1 HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1115+896G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54708183 | ||||||
chr4:54708314
|
G | A | 1 | a0001c0001t0005g0074 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1115+1027G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54708314 | ||||||
chr4:54708337
|
A | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0038 | 2 | HG00423.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.1115+1050A>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54708337 | ||||||
chr4:54708504
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1116-920C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54708504 | ||||||
chr4:54708639
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1116-785G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54708639 | ||||||
chr4:54708641
|
C | T | 1 | a0002c0002t0003g0129 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1116-783C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54708641 | ||||||
chr4:54708764
|
G | A | 73 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(70): Show | 74 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.1116-660G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54708764 | ||||||
chr4:54708777
|
A | G | 246 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(243): Show | 250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1116-647A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54708777 | ||||||
chr4:54708978
|
G | A | 81 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(78): Show | 81 | HG00544.hp1 HG00735.hp2 HG00741.hp1 others(78): Show |
intron_variant | MODIFIER | c.1116-446G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54708978 | ||||||
chr4:54708988
|
C | T | 73 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0040others(70): Show | 76 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1116-436C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54708988 | ||||||
chr4:54709108
|
C | G | 257 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(254): Show | 261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1116-316C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54709108 | ||||||
chr4:54709142
|
C | T | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1116-282C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54709142 | ||||||
chr4:54709233
|
C | T | 6 | a0001c0001t0001g0075a0001c0003t0004g0118a0001c0003t0004g0259others(3): Show | 6 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1116-191C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54709233 | ||||||
chr4:54709234
|
G | A | 2 | a0001c0006t0006g0255a0001c0006t0006g0256 | 2 | HG02572.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1116-190G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54709234 | ||||||
chr4:54709311
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1116-113A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 6/20 | chr4 | 54709311 | ||||||
chr4:54709913
|
C | T | 6 | a0001c0005t0003g0136a0001c0005t0003g0141a0001c0005t0004g0140others(3): Show | 6 | HG01255.hp2 HG01884.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231+374C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54709913 | ||||||
chr4:54709923
|
C | T | 3 | a0001c0001t0005g0074a0001c0003t0001g0135a0001c0003t0003g0049 | 3 | HG01891.hp1 HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1231+384C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54709923 | ||||||
chr4:54710128
|
C | G | 8 | a0001c0001t0001g0056a0001c0001t0001g0244a0001c0001t0001g0247others(5): Show | 8 | HG01891.hp2 HG02572.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1231+589C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54710128 | ||||||
chr4:54710351
|
A | G | 1 | a0001c0003t0001g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1231+812A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54710351 | ||||||
chr4:54710457
|
G | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(3): Show | 6 | HG02257.hp2 HG02451.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231+918G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54710457 | ||||||
chr4:54710607
|
C | CATG | 258 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(255): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.1231+1070_1231+107 others(7): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 54710607 | |||||
chr4:54710830
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1231+1291C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54710830 | ||||||
chr4:54710833
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1231+1294G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54710833 | ||||||
chr4:54711086
|
G | C | 5 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0002g0023others(2): Show | 5 | HG01070.hp2 HG02129.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.1231+1547G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54711086 | ||||||
chr4:54711206
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1231+1667T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54711206 | ||||||
chr4:54711323
|
C | T | 2 | a0001c0001t0001g0164a0001c0001t0002g0197 | 2 | HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1231+1784C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54711323 | ||||||
chr4:54711494
|
A | T | 1 | a0001c0016t0001g0137 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1231+1955A>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54711494 | ||||||
chr4:54711599
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1231+2060A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54711599 | ||||||
chr4:54711649
|
CGGTGGCT others(67): Show |
C | 72 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0040others(69): Show | 75 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1231+2111_1231+218 others(78): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54711649 | ||||||
chr4:54711691
|
G | A | 6 | a0001c0005t0003g0136a0001c0005t0003g0141a0001c0005t0004g0140others(3): Show | 6 | HG01255.hp2 HG01884.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231+2152G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54711691 | ||||||
chr4:54711725
|
C | T | 72 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0040others(69): Show | 75 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1231+2186C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54711725 | ||||||
chr4:54711726
|
A | T | 72 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0040others(69): Show | 75 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1231+2187A>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54711726 | ||||||
chr4:54711798
|
G | C | 7 | a0001c0001t0001g0056a0001c0001t0001g0147a0001c0001t0007g0246others(4): Show | 7 | HG01243.hp1 HG02145.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231+2259G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54711798 | ||||||
chr4:54711907
|
C | T | 1 | a0001c0001t0002g0179 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1231+2368C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54711907 | ||||||
chr4:54711911
|
T | A | 242 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(239): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1231+2372T>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54711911 | ||||||
chr4:54711924
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0002g0180 | 2 | NA18946.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.1231+2385G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54711924 | ||||||
chr4:54711928
|
C | CA | 7 | a0001c0001t0001g0022a0001c0001t0001g0063a0001c0001t0001g0064others(4): Show | 7 | HG01175.hp1 HG02165.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231+2407dupA | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 54711928 | |||||
chr4:54711928
|
CA | C | 6 | a0001c0001t0001g0126a0001c0001t0001g0183a0001c0001t0001g0213others(3): Show | 6 | HG01070.hp2 HG01891.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1231+2407delA | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 54711928 | |||||
chr4:54711952
|
T | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0150 | 2 | HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1231+2413T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54711952 | ||||||
chr4:54712048
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1231+2509C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54712048 | ||||||
chr4:54712146
|
T | C | 242 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(239): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1231+2607T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54712146 | ||||||
chr4:54712162
|
C | A | 2 | a0001c0001t0007g0078a0001c0001t0014g0144 | 2 | HG02630.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1231+2623C>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54712162 | ||||||
chr4:54712164
|
A | G | 6 | a0001c0001t0001g0075a0001c0003t0004g0118a0001c0003t0004g0259others(3): Show | 6 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1231+2625A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54712164 | ||||||
chr4:54712784
|
C | T | 1 | a0001c0001t0001g0031 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1231+3245C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54712784 | ||||||
chr4:54712915
|
G | A | 90 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(87): Show | 91 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.1231+3376G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54712915 | ||||||
chr4:54713019
|
C | T | 13 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0038others(10): Show | 13 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.1231+3480C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54713019 | ||||||
chr4:54713061
|
A | AT | 73 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0040others(70): Show | 76 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1231+3530dupT | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 54713061 | |||||
chr4:54713083
|
T | A | 8 | a0001c0001t0001g0016a0001c0001t0001g0056a0001c0001t0001g0147others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1231+3544T>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54713083 | ||||||
chr4:54713120
|
T | A | 1 | a0001c0001t0001g0040 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1231+3581T>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54713120 | ||||||
chr4:54713132
|
A | G | 1 | a0001c0004t0001g0087 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1231+3593A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54713132 | ||||||
chr4:54713177
|
T | C | 1 | a0001c0003t0004g0261 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1231+3638T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54713177 | ||||||
chr4:54713318
|
T | A | 154 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(151): Show | 157 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.1231+3779T>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54713318 | ||||||
chr4:54713335
|
G | A | 249 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(246): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1231+3796G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54713335 | ||||||
chr4:54713528
|
C | A | 78 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(75): Show | 78 | HG00544.hp1 HG00735.hp2 HG00741.hp1 others(75): Show |
intron_variant | MODIFIER | c.1231+3989C>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54713528 | ||||||
chr4:54713607
|
T | C | 8 | a0001c0001t0001g0016a0001c0001t0001g0056a0001c0001t0001g0147others(5): Show | 8 | HG01243.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1231+4068T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54713607 | ||||||
chr4:54714008
|
T | A | 1 | a0001c0001t0001g0210 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1231+4469T>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54714008 | ||||||
chr4:54714152
|
G | A | 2 | a0001c0001t0007g0078a0001c0001t0014g0144 | 2 | HG02630.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1231+4613G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54714152 | ||||||
chr4:54714366
|
GT | G | 88 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(85): Show | 89 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1231+4836delT | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 54714366 | |||||
chr4:54714430
|
A | T | 69 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0040others(66): Show | 72 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1231+4891A>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54714430 | ||||||
chr4:54714738
|
C | T | 248 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(245): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1231+5199C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54714738 | ||||||
chr4:54714836
|
C | T | 7 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0040others(4): Show | 7 | HG01109.hp1 HG02080.hp2 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.1231+5297C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54714836 | ||||||
chr4:54714848
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0002g0197 | 2 | HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1231+5309G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54714848 | ||||||
chr4:54714984
|
C | T | 4 | a0001c0001t0001g0081a0001c0001t0001g0082a0003c0008t0001g0011others(1): Show | 4 | HG01884.hp1 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1231+5445C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54714984 | ||||||
chr4:54715167
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG00735.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1231+5628C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54715167 | ||||||
chr4:54715350
|
G | A | 1 | a0001c0001t0002g0197 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1231+5811G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54715350 | ||||||
chr4:54715368
|
T | TA | 107 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(104): Show | 110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1231+5847dupA | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 54715368 | |||||
chr4:54715368
|
T | TAA | 7 | a0001c0001t0001g0032a0001c0001t0001g0084a0001c0001t0001g0127others(4): Show | 7 | HG01074.hp2 HG01934.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231+5846_1231+584 others(6): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 54715368 | |||||
chr4:54715368
|
TA | T | 97 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0019others(94): Show | 97 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1231+5847delA | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 54715368 | |||||
chr4:54715368
|
TAA | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0071a0001c0001t0001g0133others(3): Show | 7 | HG02615.hp1 HG03041.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.1231+5846_1231+584 others(6): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 54715368 | |||||
chr4:54715368
|
TAAAA | T | 19 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(16): Show | 19 | HG01884.hp1 HG02055.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1231+5844_1231+584 others(8): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 54715368 | |||||
chr4:54715585
|
C | T | 41 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0029others(38): Show | 41 | HG00544.hp1 HG00735.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1231+6046C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54715585 | ||||||
chr4:54715700
|
C | G | 1 | a0001c0001t0001g0083 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1231+6161C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54715700 | ||||||
chr4:54715715
|
A | G | 7 | a0001c0001t0001g0009a0001c0005t0003g0136a0001c0005t0003g0141others(4): Show | 7 | HG02572.hp1 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231+6176A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54715715 | ||||||
chr4:54715743
|
C | G | 1 | a0001c0001t0001g0152 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1231+6204C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54715743 | ||||||
chr4:54715792
|
G | A | 2 | a0001c0006t0006g0262a0001c0013t0001g0257 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1231+6253G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54715792 | ||||||
chr4:54715871
|
C | T | 30 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(27): Show | 31 | HG00280.hp2 HG00423.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1231+6332C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54715871 | ||||||
chr4:54715902
|
T | C | 178 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(175): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.1231+6363T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54715902 | ||||||
chr4:54715924
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1231+6385C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54715924 | ||||||
chr4:54715956
|
GT | G | 82 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0027others(79): Show | 85 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.1231+6419delT | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 54715956 | |||||
chr4:54715971
|
A | G | 2 | a0001c0001t0007g0078a0001c0001t0014g0144 | 2 | HG02630.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1231+6432A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54715971 | ||||||
chr4:54716067
|
G | A | 1 | a0001c0001t0007g0246 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1231+6528G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54716067 | ||||||
chr4:54716069
|
G | A | 1 | a0001c0007t0001g0101 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1231+6530G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54716069 | ||||||
chr4:54716081
|
C | T | 1 | a0001c0003t0001g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1231+6542C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54716081 | ||||||
chr4:54716205
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1231+6666T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54716205 | ||||||
chr4:54716231
|
C | T | 51 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0029others(48): Show | 51 | HG00544.hp1 HG00735.hp2 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.1231+6692C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54716231 | ||||||
chr4:54716246
|
T | C | 1 | a0001c0001t0001g0041 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1231+6707T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54716246 | ||||||
chr4:54716637
|
T | C | 1 | a0001c0009t0001g0145 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1232-6947T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54716637 | ||||||
chr4:54716857
|
A | G | 19 | a0001c0001t0008g0252a0001c0003t0001g0135a0001c0003t0004g0076others(16): Show | 19 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1232-6727A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54716857 | ||||||
chr4:54717149
|
T | G | 22 | a0001c0001t0008g0252a0001c0003t0001g0135a0001c0003t0004g0076others(19): Show | 22 | HG01243.hp1 HG01255.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1232-6435T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54717149 | ||||||
chr4:54717189
|
A | G | 3 | a0001c0006t0006g0255a0001c0006t0006g0256a0001c0006t0006g0262 | 3 | HG02572.hp1 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1232-6395A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54717189 | ||||||
chr4:54717679
|
A | G | 1 | a0001c0004t0001g0114 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1232-5905A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54717679 | ||||||
chr4:54717905
|
C | G | 1 | a0001c0003t0003g0018 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1232-5679C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54717905 | ||||||
chr4:54717907
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1232-5677C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54717907 | ||||||
chr4:54717935
|
T | A | 34 | a0001c0001t0001g0056a0001c0001t0001g0164a0001c0001t0002g0001others(31): Show | 35 | HG00735.hp1 HG01099.hp1 HG02004.hp1 others(32): Show |
intron_variant | MODIFIER | c.1232-5649T>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54717935 | ||||||
chr4:54718068
|
G | A | 16 | a0001c0001t0008g0252a0001c0003t0001g0135a0001c0003t0004g0076others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1232-5516G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54718068 | ||||||
chr4:54718121
|
G | T | 1 | a0001c0001t0002g0116 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1232-5463G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54718121 | ||||||
chr4:54718267
|
A | G | 28 | a0001c0001t0002g0002a0001c0001t0002g0111a0001c0003t0003g0044others(25): Show | 31 | HG00140.hp2 HG00280.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1232-5317A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54718267 | ||||||
chr4:54718367
|
A | G | 202 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(199): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1232-5217A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54718367 | ||||||
chr4:54718843
|
A | G | 1 | a0002c0002t0003g0124 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1232-4741A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54718843 | ||||||
chr4:54718869
|
C | T | 19 | a0001c0001t0008g0252a0001c0003t0001g0135a0001c0003t0004g0076others(16): Show | 19 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1232-4715C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54718869 | ||||||
chr4:54719020
|
C | T | 19 | a0001c0001t0008g0252a0001c0003t0001g0135a0001c0003t0004g0076others(16): Show | 19 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1232-4564C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54719020 | ||||||
chr4:54719517
|
T | C | 3 | a0001c0001t0001g0026a0001c0001t0001g0055a0001c0001t0001g0239 | 3 | HG00423.hp1 NA18988.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1232-4067T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54719517 | ||||||
chr4:54719522
|
G | A | 32 | a0001c0001t0001g0056a0001c0001t0001g0164a0001c0001t0002g0001others(29): Show | 32 | HG00735.hp1 HG01099.hp1 HG02004.hp1 others(29): Show |
intron_variant | MODIFIER | c.1232-4062G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54719522 | ||||||
chr4:54719570
|
A | AT | 152 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(149): Show | 154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1232-4005dupT | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 54719570 | |||||
chr4:54719772
|
C | T | 16 | a0001c0001t0008g0252a0001c0003t0001g0135a0001c0003t0004g0076others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1232-3812C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54719772 | ||||||
chr4:54719916
|
C | T | 1 | a0001c0001t0014g0144 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1232-3668C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54719916 | ||||||
chr4:54720177
|
C | T | 4 | a0002c0002t0003g0189a0002c0002t0003g0192a0002c0002t0003g0224others(1): Show | 4 | HG01074.hp1 HG01433.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1232-3407C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54720177 | ||||||
chr4:54720402
|
C | T | 34 | a0001c0001t0001g0056a0001c0001t0001g0164a0001c0001t0001g0171others(31): Show | 34 | HG00639.hp2 HG00735.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.1232-3182C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54720402 | ||||||
chr4:54720893
|
G | A | 19 | a0001c0001t0008g0252a0001c0003t0001g0135a0001c0003t0004g0076others(16): Show | 19 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1232-2691G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54720893 | ||||||
chr4:54721054
|
A | G | 19 | a0001c0001t0008g0252a0001c0003t0001g0135a0001c0003t0004g0076others(16): Show | 19 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1232-2530A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54721054 | ||||||
chr4:54721092
|
T | G | 19 | a0001c0001t0008g0252a0001c0003t0001g0135a0001c0003t0004g0076others(16): Show | 19 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1232-2492T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54721092 | ||||||
chr4:54721136
|
G | A | 16 | a0001c0001t0008g0252a0001c0003t0001g0135a0001c0003t0004g0076others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1232-2448G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54721136 | ||||||
chr4:54721236
|
G | A | 1 | a0001c0004t0001g0053 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1232-2348G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54721236 | ||||||
chr4:54721413
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0002g0180 | 2 | HG01106.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.1232-2171C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54721413 | ||||||
chr4:54721457
|
C | T | 16 | a0001c0001t0008g0252a0001c0003t0001g0135a0001c0003t0004g0076others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1232-2127C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54721457 | ||||||
chr4:54721633
|
C | G | 1 | a0001c0003t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1232-1951C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54721633 | ||||||
chr4:54721646
|
A | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0150 | 2 | HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1232-1938A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54721646 | ||||||
chr4:54721710
|
T | C | 1 | a0001c0003t0001g0006 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1232-1874T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54721710 | ||||||
chr4:54721893
|
G | A | 5 | a0001c0003t0004g0118a0001c0003t0004g0259a0001c0003t0004g0260others(2): Show | 5 | HG01255.hp2 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1232-1691G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54721893 | ||||||
chr4:54722112
|
A | G | 19 | a0001c0001t0008g0252a0001c0003t0001g0135a0001c0003t0004g0076others(16): Show | 19 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1232-1472A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54722112 | ||||||
chr4:54722370
|
A | G | 26 | a0001c0003t0003g0044a0001c0003t0003g0049a0001c0003t0003g0054others(23): Show | 28 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1232-1214A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54722370 | ||||||
chr4:54722479
|
A | C | 3 | a0001c0006t0006g0255a0001c0006t0006g0256a0001c0006t0006g0262 | 3 | HG02572.hp1 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1232-1105A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54722479 | ||||||
chr4:54722503
|
A | G | 3 | a0001c0006t0006g0255a0001c0006t0006g0256a0001c0006t0006g0262 | 3 | HG02572.hp1 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1232-1081A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54722503 | ||||||
chr4:54722542
|
C | T | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1232-1042C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54722542 | ||||||
chr4:54722553
|
A | C | 27 | a0001c0001t0001g0007a0001c0001t0001g0070a0001c0001t0001g0075others(24): Show | 27 | HG01070.hp1 HG01071.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1232-1031A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54722553 | ||||||
chr4:54722560
|
A | C | 262 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(259): Show | 267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.1232-1024A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54722560 | ||||||
chr4:54722631
|
G | A | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1232-953G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54722631 | ||||||
chr4:54722632
|
T | G | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1232-952T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54722632 | ||||||
chr4:54722746
|
G | C | 1 | a0001c0001t0001g0203 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1232-838G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54722746 | ||||||
chr4:54722815
|
TTA | T | 224 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(221): Show | 228 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.1232-757_1232-756d others(4): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 54722815 | |||||
chr4:54722843
|
TTA | T | 28 | a0001c0001t0007g0078a0001c0001t0007g0246a0001c0003t0003g0044others(25): Show | 30 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.1232-733_1232-732d others(4): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 54722843 | |||||
chr4:54722849
|
ATATT | A | 16 | a0001c0001t0008g0252a0001c0003t0001g0135a0001c0003t0004g0076others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1232-733_1232-730d others(6): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 54722849 | |||||
chr4:54722859
|
ATATATG | A | 32 | a0001c0001t0007g0078a0001c0001t0007g0246a0001c0003t0001g0135others(29): Show | 34 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.1232-719_1232-714d others(8): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 54722859 | |||||
chr4:54722861
|
ATATG | A | 12 | a0001c0001t0008g0252a0001c0003t0004g0076a0001c0003t0004g0118others(9): Show | 12 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1232-719_1232-716d others(6): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 54722861 | |||||
chr4:54722889
|
TTA | T | 40 | a0001c0001t0007g0078a0001c0001t0007g0246a0001c0001t0008g0252others(37): Show | 42 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.1232-683_1232-682d others(4): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 54722889 | |||||
chr4:54722889
|
TTATATA | T | 5 | a0001c0003t0004g0118a0001c0003t0004g0259a0001c0003t0004g0260others(2): Show | 5 | HG01255.hp2 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1232-687_1232-682d others(8): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 54722889 | |||||
chr4:54722916
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1232-668A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54722916 | ||||||
chr4:54722935
|
T | TTAG | 37 | a0001c0001t0001g0056a0001c0001t0001g0164a0001c0001t0001g0171others(34): Show | 38 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1232-648_1232-646d others(5): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr4 | 54722935 | |||||
chr4:54722942
|
G | T | 44 | a0001c0001t0007g0078a0001c0001t0007g0246a0001c0001t0008g0252others(41): Show | 46 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.1232-642G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54722942 | ||||||
chr4:54723086
|
C | T | 1 | a0001c0001t0001g0240 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1232-498C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54723086 | ||||||
chr4:54723111
|
G | C | 1 | a0001c0003t0001g0006 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1232-473G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54723111 | ||||||
chr4:54723128
|
A | T | 3 | a0001c0006t0006g0255a0001c0006t0006g0256a0001c0006t0006g0262 | 3 | HG02572.hp1 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1232-456A>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54723128 | ||||||
chr4:54723492
|
C | G | 5 | a0001c0001t0002g0001a0001c0001t0002g0067a0001c0001t0002g0077others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1232-92C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 7/20 | chr4 | 54723492 | ||||||
chr4:54723705
|
T | C | 1 | a0002c0002t0003g0189 | 1 | HG01074.hp1 | splice_region_variant&intron_variant | LOW | c.1346+7T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 8/20 | chr4 | 54723705 | ||||||
chr4:54723787
|
T | A | 1 | a0001c0001t0005g0157 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1346+89T>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 8/20 | chr4 | 54723787 | ||||||
chr4:54723845
|
A | G | 1 | a0001c0003t0001g0006 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1346+147A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 8/20 | chr4 | 54723845 | ||||||
chr4:54723897
|
T | C | 1 | a0001c0001t0002g0159 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1346+199T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 8/20 | chr4 | 54723897 | ||||||
chr4:54723901
|
T | C | 1 | a0001c0012t0002g0250 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1346+203T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 8/20 | chr4 | 54723901 | ||||||
chr4:54724105
|
G | A | 2 | a0001c0001t0008g0252a0004c0010t0008g0253 | 2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1346+407G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 8/20 | chr4 | 54724105 | ||||||
chr4:54724455
|
G | T | 87 | a0001c0001t0001g0056a0001c0001t0001g0164a0001c0001t0002g0001others(84): Show | 91 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.1346+757G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 8/20 | chr4 | 54724455 | ||||||
chr4:54724564
|
T | A | 18 | a0001c0001t0007g0078a0001c0001t0007g0246a0001c0001t0008g0252others(15): Show | 18 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1346+866T>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 8/20 | chr4 | 54724564 | ||||||
chr4:54724696
|
A | G | 18 | a0001c0001t0007g0078a0001c0001t0007g0246a0001c0001t0008g0252others(15): Show | 18 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1346+998A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 8/20 | chr4 | 54724696 | ||||||
chr4:54724699
|
A | C | 1 | a0001c0001t0001g0206 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1346+1001A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 8/20 | chr4 | 54724699 | ||||||
chr4:54724735
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1346+1037C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 8/20 | chr4 | 54724735 | ||||||
chr4:54724756
|
TA | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0012others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1346+1072delA | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr4 | 54724756 | |||||
chr4:54724833
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1347-1024G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 8/20 | chr4 | 54724833 | ||||||
chr4:54725141
|
C | G | 18 | a0001c0001t0008g0252a0001c0001t0012g0014a0001c0003t0001g0135others(15): Show | 18 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1347-716C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 8/20 | chr4 | 54725141 | ||||||
chr4:54725401
|
G | C | 2 | a0001c0003t0003g0018a0001c0003t0003g0054 | 2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1347-456G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 8/20 | chr4 | 54725401 | ||||||
chr4:54725440
|
A | G | 2 | a0001c0003t0001g0135a0001c0013t0001g0257 | 2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1347-417A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 8/20 | chr4 | 54725440 | ||||||
chr4:54725458
|
G | A | 10 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0108others(7): Show | 10 | HG01071.hp2 HG01099.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.1347-399G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 8/20 | chr4 | 54725458 | ||||||
chr4:54725605
|
G | C | 20 | a0001c0001t0007g0078a0001c0001t0007g0246a0001c0001t0008g0252others(17): Show | 20 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1347-252G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 8/20 | chr4 | 54725605 | ||||||
chr4:54725650
|
C | T | 7 | a0001c0001t0008g0252a0001c0003t0004g0076a0001c0003t0004g0220others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1347-207C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 8/20 | chr4 | 54725650 | ||||||
chr4:54726132
|
A | G | 4 | a0001c0001t0007g0078a0001c0001t0007g0246a0001c0001t0012g0014others(1): Show | 4 | HG02886.hp2 HG03195.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540+82A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 9/20 | chr4 | 54726132 | ||||||
chr4:54726159
|
T | C | 27 | a0001c0003t0003g0018a0001c0003t0003g0044a0001c0003t0003g0049others(24): Show | 29 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.1540+109T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 9/20 | chr4 | 54726159 | ||||||
chr4:54726412
|
A | G | 2 | a0001c0001t0007g0078a0001c0001t0007g0246 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1540+362A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 9/20 | chr4 | 54726412 | ||||||
chr4:54726684
|
G | A | 2 | a0001c0001t0007g0078a0001c0001t0007g0246 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1541-534G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 9/20 | chr4 | 54726684 | ||||||
chr4:54726761
|
G | A | 16 | a0001c0001t0008g0252a0001c0003t0001g0135a0001c0003t0004g0076others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1541-457G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 9/20 | chr4 | 54726761 | ||||||
chr4:54726781
|
G | GT | 5 | a0001c0001t0001g0152a0001c0001t0001g0188a0001c0001t0001g0237others(2): Show | 5 | HG01934.hp2 HG02135.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1541-423dupT | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 54726781 | |||||
chr4:54726781
|
GT | G | 27 | a0001c0001t0012g0014a0001c0003t0003g0018a0001c0003t0003g0044others(24): Show | 29 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.1541-423delT | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr4 | 54726781 | |||||
chr4:54726922
|
T | C | 1 | a0001c0001t0007g0246 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1541-296T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 9/20 | chr4 | 54726922 | ||||||
chr4:54726993
|
A | G | 3 | a0001c0006t0006g0255a0001c0006t0006g0256a0001c0006t0006g0262 | 3 | HG02572.hp1 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1541-225A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 9/20 | chr4 | 54726993 | ||||||
chr4:54727692
|
G | C | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1775-131G>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 11/20 | chr4 | 54727692 | ||||||
chr4:54727699
|
G | A | 22 | a0001c0003t0003g0018a0001c0003t0003g0044a0001c0003t0003g0054others(19): Show | 24 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.1775-124G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 11/20 | chr4 | 54727699 | ||||||
chr4:54727753
|
C | G | 9 | a0001c0001t0001g0093a0001c0001t0001g0169a0001c0001t0001g0183others(6): Show | 9 | HG00735.hp2 HG00741.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1775-70C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 11/20 | chr4 | 54727753 | ||||||
chr4:54728253
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1990+132C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 13/20 | chr4 | 54728253 | ||||||
chr4:54728606
|
G | T | 1 | a0001c0001t0001g0093 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1990+485G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 13/20 | chr4 | 54728606 | ||||||
chr4:54728768
|
C | G | 1 | a0001c0001t0001g0161 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1991-567C>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 13/20 | chr4 | 54728768 | ||||||
chr4:54728801
|
A | G | 1 | a0001c0004t0001g0114 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1991-534A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 13/20 | chr4 | 54728801 | ||||||
chr4:54729140
|
C | T | 2 | a0001c0001t0007g0078a0001c0001t0007g0246 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1991-195C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 13/20 | chr4 | 54729140 | ||||||
chr4:54729164
|
G | T | 1 | a0001c0001t0001g0200 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1991-171G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 13/20 | chr4 | 54729164 | ||||||
chr4:54729185
|
T | C | 19 | a0001c0001t0008g0252a0001c0003t0001g0135a0001c0003t0004g0076others(16): Show | 19 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1991-150T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 13/20 | chr4 | 54729185 | ||||||
chr4:54729669
|
A | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0155 | 2 | HG00597.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.2141+184A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 14/20 | chr4 | 54729669 | ||||||
chr4:54729767
|
G | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0187a0001c0001t0001g0226 | 3 | HG01257.hp1 NA18979.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.2141+282G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 14/20 | chr4 | 54729767 | ||||||
chr4:54729803
|
A | C | 3 | a0001c0006t0006g0255a0001c0006t0006g0256a0001c0006t0006g0262 | 3 | HG02572.hp1 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2141+318A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 14/20 | chr4 | 54729803 | ||||||
chr4:54729842
|
T | A | 28 | a0001c0001t0012g0014a0001c0003t0003g0018a0001c0003t0003g0044others(25): Show | 30 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.2141+357T>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 14/20 | chr4 | 54729842 | ||||||
chr4:54729933
|
A | G | 7 | a0001c0001t0008g0252a0001c0003t0004g0076a0001c0003t0004g0220others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2141+448A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 14/20 | chr4 | 54729933 | ||||||
chr4:54730104
|
G | A | 2 | a0001c0001t0007g0078a0001c0001t0007g0246 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2141+619G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 14/20 | chr4 | 54730104 | ||||||
chr4:54730189
|
G | A | 1 | a0001c0001t0007g0078 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2141+704G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 14/20 | chr4 | 54730189 | ||||||
chr4:54730286
|
G | A | 3 | a0001c0001t0007g0078a0001c0001t0007g0246a0001c0003t0001g0258 | 3 | HG02886.hp2 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2141+801G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 14/20 | chr4 | 54730286 | ||||||
chr4:54730313
|
A | G | 1 | a0001c0001t0014g0144 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2141+828A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 14/20 | chr4 | 54730313 | ||||||
chr4:54730759
|
C | T | 1 | a0001c0001t0015g0028 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2142-569C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 14/20 | chr4 | 54730759 | ||||||
chr4:54730917
|
G | A | 16 | a0001c0001t0008g0252a0001c0003t0001g0135a0001c0003t0004g0076others(13): Show | 16 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2142-411G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 14/20 | chr4 | 54730917 | ||||||
chr4:54731116
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2142-212T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 14/20 | chr4 | 54731116 | ||||||
chr4:54731142
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2142-186C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 14/20 | chr4 | 54731142 | ||||||
chr4:54731186
|
C | T | 1 | a0001c0012t0002g0250 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2142-142C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 14/20 | chr4 | 54731186 | ||||||
chr4:54731211
|
C | T | 1 | a0002c0002t0004g0057 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2142-117C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 14/20 | chr4 | 54731211 | ||||||
chr4:54731292
|
A | G | 7 | a0001c0001t0008g0252a0001c0003t0004g0076a0001c0003t0004g0220others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2142-36A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 14/20 | chr4 | 54731292 | ||||||
chr4:54731821
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2234-50C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 15/20 | chr4 | 54731821 | ||||||
chr4:54732045
|
A | AT | 27 | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0027others(24): Show | 27 | HG00423.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.2361+72dupT | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr4 | 54732045 | |||||
chr4:54732045
|
A | ATT | 5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0160others(2): Show | 5 | HG00639.hp2 HG01081.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.2361+71_2361+72dup others(2): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr4 | 54732045 | |||||
chr4:54732045
|
AT | A | 73 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0064others(70): Show | 76 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.2361+72delT | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr4 | 54732045 | |||||
chr4:54732045
|
ATT | A | 20 | a0001c0001t0002g0036a0001c0001t0002g0047a0001c0001t0008g0252others(17): Show | 20 | HG01070.hp2 HG01255.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.2361+71_2361+72del others(2): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr4 | 54732045 | |||||
chr4:54732088
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2361+90G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 16/20 | chr4 | 54732088 | ||||||
chr4:54732312
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2361+314A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 16/20 | chr4 | 54732312 | ||||||
chr4:54732540
|
G | A | 27 | a0001c0003t0003g0018a0001c0003t0003g0044a0001c0003t0003g0049others(24): Show | 29 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.2362-530G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 16/20 | chr4 | 54732540 | ||||||
chr4:54732561
|
T | C | 1 | a0001c0013t0001g0257 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2362-509T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 16/20 | chr4 | 54732561 | ||||||
chr4:54732574
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2362-496A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 16/20 | chr4 | 54732574 | ||||||
chr4:54732737
|
A | T | 35 | a0001c0001t0001g0164a0001c0001t0002g0001a0001c0001t0002g0002others(32): Show | 36 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.2362-333A>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 16/20 | chr4 | 54732737 | ||||||
chr4:54732786
|
T | C | 3 | a0001c0001t0001g0026a0001c0001t0001g0055a0001c0001t0001g0239 | 3 | HG00423.hp1 NA18988.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.2362-284T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 16/20 | chr4 | 54732786 | ||||||
chr4:54732963
|
T | A | 49 | a0001c0001t0007g0078a0001c0001t0007g0246a0001c0001t0008g0252others(46): Show | 52 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.2362-107T>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 16/20 | chr4 | 54732963 | ||||||
chr4:54732993
|
G | A | 85 | a0001c0001t0001g0164a0001c0001t0002g0001a0001c0001t0002g0002others(82): Show | 89 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(86): Show |
intron_variant | MODIFIER | c.2362-77G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 16/20 | chr4 | 54732993 | ||||||
chr4:54733263
|
C | T | 4 | a0002c0002t0003g0189a0002c0002t0003g0192a0002c0002t0003g0224others(1): Show | 4 | HG01074.hp1 HG01433.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.2484+71C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54733263 | ||||||
chr4:54733270
|
T | C | 116 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(113): Show | 117 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.2484+78T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54733270 | ||||||
chr4:54733316
|
T | C | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2484+124T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54733316 | ||||||
chr4:54733351
|
A | G | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2484+159A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54733351 | ||||||
chr4:54733490
|
A | G | 47 | a0001c0001t0008g0252a0001c0003t0001g0006a0001c0003t0001g0135others(44): Show | 50 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.2484+298A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54733490 | ||||||
chr4:54733629
|
G | A | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2484+437G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54733629 | ||||||
chr4:54733827
|
A | G | 1 | a0001c0001t0007g0078 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2484+635A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54733827 | ||||||
chr4:54733832
|
A | G | 47 | a0001c0001t0007g0078a0001c0001t0007g0246a0001c0001t0008g0252others(44): Show | 50 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.2484+640A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54733832 | ||||||
chr4:54734018
|
T | C | 1 | a0001c0003t0003g0044 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2484+826T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54734018 | ||||||
chr4:54734088
|
A | C | 2 | a0001c0001t0001g0164a0001c0001t0002g0197 | 2 | HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2484+896A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54734088 | ||||||
chr4:54734212
|
G | A | 35 | a0001c0001t0001g0164a0001c0001t0002g0001a0001c0001t0002g0002others(32): Show | 36 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.2484+1020G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54734212 | ||||||
chr4:54734463
|
C | T | 1 | a0001c0001t0002g0204 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2484+1271C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54734463 | ||||||
chr4:54734517
|
C | T | 35 | a0001c0001t0001g0164a0001c0001t0002g0001a0001c0001t0002g0002others(32): Show | 36 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.2484+1325C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54734517 | ||||||
chr4:54734528
|
A | T | 35 | a0001c0001t0001g0164a0001c0001t0002g0001a0001c0001t0002g0002others(32): Show | 36 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.2484+1336A>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54734528 | ||||||
chr4:54734844
|
T | A | 1 | a0001c0001t0001g0158 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2484+1652T>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54734844 | ||||||
chr4:54734949
|
G | A | 5 | a0001c0001t0008g0252a0001c0009t0001g0015a0001c0009t0001g0145others(2): Show | 5 | HG03453.hp1 HG03486.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2485-1549G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54734949 | ||||||
chr4:54735161
|
T | G | 37 | a0001c0001t0001g0164a0001c0001t0001g0171a0001c0001t0001g0173others(34): Show | 38 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.2485-1337T>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54735161 | ||||||
chr4:54735225
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2485-1273G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54735225 | ||||||
chr4:54735283
|
C | A | 5 | a0001c0001t0008g0252a0001c0009t0001g0015a0001c0009t0001g0145others(2): Show | 5 | HG03453.hp1 HG03486.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2485-1215C>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54735283 | ||||||
chr4:54735357
|
C | CT | 3 | a0001c0006t0006g0255a0001c0006t0006g0256a0001c0006t0006g0262 | 3 | HG02572.hp1 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2485-1138dupT | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr4 | 54735357 | |||||
chr4:54735363
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2485-1135C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54735363 | ||||||
chr4:54735366
|
CA | C | 46 | a0001c0001t0007g0078a0001c0001t0007g0246a0001c0001t0008g0252others(43): Show | 49 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.2485-1120delA | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr4 | 54735366 | |||||
chr4:54735369
|
AAAAAAAA others(3): Show |
A | 35 | a0001c0001t0001g0164a0001c0001t0002g0001a0001c0001t0002g0002others(32): Show | 36 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.2485-1119_2485-111 others(14): Show |
KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr4 | 54735369 | |||||
chr4:54735379
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2485-1119G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54735379 | ||||||
chr4:54735379
|
GA | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0070others(2): Show | 6 | HG02615.hp1 HG02735.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2485-1106delA | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr4 | 54735379 | |||||
chr4:54735393
|
G | A | 35 | a0001c0001t0001g0164a0001c0001t0002g0001a0001c0001t0002g0002others(32): Show | 36 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.2485-1105G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54735393 | ||||||
chr4:54735995
|
G | A | 1 | a0001c0003t0003g0149 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2485-503G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54735995 | ||||||
chr4:54736017
|
G | A | 34 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(31): Show | 35 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.2485-481G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54736017 | ||||||
chr4:54736156
|
G | A | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2485-342G>A | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54736156 | ||||||
chr4:54736166
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2485-332T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54736166 | ||||||
chr4:54736243
|
A | G | 1 | a0001c0001t0012g0014 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2485-255A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54736243 | ||||||
chr4:54736285
|
C | T | 34 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(31): Show | 35 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.2485-213C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 17/20 | chr4 | 54736285 | ||||||
chr4:54736634
|
A | G | 1 | a0001c0003t0001g0258 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2596+25A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 18/20 | chr4 | 54736634 | ||||||
chr4:54736923
|
A | C | 1 | a0001c0003t0001g0135 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2696+103A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 19/20 | chr4 | 54736923 | ||||||
chr4:54737051
|
A | G | 34 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0023others(31): Show | 35 | HG00140.hp2 HG00735.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.2697-124A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 19/20 | chr4 | 54737051 | ||||||
chr4:54737315
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2802+35T>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 20/20 | chr4 | 54737315 | ||||||
chr4:54737498
|
G | T | 1 | a0001c0003t0003g0066 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2802+218G>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 20/20 | chr4 | 54737498 | ||||||
chr4:54737610
|
A | C | 3 | a0001c0006t0006g0255a0001c0006t0006g0256a0001c0006t0006g0262 | 3 | HG02572.hp1 HG02723.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2802+330A>C | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 20/20 | chr4 | 54737610 | ||||||
chr4:54737932
|
C | T | 2 | a0001c0001t0007g0078a0001c0001t0007g0246 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2803-497C>T | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 20/20 | chr4 | 54737932 | ||||||
chr4:54738090
|
A | G | 5 | a0001c0001t0008g0252a0001c0009t0001g0015a0001c0009t0001g0145others(2): Show | 5 | HG03453.hp1 HG03486.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.2803-339A>G | KIT | ENSG00000157404.17 | transcript | ENST00000288135.6 | protein_coding | 20/20 | chr4 | 54738090 |