geneid | 10787 |
---|---|
ensemblid | ENSG00000061676.16 |
hgncid | 7666 |
symbol | NCKAP1 |
name | NCK associated protein 1 |
refseq_nuc | NM_013436.5 |
refseq_prot | NP_038464.1 |
ensembl_nuc | ENST00000361354.9 |
ensembl_prot | ENSP00000355348.3 |
mane_status | MANE Select |
chr | chr2 |
start | 182909115 |
end | 183038457 |
strand | - |
ver | v1.2 |
region | chr2:182909115-183038457 |
region5000 | chr2:182904115-183043457 |
regionname0 | NCKAP1_chr2_182909115_183038457 |
regionname5000 | NCKAP1_chr2_182904115_183043457 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1128 | 217 | 82 | 29 | 78 | 4 | 22 | 60 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0002 | 0/0 | 1128 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 3387 | 124 | 21 | 19 | 66 | 2 | 15 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
c0002 | 1/0 | 3387 | 45 | 34 | 4 | 1 | 2 | 3 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
c0003 | 0/0 | 3387 | 31 | 17 | 2 | 9 | 0 | 3 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
c0004 | 0/0 | 3387 | 8 | 4 | 4 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
c0005 | 0/0 | 3387 | 3 | 3 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
c0006 | 0/0 | 3387 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
c0007 | 0/0 | 3387 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
c0008 | 0/0 | 3387 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
c0009 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
c0010 | 0/0 | 3387 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
c0011 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
c0012 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 16963 | 12 | 0 | 2 | 8 | 0 | 2 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0002 | 0/0 | 16985 | 10 | 7 | 0 | 3 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0003 | 0/0 | 16946 | 9 | 4 | 0 | 1 | 1 | 3 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0004 | 0/0 | 16951 | 8 | 8 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0005 | 0/0 | 16964 | 6 | 0 | 3 | 0 | 0 | 3 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0006 | 0/0 | 16951 | 6 | 2 | 1 | 1 | 0 | 2 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0007 | 0/0 | 16988 | 6 | 0 | 1 | 5 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0008 | 0/0 | 16984 | 6 | 0 | 1 | 5 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0009 | 0/0 | 16956 | 5 | 5 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0010 | 0/0 | 16989 | 5 | 0 | 1 | 4 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0011 | 0/0 | 16965 | 4 | 0 | 0 | 4 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0012 | 0/0 | 16952 | 4 | 1 | 0 | 3 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0013 | 0/0 | 16957 | 4 | 4 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0014 | 0/0 | 16987 | 4 | 0 | 0 | 3 | 1 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0015 | 0/0 | 16951 | 3 | 2 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0016 | 0/0 | 16952 | 3 | 0 | 3 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0017 | 0/0 | 16963 | 3 | 0 | 0 | 3 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0018 | 0/0 | 16962 | 3 | 3 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0019 | 0/0 | 16962 | 3 | 0 | 0 | 3 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0020 | 0/0 | 16947 | 3 | 0 | 0 | 3 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0021 | 0/0 | 16992 | 3 | 0 | 1 | 2 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0022 | 0/0 | 16991 | 3 | 2 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0023 | 0/0 | 16986 | 3 | 3 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0024 | 0/0 | 16985 | 3 | 0 | 1 | 2 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0025 | 0/0 | 16962 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0026 | 0/0 | 16950 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0027 | 0/0 | 16956 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0028 | 0/0 | 16967 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0029 | 0/1 | 16995 | 2 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0030 | 0/0 | 16983 | 2 | 0 | 1 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0031 | 0/0 | 16981 | 2 | 0 | 0 | 0 | 0 | 2 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0032 | 0/0 | 16979 | 2 | 0 | 2 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0033 | 0/0 | 16977 | 2 | 1 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0034 | 0/0 | 16990 | 2 | 0 | 1 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0035 | 0/0 | 16946 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0036 | 0/0 | 16946 | 2 | 1 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0037 | 0/0 | 16958 | 2 | 0 | 1 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0038 | 0/0 | 16975 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0039 | 0/0 | 16960 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0040 | 0/0 | 16956 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0041 | 0/0 | 16955 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0042 | 0/0 | 16955 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0043 | 0/0 | 16951 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0044 | 0/0 | 16962 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0045 | 0/0 | 16964 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0046 | 0/0 | 16963 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0047 | 0/0 | 16952 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0048 | 0/0 | 16962 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0049 | 0/0 | 16961 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0050 | 0/0 | 16961 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0051 | 0/0 | 16961 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0052 | 0/0 | 16962 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0053 | 0/0 | 16964 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0054 | 0/0 | 16963 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0055 | 0/0 | 16967 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0056 | 0/0 | 16959 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0057 | 0/0 | 16963 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0058 | 0/0 | 16947 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0059 | 0/0 | 16952 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0060 | 0/0 | 16959 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0061 | 0/0 | 16955 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0062 | 0/0 | 16952 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0063 | 0/0 | 16959 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0064 | 0/0 | 16955 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0065 | 0/0 | 16948 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0066 | 0/0 | 16963 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0067 | 0/0 | 16957 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0068 | 0/0 | 16953 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0069 | 0/0 | 16954 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0070 | 0/0 | 16948 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0071 | 0/0 | 16972 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0072 | 0/0 | 16968 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0073 | 0/0 | 16960 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0074 | 0/0 | 16964 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0075 | 0/0 | 16985 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0076 | 0/0 | 16986 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0077 | 0/0 | 16980 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0078 | 0/0 | 16988 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0079 | 0/0 | 16987 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0080 | 0/0 | 16983 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0081 | 0/0 | 16989 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0082 | 0/0 | 16993 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0083 | 0/0 | 16990 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0084 | 0/0 | 16989 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0085 | 0/0 | 16981 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0086 | 0/0 | 16976 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0087 | 0/0 | 16967 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0088 | 0/0 | 16989 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0089 | 0/0 | 16987 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0090 | 0/0 | 16986 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0091 | 0/0 | 16984 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0092 | 0/0 | 16982 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0093 | 0/0 | 16981 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0094 | 0/0 | 16984 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0095 | 0/0 | 16984 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0096 | 0/0 | 16988 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0097 | 0/0 | 16992 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0098 | 0/0 | 16984 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0099 | 0/0 | 16983 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0100 | 0/0 | 16988 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0101 | 0/0 | 16988 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0102 | 0/0 | 16946 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0103 | 0/0 | 16946 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0104 | 0/0 | 16946 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0105 | 1/0 | 16946 | 1 | 0 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0106 | 0/0 | 16946 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0107 | 0/0 | 16947 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0108 | 0/0 | 16946 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0109 | 0/0 | 16962 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
t0110 | 0/0 | 16949 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0069 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3387 | 124 | 21 | 19 | 66 | 2 | 15 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002 | 1/0 | 3387 | 45 | 34 | 4 | 1 | 2 | 3 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0003 | 0/0 | 3387 | 31 | 17 | 2 | 9 | 0 | 3 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0004 | 0/0 | 3387 | 8 | 4 | 4 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0005 | 0/0 | 3387 | 3 | 3 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0006 | 0/0 | 3387 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0007 | 0/0 | 3387 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0009 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0010 | 0/0 | 3387 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0011 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0012 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0002c0008 | 0/0 | 3387 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 20349 | 11 | 0 | 2 | 7 | 0 | 2 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0002 | 0/0 | 20371 | 9 | 7 | 0 | 2 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0005 | 0/0 | 20350 | 6 | 0 | 3 | 0 | 0 | 3 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0007 | 0/0 | 20374 | 6 | 0 | 1 | 5 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0008 | 0/0 | 20370 | 6 | 0 | 1 | 5 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0010 | 0/0 | 20375 | 5 | 0 | 1 | 4 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0011 | 0/0 | 20351 | 4 | 0 | 0 | 4 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0014 | 0/0 | 20373 | 4 | 0 | 0 | 3 | 1 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0017 | 0/0 | 20349 | 3 | 0 | 0 | 3 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0018 | 0/0 | 20348 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0019 | 0/0 | 20348 | 3 | 0 | 0 | 3 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0021 | 0/0 | 20378 | 3 | 0 | 1 | 2 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0022 | 0/0 | 20377 | 3 | 2 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0023 | 0/0 | 20372 | 3 | 3 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0024 | 0/0 | 20371 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0025 | 0/0 | 20348 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0029 | 0/1 | 20381 | 2 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0030 | 0/0 | 20369 | 2 | 0 | 1 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0031 | 0/0 | 20367 | 2 | 0 | 0 | 0 | 0 | 2 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0032 | 0/0 | 20365 | 2 | 0 | 2 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0033 | 0/0 | 20363 | 2 | 1 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0034 | 0/0 | 20376 | 2 | 0 | 1 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0044 | 0/0 | 20348 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0045 | 0/0 | 20350 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0046 | 0/0 | 20349 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0048 | 0/0 | 20348 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0049 | 0/0 | 20347 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0050 | 0/0 | 20347 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0051 | 0/0 | 20347 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0052 | 0/0 | 20348 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0053 | 0/0 | 20350 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0054 | 0/0 | 20349 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0055 | 0/0 | 20353 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0056 | 0/0 | 20345 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0057 | 0/0 | 20349 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0075 | 0/0 | 20371 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0076 | 0/0 | 20372 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0077 | 0/0 | 20366 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0078 | 0/0 | 20374 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0079 | 0/0 | 20373 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0080 | 0/0 | 20369 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0081 | 0/0 | 20375 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0082 | 0/0 | 20379 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0083 | 0/0 | 20376 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0084 | 0/0 | 20375 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0085 | 0/0 | 20367 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0086 | 0/0 | 20362 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0087 | 0/0 | 20353 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0088 | 0/0 | 20375 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0089 | 0/0 | 20373 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0090 | 0/0 | 20372 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0091 | 0/0 | 20370 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0092 | 0/0 | 20368 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0093 | 0/0 | 20367 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0094 | 0/0 | 20370 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0095 | 0/0 | 20370 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0096 | 0/0 | 20374 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0097 | 0/0 | 20378 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0098 | 0/0 | 20370 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0099 | 0/0 | 20369 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0100 | 0/0 | 20374 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0001t0101 | 0/0 | 20374 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0003 | 0/0 | 20332 | 8 | 4 | 0 | 1 | 1 | 2 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0009 | 0/0 | 20342 | 5 | 5 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0013 | 0/0 | 20343 | 4 | 4 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0035 | 0/0 | 20332 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0036 | 0/0 | 20332 | 2 | 1 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0037 | 0/0 | 20344 | 2 | 0 | 1 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0039 | 0/0 | 20346 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0040 | 0/0 | 20342 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0041 | 0/0 | 20341 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0042 | 0/0 | 20341 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0043 | 0/0 | 20337 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0060 | 0/0 | 20345 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0063 | 0/0 | 20345 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0064 | 0/0 | 20341 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0065 | 0/0 | 20334 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0067 | 0/0 | 20343 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0068 | 0/0 | 20339 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0069 | 0/0 | 20340 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0070 | 0/0 | 20334 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0074 | 0/0 | 20350 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0102 | 0/0 | 20332 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0103 | 0/0 | 20332 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0104 | 0/0 | 20332 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0105 | 1/0 | 20332 | 1 | 0 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0106 | 0/0 | 20332 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0107 | 0/0 | 20333 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0108 | 0/0 | 20332 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0002t0110 | 0/0 | 20335 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0003t0004 | 0/0 | 20337 | 8 | 8 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0003t0006 | 0/0 | 20337 | 6 | 2 | 1 | 1 | 0 | 2 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0003t0012 | 0/0 | 20338 | 4 | 1 | 0 | 3 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0003t0015 | 0/0 | 20337 | 3 | 2 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0003t0020 | 0/0 | 20333 | 3 | 0 | 0 | 3 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0003t0026 | 0/0 | 20336 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0003t0027 | 0/0 | 20342 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0003t0047 | 0/0 | 20338 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0003t0058 | 0/0 | 20333 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0003t0059 | 0/0 | 20338 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0004t0016 | 0/0 | 20338 | 3 | 0 | 3 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0004t0028 | 0/0 | 20353 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0004t0038 | 0/0 | 20361 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0004t0062 | 0/0 | 20338 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0004t0066 | 0/0 | 20349 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0005t0071 | 0/0 | 20358 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0005t0072 | 0/0 | 20354 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0005t0073 | 0/0 | 20346 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0006t0001 | 0/0 | 20349 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0007t0003 | 0/0 | 20332 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0009t0061 | 0/0 | 20341 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0010t0002 | 0/0 | 20371 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0011t0109 | 0/0 | 20348 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0001c0012t0018 | 0/0 | 20348 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
a0002c0008t0024 | 0/0 | 20371 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | copy fasta | chr2 | 182904115 | 183043457 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0005g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0005g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0007g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0007g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0007g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0007g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0007g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0008g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0008g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0008g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0008g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0008g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0008g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0010g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0010g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0010g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0010g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0010g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0011g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0011g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0011g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0011g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0014g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0014g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0014g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0014g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0017g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0017g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0017g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0018g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0018g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0019g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0019g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0021g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0021g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0021g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0022g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0022g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0022g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0023g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0023g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0023g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0024g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0024g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0025g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0025g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0029g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0029g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0030g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0030g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0031g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0031g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0032g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0032g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0033g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0033g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0034g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0034g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0044g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0045g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0046g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0048g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0049g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0050g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0051g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0052g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0053g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0054g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0055g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0056g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0057g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0075g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0076g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0077g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0078g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0079g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0080g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0081g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0082g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0083g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0084g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0085g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0086g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0087g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0088g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0089g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0090g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0091g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0092g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0093g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0094g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0095g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0096g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0097g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0098g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0099g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0100g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0001t0101g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0009g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0009g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0009g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0013g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0013g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0013g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0013g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0035g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0035g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0036g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0036g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0037g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0037g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0039g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0040g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0041g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0042g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0043g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0060g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0063g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0064g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0065g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0067g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0068g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0069g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0070g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0074g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0102g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0103g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0104g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0105g0069 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0106g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0107g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0108g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0002t0110g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0006g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0006g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0006g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0006g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0012g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0012g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0012g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0012g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0015g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0015g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0015g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0020g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0020g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0020g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0026g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0026g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0027g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0027g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0047g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0058g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0003t0059g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0004t0016g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0004t0016g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0004t0028g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0004t0028g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0004t0038g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0004t0062g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0004t0066g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0005t0071g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0005t0072g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0005t0073g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0006t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0007t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0009t0061g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0010t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0011t0109g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0001c0012t0018g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
a0002c0008t0024g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00438 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG00438 | hp2 | a0001 | c0001 | t0082 | g0085 | EAS | CHS | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | CHS | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG00597 | hp2 | a0001 | c0002 | t0003 | g0204 | EAS | CHS | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG00609 | hp1 | a0001 | c0001 | t0007 | g0060 | EAS | CHS | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG00609 | hp2 | a0001 | c0003 | t0012 | g0177 | EAS | CHS | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG00621 | hp1 | a0001 | c0003 | t0012 | g0174 | EAS | CHS | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01069 | hp1 | a0001 | c0001 | t0091 | g0068 | AMR | PUR | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01071 | hp2 | a0001 | c0001 | t0010 | g0132 | AMR | PUR | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01081 | hp1 | a0001 | c0001 | t0076 | g0066 | AMR | PUR | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01081 | hp2 | a0001 | c0003 | t0015 | g0009 | AMR | PUR | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01099 | hp1 | a0001 | c0004 | t0016 | g0001 | AMR | PUR | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01099 | hp2 | a0001 | c0001 | t0021 | g0120 | AMR | PUR | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01109 | hp1 | a0001 | c0002 | t0037 | g0213 | AMR | PUR | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01109 | hp2 | a0001 | c0001 | t0032 | g0131 | AMR | PUR | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01169 | hp1 | a0001 | c0002 | t0042 | g0011 | AMR | PUR | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01169 | hp2 | a0001 | c0001 | t0032 | g0088 | AMR | PUR | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01192 | hp1 | a0001 | c0001 | t0005 | g0036 | AMR | PUR | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01192 | hp2 | a0001 | c0001 | t0075 | g0118 | AMR | PUR | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01243 | hp1 | a0001 | c0001 | t0101 | g0103 | AMR | PUR | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01243 | hp2 | a0001 | c0003 | t0006 | g0170 | AMR | PUR | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01255 | hp1 | a0001 | c0001 | t0007 | g0117 | AMR | CLM | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01255 | hp2 | a0001 | c0004 | t0062 | g0194 | AMR | CLM | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01256 | hp1 | a0001 | c0001 | t0086 | g0072 | AMR | CLM | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01256 | hp2 | a0001 | c0001 | t0030 | g0087 | AMR | CLM | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01261 | hp1 | a0001 | c0002 | t0036 | g0197 | AMR | CLM | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01261 | hp2 | a0001 | c0001 | t0034 | g0106 | AMR | CLM | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01346 | hp1 | a0001 | c0001 | t0008 | g0122 | AMR | CLM | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01346 | hp2 | a0001 | c0002 | t0041 | g0012 | AMR | CLM | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01358 | hp1 | a0001 | c0004 | t0016 | g0010 | AMR | CLM | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01358 | hp2 | a0001 | c0001 | t0100 | g0104 | AMR | CLM | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01361 | hp1 | a0001 | c0001 | t0005 | g0019 | AMR | CLM | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01361 | hp2 | a0001 | c0004 | t0016 | g0001 | AMR | CLM | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01884 | hp1 | a0001 | c0002 | t0106 | g0143 | AFR | ACB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01884 | hp2 | a0001 | c0003 | t0004 | g0166 | AFR | ACB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01978 | hp1 | a0002 | c0008 | t0024 | g0135 | AMR | PEL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG01978 | hp2 | a0001 | c0001 | t0005 | g0018 | AMR | PEL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | ACB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02055 | hp2 | a0001 | c0001 | t0098 | g0079 | AFR | ACB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02056 | hp1 | a0001 | c0001 | t0092 | g0137 | EAS | KHV | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02074 | hp1 | a0001 | c0001 | t0008 | g0095 | EAS | KHV | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02074 | hp2 | a0001 | c0006 | t0001 | g0026 | EAS | KHV | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02080 | hp1 | a0001 | c0001 | t0024 | g0096 | EAS | KHV | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02080 | hp2 | a0001 | c0001 | t0055 | g0043 | EAS | KHV | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02145 | hp1 | a0001 | c0002 | t0107 | g0207 | AFR | ACB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02145 | hp2 | a0001 | c0003 | t0027 | g0185 | AFR | ACB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02257 | hp1 | a0001 | c0002 | t0068 | g0154 | AFR | ACB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02257 | hp2 | a0001 | c0003 | t0004 | g0163 | AFR | ACB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02258 | hp1 | a0001 | c0003 | t0004 | g0080 | AFR | ACB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02258 | hp2 | a0001 | c0002 | t0003 | g0201 | AFR | ACB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | ACB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02280 | hp2 | a0001 | c0001 | t0018 | g0070 | AFR | ACB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02451 | hp1 | a0001 | c0002 | t0069 | g0158 | AFR | ACB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02451 | hp2 | a0001 | c0002 | t0063 | g0190 | AFR | ACB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02523 | hp1 | a0001 | c0001 | t0080 | g0062 | EAS | KHV | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02523 | hp2 | a0001 | c0001 | t0046 | g0045 | EAS | KHV | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02572 | hp1 | a0001 | c0001 | t0090 | g0078 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02572 | hp2 | a0001 | c0003 | t0026 | g0171 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02615 | hp2 | a0001 | c0012 | t0018 | g0211 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02622 | hp1 | a0001 | c0003 | t0004 | g0161 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02622 | hp2 | a0001 | c0002 | t0013 | g0149 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02630 | hp1 | a0001 | c0001 | t0085 | g0083 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02630 | hp2 | a0001 | c0003 | t0026 | g0173 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02647 | hp1 | a0001 | c0005 | t0073 | g0156 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02647 | hp2 | a0001 | c0001 | t0095 | g0112 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02698 | hp1 | a0001 | c0001 | t0031 | g0127 | SAS | PJL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02698 | hp2 | a0001 | c0003 | t0047 | g0179 | SAS | PJL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02717 | hp1 | a0001 | c0001 | t0018 | g0195 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02717 | hp2 | a0001 | c0002 | t0074 | g0159 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02723 | hp1 | a0001 | c0003 | t0015 | g0008 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02723 | hp2 | a0001 | c0002 | t0103 | g0144 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02735 | hp1 | a0001 | c0002 | t0003 | g0198 | SAS | PJL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02818 | hp1 | a0001 | c0004 | t0028 | g0056 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02818 | hp2 | a0001 | c0002 | t0065 | g0191 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02886 | hp1 | a0001 | c0003 | t0004 | g0162 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02886 | hp2 | a0001 | c0004 | t0066 | g0055 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02896 | hp1 | a0001 | c0003 | t0012 | g0175 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02896 | hp2 | a0001 | c0001 | t0022 | g0111 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02897 | hp1 | a0001 | c0001 | t0022 | g0110 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02897 | hp2 | a0001 | c0002 | t0102 | g0200 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02922 | hp1 | a0001 | c0011 | t0109 | g0215 | AFR | ESN | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02922 | hp2 | a0001 | c0003 | t0006 | g0168 | AFR | ESN | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02965 | hp1 | a0001 | c0003 | t0004 | g0160 | AFR | ESN | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02965 | hp2 | a0001 | c0002 | t0009 | g0145 | AFR | ESN | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02970 | hp1 | a0001 | c0003 | t0006 | g0169 | AFR | ESN | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02970 | hp2 | a0001 | c0002 | t0003 | g0199 | AFR | ESN | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02976 | hp1 | a0001 | c0001 | t0048 | g0196 | AFR | ESN | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | ESN | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03017 | hp1 | a0001 | c0002 | t0037 | g0212 | SAS | PJL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03017 | hp2 | a0001 | c0001 | t0099 | g0089 | SAS | PJL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03041 | hp1 | a0001 | c0002 | t0036 | g0208 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03041 | hp2 | a0001 | c0002 | t0039 | g0005 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03098 | hp1 | a0001 | c0001 | t0023 | g0097 | AFR | MSL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03098 | hp2 | a0001 | c0003 | t0004 | g0165 | AFR | MSL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03139 | hp1 | a0001 | c0001 | t0023 | g0075 | AFR | ESN | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03139 | hp2 | a0001 | c0002 | t0009 | g0151 | AFR | ESN | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03195 | hp1 | a0001 | c0002 | t0108 | g0014 | AFR | ESN | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03195 | hp2 | a0001 | c0001 | t0089 | g0076 | AFR | ESN | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03209 | hp1 | a0001 | c0002 | t0035 | g0209 | AFR | MSL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03209 | hp2 | a0001 | c0002 | t0013 | g0147 | AFR | MSL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03225 | hp1 | a0001 | c0002 | t0003 | g0206 | AFR | MSL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03225 | hp2 | a0001 | c0003 | t0004 | g0164 | AFR | MSL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03453 | hp1 | a0001 | c0002 | t0043 | g0013 | AFR | MSL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03453 | hp2 | a0001 | c0001 | t0033 | g0077 | AFR | MSL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03486 | hp1 | a0001 | c0002 | t0040 | g0006 | AFR | MSL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | MSL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03540 | hp1 | a0001 | c0002 | t0009 | g0153 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03540 | hp2 | a0001 | c0002 | t0003 | g0192 | AFR | GWD | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03579 | hp1 | a0001 | c0005 | t0072 | g0157 | AFR | MSL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03579 | hp2 | a0001 | c0002 | t0067 | g0152 | AFR | MSL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03654 | hp1 | a0001 | c0003 | t0006 | g0057 | SAS | PJL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03654 | hp2 | a0001 | c0002 | t0003 | g0203 | SAS | PJL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03710 | hp1 | a0001 | c0001 | t0005 | g0031 | SAS | PJL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03710 | hp2 | a0001 | c0001 | t0005 | g0140 | SAS | PJL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03831 | hp1 | a0001 | c0001 | t0057 | g0037 | SAS | BEB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03831 | hp2 | a0001 | c0001 | t0031 | g0093 | SAS | BEB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03834 | hp1 | a0001 | c0007 | t0003 | g0205 | SAS | BEB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03927 | hp1 | a0001 | c0001 | t0034 | g0116 | SAS | BEB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03927 | hp2 | a0001 | c0001 | t0005 | g0021 | SAS | BEB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03942 | hp1 | a0001 | c0001 | t0029 | g0187 | SAS | BEB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03942 | hp2 | a0001 | c0001 | t0096 | g0073 | SAS | BEB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG04115 | hp1 | a0001 | c0001 | t0088 | g0141 | SAS | STU | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG04115 | hp2 | a0001 | c0003 | t0006 | g0058 | SAS | STU | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG04199 | hp1 | a0001 | c0001 | t0030 | g0133 | SAS | STU | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG04199 | hp2 | a0001 | c0001 | t0056 | g0029 | SAS | STU | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18612 | hp2 | a0001 | c0001 | t0008 | g0063 | EAS | CHB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18939 | hp1 | a0001 | c0001 | t0054 | g0042 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18939 | hp2 | a0001 | c0001 | t0079 | g0125 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18942 | hp1 | a0001 | c0001 | t0053 | g0022 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18942 | hp2 | a0001 | c0001 | t0007 | g0107 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18944 | hp1 | a0001 | c0001 | t0007 | g0100 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18944 | hp2 | a0001 | c0001 | t0019 | g0002 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18949 | hp1 | a0001 | c0001 | t0014 | g0139 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18949 | hp2 | a0001 | c0001 | t0025 | g0035 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18960 | hp1 | a0001 | c0001 | t0008 | g0098 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18960 | hp2 | a0001 | c0001 | t0019 | g0002 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18964 | hp1 | a0001 | c0001 | t0010 | g0188 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18964 | hp2 | a0001 | c0001 | t0010 | g0186 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18969 | hp1 | a0001 | c0001 | t0022 | g0119 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18969 | hp2 | a0001 | c0003 | t0020 | g0181 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18970 | hp1 | a0001 | c0001 | t0087 | g0123 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18972 | hp1 | a0001 | c0001 | t0078 | g0136 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18972 | hp2 | a0001 | c0003 | t0006 | g0182 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18973 | hp1 | a0001 | c0001 | t0011 | g0023 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18973 | hp2 | a0001 | c0001 | t0021 | g0121 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18975 | hp1 | a0001 | c0001 | t0093 | g0064 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18975 | hp2 | a0001 | c0001 | t0011 | g0024 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18978 | hp1 | a0001 | c0001 | t0084 | g0126 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18983 | hp1 | a0001 | c0001 | t0077 | g0130 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18983 | hp2 | a0001 | c0001 | t0017 | g0046 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18985 | hp1 | a0001 | c0001 | t0010 | g0094 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18985 | hp2 | a0001 | c0001 | t0025 | g0027 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18992 | hp2 | a0001 | c0001 | t0010 | g0128 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18995 | hp1 | a0001 | c0001 | t0050 | g0033 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18995 | hp2 | a0001 | c0003 | t0020 | g0142 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18998 | hp1 | a0001 | c0001 | t0007 | g0065 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18998 | hp2 | a0001 | c0001 | t0051 | g0034 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18999 | hp1 | a0001 | c0001 | t0017 | g0047 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18999 | hp2 | a0001 | c0001 | t0024 | g0086 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19004 | hp1 | a0001 | c0001 | t0017 | g0049 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19004 | hp2 | a0001 | c0001 | t0083 | g0129 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19005 | hp1 | a0001 | c0001 | t0097 | g0061 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19005 | hp2 | a0001 | c0003 | t0058 | g0180 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19010 | hp1 | a0001 | c0001 | t0044 | g0044 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19010 | hp2 | a0001 | c0001 | t0033 | g0101 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19043 | hp1 | a0001 | c0005 | t0071 | g0155 | AFR | LWK | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19043 | hp2 | a0001 | c0009 | t0061 | g0184 | AFR | LWK | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19056 | hp1 | a0001 | c0003 | t0012 | g0167 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19056 | hp2 | a0001 | c0001 | t0011 | g0015 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19058 | hp1 | a0001 | c0001 | t0008 | g0102 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19058 | hp2 | a0001 | c0001 | t0011 | g0025 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19060 | hp1 | a0001 | c0010 | t0002 | g0105 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19060 | hp2 | a0001 | c0003 | t0020 | g0172 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19062 | hp1 | a0001 | c0001 | t0052 | g0041 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19062 | hp2 | a0001 | c0001 | t0014 | g0092 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19072 | hp1 | a0001 | c0001 | t0008 | g0115 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19072 | hp2 | a0001 | c0001 | t0019 | g0053 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19078 | hp1 | a0001 | c0001 | t0081 | g0091 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19078 | hp2 | a0001 | c0001 | t0049 | g0040 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19080 | hp1 | a0001 | c0001 | t0021 | g0113 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19080 | hp2 | a0001 | c0001 | t0045 | g0048 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19086 | hp1 | a0001 | c0001 | t0007 | g0114 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19086 | hp2 | a0001 | c0003 | t0059 | g0178 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19240 | hp1 | a0001 | c0002 | t0009 | g0003 | AFR | YRI | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA19240 | hp2 | a0001 | c0003 | t0027 | g0176 | AFR | YRI | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA20752 | hp1 | a0001 | c0001 | t0094 | g0067 | EUR | TSI | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA20752 | hp2 | a0001 | c0002 | t0003 | g0202 | EUR | TSI | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA20805 | hp1 | a0001 | c0002 | t0110 | g0214 | EUR | TSI | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA20805 | hp2 | a0001 | c0001 | t0014 | g0134 | EUR | TSI | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02109 | hp1 | a0001 | c0002 | t0064 | g0189 | AFR | ACB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02109 | hp2 | a0001 | c0004 | t0028 | g0054 | AFR | ACB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02486 | hp1 | a0001 | c0002 | t0035 | g0210 | AFR | ACB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02486 | hp2 | a0001 | c0004 | t0038 | g0004 | AFR | ACB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02559 | hp1 | a0001 | c0003 | t0015 | g0007 | AFR | ACB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG02559 | hp2 | a0001 | c0002 | t0009 | g0003 | AFR | ACB | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | MSL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG03471 | hp2 | a0001 | c0002 | t0070 | g0150 | AFR | MSL | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG06807 | hp1 | a0001 | c0002 | t0104 | g0193 | AFR | USA | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | USA | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA18955 | hp2 | a0001 | c0001 | t0014 | g0109 | EAS | JPT | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA20300 | hp1 | a0001 | c0001 | t0023 | g0074 | AFR | USA | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA20300 | hp2 | a0001 | c0002 | t0013 | g0148 | AFR | USA | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA21309 | hp1 | a0001 | c0002 | t0013 | g0146 | AFR | LWK | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
NA21309 | hp2 | a0001 | c0002 | t0060 | g0183 | AFR | LWK | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0029 | g0138 | REF | REF | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0105 | g0069 | REF | REF | NCKAP1_chr2_182904115_183043457 | NCKAP1 | chr2 | 182904115 | 183043457 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:182989153
|
G | C | 1 | a0002 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.824C>G | p.Thr275Ser | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 9/31 | 1182/20332 | 824/3387 | 275/1128 | chr2 | 182989153 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:182934830
|
G | C | 6 | a0001c0001a0001c0006a0001c0010others(3): Show | 129 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(126): Show |
splice_region_variant&synonymous_variant | LOW | c.2781C>G | p.Val927Val | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/31 | 3139/20332 | 2781/3387 | 927/1128 | chr2 | 182934830 | ||
chr2:182952426
|
T | C | 1 | a0001c0005 | 3 | HG02647.hp1 HG03579.hp1 NA19043.hp1 |
synonymous_variant | LOW | c.2580A>G | p.Ser860Ser | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/31 | 2938/20332 | 2580/3387 | 860/1128 | chr2 | 182952426 | ||
chr2:182952857
|
C | T | 1 | a0001c0007 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.2439G>A | p.Ala813Ala | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 22/31 | 2797/20332 | 2439/3387 | 813/1128 | chr2 | 182952857 | ||
chr2:182953229
|
T | A | 1 | a0001c0003 | 31 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
synonymous_variant | LOW | c.2256A>T | p.Ser752Ser | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 21/31 | 2614/20332 | 2256/3387 | 752/1128 | chr2 | 182953229 | ||
chr2:182983325
|
A | G | 1 | a0001c0004 | 8 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(5): Show |
synonymous_variant | LOW | c.1062T>C | p.Ala354Ala | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 11/31 | 1420/20332 | 1062/3387 | 354/1128 | chr2 | 182983325 | ||
chr2:182995707
|
G | A | 1 | a0001c0009 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.735C>T | p.Ser245Ser | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 7/31 | 1093/20332 | 735/3387 | 245/1128 | chr2 | 182995707 | ||
chr2:183002203
|
G | A | 1 | a0001c0010 | 1 | NA19060.hp1 | synonymous_variant | LOW | c.436C>T | p.Leu146Leu | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 5/31 | 794/20332 | 436/3387 | 146/1128 | chr2 | 183002203 | ||
chr2:183023842
|
G | T | 1 | a0001c0006 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.183C>A | p.Val61Val | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/31 | 541/20332 | 183/3387 | 61/1128 | chr2 | 183023842 | ||
chr2:183038007
|
G | A | 1 | a0001c0011 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.93C>T | p.Leu31Leu | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/31 | 451/20332 | 93/3387 | 31/1128 | chr2 | 183038007 | ||
chr2:183038040
|
G | A | 1 | a0001c0012 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.60C>T | p.Leu20Leu | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/31 | 418/20332 | 60/3387 | 20/1128 | chr2 | 183038040 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:182909127
|
T | C | 2 | a0001c0004t0028a0001c0004t0066 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*16575A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 16575 | chr2 | 182909127 | |||||
chr2:182909361
|
C | T | 1 | a0001c0003t0026 | 2 | HG02572.hp2 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*16341G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 16341 | chr2 | 182909361 | |||||
chr2:182909564
|
C | T | 1 | a0001c0011t0109 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*16138G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 16138 | chr2 | 182909564 | |||||
chr2:182909568
|
C | A | 2 | a0001c0001t0079a0001c0001t0084 | 2 | NA18939.hp2 NA18978.hp1 |
3_prime_UTR_variant | MODIFIER | c.*16134G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 16134 | chr2 | 182909568 | |||||
chr2:182909613
|
C | T | 1 | a0001c0003t0004 | 8 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*16089G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 16089 | chr2 | 182909613 | |||||
chr2:182909908
|
G | A | 1 | a0001c0001t0085 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*15794C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 15794 | chr2 | 182909908 | |||||
chr2:182909942
|
G | A | 1 | a0001c0004t0062 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15760C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 15760 | chr2 | 182909942 | |||||
chr2:182910141
|
A | C | 75 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(72): Show | 141 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*15561T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 15561 | chr2 | 182910141 | |||||
chr2:182910182
|
C | T | 8 | a0001c0002t0009a0001c0002t0013a0001c0002t0039others(5): Show | 15 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*15520G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 15520 | chr2 | 182910182 | |||||
chr2:182910236
|
C | A | 1 | a0001c0004t0062 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15466G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 15466 | chr2 | 182910236 | |||||
chr2:182910312
|
T | C | 19 | a0001c0001t0001a0001c0001t0005a0001c0001t0011others(16): Show | 42 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*15390A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 15390 | chr2 | 182910312 | |||||
chr2:182910377
|
G | A | 3 | a0001c0001t0018a0001c0001t0048a0001c0012t0018 | 4 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*15325C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 15325 | chr2 | 182910377 | |||||
chr2:182910480
|
G | A | 1 | a0001c0004t0062 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15222C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 15222 | chr2 | 182910480 | |||||
chr2:182910850
|
A | G | 1 | a0001c0003t0026 | 2 | HG02572.hp2 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*14852T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 14852 | chr2 | 182910850 | |||||
chr2:182910948
|
G | GC | 23 | a0001c0001t0001a0001c0001t0017a0001c0001t0018others(20): Show | 39 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*14753dupG | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 14753 | chr2 | 182910948 | |||||
chr2:182910948
|
G | GCA | 9 | a0001c0001t0014a0001c0001t0022a0001c0001t0029others(6): Show | 17 | HG01069.hp1 HG01109.hp2 HG01169.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*14753_*14754insTG | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 14753 | chr2 | 182910948 | |||||
chr2:182910948
|
G | GCAC | 19 | a0001c0001t0007a0001c0001t0008a0001c0001t0021others(16): Show | 32 | HG00609.hp1 HG01099.hp2 HG01192.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*14753_*14754insGT others(1): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 14753 | chr2 | 182910948 | |||||
chr2:182910948
|
G | GCACC | 13 | a0001c0001t0002a0001c0001t0010a0001c0001t0031others(10): Show | 28 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*14753_*14754insGG others(2): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 14753 | chr2 | 182910948 | |||||
chr2:182910948
|
G | GCACCC | 3 | a0001c0001t0023a0001c0001t0083a0001c0001t0089 | 5 | HG03098.hp1 HG03139.hp1 HG03195.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*14753_*14754insGG others(3): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 14753 | chr2 | 182910948 | |||||
chr2:182910948
|
G | GCC | 3 | a0001c0001t0005a0001c0001t0045a0001c0001t0049 | 8 | HG01192.hp1 HG01361.hp1 HG01978.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*14753_*14754insGG | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 14753 | chr2 | 182910948 | |||||
chr2:182910948
|
G | GCCC | 3 | a0001c0001t0011a0001c0001t0053a0001c0011t0109 | 6 | HG02922.hp1 NA18942.hp1 NA18973.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*14753_*14754insGG others(1): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 14753 | chr2 | 182910948 | |||||
chr2:182910949
|
CT | C | 3 | a0001c0002t0037a0001c0002t0041a0001c0002t0042 | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*14752delA | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 14752 | chr2 | 182910949 | |||||
chr2:182910950
|
T | C | 103 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(100): Show | 196 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*14752A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 14752 | chr2 | 182910950 | |||||
chr2:182910959
|
A | C | 67 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(64): Show | 129 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*14743T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 14743 | chr2 | 182910959 | |||||
chr2:182910972
|
C | T | 75 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(72): Show | 141 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*14730G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 14730 | chr2 | 182910972 | |||||
chr2:182911025
|
C | T | 2 | a0001c0002t0043a0001c0002t0065 | 2 | HG02818.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*14677G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 14677 | chr2 | 182911025 | |||||
chr2:182911037
|
G | A | 3 | a0001c0001t0018a0001c0001t0048a0001c0012t0018 | 4 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*14665C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 14665 | chr2 | 182911037 | |||||
chr2:182911050
|
G | A | 1 | a0001c0003t0059 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14652C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 14652 | chr2 | 182911050 | |||||
chr2:182911361
|
T | C | 12 | a0001c0002t0060a0001c0003t0004a0001c0003t0006others(9): Show | 33 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*14341A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 14341 | chr2 | 182911361 | |||||
chr2:182911395
|
A | G | 2 | a0001c0002t0060a0001c0009t0061 | 2 | NA19043.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*14307T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 14307 | chr2 | 182911395 | |||||
chr2:182911413
|
A | G | 2 | a0001c0002t0063a0001c0002t0064 | 2 | HG02109.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*14289T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 14289 | chr2 | 182911413 | |||||
chr2:182911550
|
A | T | 67 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(64): Show | 129 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*14152T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 14152 | chr2 | 182911550 | |||||
chr2:182911739
|
A | T | 20 | a0001c0002t0009a0001c0002t0013a0001c0002t0037others(17): Show | 31 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*13963T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 13963 | chr2 | 182911739 | |||||
chr2:182911750
|
AC | A | 1 | a0001c0003t0026 | 2 | HG02572.hp2 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*13951delG | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 13951 | chr2 | 182911750 | |||||
chr2:182911850
|
T | C | 3 | a0001c0005t0071a0001c0005t0072a0001c0005t0073 | 3 | HG02647.hp1 HG03579.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*13852A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 13852 | chr2 | 182911850 | |||||
chr2:182911868
|
G | GCAGTAAC others(1): Show |
67 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(64): Show | 129 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*13826_*13833dupAG others(6): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 13833 | chr2 | 182911868 | |||||
chr2:182911885
|
G | C | 1 | a0001c0002t0069 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13817C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 13817 | chr2 | 182911885 | |||||
chr2:182912036
|
A | G | 1 | a0001c0002t0067 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*13666T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 13666 | chr2 | 182912036 | |||||
chr2:182912086
|
A | T | 7 | a0001c0002t0009a0001c0002t0013a0001c0002t0039others(4): Show | 14 | HG02257.hp1 HG02559.hp2 HG02622.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*13616T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 13616 | chr2 | 182912086 | |||||
chr2:182912178
|
T | C | 2 | a0001c0002t0063a0001c0002t0064 | 2 | HG02109.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*13524A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 13524 | chr2 | 182912178 | |||||
chr2:182912253
|
G | T | 3 | a0001c0002t0037a0001c0002t0041a0001c0002t0042 | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*13449C>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 13449 | chr2 | 182912253 | |||||
chr2:182912547
|
G | A | 1 | a0001c0001t0046 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*13155C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 13155 | chr2 | 182912547 | |||||
chr2:182912717
|
T | C | 1 | a0001c0004t0038 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12985A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 12985 | chr2 | 182912717 | |||||
chr2:182912849
|
A | AAAGG | 31 | a0001c0001t0001a0001c0001t0005a0001c0001t0011others(28): Show | 75 | HG00609.hp2 HG00621.hp1 HG00621.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*12849_*12852dupCC others(2): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 12852 | chr2 | 182912849 | |||||
chr2:182912849
|
A | AAAGGAAG others(1): Show |
10 | a0001c0001t0055a0001c0001t0087a0001c0002t0037others(7): Show | 12 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*12845_*12852dupCC others(6): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 12852 | chr2 | 182912849 | |||||
chr2:182912849
|
A | AAAGGAAG others(5): Show |
8 | a0001c0002t0009a0001c0002t0013a0001c0002t0040others(5): Show | 15 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*12841_*12852dupCC others(10): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 12852 | chr2 | 182912849 | |||||
chr2:182912849
|
A | AAAGGAAG others(9): Show |
5 | a0001c0001t0033a0001c0001t0086a0001c0002t0039others(2): Show | 7 | HG01256.hp1 HG02109.hp2 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*12837_*12852dupCC others(14): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 12852 | chr2 | 182912849 | |||||
chr2:182912849
|
A | AAAGGAAG others(13): Show |
7 | a0001c0001t0031a0001c0001t0032a0001c0001t0077others(4): Show | 9 | HG01109.hp2 HG01169.hp2 HG02056.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*12833_*12852dupCC others(18): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 12852 | chr2 | 182912849 | |||||
chr2:182912849
|
A | AAAGGAAG others(17): Show |
18 | a0001c0001t0002a0001c0001t0008a0001c0001t0023others(15): Show | 35 | HG00438.hp1 HG00597.hp1 HG01069.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*12829_*12852dupCC others(22): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 12852 | chr2 | 182912849 | |||||
chr2:182912849
|
A | AAAGGAAG others(21): Show |
14 | a0001c0001t0007a0001c0001t0010a0001c0001t0014others(11): Show | 27 | HG00609.hp1 HG01071.hp2 HG01243.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*12825_*12852dupCC others(26): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 12852 | chr2 | 182912849 | |||||
chr2:182912849
|
A | AAAGGAAG others(25): Show |
4 | a0001c0001t0021a0001c0001t0022a0001c0001t0082others(1): Show | 8 | HG00438.hp2 HG01099.hp2 HG02896.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*12821_*12852dupCC others(30): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 12852 | chr2 | 182912849 | |||||
chr2:182912849
|
A | AAAGGAAG others(29): Show |
1 | a0001c0001t0029 | 2 | HG03942.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12817_*12852dupCC others(34): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 12852 | chr2 | 182912849 | |||||
chr2:182913010
|
G | C | 1 | a0001c0002t0065 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12692C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 12692 | chr2 | 182913010 | |||||
chr2:182913073
|
C | T | 1 | a0001c0002t0036 | 2 | HG01261.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12629G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 12629 | chr2 | 182913073 | |||||
chr2:182913284
|
G | A | 1 | a0001c0011t0109 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12418C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 12418 | chr2 | 182913284 | |||||
chr2:182913319
|
G | A | 1 | a0001c0001t0094 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12383C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 12383 | chr2 | 182913319 | |||||
chr2:182913856
|
C | A | 1 | a0001c0003t0058 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11846G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 11846 | chr2 | 182913856 | |||||
chr2:182913889
|
T | G | 1 | a0001c0004t0038 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11813A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 11813 | chr2 | 182913889 | |||||
chr2:182913938
|
A | G | 1 | a0001c0001t0054 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11764T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 11764 | chr2 | 182913938 | |||||
chr2:182914468
|
T | A | 1 | a0001c0003t0004 | 8 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*11234A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 11234 | chr2 | 182914468 | |||||
chr2:182914500
|
A | AC | 103 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(100): Show | 197 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*11201_*11202insG | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 11201 | chr2 | 182914500 | |||||
chr2:182914530
|
T | A | 1 | a0001c0001t0081 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11172A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 11172 | chr2 | 182914530 | |||||
chr2:182914807
|
G | A | 8 | a0001c0002t0037a0001c0002t0041a0001c0002t0042others(5): Show | 12 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*10895C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 10895 | chr2 | 182914807 | |||||
chr2:182914827
|
C | G | 3 | a0001c0002t0037a0001c0002t0041a0001c0002t0042 | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10875G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 10875 | chr2 | 182914827 | |||||
chr2:182915304
|
GT | G | 4 | a0001c0002t0043a0001c0002t0063a0001c0002t0064others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*10397delA | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 10397 | chr2 | 182915304 | |||||
chr2:182915680
|
T | C | 67 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(64): Show | 129 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*10022A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 10022 | chr2 | 182915680 | |||||
chr2:182915816
|
T | C | 1 | a0001c0002t0106 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9886A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 9886 | chr2 | 182915816 | |||||
chr2:182915978
|
A | G | 1 | a0001c0001t0081 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9724T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 9724 | chr2 | 182915978 | |||||
chr2:182916120
|
T | C | 106 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(103): Show | 200 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*9582A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 9582 | chr2 | 182916120 | |||||
chr2:182916148
|
T | C | 1 | a0001c0002t0042 | 1 | HG01169.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9554A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 9554 | chr2 | 182916148 | |||||
chr2:182916169
|
C | CA | 51 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(48): Show | 97 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*9532dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 9532 | chr2 | 182916169 | |||||
chr2:182916169
|
C | CAA | 25 | a0001c0001t0001a0001c0001t0005a0001c0001t0011others(22): Show | 50 | HG00621.hp2 HG01069.hp1 HG01069.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*9531_*9532dupTT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 9532 | chr2 | 182916169 | |||||
chr2:182916182
|
A | C | 3 | a0001c0005t0071a0001c0005t0072a0001c0005t0073 | 3 | HG02647.hp1 HG03579.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9520T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 9520 | chr2 | 182916182 | |||||
chr2:182916317
|
A | C | 1 | a0001c0004t0016 | 3 | HG01099.hp1 HG01358.hp1 HG01361.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9385T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 9385 | chr2 | 182916317 | |||||
chr2:182917046
|
A | G | 1 | a0001c0001t0048 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8656T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 8656 | chr2 | 182917046 | |||||
chr2:182917129
|
T | G | 1 | a0001c0001t0095 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8573A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 8573 | chr2 | 182917129 | |||||
chr2:182917290
|
G | A | 1 | a0001c0002t0035 | 2 | HG02486.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8412C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 8412 | chr2 | 182917290 | |||||
chr2:182917387
|
G | A | 113 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(110): Show | 215 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*8315C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 8315 | chr2 | 182917387 | |||||
chr2:182917412
|
G | A | 1 | a0001c0001t0078 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8290C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 8290 | chr2 | 182917412 | |||||
chr2:182917672
|
A | G | 1 | a0001c0002t0060 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8030T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 8030 | chr2 | 182917672 | |||||
chr2:182917865
|
G | A | 1 | a0001c0004t0038 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7837C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 7837 | chr2 | 182917865 | |||||
chr2:182918432
|
C | T | 1 | a0001c0002t0042 | 1 | HG01169.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7270G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 7270 | chr2 | 182918432 | |||||
chr2:182918717
|
A | G | 1 | a0001c0004t0066 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6985T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 6985 | chr2 | 182918717 | |||||
chr2:182919420
|
C | A | 1 | a0001c0002t0074 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6282G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 6282 | chr2 | 182919420 | |||||
chr2:182919447
|
A | G | 1 | a0001c0002t0069 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6255T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 6255 | chr2 | 182919447 | |||||
chr2:182919632
|
C | T | 102 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(99): Show | 196 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*6070G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 6070 | chr2 | 182919632 | |||||
chr2:182919798
|
C | T | 10 | a0001c0003t0004a0001c0003t0006a0001c0003t0012others(7): Show | 31 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*5904G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 5904 | chr2 | 182919798 | |||||
chr2:182919896
|
T | C | 103 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(100): Show | 197 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*5806A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 5806 | chr2 | 182919896 | |||||
chr2:182919967
|
A | C | 1 | a0001c0001t0057 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5735T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 5735 | chr2 | 182919967 | |||||
chr2:182920129
|
G | A | 1 | a0001c0001t0096 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5573C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 5573 | chr2 | 182920129 | |||||
chr2:182920342
|
G | T | 1 | a0001c0002t0104 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5360C>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 5360 | chr2 | 182920342 | |||||
chr2:182920375
|
A | G | 2 | a0001c0004t0016a0001c0004t0062 | 4 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5327T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 5327 | chr2 | 182920375 | |||||
chr2:182920467
|
C | T | 1 | a0001c0011t0109 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5235G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 5235 | chr2 | 182920467 | |||||
chr2:182920759
|
C | A | 1 | a0001c0001t0097 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4943G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 4943 | chr2 | 182920759 | |||||
chr2:182920852
|
C | T | 103 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(100): Show | 197 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*4850G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 4850 | chr2 | 182920852 | |||||
chr2:182920870
|
G | A | 44 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(41): Show | 82 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*4832C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 4832 | chr2 | 182920870 | |||||
chr2:182920889
|
T | TA | 68 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(65): Show | 131 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*4812dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 4812 | chr2 | 182920889 | |||||
chr2:182920964
|
C | T | 2 | a0001c0002t0067a0001c0002t0068 | 2 | HG02257.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4738G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 4738 | chr2 | 182920964 | |||||
chr2:182920991
|
G | C | 1 | a0001c0001t0057 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4711C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 4711 | chr2 | 182920991 | |||||
chr2:182921119
|
G | A | 20 | a0001c0001t0001a0001c0001t0005a0001c0001t0011others(17): Show | 43 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*4583C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 4583 | chr2 | 182921119 | |||||
chr2:182921148
|
ATAAC | A | 8 | a0001c0002t0009a0001c0002t0013a0001c0002t0039others(5): Show | 15 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4550_*4553delGTTA | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 4550 | chr2 | 182921148 | |||||
chr2:182921322
|
G | A | 1 | a0001c0002t0103 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4380C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 4380 | chr2 | 182921322 | |||||
chr2:182921654
|
C | T | 3 | a0001c0001t0018a0001c0001t0048a0001c0012t0018 | 4 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4048G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 4048 | chr2 | 182921654 | |||||
chr2:182921692
|
C | A | 3 | a0001c0002t0037a0001c0002t0041a0001c0002t0042 | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4010G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 4010 | chr2 | 182921692 | |||||
chr2:182921997
|
C | T | 1 | a0001c0001t0077 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3705G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 3705 | chr2 | 182921997 | |||||
chr2:182922035
|
C | T | 67 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(64): Show | 129 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*3667G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 3667 | chr2 | 182922035 | |||||
chr2:182922085
|
C | T | 1 | a0001c0003t0047 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3617G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 3617 | chr2 | 182922085 | |||||
chr2:182922091
|
A | C | 1 | a0001c0002t0103 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3611T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 3611 | chr2 | 182922091 | |||||
chr2:182922414
|
A | G | 91 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(88): Show | 178 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*3288T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 3288 | chr2 | 182922414 | |||||
chr2:182922493
|
G | A | 1 | a0001c0003t0015 | 3 | HG01081.hp2 HG02559.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3209C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 3209 | chr2 | 182922493 | |||||
chr2:182922602
|
C | T | 1 | a0001c0001t0076 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3100G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 3100 | chr2 | 182922602 | |||||
chr2:182923023
|
G | A | 1 | a0001c0002t0108 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2679C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 2679 | chr2 | 182923023 | |||||
chr2:182923092
|
T | C | 2 | a0001c0001t0098a0001c0001t0099 | 2 | HG02055.hp2 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2610A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 2610 | chr2 | 182923092 | |||||
chr2:182923093
|
A | C | 2 | a0001c0004t0028a0001c0004t0066 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2609T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 2609 | chr2 | 182923093 | |||||
chr2:182923217
|
T | C | 2 | a0001c0004t0028a0001c0004t0066 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2485A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 2485 | chr2 | 182923217 | |||||
chr2:182923281
|
C | CT | 7 | a0001c0001t0075a0001c0002t0043a0001c0002t0063others(4): Show | 8 | HG01192.hp2 HG02109.hp1 HG02109.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2420dupA | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 2420 | chr2 | 182923281 | |||||
chr2:182923625
|
G | A | 1 | a0001c0011t0109 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2077C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 2077 | chr2 | 182923625 | |||||
chr2:182923641
|
C | T | 8 | a0001c0002t0037a0001c0002t0041a0001c0002t0042others(5): Show | 12 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2061G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 2061 | chr2 | 182923641 | |||||
chr2:182923727
|
G | A | 99 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(96): Show | 193 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*1975C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 1975 | chr2 | 182923727 | |||||
chr2:182923755
|
A | G | 1 | a0001c0002t0102 | 1 | HG02897.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1947T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 1947 | chr2 | 182923755 | |||||
chr2:182923758
|
T | C | 2 | a0001c0004t0016a0001c0004t0062 | 4 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1944A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 1944 | chr2 | 182923758 | |||||
chr2:182924030
|
T | C | 2 | a0001c0004t0028a0001c0004t0066 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1672A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 1672 | chr2 | 182924030 | |||||
chr2:182924050
|
C | T | 2 | a0001c0002t0041a0001c0003t0004 | 9 | HG01346.hp2 HG01884.hp2 HG02257.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1652G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 1652 | chr2 | 182924050 | |||||
chr2:182924096
|
T | C | 4 | a0001c0001t0017a0001c0001t0044a0001c0001t0045others(1): Show | 6 | HG02523.hp2 NA18983.hp2 NA18999.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1606A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 1606 | chr2 | 182924096 | |||||
chr2:182924265
|
T | A | 4 | a0001c0002t0043a0001c0002t0063a0001c0002t0064others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1437A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 1437 | chr2 | 182924265 | |||||
chr2:182924274
|
T | C | 1 | a0001c0002t0108 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1428A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 1428 | chr2 | 182924274 | |||||
chr2:182924318
|
T | C | 3 | a0001c0004t0028a0001c0004t0038a0001c0004t0066 | 4 | HG02109.hp2 HG02486.hp2 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1384A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 1384 | chr2 | 182924318 | |||||
chr2:182924508
|
T | C | 2 | a0001c0001t0100a0001c0001t0101 | 2 | HG01243.hp1 HG01358.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1194A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 1194 | chr2 | 182924508 | |||||
chr2:182924576
|
A | AT | 8 | a0001c0002t0009a0001c0002t0013a0001c0002t0039others(5): Show | 15 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1125dupA | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 1125 | chr2 | 182924576 | |||||
chr2:182924760
|
G | C | 12 | a0001c0002t0009a0001c0002t0013a0001c0002t0039others(9): Show | 19 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*942C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 942 | chr2 | 182924760 | |||||
chr2:182924921
|
C | A | 44 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(41): Show | 82 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*781G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 781 | chr2 | 182924921 | |||||
chr2:182925344
|
A | G | 103 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(100): Show | 197 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*358T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 358 | chr2 | 182925344 | |||||
chr2:182925494
|
C | T | 4 | a0001c0001t0017a0001c0001t0044a0001c0001t0045others(1): Show | 6 | HG02523.hp2 NA18983.hp2 NA18999.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*208G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 31/31 | 208 | chr2 | 182925494 | |||||
chr2:183038181
|
C | T | 1 | a0001c0002t0043 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-82G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/31 | 82 | chr2 | 183038181 | |||||
chr2:183038215
|
G | T | 5 | a0001c0002t0037a0001c0002t0041a0001c0002t0042others(2): Show | 8 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-116C>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/31 | 116 | chr2 | 183038215 | |||||
chr2:183038274
|
C | T | 1 | a0001c0003t0015 | 3 | HG01081.hp2 HG02559.hp1 HG02723.hp1 |
5_prime_UTR_variant | MODIFIER | c.-175G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/31 | 175 | chr2 | 183038274 | |||||
chr2:183038333
|
C | T | 2 | a0001c0002t0039a0001c0002t0040 | 2 | HG03041.hp2 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-234G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/31 | 234 | chr2 | 183038333 | |||||
chr2:183038417
|
T | TGGC | 3 | a0001c0002t0037a0001c0002t0110a0001c0011t0109 | 4 | HG01109.hp1 HG02922.hp1 HG03017.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-321_-319dupGCC | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/31 | 319 | chr2 | 183038417 | |||||
chr2:183038453
|
C | T | 1 | a0001c0004t0038 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-354G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/31 | 354 | chr2 | 183038453 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:182926044
|
T | A | 2 | a0001c0002t0060g0183a0001c0009t0061g0184 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3271-226A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 30/30 | chr2 | 182926044 | ||||||
chr2:182926155
|
C | G | 128 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(125): Show | 129 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.3271-337G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 30/30 | chr2 | 182926155 | ||||||
chr2:182926350
|
G | A | 2 | a0001c0002t0063g0190a0001c0002t0064g0189 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.3270+466C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 30/30 | chr2 | 182926350 | ||||||
chr2:182926375
|
G | A | 10 | a0001c0001t0002g0071a0001c0001t0002g0081a0001c0001t0002g0082others(7): Show | 10 | HG02055.hp1 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.3270+441C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 30/30 | chr2 | 182926375 | ||||||
chr2:182926386
|
G | A | 2 | a0001c0003t0027g0176a0001c0003t0027g0185 | 2 | HG02145.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3270+430C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 30/30 | chr2 | 182926386 | ||||||
chr2:182926390
|
T | C | 14 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(11): Show | 15 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.3270+426A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 30/30 | chr2 | 182926390 | ||||||
chr2:182926414
|
C | T | 4 | a0001c0001t0018g0070a0001c0001t0018g0195a0001c0001t0048g0196others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.3270+402G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 30/30 | chr2 | 182926414 | ||||||
chr2:182926770
|
C | T | 2 | a0001c0002t0043g0013a0001c0002t0065g0191 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3270+46G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 30/30 | chr2 | 182926770 | ||||||
chr2:182927133
|
T | C | 33 | a0001c0001t0002g0059a0001c0001t0002g0071a0001c0001t0002g0081others(30): Show | 33 | HG00438.hp1 HG00438.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.3181-228A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 29/30 | chr2 | 182927133 | ||||||
chr2:182927251
|
G | A | 4 | a0001c0001t0001g0039a0001c0001t0019g0002a0001c0001t0019g0053others(1): Show | 5 | NA18944.hp2 NA18955.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.3181-346C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 29/30 | chr2 | 182927251 | ||||||
chr2:182927570
|
TAGAG | T | 31 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(28): Show | 31 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.3180+543_3180+546d others(6): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 29/30 | chr2 | 182927570 | ||||||
chr2:182927621
|
C | T | 194 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(191): Show | 197 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(194): Show |
intron_variant | MODIFIER | c.3180+496G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 29/30 | chr2 | 182927621 | ||||||
chr2:182927872
|
C | T | 1 | a0001c0001t0086g0072 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3180+245G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 29/30 | chr2 | 182927872 | ||||||
chr2:182927873
|
G | A | 1 | a0001c0001t0022g0119 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.3180+244C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 29/30 | chr2 | 182927873 | ||||||
chr2:182927876
|
C | T | 51 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(48): Show | 52 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.3180+241G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 29/30 | chr2 | 182927876 | ||||||
chr2:182927966
|
T | C | 3 | a0001c0001t0011g0023a0001c0001t0011g0024a0001c0001t0011g0025 | 3 | NA18973.hp1 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.3180+151A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 29/30 | chr2 | 182927966 | ||||||
chr2:182927968
|
T | C | 1 | a0001c0007t0003g0205 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3180+149A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 29/30 | chr2 | 182927968 | ||||||
chr2:182927988
|
A | G | 1 | a0001c0001t0021g0113 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.3180+129T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 29/30 | chr2 | 182927988 | ||||||
chr2:182928329
|
T | G | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3071-103A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 28/30 | chr2 | 182928329 | ||||||
chr2:182928352
|
C | T | 46 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(43): Show | 47 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.3071-126G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 28/30 | chr2 | 182928352 | ||||||
chr2:182928426
|
C | T | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(38): Show | 42 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.3071-200G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 28/30 | chr2 | 182928426 | ||||||
chr2:182928477
|
C | G | 1 | a0001c0001t0077g0130 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3071-251G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 28/30 | chr2 | 182928477 | ||||||
chr2:182928483
|
A | T | 33 | a0001c0002t0060g0183a0001c0003t0004g0080a0001c0003t0004g0160others(30): Show | 33 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.3071-257T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 28/30 | chr2 | 182928483 | ||||||
chr2:182928655
|
T | C | 82 | a0001c0001t0002g0059a0001c0001t0002g0071a0001c0001t0002g0081others(79): Show | 82 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.3070+128A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 28/30 | chr2 | 182928655 | ||||||
chr2:182928670
|
A | G | 128 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(125): Show | 129 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.3070+113T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 28/30 | chr2 | 182928670 | ||||||
chr2:182928717
|
A | C | 1 | a0001c0004t0062g0194 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3070+66T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 28/30 | chr2 | 182928717 | ||||||
chr2:182928925
|
A | G | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.2954-26T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 27/30 | chr2 | 182928925 | ||||||
chr2:182929205
|
G | C | 18 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(15): Show | 19 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.2954-306C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 27/30 | chr2 | 182929205 | ||||||
chr2:182929412
|
C | A | 2 | a0001c0003t0004g0165a0001c0003t0004g0166 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2954-513G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 27/30 | chr2 | 182929412 | ||||||
chr2:182929627
|
G | A | 194 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(191): Show | 197 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(194): Show |
intron_variant | MODIFIER | c.2954-728C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 27/30 | chr2 | 182929627 | ||||||
chr2:182929762
|
GA | G | 63 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(60): Show | 65 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(62): Show |
intron_variant | MODIFIER | c.2954-864delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 27/30 | chr2 | 182929762 | ||||||
chr2:182929793
|
A | G | 51 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(48): Show | 52 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.2954-894T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 27/30 | chr2 | 182929793 | ||||||
chr2:182929938
|
A | T | 1 | a0001c0002t0106g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2953+757T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 27/30 | chr2 | 182929938 | ||||||
chr2:182930000
|
C | T | 51 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(48): Show | 52 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.2953+695G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 27/30 | chr2 | 182930000 | ||||||
chr2:182930141
|
T | C | 1 | a0001c0001t0030g0087 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2953+554A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 27/30 | chr2 | 182930141 | ||||||
chr2:182930229
|
T | C | 1 | a0001c0002t0074g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2953+466A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 27/30 | chr2 | 182930229 | ||||||
chr2:182930349
|
A | C | 2 | a0001c0002t0060g0183a0001c0009t0061g0184 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2953+346T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 27/30 | chr2 | 182930349 | ||||||
chr2:182930397
|
T | A | 11 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.2953+298A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 27/30 | chr2 | 182930397 | ||||||
chr2:182930634
|
A | T | 2 | a0001c0002t0063g0190a0001c0002t0064g0189 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2953+61T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 27/30 | chr2 | 182930634 | ||||||
chr2:182930643
|
C | T | 1 | a0001c0002t0106g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2953+52G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 27/30 | chr2 | 182930643 | ||||||
chr2:182930905
|
A | C | 51 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(48): Show | 52 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.2860-117T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182930905 | ||||||
chr2:182931258
|
A | G | 1 | a0001c0001t0001g0039 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2860-470T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182931258 | ||||||
chr2:182931533
|
C | A | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2860-745G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182931533 | ||||||
chr2:182931635
|
C | G | 13 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(10): Show | 14 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.2860-847G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182931635 | ||||||
chr2:182931680
|
T | G | 31 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(28): Show | 31 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2860-892A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182931680 | ||||||
chr2:182931836
|
C | T | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(38): Show | 42 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.2860-1048G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182931836 | ||||||
chr2:182931876
|
T | C | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2860-1088A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182931876 | ||||||
chr2:182931983
|
T | C | 3 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0062g0194 | 4 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.2860-1195A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182931983 | ||||||
chr2:182932060
|
T | C | 1 | a0001c0003t0012g0175 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2860-1272A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182932060 | ||||||
chr2:182932145
|
G | A | 1 | a0001c0001t0031g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2860-1357C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182932145 | ||||||
chr2:182932285
|
CA | C | 8 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2860-1498delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182932285 | ||||||
chr2:182932311
|
T | C | 3 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0062g0194 | 4 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.2860-1523A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182932311 | ||||||
chr2:182932499
|
T | C | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.2860-1711A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182932499 | ||||||
chr2:182932559
|
A | G | 51 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(48): Show | 52 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.2860-1771T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182932559 | ||||||
chr2:182932639
|
T | C | 2 | a0001c0002t0060g0183a0001c0009t0061g0184 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2860-1851A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182932639 | ||||||
chr2:182932654
|
GT | G | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.2860-1867delA | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182932654 | ||||||
chr2:182932675
|
T | A | 2 | a0001c0001t0014g0109a0001c0001t0014g0139 | 2 | NA18949.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.2860-1887A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182932675 | ||||||
chr2:182932676
|
A | T | 1 | a0001c0004t0028g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2860-1888T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182932676 | ||||||
chr2:182932710
|
T | C | 1 | a0001c0004t0062g0194 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2860-1922A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182932710 | ||||||
chr2:182932766
|
T | C | 4 | a0001c0002t0043g0013a0001c0002t0063g0190a0001c0002t0064g0189others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2860-1978A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182932766 | ||||||
chr2:182932934
|
A | G | 128 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(125): Show | 129 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.2859+1818T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182932934 | ||||||
chr2:182932965
|
A | C | 1 | a0001c0002t0009g0145 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2859+1787T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182932965 | ||||||
chr2:182933121
|
T | C | 4 | a0001c0001t0018g0070a0001c0001t0018g0195a0001c0001t0048g0196others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2859+1631A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182933121 | ||||||
chr2:182933267
|
A | G | 3 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0062g0194 | 4 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.2859+1485T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182933267 | ||||||
chr2:182933349
|
G | A | 1 | a0001c0009t0061g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2859+1403C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182933349 | ||||||
chr2:182933389
|
A | AT | 119 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(116): Show | 121 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.2859+1362dupA | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182933389 | ||||||
chr2:182933389
|
A | ATT | 36 | a0001c0001t0007g0060a0001c0001t0010g0128a0001c0001t0010g0186others(33): Show | 37 | HG00609.hp1 HG02056.hp1 HG02145.hp2 others(34): Show |
intron_variant | MODIFIER | c.2859+1361_2859+136 others(6): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182933389 | ||||||
chr2:182933389
|
A | ATTT | 25 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(22): Show | 25 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.2859+1360_2859+136 others(7): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182933389 | ||||||
chr2:182933389
|
A | ATTTT | 6 | a0001c0002t0043g0013a0001c0002t0063g0190a0001c0002t0064g0189others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2859+1359_2859+136 others(8): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182933389 | ||||||
chr2:182933507
|
C | T | 23 | a0001c0003t0006g0057a0001c0003t0006g0058a0001c0003t0006g0168others(20): Show | 23 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.2859+1245G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182933507 | ||||||
chr2:182933619
|
C | G | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2859+1133G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182933619 | ||||||
chr2:182933754
|
A | G | 1 | a0001c0002t0064g0189 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2859+998T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182933754 | ||||||
chr2:182933861
|
G | A | 1 | a0001c0001t0054g0042 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2859+891C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182933861 | ||||||
chr2:182933949
|
A | G | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.2859+803T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182933949 | ||||||
chr2:182934033
|
T | A | 13 | a0001c0001t0002g0099a0001c0001t0007g0100a0001c0001t0008g0063others(10): Show | 13 | HG00438.hp1 HG02074.hp1 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.2859+719A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182934033 | ||||||
chr2:182934223
|
C | T | 1 | a0001c0001t0087g0123 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2859+529G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182934223 | ||||||
chr2:182934304
|
A | AT | 46 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(43): Show | 47 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.2859+447dupA | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182934304 | ||||||
chr2:182934427
|
G | A | 3 | a0001c0005t0071g0155a0001c0005t0072g0157a0001c0005t0073g0156 | 3 | HG02647.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2859+325C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 26/30 | chr2 | 182934427 | ||||||
chr2:182934842
|
A | G | 1 | a0001c0002t0041g0012 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2779-10T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 25/30 | chr2 | 182934842 | ||||||
chr2:182934957
|
G | A | 2 | a0001c0004t0028g0056a0001c0004t0066g0055 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2779-125C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 25/30 | chr2 | 182934957 | ||||||
chr2:182935134
|
T | C | 4 | a0001c0002t0043g0013a0001c0002t0063g0190a0001c0002t0064g0189others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2778+159A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 25/30 | chr2 | 182935134 | ||||||
chr2:182935754
|
AAAG | A | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.2696-382_2696-380d others(5): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182935754 | ||||||
chr2:182935814
|
G | A | 14 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(11): Show | 15 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.2696-439C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182935814 | ||||||
chr2:182935907
|
T | C | 1 | a0001c0002t0060g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2696-532A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182935907 | ||||||
chr2:182935911
|
C | T | 1 | a0001c0002t0106g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2696-536G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182935911 | ||||||
chr2:182936136
|
G | C | 3 | a0001c0005t0071g0155a0001c0005t0072g0157a0001c0005t0073g0156 | 3 | HG02647.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2696-761C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182936136 | ||||||
chr2:182936352
|
C | T | 1 | a0001c0001t0030g0087 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2696-977G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182936352 | ||||||
chr2:182936449
|
T | C | 1 | a0001c0001t0002g0124 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2696-1074A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182936449 | ||||||
chr2:182936472
|
A | G | 1 | a0001c0002t0069g0158 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2696-1097T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182936472 | ||||||
chr2:182936555
|
CAGTAACT others(5): Show |
C | 1 | a0001c0001t0001g0030 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2696-1192_2696-118 others(16): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182936555 | ||||||
chr2:182936736
|
G | A | 31 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(28): Show | 31 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2696-1361C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182936736 | ||||||
chr2:182936927
|
C | A | 1 | a0001c0002t0003g0204 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2696-1552G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182936927 | ||||||
chr2:182936985
|
C | T | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2696-1610G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182936985 | ||||||
chr2:182937001
|
G | A | 3 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0062g0194 | 4 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.2696-1626C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182937001 | ||||||
chr2:182937071
|
C | T | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.2696-1696G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182937071 | ||||||
chr2:182937114
|
C | CA | 5 | a0001c0002t0003g0203a0001c0002t0003g0204a0001c0002t0035g0210others(2): Show | 5 | HG00597.hp2 HG01261.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.2696-1740dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182937114 | ||||||
chr2:182937114
|
CAA | C | 9 | a0001c0001t0076g0066a0001c0002t0013g0147a0001c0002t0013g0148others(6): Show | 9 | HG01081.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2696-1741_2696-174 others(6): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182937114 | ||||||
chr2:182937114
|
CAAA | C | 29 | a0001c0001t0002g0090a0001c0001t0008g0095a0001c0001t0014g0092others(26): Show | 30 | HG01069.hp1 HG01109.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.2696-1742_2696-174 others(7): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182937114 | ||||||
chr2:182937114
|
CAAAA | C | 71 | a0001c0001t0001g0051a0001c0001t0002g0059a0001c0001t0002g0071others(68): Show | 71 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.2696-1743_2696-174 others(8): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182937114 | ||||||
chr2:182937114
|
CAAAAA | C | 59 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(56): Show | 61 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.2696-1744_2696-174 others(9): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182937114 | ||||||
chr2:182937114
|
CAAAAAA | C | 21 | a0001c0003t0006g0057a0001c0003t0006g0168a0001c0003t0006g0169others(18): Show | 21 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.2696-1745_2696-174 others(10): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182937114 | ||||||
chr2:182937114
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0003t0004g0080 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2696-1749_2696-174 others(14): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182937114 | ||||||
chr2:182937298
|
A | G | 51 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(48): Show | 52 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.2696-1923T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182937298 | ||||||
chr2:182937300
|
A | T | 1 | a0001c0004t0062g0194 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2696-1925T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182937300 | ||||||
chr2:182937301
|
C | A | 1 | a0001c0003t0004g0162 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2696-1926G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182937301 | ||||||
chr2:182937392
|
A | G | 194 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(191): Show | 197 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(194): Show |
intron_variant | MODIFIER | c.2696-2017T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182937392 | ||||||
chr2:182937542
|
G | A | 1 | a0001c0002t0060g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2696-2167C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182937542 | ||||||
chr2:182937708
|
C | T | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(38): Show | 42 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.2696-2333G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182937708 | ||||||
chr2:182937819
|
T | G | 5 | a0001c0002t0009g0145a0001c0002t0013g0146a0001c0002t0013g0147others(2): Show | 5 | HG02622.hp2 HG02965.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2696-2444A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182937819 | ||||||
chr2:182937845
|
G | A | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.2696-2470C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182937845 | ||||||
chr2:182938094
|
T | C | 2 | a0001c0004t0016g0001a0001c0004t0016g0010 | 3 | HG01099.hp1 HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.2696-2719A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182938094 | ||||||
chr2:182938203
|
T | C | 1 | a0001c0011t0109g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2696-2828A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182938203 | ||||||
chr2:182938283
|
G | A | 1 | a0001c0002t0060g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2696-2908C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182938283 | ||||||
chr2:182938416
|
A | T | 1 | a0001c0001t0029g0138 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2696-3041T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182938416 | ||||||
chr2:182938524
|
C | T | 4 | a0001c0002t0043g0013a0001c0002t0063g0190a0001c0002t0064g0189others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2696-3149G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182938524 | ||||||
chr2:182938786
|
T | C | 7 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0028g0054others(4): Show | 8 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.2695+3284A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182938786 | ||||||
chr2:182938867
|
C | T | 205 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(202): Show | 208 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(205): Show |
intron_variant | MODIFIER | c.2695+3203G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182938867 | ||||||
chr2:182939127
|
T | C | 193 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(190): Show | 196 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(193): Show |
intron_variant | MODIFIER | c.2695+2943A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182939127 | ||||||
chr2:182939170
|
T | C | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(38): Show | 42 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.2695+2900A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182939170 | ||||||
chr2:182939224
|
T | C | 1 | a0001c0002t0009g0145 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2695+2846A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182939224 | ||||||
chr2:182939226
|
G | A | 128 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(125): Show | 129 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.2695+2844C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182939226 | ||||||
chr2:182939228
|
A | G | 4 | a0001c0001t0002g0059a0001c0001t0082g0085a0001c0001t0085g0083others(1): Show | 4 | HG00438.hp2 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2695+2842T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182939228 | ||||||
chr2:182939967
|
A | C | 18 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(15): Show | 19 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.2695+2103T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182939967 | ||||||
chr2:182940116
|
C | T | 1 | a0001c0001t0030g0087 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2695+1954G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182940116 | ||||||
chr2:182940298
|
CAAAAGAA others(17): Show |
C | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.2695+1748_2695+177 others(28): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182940298 | ||||||
chr2:182940368
|
A | G | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(38): Show | 42 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.2695+1702T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182940368 | ||||||
chr2:182940435
|
C | T | 1 | a0001c0002t0063g0190 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2695+1635G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182940435 | ||||||
chr2:182940554
|
C | G | 1 | a0001c0001t0048g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2695+1516G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182940554 | ||||||
chr2:182940639
|
T | C | 1 | a0001c0011t0109g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2695+1431A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182940639 | ||||||
chr2:182941132
|
A | T | 128 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(125): Show | 129 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.2695+938T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182941132 | ||||||
chr2:182941431
|
C | G | 1 | a0001c0001t0029g0187 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2695+639G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182941431 | ||||||
chr2:182941534
|
T | G | 1 | a0001c0001t0007g0100 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2695+536A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182941534 | ||||||
chr2:182941702
|
G | A | 17 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0050others(14): Show | 18 | HG00621.hp2 HG02056.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.2695+368C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182941702 | ||||||
chr2:182941946
|
T | G | 2 | a0001c0002t0060g0183a0001c0009t0061g0184 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2695+124A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182941946 | ||||||
chr2:182942061
|
G | A | 2 | a0001c0002t0060g0183a0001c0009t0061g0184 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2695+9C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 24/30 | chr2 | 182942061 | ||||||
chr2:182942165
|
TA | T | 11 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.2602-3delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182942165 | ||||||
chr2:182942252
|
T | C | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.2602-89A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182942252 | ||||||
chr2:182942304
|
G | A | 1 | a0001c0002t0103g0144 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2602-141C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182942304 | ||||||
chr2:182942445
|
G | A | 1 | a0001c0004t0028g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2602-282C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182942445 | ||||||
chr2:182942699
|
C | T | 2 | a0001c0004t0016g0001a0001c0004t0016g0010 | 3 | HG01099.hp1 HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.2602-536G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182942699 | ||||||
chr2:182942864
|
A | C | 31 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(28): Show | 31 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2602-701T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182942864 | ||||||
chr2:182943134
|
A | G | 3 | a0001c0003t0006g0170a0001c0003t0026g0171a0001c0003t0026g0173 | 3 | HG01243.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2602-971T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182943134 | ||||||
chr2:182943196
|
T | C | 1 | a0001c0011t0109g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2602-1033A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182943196 | ||||||
chr2:182943293
|
A | G | 1 | a0001c0009t0061g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2602-1130T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182943293 | ||||||
chr2:182943411
|
G | A | 1 | a0001c0001t0005g0140 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2602-1248C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182943411 | ||||||
chr2:182943475
|
T | G | 31 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(28): Show | 31 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2602-1312A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182943475 | ||||||
chr2:182943523
|
A | G | 1 | a0001c0003t0015g0009 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2602-1360T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182943523 | ||||||
chr2:182943575
|
C | A | 193 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(190): Show | 196 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(193): Show |
intron_variant | MODIFIER | c.2602-1412G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182943575 | ||||||
chr2:182943643
|
G | GA | 42 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(39): Show | 43 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.2602-1481dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182943643 | ||||||
chr2:182943652
|
A | C | 2 | a0001c0004t0016g0001a0001c0004t0016g0010 | 3 | HG01099.hp1 HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.2602-1489T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182943652 | ||||||
chr2:182943696
|
C | T | 193 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(190): Show | 196 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(193): Show |
intron_variant | MODIFIER | c.2602-1533G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182943696 | ||||||
chr2:182943894
|
C | T | 1 | a0001c0001t0005g0019 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2602-1731G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182943894 | ||||||
chr2:182944017
|
G | A | 194 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(191): Show | 197 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(194): Show |
intron_variant | MODIFIER | c.2602-1854C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182944017 | ||||||
chr2:182944242
|
A | G | 1 | a0001c0002t0063g0190 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2602-2079T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182944242 | ||||||
chr2:182944287
|
T | A | 7 | a0001c0003t0004g0080a0001c0003t0004g0164a0001c0003t0004g0165others(4): Show | 7 | HG01884.hp2 HG02258.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2602-2124A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182944287 | ||||||
chr2:182944288
|
A | T | 7 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(4): Show | 8 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.2602-2125T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182944288 | ||||||
chr2:182944344
|
C | A | 2 | a0001c0004t0016g0001a0001c0004t0016g0010 | 3 | HG01099.hp1 HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.2602-2181G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182944344 | ||||||
chr2:182944482
|
C | T | 1 | a0001c0001t0018g0070 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2602-2319G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182944482 | ||||||
chr2:182944506
|
A | C | 128 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(125): Show | 129 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.2602-2343T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182944506 | ||||||
chr2:182944538
|
T | C | 2 | a0001c0002t0043g0013a0001c0002t0065g0191 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2602-2375A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182944538 | ||||||
chr2:182944609
|
A | G | 1 | a0001c0002t0074g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2602-2446T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182944609 | ||||||
chr2:182944711
|
A | G | 1 | a0001c0012t0018g0211 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2602-2548T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182944711 | ||||||
chr2:182944962
|
T | C | 189 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(186): Show | 192 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(189): Show |
intron_variant | MODIFIER | c.2602-2799A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182944962 | ||||||
chr2:182944963
|
G | A | 3 | a0001c0005t0071g0155a0001c0005t0072g0157a0001c0005t0073g0156 | 3 | HG02647.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2602-2800C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182944963 | ||||||
chr2:182945010
|
G | A | 1 | a0001c0001t0008g0115 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2602-2847C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182945010 | ||||||
chr2:182945098
|
G | A | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2602-2935C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182945098 | ||||||
chr2:182945128
|
G | A | 1 | a0001c0001t0010g0132 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2602-2965C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182945128 | ||||||
chr2:182945222
|
C | T | 2 | a0001c0002t0043g0013a0001c0002t0065g0191 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2602-3059G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182945222 | ||||||
chr2:182945247
|
CA | C | 193 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(190): Show | 196 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(193): Show |
intron_variant | MODIFIER | c.2602-3085delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182945247 | ||||||
chr2:182945632
|
T | C | 194 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(191): Show | 197 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(194): Show |
intron_variant | MODIFIER | c.2602-3469A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182945632 | ||||||
chr2:182945647
|
T | C | 1 | a0001c0012t0018g0211 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2602-3484A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182945647 | ||||||
chr2:182945747
|
A | G | 2 | a0001c0002t0063g0190a0001c0002t0064g0189 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2602-3584T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182945747 | ||||||
chr2:182945862
|
A | T | 10 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(7): Show | 11 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.2602-3699T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182945862 | ||||||
chr2:182945880
|
A | T | 3 | a0001c0001t0007g0117a0001c0001t0022g0119a0001c0001t0075g0118 | 3 | HG01192.hp2 HG01255.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.2602-3717T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182945880 | ||||||
chr2:182946020
|
G | C | 31 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(28): Show | 31 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2602-3857C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182946020 | ||||||
chr2:182946112
|
T | C | 4 | a0001c0003t0012g0167a0001c0003t0012g0174a0001c0003t0012g0177others(1): Show | 4 | HG00609.hp2 HG00621.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.2602-3949A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182946112 | ||||||
chr2:182946125
|
T | G | 1 | a0001c0001t0005g0031 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2602-3962A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182946125 | ||||||
chr2:182946147
|
C | G | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.2602-3984G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182946147 | ||||||
chr2:182946154
|
T | C | 194 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(191): Show | 197 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(194): Show |
intron_variant | MODIFIER | c.2602-3991A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182946154 | ||||||
chr2:182946314
|
G | A | 82 | a0001c0001t0002g0059a0001c0001t0002g0071a0001c0001t0002g0081others(79): Show | 82 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.2602-4151C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182946314 | ||||||
chr2:182946401
|
C | CA | 18 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(15): Show | 19 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.2602-4239dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182946401 | ||||||
chr2:182946414
|
A | G | 42 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(39): Show | 43 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.2602-4251T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182946414 | ||||||
chr2:182946476
|
T | C | 1 | a0001c0002t0035g0209 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2602-4313A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182946476 | ||||||
chr2:182946603
|
GA | G | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(38): Show | 42 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.2602-4441delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182946603 | ||||||
chr2:182946666
|
T | G | 4 | a0001c0001t0018g0070a0001c0001t0018g0195a0001c0001t0048g0196others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2602-4503A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182946666 | ||||||
chr2:182946702
|
T | G | 1 | a0001c0001t0005g0019 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2602-4539A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182946702 | ||||||
chr2:182946739
|
C | CA | 146 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(143): Show | 148 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.2602-4577dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182946739 | ||||||
chr2:182946739
|
C | CAA | 46 | a0001c0001t0018g0070a0001c0001t0018g0195a0001c0001t0048g0196others(43): Show | 47 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.2602-4578_2602-457 others(6): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182946739 | ||||||
chr2:182946834
|
G | A | 1 | a0001c0002t0041g0012 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2602-4671C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182946834 | ||||||
chr2:182946981
|
C | A | 4 | a0001c0002t0043g0013a0001c0002t0063g0190a0001c0002t0064g0189others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2602-4818G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182946981 | ||||||
chr2:182947072
|
A | G | 1 | a0001c0011t0109g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2602-4909T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182947072 | ||||||
chr2:182947171
|
T | C | 31 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(28): Show | 31 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2602-5008A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182947171 | ||||||
chr2:182947290
|
C | T | 3 | a0001c0003t0004g0164a0001c0003t0004g0165a0001c0003t0004g0166 | 3 | HG01884.hp2 HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2601+5115G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182947290 | ||||||
chr2:182947539
|
C | T | 46 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(43): Show | 47 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.2601+4866G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182947539 | ||||||
chr2:182947743
|
G | A | 1 | a0001c0004t0028g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2601+4662C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182947743 | ||||||
chr2:182947749
|
TA | T | 31 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(28): Show | 31 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2601+4655delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182947749 | ||||||
chr2:182947789
|
G | C | 8 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2601+4616C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182947789 | ||||||
chr2:182947792
|
T | G | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2601+4613A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182947792 | ||||||
chr2:182947809
|
A | G | 2 | a0001c0003t0006g0168a0001c0003t0006g0169 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2601+4596T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182947809 | ||||||
chr2:182947825
|
C | A | 128 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(125): Show | 129 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.2601+4580G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182947825 | ||||||
chr2:182947911
|
TAC | T | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.2601+4492_2601+449 others(6): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182947911 | ||||||
chr2:182948057
|
G | A | 11 | a0001c0003t0006g0057a0001c0003t0006g0058a0001c0003t0006g0170others(8): Show | 11 | HG01243.hp2 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.2601+4348C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182948057 | ||||||
chr2:182948246
|
T | C | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2601+4159A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182948246 | ||||||
chr2:182948410
|
C | T | 13 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(10): Show | 14 | HG02257.hp1 HG02559.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.2601+3995G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182948410 | ||||||
chr2:182948411
|
G | A | 1 | a0001c0002t0108g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2601+3994C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182948411 | ||||||
chr2:182948445
|
G | A | 4 | a0001c0001t0018g0070a0001c0001t0018g0195a0001c0001t0048g0196others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2601+3960C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182948445 | ||||||
chr2:182948568
|
G | C | 1 | a0001c0001t0057g0037 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2601+3837C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182948568 | ||||||
chr2:182948684
|
C | T | 128 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(125): Show | 129 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.2601+3721G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182948684 | ||||||
chr2:182948784
|
T | G | 4 | a0001c0003t0012g0167a0001c0003t0012g0174a0001c0003t0012g0177others(1): Show | 4 | HG00609.hp2 HG00621.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.2601+3621A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182948784 | ||||||
chr2:182949375
|
G | A | 13 | a0001c0003t0006g0057a0001c0003t0006g0058a0001c0003t0006g0168others(10): Show | 13 | HG01243.hp2 HG02572.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.2601+3030C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182949375 | ||||||
chr2:182949417
|
T | G | 1 | a0001c0001t0033g0077 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2601+2988A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182949417 | ||||||
chr2:182949453
|
A | C | 3 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0062g0194 | 4 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.2601+2952T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182949453 | ||||||
chr2:182949633
|
C | T | 1 | a0001c0001t0029g0187 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2601+2772G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182949633 | ||||||
chr2:182949741
|
G | A | 1 | a0001c0006t0001g0026 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2601+2664C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182949741 | ||||||
chr2:182949968
|
T | C | 1 | a0001c0001t0082g0085 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2601+2437A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182949968 | ||||||
chr2:182950245
|
G | A | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2601+2160C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182950245 | ||||||
chr2:182950628
|
C | T | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2601+1777G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182950628 | ||||||
chr2:182950643
|
A | G | 1 | a0001c0001t0083g0129 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2601+1762T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182950643 | ||||||
chr2:182950774
|
C | T | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.2601+1631G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182950774 | ||||||
chr2:182950785
|
C | T | 1 | a0001c0002t0060g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2601+1620G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182950785 | ||||||
chr2:182950914
|
C | T | 1 | a0001c0004t0016g0010 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2601+1491G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182950914 | ||||||
chr2:182951271
|
A | G | 1 | a0001c0002t0074g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2601+1134T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182951271 | ||||||
chr2:182951496
|
C | T | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.2601+909G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182951496 | ||||||
chr2:182951636
|
C | CA | 108 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(105): Show | 109 | HG00609.hp1 HG00621.hp2 HG01069.hp1 others(106): Show |
intron_variant | MODIFIER | c.2601+768dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182951636 | ||||||
chr2:182951636
|
C | CAA | 22 | a0001c0001t0001g0028a0001c0001t0001g0051a0001c0001t0002g0071others(19): Show | 22 | HG00438.hp1 HG00597.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.2601+767_2601+768d others(4): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182951636 | ||||||
chr2:182951636
|
CA | C | 9 | a0001c0002t0009g0003a0001c0002t0009g0151a0001c0002t0009g0153others(6): Show | 10 | HG02109.hp2 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2601+768delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182951636 | ||||||
chr2:182951649
|
A | C | 1 | a0001c0004t0028g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2601+756T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182951649 | ||||||
chr2:182951653
|
C | A | 83 | a0001c0001t0002g0059a0001c0001t0002g0071a0001c0001t0002g0081others(80): Show | 83 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.2601+752G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182951653 | ||||||
chr2:182951657
|
C | A | 1 | a0001c0001t0082g0085 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2601+748G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182951657 | ||||||
chr2:182951679
|
G | A | 128 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(125): Show | 129 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.2601+726C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182951679 | ||||||
chr2:182951708
|
G | A | 44 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(41): Show | 45 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.2601+697C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182951708 | ||||||
chr2:182951847
|
G | A | 17 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(14): Show | 18 | HG02257.hp1 HG02559.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.2601+558C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182951847 | ||||||
chr2:182952053
|
C | T | 1 | a0001c0001t0031g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2601+352G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182952053 | ||||||
chr2:182952084
|
G | C | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2601+321C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 23/30 | chr2 | 182952084 | ||||||
chr2:182952708
|
C | G | 3 | a0001c0003t0015g0007a0001c0003t0015g0008a0001c0003t0015g0009 | 3 | HG01081.hp2 HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2503+85G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 22/30 | chr2 | 182952708 | ||||||
chr2:182952996
|
A | G | 31 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(28): Show | 31 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2373-73T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 21/30 | chr2 | 182952996 | ||||||
chr2:182953017
|
T | C | 1 | a0001c0001t0086g0072 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2373-94A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 21/30 | chr2 | 182953017 | ||||||
chr2:182953052
|
T | A | 14 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(11): Show | 15 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.2372+61A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 21/30 | chr2 | 182953052 | ||||||
chr2:182953346
|
T | C | 5 | a0001c0001t0018g0070a0001c0001t0018g0195a0001c0001t0048g0196others(2): Show | 5 | HG02109.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2154-15A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182953346 | ||||||
chr2:182953370
|
C | A | 1 | a0001c0003t0004g0161 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2154-39G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182953370 | ||||||
chr2:182953571
|
C | T | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2154-240G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182953571 | ||||||
chr2:182953642
|
A | T | 5 | a0001c0002t0009g0145a0001c0002t0013g0146a0001c0002t0013g0147others(2): Show | 5 | HG02622.hp2 HG02965.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2154-311T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182953642 | ||||||
chr2:182953674
|
T | C | 8 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2154-343A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182953674 | ||||||
chr2:182953751
|
T | C | 16 | a0001c0003t0006g0057a0001c0003t0006g0058a0001c0003t0006g0168others(13): Show | 16 | HG01081.hp2 HG01243.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.2154-420A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182953751 | ||||||
chr2:182953771
|
C | T | 1 | a0001c0001t0005g0036 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2154-440G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182953771 | ||||||
chr2:182953780
|
A | G | 1 | a0001c0004t0062g0194 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2154-449T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182953780 | ||||||
chr2:182954168
|
CCTGA | C | 6 | a0001c0003t0012g0167a0001c0003t0012g0174a0001c0003t0012g0177others(3): Show | 6 | HG00609.hp2 HG00621.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.2154-841_2154-838d others(6): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182954168 | ||||||
chr2:182954191
|
C | T | 3 | a0001c0001t0007g0107a0001c0001t0010g0094a0001c0001t0034g0106 | 3 | HG01261.hp2 NA18942.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.2154-860G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182954191 | ||||||
chr2:182954249
|
C | T | 1 | a0001c0001t0007g0117 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2154-918G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182954249 | ||||||
chr2:182954263
|
A | AAC | 194 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(191): Show | 197 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(194): Show |
intron_variant | MODIFIER | c.2154-934_2154-933d others(4): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182954263 | ||||||
chr2:182954363
|
C | T | 6 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0028g0054others(3): Show | 7 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.2154-1032G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182954363 | ||||||
chr2:182954477
|
C | T | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2154-1146G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182954477 | ||||||
chr2:182954521
|
A | T | 1 | a0001c0004t0062g0194 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2154-1190T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182954521 | ||||||
chr2:182954781
|
G | A | 1 | a0001c0002t0069g0158 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2154-1450C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182954781 | ||||||
chr2:182954807
|
T | A | 194 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(191): Show | 197 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(194): Show |
intron_variant | MODIFIER | c.2154-1476A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182954807 | ||||||
chr2:182954897
|
C | T | 9 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(6): Show | 9 | HG01109.hp1 HG01169.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.2153+1565G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182954897 | ||||||
chr2:182954982
|
G | C | 194 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(191): Show | 197 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(194): Show |
intron_variant | MODIFIER | c.2153+1480C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182954982 | ||||||
chr2:182955164
|
C | A | 9 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(6): Show | 9 | HG01109.hp1 HG01169.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.2153+1298G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182955164 | ||||||
chr2:182955183
|
C | G | 4 | a0001c0002t0003g0192a0001c0002t0063g0190a0001c0002t0064g0189others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2153+1279G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182955183 | ||||||
chr2:182955728
|
G | A | 21 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(18): Show | 21 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.2153+734C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182955728 | ||||||
chr2:182955982
|
T | C | 1 | a0001c0002t0013g0146 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2153+480A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182955982 | ||||||
chr2:182956248
|
G | A | 4 | a0001c0002t0043g0013a0001c0002t0063g0190a0001c0002t0064g0189others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2153+214C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 20/30 | chr2 | 182956248 | ||||||
chr2:182956612
|
C | G | 1 | a0001c0002t0106g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2022-19G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 19/30 | chr2 | 182956612 | ||||||
chr2:182956847
|
A | C | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2022-254T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 19/30 | chr2 | 182956847 | ||||||
chr2:182956904
|
G | A | 2 | a0001c0002t0063g0190a0001c0002t0064g0189 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.2022-311C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 19/30 | chr2 | 182956904 | ||||||
chr2:182956967
|
C | A | 3 | a0001c0005t0071g0155a0001c0005t0072g0157a0001c0005t0073g0156 | 3 | HG02647.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2022-374G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 19/30 | chr2 | 182956967 | ||||||
chr2:182957303
|
T | C | 1 | a0001c0001t0099g0089 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2021+154A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 19/30 | chr2 | 182957303 | ||||||
chr2:182957636
|
T | C | 1 | a0001c0001t0007g0107 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1882-40A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182957636 | ||||||
chr2:182957640
|
C | G | 2 | a0001c0002t0103g0144a0001c0002t0108g0014 | 2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1882-44G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182957640 | ||||||
chr2:182957646
|
G | C | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1882-50C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182957646 | ||||||
chr2:182957969
|
T | C | 1 | a0001c0009t0061g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1882-373A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182957969 | ||||||
chr2:182958056
|
T | C | 8 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1882-460A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182958056 | ||||||
chr2:182958105
|
G | A | 1 | a0001c0002t0065g0191 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1882-509C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182958105 | ||||||
chr2:182958172
|
A | C | 1 | a0001c0003t0004g0161 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1882-576T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182958172 | ||||||
chr2:182958686
|
C | T | 1 | a0001c0001t0082g0085 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1882-1090G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182958686 | ||||||
chr2:182958728
|
C | A | 1 | a0001c0003t0012g0177 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1882-1132G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182958728 | ||||||
chr2:182958815
|
G | A | 11 | a0001c0001t0002g0124a0001c0001t0007g0117a0001c0001t0008g0122others(8): Show | 11 | HG00597.hp1 HG01099.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1882-1219C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182958815 | ||||||
chr2:182958845
|
C | G | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1882-1249G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182958845 | ||||||
chr2:182959042
|
T | C | 1 | a0001c0001t0095g0112 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1882-1446A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182959042 | ||||||
chr2:182959314
|
G | C | 31 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(28): Show | 31 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1882-1718C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182959314 | ||||||
chr2:182959359
|
CAAGA | C | 4 | a0001c0002t0043g0013a0001c0002t0063g0190a0001c0002t0064g0189others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1882-1767_1882-176 others(8): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182959359 | ||||||
chr2:182959396
|
G | A | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1882-1800C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182959396 | ||||||
chr2:182959432
|
C | T | 31 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(28): Show | 31 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1882-1836G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182959432 | ||||||
chr2:182959436
|
T | C | 3 | a0001c0002t0003g0198a0001c0002t0003g0202a0001c0002t0110g0214 | 3 | HG02735.hp1 NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1882-1840A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182959436 | ||||||
chr2:182959477
|
C | A | 4 | a0001c0002t0043g0013a0001c0002t0063g0190a0001c0002t0064g0189others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1882-1881G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182959477 | ||||||
chr2:182959477
|
C | T | 8 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1882-1881G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182959477 | ||||||
chr2:182959641
|
G | T | 10 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(7): Show | 11 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.1882-2045C>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182959641 | ||||||
chr2:182959744
|
C | T | 1 | a0001c0003t0006g0058 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1882-2148G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182959744 | ||||||
chr2:182959817
|
A | G | 1 | a0001c0007t0003g0205 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1882-2221T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182959817 | ||||||
chr2:182959837
|
C | A | 2 | a0001c0002t0043g0013a0001c0002t0065g0191 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1882-2241G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182959837 | ||||||
chr2:182960068
|
A | G | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1881+2091T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182960068 | ||||||
chr2:182960083
|
G | T | 1 | a0001c0002t0108g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1881+2076C>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182960083 | ||||||
chr2:182960137
|
G | A | 2 | a0001c0002t0063g0190a0001c0002t0064g0189 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1881+2022C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182960137 | ||||||
chr2:182960148
|
T | C | 11 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1881+2011A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182960148 | ||||||
chr2:182960312
|
C | T | 1 | a0001c0002t0063g0190 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1881+1847G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182960312 | ||||||
chr2:182960313
|
G | T | 18 | a0001c0002t0003g0198a0001c0002t0003g0199a0001c0002t0003g0201others(15): Show | 18 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1881+1846C>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182960313 | ||||||
chr2:182960368
|
T | G | 210 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(207): Show | 213 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(210): Show |
intron_variant | MODIFIER | c.1881+1791A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182960368 | ||||||
chr2:182960395
|
T | C | 1 | a0001c0006t0001g0026 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1881+1764A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182960395 | ||||||
chr2:182960463
|
G | C | 8 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1881+1696C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182960463 | ||||||
chr2:182960484
|
T | G | 2 | a0001c0001t0002g0108a0001c0001t0023g0097 | 2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1881+1675A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182960484 | ||||||
chr2:182960508
|
C | T | 4 | a0001c0001t0007g0060a0001c0001t0021g0113a0001c0001t0092g0137others(1): Show | 4 | HG00609.hp1 HG02056.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1881+1651G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182960508 | ||||||
chr2:182960706
|
A | G | 1 | a0001c0001t0033g0101 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1881+1453T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182960706 | ||||||
chr2:182960710
|
A | G | 1 | a0001c0001t0033g0101 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1881+1449T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182960710 | ||||||
chr2:182960809
|
G | C | 2 | a0001c0002t0060g0183a0001c0009t0061g0184 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1881+1350C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182960809 | ||||||
chr2:182960886
|
G | GAAA | 11 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1881+1270_1881+127 others(7): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182960886 | ||||||
chr2:182960955
|
A | G | 14 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(11): Show | 15 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1881+1204T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182960955 | ||||||
chr2:182961058
|
C | T | 1 | a0001c0002t0065g0191 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1881+1101G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182961058 | ||||||
chr2:182961133
|
G | A | 2 | a0001c0001t0082g0085a0001c0001t0096g0073 | 2 | HG00438.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1881+1026C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182961133 | ||||||
chr2:182961145
|
T | C | 1 | a0001c0001t0076g0066 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1881+1014A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182961145 | ||||||
chr2:182961175
|
G | C | 1 | a0001c0001t0002g0099 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1881+984C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182961175 | ||||||
chr2:182961473
|
G | A | 1 | a0001c0001t0029g0138 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1881+686C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182961473 | ||||||
chr2:182961521
|
T | C | 1 | a0001c0006t0001g0026 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1881+638A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182961521 | ||||||
chr2:182961594
|
G | A | 1 | a0001c0003t0004g0161 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1881+565C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182961594 | ||||||
chr2:182961600
|
G | T | 4 | a0001c0001t0007g0060a0001c0001t0021g0113a0001c0001t0092g0137others(1): Show | 4 | HG00609.hp1 HG02056.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1881+559C>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182961600 | ||||||
chr2:182961666
|
G | A | 3 | a0001c0005t0071g0155a0001c0005t0072g0157a0001c0005t0073g0156 | 3 | HG02647.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1881+493C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182961666 | ||||||
chr2:182961684
|
C | G | 1 | a0001c0004t0066g0055 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1881+475G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182961684 | ||||||
chr2:182961697
|
T | C | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1881+462A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182961697 | ||||||
chr2:182961726
|
T | C | 1 | a0001c0001t0052g0041 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1881+433A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182961726 | ||||||
chr2:182961768
|
G | A | 1 | a0001c0002t0003g0203 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1881+391C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182961768 | ||||||
chr2:182961983
|
C | A | 1 | a0001c0002t0106g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1881+176G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 18/30 | chr2 | 182961983 | ||||||
chr2:182962290
|
G | A | 82 | a0001c0001t0002g0059a0001c0001t0002g0071a0001c0001t0002g0081others(79): Show | 82 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1762-12C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182962290 | ||||||
chr2:182962376
|
C | T | 2 | a0001c0002t0063g0190a0001c0002t0064g0189 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1762-98G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182962376 | ||||||
chr2:182962381
|
C | T | 1 | a0001c0001t0048g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1762-103G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182962381 | ||||||
chr2:182962453
|
TG | T | 2 | a0001c0002t0063g0190a0001c0002t0064g0189 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1762-176delC | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182962453 | ||||||
chr2:182962496
|
A | G | 1 | a0001c0002t0042g0011 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1762-218T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182962496 | ||||||
chr2:182962609
|
A | C | 14 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(11): Show | 15 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1762-331T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182962609 | ||||||
chr2:182962614
|
T | A | 1 | a0001c0001t0007g0107 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1762-336A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182962614 | ||||||
chr2:182962708
|
G | T | 6 | a0001c0002t0003g0198a0001c0002t0003g0202a0001c0002t0003g0203others(3): Show | 6 | HG00597.hp2 HG02735.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.1762-430C>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182962708 | ||||||
chr2:182962725
|
GA | G | 4 | a0001c0002t0043g0013a0001c0002t0063g0190a0001c0002t0064g0189others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1762-448delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182962725 | ||||||
chr2:182962793
|
T | C | 1 | a0001c0002t0064g0189 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1762-515A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182962793 | ||||||
chr2:182962807
|
C | T | 2 | a0001c0002t0063g0190a0001c0002t0064g0189 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1762-529G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182962807 | ||||||
chr2:182962823
|
G | GA | 13 | a0001c0001t0001g0028a0001c0001t0014g0139a0001c0001t0021g0113others(10): Show | 13 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.1762-546dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182962823 | ||||||
chr2:182962841
|
T | C | 1 | a0001c0004t0062g0194 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1762-563A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182962841 | ||||||
chr2:182963043
|
A | G | 1 | a0001c0003t0004g0161 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1762-765T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182963043 | ||||||
chr2:182963182
|
A | G | 1 | a0001c0001t0054g0042 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1762-904T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182963182 | ||||||
chr2:182963252
|
A | G | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1762-974T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182963252 | ||||||
chr2:182963505
|
C | T | 1 | a0001c0009t0061g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1761+1171G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182963505 | ||||||
chr2:182963609
|
G | A | 1 | a0001c0003t0026g0173 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1761+1067C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182963609 | ||||||
chr2:182963997
|
C | T | 1 | a0001c0003t0012g0175 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1761+679G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182963997 | ||||||
chr2:182964458
|
C | T | 18 | a0001c0002t0003g0198a0001c0002t0003g0199a0001c0002t0003g0201others(15): Show | 18 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1761+218G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182964458 | ||||||
chr2:182964460
|
A | C | 1 | a0001c0001t0008g0098 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1761+216T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182964460 | ||||||
chr2:182964508
|
T | C | 49 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(46): Show | 50 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.1761+168A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 17/30 | chr2 | 182964508 | ||||||
chr2:182964907
|
C | T | 50 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(47): Show | 51 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.1629-99G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182964907 | ||||||
chr2:182964973
|
C | A | 1 | a0001c0003t0015g0009 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1629-165G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182964973 | ||||||
chr2:182965144
|
A | G | 24 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(21): Show | 24 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.1629-336T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182965144 | ||||||
chr2:182965211
|
T | C | 1 | a0001c0002t0036g0197 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1629-403A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182965211 | ||||||
chr2:182965277
|
G | GA | 207 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(204): Show | 209 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(206): Show |
intron_variant | MODIFIER | c.1629-470dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182965277 | ||||||
chr2:182965277
|
G | GAA | 7 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0028g0054others(4): Show | 8 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.1629-471_1629-470d others(4): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182965277 | ||||||
chr2:182965323
|
A | AT | 20 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(17): Show | 21 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.1629-516dupA | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182965323 | ||||||
chr2:182965327
|
T | TA | 4 | a0001c0002t0003g0192a0001c0002t0063g0190a0001c0002t0064g0189others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1629-520_1629-519i others(3): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182965327 | ||||||
chr2:182965405
|
T | A | 18 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(15): Show | 19 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.1629-597A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182965405 | ||||||
chr2:182965409
|
T | C | 1 | a0001c0003t0047g0179 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1629-601A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182965409 | ||||||
chr2:182965417
|
T | C | 1 | a0001c0002t0108g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1629-609A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182965417 | ||||||
chr2:182965641
|
T | C | 1 | a0001c0002t0103g0144 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1629-833A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182965641 | ||||||
chr2:182965721
|
T | C | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1629-913A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182965721 | ||||||
chr2:182965921
|
A | G | 82 | a0001c0001t0002g0059a0001c0001t0002g0071a0001c0001t0002g0081others(79): Show | 82 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1629-1113T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182965921 | ||||||
chr2:182965962
|
C | T | 1 | a0001c0001t0025g0035 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1629-1154G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182965962 | ||||||
chr2:182966253
|
G | A | 1 | a0001c0002t0070g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1628+963C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182966253 | ||||||
chr2:182966561
|
T | A | 4 | a0001c0002t0043g0013a0001c0002t0063g0190a0001c0002t0064g0189others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1628+655A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182966561 | ||||||
chr2:182966578
|
G | A | 2 | a0001c0001t0030g0087a0001c0001t0087g0123 | 2 | HG01256.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1628+638C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182966578 | ||||||
chr2:182966610
|
A | C | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1628+606T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182966610 | ||||||
chr2:182966623
|
C | T | 1 | a0001c0002t0042g0011 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1628+593G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182966623 | ||||||
chr2:182966961
|
A | C | 2 | a0001c0001t0100g0104a0001c0001t0101g0103 | 2 | HG01243.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1628+255T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182966961 | ||||||
chr2:182967184
|
C | G | 1 | a0001c0002t0074g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1628+32G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 16/30 | chr2 | 182967184 | ||||||
chr2:182967372
|
C | CA | 14 | a0001c0001t0030g0087a0001c0002t0037g0212a0001c0002t0037g0213others(11): Show | 15 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1483-12dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182967372 | ||||||
chr2:182967423
|
T | C | 4 | a0001c0002t0003g0192a0001c0002t0063g0190a0001c0002t0064g0189others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1483-62A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182967423 | ||||||
chr2:182967427
|
C | T | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(38): Show | 42 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.1483-66G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182967427 | ||||||
chr2:182967634
|
A | G | 2 | a0001c0002t0060g0183a0001c0009t0061g0184 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1483-273T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182967634 | ||||||
chr2:182967710
|
C | T | 81 | a0001c0001t0002g0059a0001c0001t0002g0071a0001c0001t0002g0081others(78): Show | 81 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.1483-349G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182967710 | ||||||
chr2:182967753
|
T | C | 1 | a0001c0001t0046g0045 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1483-392A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182967753 | ||||||
chr2:182967812
|
T | C | 12 | a0001c0001t0030g0087a0001c0002t0037g0212a0001c0002t0037g0213others(9): Show | 13 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.1483-451A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182967812 | ||||||
chr2:182967853
|
T | C | 3 | a0001c0001t0002g0084a0001c0001t0023g0074a0001c0001t0090g0078 | 3 | HG02572.hp1 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1483-492A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182967853 | ||||||
chr2:182968035
|
T | G | 1 | a0001c0001t0081g0091 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1483-674A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182968035 | ||||||
chr2:182968185
|
T | C | 2 | a0001c0001t0007g0065a0001c0001t0077g0130 | 2 | NA18983.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1483-824A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182968185 | ||||||
chr2:182968259
|
G | A | 1 | a0001c0001t0056g0029 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1483-898C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182968259 | ||||||
chr2:182968612
|
T | C | 1 | a0001c0001t0008g0115 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1483-1251A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182968612 | ||||||
chr2:182968679
|
G | A | 8 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1483-1318C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182968679 | ||||||
chr2:182968786
|
G | A | 18 | a0001c0002t0003g0198a0001c0002t0003g0199a0001c0002t0003g0201others(15): Show | 18 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1483-1425C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182968786 | ||||||
chr2:182969291
|
C | T | 2 | a0001c0001t0022g0110a0001c0001t0022g0111 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1483-1930G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182969291 | ||||||
chr2:182969399
|
C | T | 2 | a0001c0003t0020g0142a0001c0003t0020g0181 | 2 | NA18969.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1483-2038G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182969399 | ||||||
chr2:182969401
|
A | T | 1 | a0001c0002t0064g0189 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1483-2040T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182969401 | ||||||
chr2:182969686
|
T | C | 1 | a0001c0007t0003g0205 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1483-2325A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182969686 | ||||||
chr2:182969742
|
C | T | 1 | a0001c0004t0062g0194 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1483-2381G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182969742 | ||||||
chr2:182969793
|
G | A | 1 | a0001c0002t0060g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1483-2432C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182969793 | ||||||
chr2:182969809
|
A | C | 5 | a0001c0001t0030g0087a0001c0002t0037g0212a0001c0002t0037g0213others(2): Show | 5 | HG01109.hp1 HG01169.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.1483-2448T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182969809 | ||||||
chr2:182969920
|
A | C | 1 | a0001c0001t0005g0140 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1483-2559T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182969920 | ||||||
chr2:182969944
|
G | C | 1 | a0001c0002t0069g0158 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1483-2583C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182969944 | ||||||
chr2:182969948
|
T | G | 2 | a0001c0001t0079g0125a0001c0001t0084g0126 | 2 | NA18939.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1483-2587A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182969948 | ||||||
chr2:182970019
|
G | A | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1483-2658C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182970019 | ||||||
chr2:182970253
|
C | T | 81 | a0001c0001t0002g0059a0001c0001t0002g0071a0001c0001t0002g0081others(78): Show | 81 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.1483-2892G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182970253 | ||||||
chr2:182970275
|
C | G | 3 | a0001c0003t0004g0160a0001c0003t0004g0162a0001c0003t0004g0163 | 3 | HG02257.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1483-2914G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182970275 | ||||||
chr2:182970450
|
C | CATGA | 12 | a0001c0001t0030g0087a0001c0002t0037g0212a0001c0002t0037g0213others(9): Show | 13 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.1483-3090_1483-308 others(8): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182970450 | ||||||
chr2:182970556
|
C | T | 2 | a0001c0001t0002g0090a0001c0001t0098g0079 | 2 | HG02055.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1483-3195G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182970556 | ||||||
chr2:182970574
|
A | G | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1483-3213T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182970574 | ||||||
chr2:182970647
|
C | T | 1 | a0001c0002t0074g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1483-3286G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182970647 | ||||||
chr2:182970719
|
T | C | 81 | a0001c0001t0002g0059a0001c0001t0002g0071a0001c0001t0002g0081others(78): Show | 81 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.1483-3358A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182970719 | ||||||
chr2:182970872
|
A | ACT | 213 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(210): Show | 216 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(213): Show |
intron_variant | MODIFIER | c.1483-3513_1483-351 others(6): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182970872 | ||||||
chr2:182971116
|
C | T | 18 | a0001c0002t0003g0198a0001c0002t0003g0199a0001c0002t0003g0201others(15): Show | 18 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1483-3755G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182971116 | ||||||
chr2:182971122
|
C | T | 1 | a0001c0001t0088g0141 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1483-3761G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182971122 | ||||||
chr2:182971149
|
C | T | 7 | a0001c0001t0002g0099a0001c0001t0007g0100a0001c0001t0008g0063others(4): Show | 7 | HG00438.hp1 HG02523.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.1483-3788G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182971149 | ||||||
chr2:182971381
|
G | A | 20 | a0001c0001t0002g0099a0001c0001t0007g0100a0001c0001t0008g0063others(17): Show | 20 | HG00438.hp1 HG01071.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1483-4020C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182971381 | ||||||
chr2:182971388
|
C | T | 2 | a0001c0002t0063g0190a0001c0002t0064g0189 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1483-4027G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182971388 | ||||||
chr2:182971391
|
C | CT | 2 | a0001c0003t0006g0170a0001c0009t0061g0184 | 2 | HG01243.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1483-4031dupA | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182971391 | ||||||
chr2:182971392
|
TCAAAAAA others(1): Show |
T | 8 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1483-4039_1483-403 others(12): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182971392 | ||||||
chr2:182971393
|
C | A | 3 | a0001c0002t0060g0183a0001c0003t0006g0170a0001c0009t0061g0184 | 3 | HG01243.hp2 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1483-4032G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182971393 | ||||||
chr2:182971393
|
C | CA | 14 | a0001c0001t0002g0090a0001c0001t0010g0128a0001c0001t0014g0139others(11): Show | 14 | HG00438.hp2 HG01261.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1483-4033dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182971393 | ||||||
chr2:182971393
|
C | CAA | 15 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(12): Show | 15 | HG00597.hp2 HG01884.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1483-4034_1483-403 others(6): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182971393 | ||||||
chr2:182971393
|
C | T | 22 | a0001c0003t0006g0057a0001c0003t0006g0058a0001c0003t0006g0168others(19): Show | 22 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.1483-4032G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182971393 | ||||||
chr2:182971393
|
CA | C | 12 | a0001c0001t0001g0030a0001c0001t0001g0051a0001c0001t0001g0052others(9): Show | 12 | HG00621.hp2 HG01169.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.1483-4033delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182971393 | ||||||
chr2:182971393
|
CAA | C | 5 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0004t0016g0001others(2): Show | 6 | HG01099.hp1 HG01109.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1483-4034_1483-403 others(6): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182971393 | ||||||
chr2:182971393
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1483-4043_1483-403 others(15): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182971393 | ||||||
chr2:182971401
|
A | T | 8 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1483-4040T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182971401 | ||||||
chr2:182971575
|
A | C | 2 | a0001c0002t0003g0203a0001c0004t0028g0054 | 2 | HG02109.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1483-4214T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182971575 | ||||||
chr2:182971666
|
T | C | 81 | a0001c0001t0002g0059a0001c0001t0002g0071a0001c0001t0002g0081others(78): Show | 81 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.1483-4305A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182971666 | ||||||
chr2:182971732
|
G | A | 2 | a0001c0002t0043g0013a0001c0002t0065g0191 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1483-4371C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182971732 | ||||||
chr2:182972220
|
A | T | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1482+4673T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182972220 | ||||||
chr2:182972221
|
T | C | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1482+4672A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182972221 | ||||||
chr2:182972224
|
CA | C | 156 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(153): Show | 158 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(155): Show |
intron_variant | MODIFIER | c.1482+4668delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182972224 | ||||||
chr2:182972224
|
CAA | C | 12 | a0001c0002t0013g0146a0001c0002t0013g0147a0001c0002t0013g0148others(9): Show | 12 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.1482+4667_1482+466 others(6): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182972224 | ||||||
chr2:182972242
|
A | C | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1482+4651T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182972242 | ||||||
chr2:182972245
|
AC | A | 4 | a0001c0001t0076g0066a0001c0001t0087g0123a0001c0001t0091g0068others(1): Show | 4 | HG01069.hp1 HG01081.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1482+4647delG | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182972245 | ||||||
chr2:182972246
|
C | A | 3 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0062g0194 | 4 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1482+4647G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182972246 | ||||||
chr2:182972556
|
T | G | 1 | a0001c0001t0008g0115 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1482+4337A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182972556 | ||||||
chr2:182972656
|
C | A | 1 | a0001c0002t0003g0192 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1482+4237G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182972656 | ||||||
chr2:182973462
|
T | G | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1482+3431A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182973462 | ||||||
chr2:182973689
|
T | A | 3 | a0001c0001t0022g0110a0001c0001t0022g0111a0001c0001t0095g0112 | 3 | HG02647.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1482+3204A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182973689 | ||||||
chr2:182974091
|
C | G | 1 | a0001c0001t0024g0086 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1482+2802G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182974091 | ||||||
chr2:182974259
|
T | TA | 16 | a0001c0001t0056g0029a0001c0001t0092g0137a0001c0001t0100g0104others(13): Show | 17 | HG01099.hp1 HG01346.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.1482+2633dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182974259 | ||||||
chr2:182974259
|
TA | T | 7 | a0001c0001t0005g0018a0001c0001t0011g0025a0001c0001t0022g0110others(4): Show | 7 | HG01081.hp1 HG01081.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.1482+2633delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182974259 | ||||||
chr2:182974423
|
G | A | 13 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(10): Show | 14 | HG02257.hp1 HG02559.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.1482+2470C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182974423 | ||||||
chr2:182974579
|
A | G | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1482+2314T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182974579 | ||||||
chr2:182974580
|
G | A | 1 | a0001c0001t0031g0127 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1482+2313C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182974580 | ||||||
chr2:182974596
|
A | T | 3 | a0001c0001t0022g0110a0001c0001t0022g0111a0001c0001t0095g0112 | 3 | HG02647.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1482+2297T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182974596 | ||||||
chr2:182974699
|
C | T | 2 | a0001c0002t0063g0190a0001c0002t0064g0189 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1482+2194G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182974699 | ||||||
chr2:182974891
|
A | G | 1 | a0001c0003t0012g0175 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1482+2002T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182974891 | ||||||
chr2:182974932
|
C | T | 1 | a0001c0004t0028g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1482+1961G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182974932 | ||||||
chr2:182975061
|
A | G | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1482+1832T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182975061 | ||||||
chr2:182975089
|
C | G | 8 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(5): Show | 8 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1482+1804G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182975089 | ||||||
chr2:182975352
|
A | G | 1 | a0001c0001t0024g0086 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1482+1541T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182975352 | ||||||
chr2:182975414
|
T | C | 86 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(83): Show | 88 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.1482+1479A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182975414 | ||||||
chr2:182975579
|
A | C | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1482+1314T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182975579 | ||||||
chr2:182975637
|
T | C | 4 | a0001c0001t0007g0117a0001c0001t0022g0119a0001c0001t0075g0118others(1): Show | 4 | HG01192.hp2 HG01255.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1482+1256A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182975637 | ||||||
chr2:182975744
|
A | T | 2 | a0001c0002t0013g0148a0001c0002t0013g0149 | 2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1482+1149T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182975744 | ||||||
chr2:182975838
|
G | A | 7 | a0001c0001t0011g0015a0001c0001t0011g0023a0001c0001t0011g0024others(4): Show | 7 | NA18942.hp1 NA18949.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.1482+1055C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182975838 | ||||||
chr2:182975848
|
T | G | 1 | a0001c0001t0001g0050 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1482+1045A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182975848 | ||||||
chr2:182975919
|
A | G | 1 | a0001c0001t0008g0115 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1482+974T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182975919 | ||||||
chr2:182976197
|
A | T | 1 | a0001c0002t0060g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1482+696T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182976197 | ||||||
chr2:182976340
|
GT | G | 17 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0050others(14): Show | 18 | HG00621.hp2 HG02056.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.1482+552delA | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182976340 | ||||||
chr2:182976356
|
G | A | 3 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0062g0194 | 4 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1482+537C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182976356 | ||||||
chr2:182976647
|
G | C | 1 | a0001c0001t0007g0114 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1482+246C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182976647 | ||||||
chr2:182976813
|
T | A | 2 | a0001c0002t0043g0013a0001c0002t0065g0191 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1482+80A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182976813 | ||||||
chr2:182976863
|
A | G | 1 | a0001c0002t0043g0013 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1482+30T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 15/30 | chr2 | 182976863 | ||||||
chr2:182976963
|
GA | G | 8 | a0001c0001t0082g0085a0001c0002t0037g0212a0001c0002t0037g0213others(5): Show | 8 | HG00438.hp2 HG01109.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1424-13delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 14/30 | chr2 | 182976963 | ||||||
chr2:182977163
|
A | G | 2 | a0001c0002t0003g0198a0001c0002t0003g0202 | 2 | HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1424-212T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 14/30 | chr2 | 182977163 | ||||||
chr2:182977175
|
A | G | 14 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(11): Show | 15 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1424-224T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 14/30 | chr2 | 182977175 | ||||||
chr2:182977226
|
T | C | 1 | a0001c0001t0002g0084 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1424-275A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 14/30 | chr2 | 182977226 | ||||||
chr2:182977276
|
G | A | 10 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(7): Show | 11 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.1424-325C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 14/30 | chr2 | 182977276 | ||||||
chr2:182977355
|
T | A | 1 | a0001c0003t0015g0007 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1424-404A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 14/30 | chr2 | 182977355 | ||||||
chr2:182977367
|
G | A | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1424-416C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 14/30 | chr2 | 182977367 | ||||||
chr2:182977526
|
T | G | 1 | a0001c0001t0022g0119 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1424-575A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 14/30 | chr2 | 182977526 | ||||||
chr2:182977779
|
G | A | 1 | a0001c0002t0065g0191 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1424-828C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 14/30 | chr2 | 182977779 | ||||||
chr2:182977782
|
T | C | 31 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(28): Show | 31 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1424-831A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 14/30 | chr2 | 182977782 | ||||||
chr2:182978126
|
A | C | 1 | a0001c0001t0031g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1423+708T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 14/30 | chr2 | 182978126 | ||||||
chr2:182978426
|
T | C | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1423+408A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 14/30 | chr2 | 182978426 | ||||||
chr2:182979016
|
T | C | 51 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(48): Show | 52 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1342-101A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182979016 | ||||||
chr2:182979188
|
C | T | 1 | a0001c0001t0023g0097 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1342-273G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182979188 | ||||||
chr2:182979198
|
A | G | 86 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(83): Show | 88 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.1342-283T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182979198 | ||||||
chr2:182979372
|
T | C | 1 | a0001c0002t0069g0158 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1342-457A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182979372 | ||||||
chr2:182979429
|
C | T | 2 | a0001c0003t0006g0168a0001c0003t0006g0169 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1342-514G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182979429 | ||||||
chr2:182979504
|
G | C | 17 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(14): Show | 18 | HG02257.hp1 HG02559.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.1342-589C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182979504 | ||||||
chr2:182979572
|
T | C | 3 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0062g0194 | 4 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1342-657A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182979572 | ||||||
chr2:182979611
|
A | C | 2 | a0001c0002t0043g0013a0001c0002t0065g0191 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1342-696T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182979611 | ||||||
chr2:182979860
|
T | C | 23 | a0001c0003t0006g0057a0001c0003t0006g0058a0001c0003t0006g0168others(20): Show | 23 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.1342-945A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182979860 | ||||||
chr2:182979862
|
A | G | 51 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(48): Show | 52 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1342-947T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182979862 | ||||||
chr2:182979899
|
T | G | 3 | a0001c0002t0003g0192a0001c0002t0003g0199a0001c0002t0104g0193 | 3 | HG02970.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1342-984A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182979899 | ||||||
chr2:182980091
|
A | G | 1 | a0001c0001t0076g0066 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1341+1153T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182980091 | ||||||
chr2:182980196
|
C | T | 1 | a0001c0001t0005g0021 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1341+1048G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182980196 | ||||||
chr2:182980339
|
T | C | 2 | a0001c0002t0060g0183a0001c0009t0061g0184 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1341+905A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182980339 | ||||||
chr2:182980360
|
A | G | 2 | a0001c0001t0008g0095a0001c0001t0024g0096 | 2 | HG02074.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1341+884T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182980360 | ||||||
chr2:182980560
|
T | A | 1 | a0001c0001t0080g0062 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1341+684A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182980560 | ||||||
chr2:182980577
|
G | A | 3 | a0001c0001t0010g0128a0001c0001t0010g0186a0001c0001t0083g0129 | 3 | NA18964.hp2 NA18992.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1341+667C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182980577 | ||||||
chr2:182980629
|
T | A | 1 | a0001c0001t0032g0088 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1341+615A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182980629 | ||||||
chr2:182980664
|
T | G | 1 | a0001c0002t0106g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1341+580A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182980664 | ||||||
chr2:182980740
|
A | G | 1 | a0001c0002t0003g0204 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1341+504T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182980740 | ||||||
chr2:182980771
|
A | G | 5 | a0001c0003t0006g0182a0001c0003t0020g0142a0001c0003t0020g0172others(2): Show | 5 | NA18969.hp2 NA18972.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.1341+473T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182980771 | ||||||
chr2:182980778
|
C | G | 4 | a0001c0003t0012g0167a0001c0003t0012g0174a0001c0003t0012g0177others(1): Show | 4 | HG00609.hp2 HG00621.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.1341+466G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182980778 | ||||||
chr2:182980838
|
C | T | 1 | a0001c0002t0065g0191 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1341+406G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182980838 | ||||||
chr2:182981125
|
A | G | 1 | a0001c0003t0004g0162 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1341+119T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182981125 | ||||||
chr2:182981162
|
A | C | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1341+82T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 13/30 | chr2 | 182981162 | ||||||
chr2:182981433
|
T | C | 18 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(15): Show | 19 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.1209-57A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 12/30 | chr2 | 182981433 | ||||||
chr2:182981620
|
T | A | 1 | a0001c0002t0003g0206 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1209-244A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 12/30 | chr2 | 182981620 | ||||||
chr2:182981649
|
C | A | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1209-273G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 12/30 | chr2 | 182981649 | ||||||
chr2:182981651
|
G | A | 14 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(11): Show | 15 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1209-275C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 12/30 | chr2 | 182981651 | ||||||
chr2:182981703
|
G | A | 82 | a0001c0001t0002g0059a0001c0001t0002g0071a0001c0001t0002g0081others(79): Show | 82 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1209-327C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 12/30 | chr2 | 182981703 | ||||||
chr2:182981733
|
A | C | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1209-357T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 12/30 | chr2 | 182981733 | ||||||
chr2:182981802
|
G | A | 2 | a0001c0002t0003g0198a0001c0002t0003g0202 | 2 | HG02735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1209-426C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 12/30 | chr2 | 182981802 | ||||||
chr2:182981908
|
C | CA | 19 | a0001c0001t0002g0084a0001c0001t0005g0019a0001c0001t0033g0101others(16): Show | 20 | HG01099.hp1 HG01109.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.1209-533dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 12/30 | chr2 | 182981908 | ||||||
chr2:182981908
|
CA | C | 11 | a0001c0001t0011g0025a0001c0001t0032g0088a0001c0001t0054g0042others(8): Show | 11 | HG01081.hp1 HG01169.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.1209-533delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 12/30 | chr2 | 182981908 | ||||||
chr2:182982029
|
T | C | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1209-653A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 12/30 | chr2 | 182982029 | ||||||
chr2:182982175
|
A | G | 2 | a0001c0002t0060g0183a0001c0009t0061g0184 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1208+646T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 12/30 | chr2 | 182982175 | ||||||
chr2:182982306
|
T | C | 1 | a0001c0001t0005g0031 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1208+515A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 12/30 | chr2 | 182982306 | ||||||
chr2:182982386
|
A | G | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1208+435T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 12/30 | chr2 | 182982386 | ||||||
chr2:182982450
|
GAT | G | 31 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(28): Show | 31 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1208+369_1208+370d others(4): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 12/30 | chr2 | 182982450 | ||||||
chr2:182982601
|
T | C | 2 | a0001c0003t0004g0160a0001c0003t0004g0163 | 2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1208+220A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 12/30 | chr2 | 182982601 | ||||||
chr2:182982604
|
C | T | 4 | a0001c0003t0004g0080a0001c0003t0004g0164a0001c0003t0004g0165others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1208+217G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 12/30 | chr2 | 182982604 | ||||||
chr2:182983094
|
G | C | 4 | a0001c0002t0043g0013a0001c0002t0063g0190a0001c0002t0064g0189others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1102-167C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 11/30 | chr2 | 182983094 | ||||||
chr2:182983386
|
T | C | 86 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(83): Show | 88 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(85): Show |
splice_region_variant&intron_variant | LOW | c.1005-4A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182983386 | ||||||
chr2:182983562
|
C | T | 13 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(10): Show | 14 | HG02257.hp1 HG02559.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.1005-180G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182983562 | ||||||
chr2:182983624
|
C | A | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(38): Show | 42 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.1005-242G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182983624 | ||||||
chr2:182983747
|
T | C | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1005-365A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182983747 | ||||||
chr2:182983900
|
G | T | 1 | a0001c0001t0008g0115 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1005-518C>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182983900 | ||||||
chr2:182983956
|
A | G | 25 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(22): Show | 25 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1005-574T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182983956 | ||||||
chr2:182983963
|
A | T | 1 | a0001c0002t0074g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1005-581T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182983963 | ||||||
chr2:182984052
|
A | C | 1 | a0001c0003t0012g0167 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1005-670T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182984052 | ||||||
chr2:182984060
|
AACTG | A | 124 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(121): Show | 125 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.1005-682_1005-679d others(6): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182984060 | ||||||
chr2:182984094
|
T | C | 1 | a0001c0002t0074g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1005-712A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182984094 | ||||||
chr2:182984191
|
T | C | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1005-809A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182984191 | ||||||
chr2:182984423
|
G | GGGGTGTG others(31): Show |
1 | a0001c0004t0028g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1005-1042_1005-104 others(42): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182984423 | ||||||
chr2:182984423
|
G | GGGGTGTG others(41): Show |
1 | a0001c0004t0066g0055 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1005-1042_1005-104 others(52): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182984423 | ||||||
chr2:182984423
|
G | GGGTGTGT others(14): Show |
1 | a0001c0004t0016g0010 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1005-1042_1005-104 others(25): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182984423 | ||||||
chr2:182984423
|
G | GGGTGTGT others(16): Show |
1 | a0001c0004t0016g0001 | 2 | HG01099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1005-1042_1005-104 others(27): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182984423 | ||||||
chr2:182984423
|
G | GGGTGTGT others(46): Show |
1 | a0001c0004t0062g0194 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1005-1042_1005-104 others(57): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182984423 | ||||||
chr2:182984423
|
G | GGTGTGTG others(29): Show |
1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1005-1042_1005-104 others(40): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182984423 | ||||||
chr2:182984423
|
G | GGTGTGTG others(37): Show |
1 | a0001c0004t0028g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1005-1042_1005-104 others(48): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182984423 | ||||||
chr2:182984423
|
G | GGTGTGTG others(178): Show |
1 | a0001c0002t0041g0012 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1005-1042_1005-104 others(189): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182984423 | ||||||
chr2:182984423
|
G | GGTGTGTG others(162): Show |
1 | a0001c0002t0042g0011 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1005-1042_1005-104 others(173): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182984423 | ||||||
chr2:182984423
|
G | GGTGTGTG others(160): Show |
1 | a0001c0002t0037g0213 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1005-1042_1005-104 others(171): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182984423 | ||||||
chr2:182984423
|
G | GGTGTGTG others(158): Show |
1 | a0001c0002t0037g0212 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1005-1042_1005-104 others(169): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182984423 | ||||||
chr2:182984423
|
GGT | G | 78 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(75): Show | 79 | HG00609.hp2 HG00621.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.1005-1043_1005-104 others(6): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182984423 | ||||||
chr2:182984423
|
GGTGT | G | 84 | a0001c0001t0002g0059a0001c0001t0002g0071a0001c0001t0002g0081others(81): Show | 84 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1005-1045_1005-104 others(8): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182984423 | ||||||
chr2:182984423
|
GGTGTGT | G | 20 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(17): Show | 20 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1005-1047_1005-104 others(10): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182984423 | ||||||
chr2:182984427
|
T | G | 2 | a0001c0002t0060g0183a0001c0009t0061g0184 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1005-1045A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182984427 | ||||||
chr2:182984460
|
C | T | 3 | a0001c0003t0004g0164a0001c0003t0004g0165a0001c0003t0004g0166 | 3 | HG01884.hp2 HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1005-1078G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182984460 | ||||||
chr2:182984810
|
G | C | 1 | a0001c0001t0021g0113 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1004+1361C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182984810 | ||||||
chr2:182985059
|
C | T | 2 | a0001c0002t0036g0197a0001c0002t0036g0208 | 2 | HG01261.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1004+1112G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182985059 | ||||||
chr2:182985065
|
C | T | 1 | a0001c0001t0030g0087 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1004+1106G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182985065 | ||||||
chr2:182985277
|
T | C | 11 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.1004+894A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182985277 | ||||||
chr2:182985351
|
T | A | 2 | a0001c0002t0003g0206a0001c0002t0107g0207 | 2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1004+820A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182985351 | ||||||
chr2:182985352
|
C | G | 2 | a0001c0002t0003g0206a0001c0002t0107g0207 | 2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1004+819G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182985352 | ||||||
chr2:182985494
|
A | AGAGGTGT others(318): Show |
2 | a0001c0002t0060g0183a0001c0009t0061g0184 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1004+676_1004+677i others(327): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182985494 | ||||||
chr2:182985524
|
C | T | 9 | a0001c0001t0002g0071a0001c0001t0002g0081a0001c0001t0002g0082others(6): Show | 9 | HG02572.hp1 HG02615.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1004+647G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182985524 | ||||||
chr2:182985666
|
T | C | 38 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0030others(35): Show | 40 | HG00621.hp2 HG01099.hp1 HG01358.hp1 others(37): Show |
intron_variant | MODIFIER | c.1004+505A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182985666 | ||||||
chr2:182985800
|
CA | C | 6 | a0001c0001t0034g0116a0001c0001t0088g0141a0001c0002t0037g0212others(3): Show | 6 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.1004+370delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182985800 | ||||||
chr2:182986149
|
C | T | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1004+22G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 10/30 | chr2 | 182986149 | ||||||
chr2:182986330
|
C | T | 210 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(207): Show | 213 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(210): Show |
intron_variant | MODIFIER | c.948-103G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 9/30 | chr2 | 182986330 | ||||||
chr2:182986413
|
C | T | 1 | a0001c0001t0011g0015 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.948-186G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 9/30 | chr2 | 182986413 | ||||||
chr2:182986414
|
T | TA | 18 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(15): Show | 18 | HG00597.hp2 HG01261.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.948-188dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 9/30 | chr2 | 182986414 | ||||||
chr2:182986646
|
A | G | 2 | a0001c0002t0063g0190a0001c0002t0064g0189 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.948-419T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 9/30 | chr2 | 182986646 | ||||||
chr2:182986678
|
T | A | 1 | a0001c0001t0082g0085 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.948-451A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 9/30 | chr2 | 182986678 | ||||||
chr2:182986981
|
C | T | 21 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(18): Show | 21 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.948-754G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 9/30 | chr2 | 182986981 | ||||||
chr2:182987036
|
G | A | 1 | a0001c0003t0004g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.948-809C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 9/30 | chr2 | 182987036 | ||||||
chr2:182987111
|
G | A | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.948-884C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 9/30 | chr2 | 182987111 | ||||||
chr2:182987179
|
T | C | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.948-952A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 9/30 | chr2 | 182987179 | ||||||
chr2:182987460
|
T | A | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.948-1233A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 9/30 | chr2 | 182987460 | ||||||
chr2:182987476
|
T | C | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.948-1249A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 9/30 | chr2 | 182987476 | ||||||
chr2:182987554
|
C | T | 17 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(14): Show | 18 | HG02257.hp1 HG02559.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.948-1327G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 9/30 | chr2 | 182987554 | ||||||
chr2:182987883
|
G | C | 1 | a0001c0001t0088g0141 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.947+1147C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 9/30 | chr2 | 182987883 | ||||||
chr2:182987887
|
G | A | 17 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(14): Show | 18 | HG02257.hp1 HG02559.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.947+1143C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 9/30 | chr2 | 182987887 | ||||||
chr2:182988338
|
A | C | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.947+692T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 9/30 | chr2 | 182988338 | ||||||
chr2:182988430
|
A | G | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.947+600T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 9/30 | chr2 | 182988430 | ||||||
chr2:182989421
|
G | A | 2 | a0001c0001t0002g0108a0001c0001t0023g0097 | 2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.791-235C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182989421 | ||||||
chr2:182989567
|
C | T | 2 | a0001c0001t0007g0060a0001c0001t0097g0061 | 2 | HG00609.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.791-381G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182989567 | ||||||
chr2:182989629
|
T | C | 1 | a0001c0001t0002g0071 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.791-443A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182989629 | ||||||
chr2:182989681
|
C | T | 11 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.791-495G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182989681 | ||||||
chr2:182989776
|
C | T | 1 | a0001c0001t0010g0188 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.791-590G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182989776 | ||||||
chr2:182989842
|
A | C | 5 | a0001c0003t0006g0057a0001c0003t0006g0058a0001c0003t0006g0170others(2): Show | 5 | HG01243.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.791-656T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182989842 | ||||||
chr2:182989923
|
G | A | 8 | a0001c0002t0003g0198a0001c0002t0003g0202a0001c0002t0003g0203others(5): Show | 8 | HG00597.hp2 HG02486.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.791-737C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182989923 | ||||||
chr2:182990050
|
A | C | 1 | a0001c0002t0103g0144 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.791-864T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182990050 | ||||||
chr2:182990146
|
T | C | 20 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(17): Show | 20 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.791-960A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182990146 | ||||||
chr2:182990191
|
G | T | 2 | a0001c0002t0063g0190a0001c0002t0064g0189 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.791-1005C>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182990191 | ||||||
chr2:182990335
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.791-1149C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182990335 | ||||||
chr2:182990577
|
C | T | 210 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(207): Show | 213 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(210): Show |
intron_variant | MODIFIER | c.791-1391G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182990577 | ||||||
chr2:182990780
|
T | A | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.791-1594A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182990780 | ||||||
chr2:182991057
|
C | T | 23 | a0001c0003t0006g0057a0001c0003t0006g0058a0001c0003t0006g0168others(20): Show | 23 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.791-1871G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182991057 | ||||||
chr2:182991112
|
A | C | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(38): Show | 42 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.791-1926T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182991112 | ||||||
chr2:182991129
|
GCTA | G | 2 | a0001c0002t0043g0013a0001c0002t0065g0191 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.791-1946_791-1944d others(5): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182991129 | ||||||
chr2:182991305
|
C | T | 1 | a0001c0001t0086g0072 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.791-2119G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182991305 | ||||||
chr2:182991660
|
CA | C | 5 | a0001c0001t0001g0016a0001c0003t0012g0175a0001c0005t0071g0155others(2): Show | 5 | HG01069.hp2 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.791-2475delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182991660 | ||||||
chr2:182991797
|
C | T | 1 | a0001c0001t0021g0121 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.791-2611G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182991797 | ||||||
chr2:182992018
|
A | C | 17 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(14): Show | 18 | HG02257.hp1 HG02559.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.790+2821T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182992018 | ||||||
chr2:182992487
|
T | A | 1 | a0001c0003t0004g0164 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.790+2352A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182992487 | ||||||
chr2:182992501
|
A | G | 1 | a0001c0002t0070g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.790+2338T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182992501 | ||||||
chr2:182992570
|
G | C | 1 | a0001c0003t0006g0170 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.790+2269C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182992570 | ||||||
chr2:182992591
|
C | T | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.790+2248G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182992591 | ||||||
chr2:182993283
|
G | A | 1 | a0001c0001t0021g0113 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.790+1556C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182993283 | ||||||
chr2:182993440
|
T | C | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.790+1399A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182993440 | ||||||
chr2:182993486
|
A | G | 1 | a0001c0001t0078g0136 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.790+1353T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182993486 | ||||||
chr2:182993578
|
C | T | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.790+1261G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182993578 | ||||||
chr2:182993662
|
G | A | 6 | a0001c0002t0009g0003a0001c0002t0009g0151a0001c0002t0009g0153others(3): Show | 7 | HG02257.hp1 HG02559.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.790+1177C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182993662 | ||||||
chr2:182993710
|
C | T | 2 | a0001c0004t0028g0056a0001c0004t0066g0055 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.790+1129G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182993710 | ||||||
chr2:182993734
|
T | TA | 34 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(31): Show | 34 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.790+1104dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182993734 | ||||||
chr2:182993841
|
G | A | 2 | a0001c0002t0037g0212a0001c0002t0037g0213 | 2 | HG01109.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.790+998C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182993841 | ||||||
chr2:182993912
|
C | T | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.790+927G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182993912 | ||||||
chr2:182993929
|
T | C | 1 | a0001c0001t0085g0083 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.790+910A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182993929 | ||||||
chr2:182993954
|
T | C | 50 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(47): Show | 51 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.790+885A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182993954 | ||||||
chr2:182994314
|
T | A | 1 | a0001c0001t0095g0112 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.790+525A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182994314 | ||||||
chr2:182994326
|
T | C | 1 | a0001c0001t0095g0112 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.790+513A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182994326 | ||||||
chr2:182994546
|
C | T | 1 | a0001c0012t0018g0211 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.790+293G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182994546 | ||||||
chr2:182994588
|
G | A | 1 | a0001c0001t0031g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.790+251C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182994588 | ||||||
chr2:182994698
|
C | T | 4 | a0001c0002t0043g0013a0001c0002t0063g0190a0001c0002t0064g0189others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.790+141G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182994698 | ||||||
chr2:182994745
|
T | C | 19 | a0001c0001t0002g0099a0001c0001t0007g0100a0001c0001t0008g0063others(16): Show | 19 | HG00438.hp1 HG01071.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.790+94A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 8/30 | chr2 | 182994745 | ||||||
chr2:182994962
|
C | CT | 14 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(11): Show | 15 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.742-76dupA | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 7/30 | chr2 | 182994962 | ||||||
chr2:182995066
|
A | G | 1 | a0001c0002t0043g0013 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.742-179T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 7/30 | chr2 | 182995066 | ||||||
chr2:182995570
|
G | A | 85 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(82): Show | 87 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.741+131C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 7/30 | chr2 | 182995570 | ||||||
chr2:182995664
|
C | T | 1 | a0001c0001t0093g0064 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.741+37G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 7/30 | chr2 | 182995664 | ||||||
chr2:182995932
|
A | G | 1 | a0001c0002t0063g0190 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.604-94T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182995932 | ||||||
chr2:182996106
|
G | A | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(38): Show | 42 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.604-268C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182996106 | ||||||
chr2:182996261
|
T | C | 1 | a0001c0003t0012g0175 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.604-423A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182996261 | ||||||
chr2:182996317
|
TACTTA | T | 2 | a0001c0002t0043g0013a0001c0002t0065g0191 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.604-484_604-480del others(5): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182996317 | ||||||
chr2:182996476
|
G | A | 34 | a0001c0002t0043g0013a0001c0002t0063g0190a0001c0002t0064g0189others(31): Show | 34 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.604-638C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182996476 | ||||||
chr2:182996543
|
C | T | 34 | a0001c0002t0043g0013a0001c0002t0063g0190a0001c0002t0064g0189others(31): Show | 34 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.604-705G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182996543 | ||||||
chr2:182996703
|
G | C | 1 | a0001c0001t0021g0113 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.604-865C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182996703 | ||||||
chr2:182996756
|
G | T | 2 | a0001c0002t0037g0212a0001c0002t0037g0213 | 2 | HG01109.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.604-918C>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182996756 | ||||||
chr2:182996768
|
C | A | 1 | a0001c0001t0007g0065 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.604-930G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182996768 | ||||||
chr2:182997685
|
T | C | 1 | a0001c0005t0073g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.604-1847A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182997685 | ||||||
chr2:182997730
|
G | C | 211 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(208): Show | 214 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(211): Show |
intron_variant | MODIFIER | c.604-1892C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182997730 | ||||||
chr2:182997843
|
G | C | 1 | a0001c0002t0107g0207 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.604-2005C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182997843 | ||||||
chr2:182997880
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.604-2042C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182997880 | ||||||
chr2:182997951
|
C | A | 1 | a0001c0005t0071g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.604-2113G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182997951 | ||||||
chr2:182997952
|
C | T | 1 | a0001c0005t0071g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.604-2114G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182997952 | ||||||
chr2:182997976
|
C | T | 2 | a0001c0002t0003g0206a0001c0002t0107g0207 | 2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.604-2138G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182997976 | ||||||
chr2:182998014
|
T | C | 2 | a0001c0004t0016g0001a0001c0004t0016g0010 | 3 | HG01099.hp1 HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.604-2176A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182998014 | ||||||
chr2:182998220
|
C | T | 1 | a0001c0001t0096g0073 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.604-2382G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182998220 | ||||||
chr2:182998291
|
G | A | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.604-2453C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182998291 | ||||||
chr2:182998347
|
T | A | 1 | a0001c0001t0014g0139 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.604-2509A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182998347 | ||||||
chr2:182998608
|
T | C | 1 | a0001c0001t0002g0059 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.604-2770A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182998608 | ||||||
chr2:182998673
|
T | C | 1 | a0001c0001t0091g0068 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.604-2835A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182998673 | ||||||
chr2:182998738
|
G | T | 1 | a0001c0003t0012g0175 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.604-2900C>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182998738 | ||||||
chr2:182998834
|
C | CA | 5 | a0001c0002t0013g0149a0001c0002t0037g0212a0001c0002t0037g0213others(2): Show | 5 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.604-2997dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182998834 | ||||||
chr2:182998835
|
A | C | 2 | a0001c0002t0063g0190a0001c0002t0064g0189 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.604-2997T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182998835 | ||||||
chr2:182998857
|
AG | A | 182 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(179): Show | 184 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(181): Show |
intron_variant | MODIFIER | c.604-3020delC | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182998857 | ||||||
chr2:182998858
|
G | A | 23 | a0001c0001t0001g0028a0001c0001t0007g0114a0001c0001t0018g0070others(20): Show | 23 | HG00597.hp2 HG01109.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.604-3020C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182998858 | ||||||
chr2:182998982
|
C | T | 3 | a0001c0002t0003g0198a0001c0002t0003g0202a0001c0002t0110g0214 | 3 | HG02735.hp1 NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.603+2971G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182998982 | ||||||
chr2:182999032
|
C | T | 20 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(17): Show | 20 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.603+2921G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182999032 | ||||||
chr2:182999313
|
C | A | 20 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(17): Show | 20 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.603+2640G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182999313 | ||||||
chr2:182999413
|
CAG | C | 30 | a0001c0003t0004g0160a0001c0003t0004g0161a0001c0003t0004g0162others(27): Show | 30 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.603+2538_603+2539d others(4): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182999413 | ||||||
chr2:182999662
|
A | G | 30 | a0001c0003t0004g0160a0001c0003t0004g0161a0001c0003t0004g0162others(27): Show | 30 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.603+2291T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182999662 | ||||||
chr2:182999757
|
C | T | 3 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0062g0194 | 4 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.603+2196G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182999757 | ||||||
chr2:182999985
|
C | A | 4 | a0001c0001t0017g0046a0001c0001t0017g0047a0001c0001t0017g0049others(1): Show | 4 | NA18983.hp2 NA18999.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.603+1968G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 182999985 | ||||||
chr2:183000180
|
A | C | 48 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(45): Show | 49 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.603+1773T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 183000180 | ||||||
chr2:183001022
|
G | A | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(38): Show | 42 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.603+931C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 183001022 | ||||||
chr2:183001083
|
A | G | 1 | a0001c0001t0075g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.603+870T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 183001083 | ||||||
chr2:183001129
|
T | C | 1 | a0001c0001t0095g0112 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.603+824A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 183001129 | ||||||
chr2:183001335
|
T | A | 11 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.603+618A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 183001335 | ||||||
chr2:183001541
|
T | C | 1 | a0001c0001t0005g0021 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.603+412A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 183001541 | ||||||
chr2:183001585
|
A | AC | 21 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(18): Show | 21 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.603+367dupG | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 183001585 | ||||||
chr2:183001854
|
T | C | 1 | a0001c0001t0005g0031 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.603+99A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 183001854 | ||||||
chr2:183001911
|
T | C | 1 | a0001c0003t0047g0179 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.603+42A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 6/30 | chr2 | 183001911 | ||||||
chr2:183002114
|
A | G | 1 | a0001c0002t0013g0147 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.512+13T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 5/30 | chr2 | 183002114 | ||||||
chr2:183002276
|
G | GA | 11 | a0001c0001t0001g0028a0001c0002t0037g0212a0001c0002t0037g0213others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.370-8dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 4/30 | chr2 | 183002276 | ||||||
chr2:183002527
|
G | T | 1 | a0001c0002t0060g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.370-258C>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 4/30 | chr2 | 183002527 | ||||||
chr2:183002570
|
G | A | 4 | a0001c0003t0004g0080a0001c0003t0004g0164a0001c0003t0004g0165others(1): Show | 4 | HG01884.hp2 HG02258.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.370-301C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 4/30 | chr2 | 183002570 | ||||||
chr2:183002661
|
TAAGA | T | 35 | a0001c0002t0043g0013a0001c0002t0063g0190a0001c0002t0064g0189others(32): Show | 35 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.369+309_369+312del others(4): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 4/30 | chr2 | 183002661 | ||||||
chr2:183002664
|
G | C | 1 | a0001c0001t0005g0031 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.369+310C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 4/30 | chr2 | 183002664 | ||||||
chr2:183002756
|
G | A | 2 | a0001c0003t0027g0176a0001c0003t0027g0185 | 2 | HG02145.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.369+218C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 4/30 | chr2 | 183002756 | ||||||
chr2:183003557
|
G | A | 3 | a0001c0005t0071g0155a0001c0005t0072g0157a0001c0005t0073g0156 | 3 | HG02647.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.220-232C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183003557 | ||||||
chr2:183003914
|
G | C | 2 | a0001c0002t0063g0190a0001c0002t0064g0189 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.220-589C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183003914 | ||||||
chr2:183003923
|
GT | G | 212 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(209): Show | 215 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(212): Show |
intron_variant | MODIFIER | c.220-599delA | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183003923 | ||||||
chr2:183004168
|
A | G | 1 | a0001c0001t0008g0063 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.220-843T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183004168 | ||||||
chr2:183004176
|
A | C | 53 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(50): Show | 54 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.220-851T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183004176 | ||||||
chr2:183004190
|
C | T | 211 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(208): Show | 214 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(211): Show |
intron_variant | MODIFIER | c.220-865G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183004190 | ||||||
chr2:183004220
|
CA | C | 14 | a0001c0001t0002g0059a0001c0001t0002g0071a0001c0001t0002g0081others(11): Show | 14 | HG00438.hp2 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.220-896delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183004220 | ||||||
chr2:183004354
|
G | A | 210 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(207): Show | 213 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(210): Show |
intron_variant | MODIFIER | c.220-1029C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183004354 | ||||||
chr2:183004488
|
C | CA | 26 | a0001c0001t0001g0028a0001c0001t0001g0038a0001c0001t0002g0081others(23): Show | 26 | HG01261.hp2 HG02109.hp2 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.220-1164dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183004488 | ||||||
chr2:183004488
|
C | CAA | 42 | a0001c0001t0017g0047a0001c0002t0009g0003a0001c0002t0009g0145others(39): Show | 43 | HG00609.hp2 HG00621.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.220-1165_220-1164d others(4): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183004488 | ||||||
chr2:183004488
|
CA | C | 38 | a0001c0001t0001g0039a0001c0001t0002g0099a0001c0001t0007g0100others(35): Show | 39 | HG00438.hp1 HG01099.hp1 HG01261.hp1 others(36): Show |
intron_variant | MODIFIER | c.220-1164delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183004488 | ||||||
chr2:183004640
|
T | C | 1 | a0001c0005t0071g0155 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.220-1315A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183004640 | ||||||
chr2:183004682
|
G | A | 1 | a0001c0001t0033g0101 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.220-1357C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183004682 | ||||||
chr2:183004861
|
G | T | 1 | a0001c0011t0109g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.220-1536C>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183004861 | ||||||
chr2:183004884
|
C | CA | 207 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0028others(204): Show | 210 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(207): Show |
intron_variant | MODIFIER | c.220-1560dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183004884 | ||||||
chr2:183004987
|
A | C | 1 | a0001c0002t0035g0209 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.220-1662T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183004987 | ||||||
chr2:183004989
|
C | T | 20 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(17): Show | 20 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.220-1664G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183004989 | ||||||
chr2:183005024
|
C | T | 1 | a0001c0003t0012g0175 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.220-1699G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183005024 | ||||||
chr2:183005028
|
ATC | A | 31 | a0001c0003t0004g0080a0001c0003t0004g0160a0001c0003t0004g0161others(28): Show | 31 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.220-1705_220-1704d others(4): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183005028 | ||||||
chr2:183005042
|
G | A | 1 | a0001c0002t0074g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.220-1717C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183005042 | ||||||
chr2:183005060
|
A | G | 1 | a0001c0003t0004g0161 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.220-1735T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183005060 | ||||||
chr2:183005282
|
C | T | 2 | a0001c0002t0043g0013a0001c0002t0065g0191 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.220-1957G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183005282 | ||||||
chr2:183005299
|
T | A | 1 | a0001c0001t0034g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.220-1974A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183005299 | ||||||
chr2:183005317
|
T | A | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-1992A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183005317 | ||||||
chr2:183005369
|
C | T | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.220-2044G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183005369 | ||||||
chr2:183005418
|
A | G | 82 | a0001c0001t0002g0059a0001c0001t0002g0071a0001c0001t0002g0081others(79): Show | 82 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.220-2093T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183005418 | ||||||
chr2:183005817
|
T | C | 3 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0062g0194 | 4 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-2492A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183005817 | ||||||
chr2:183005828
|
T | G | 1 | a0001c0001t0002g0124 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.220-2503A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183005828 | ||||||
chr2:183005835
|
T | C | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.220-2510A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183005835 | ||||||
chr2:183006214
|
C | A | 17 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(14): Show | 18 | HG02257.hp1 HG02559.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.220-2889G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183006214 | ||||||
chr2:183006344
|
A | G | 1 | a0001c0001t0048g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.220-3019T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183006344 | ||||||
chr2:183006720
|
C | A | 85 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(82): Show | 87 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.220-3395G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183006720 | ||||||
chr2:183006775
|
C | G | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(38): Show | 42 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.220-3450G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183006775 | ||||||
chr2:183006776
|
CTAAGAAC others(5): Show |
C | 3 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0062g0194 | 4 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-3463_220-3452d others(14): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183006776 | ||||||
chr2:183006892
|
G | C | 1 | a0001c0001t0002g0059 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.220-3567C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183006892 | ||||||
chr2:183006990
|
C | G | 2 | a0001c0001t0007g0065a0001c0001t0077g0130 | 2 | NA18983.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.220-3665G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183006990 | ||||||
chr2:183007161
|
C | T | 2 | a0001c0002t0060g0183a0001c0009t0061g0184 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.220-3836G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183007161 | ||||||
chr2:183007179
|
C | T | 1 | a0001c0003t0058g0180 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.220-3854G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183007179 | ||||||
chr2:183007554
|
G | A | 1 | a0001c0002t0067g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.220-4229C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183007554 | ||||||
chr2:183007673
|
C | A | 1 | a0001c0001t0033g0101 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.220-4348G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183007673 | ||||||
chr2:183007755
|
G | A | 5 | a0001c0003t0006g0057a0001c0003t0006g0058a0001c0003t0006g0170others(2): Show | 5 | HG01243.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-4430C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183007755 | ||||||
chr2:183007937
|
T | C | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-4612A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183007937 | ||||||
chr2:183007998
|
C | T | 2 | a0001c0004t0016g0001a0001c0004t0016g0010 | 3 | HG01099.hp1 HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.220-4673G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183007998 | ||||||
chr2:183008069
|
C | G | 11 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.220-4744G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183008069 | ||||||
chr2:183008355
|
C | G | 210 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(207): Show | 213 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(210): Show |
intron_variant | MODIFIER | c.220-5030G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183008355 | ||||||
chr2:183008393
|
C | T | 2 | a0001c0001t0079g0125a0001c0001t0084g0126 | 2 | NA18939.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.220-5068G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183008393 | ||||||
chr2:183008427
|
T | C | 1 | a0001c0002t0106g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.220-5102A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183008427 | ||||||
chr2:183008428
|
A | C | 86 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(83): Show | 88 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.220-5103T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183008428 | ||||||
chr2:183008540
|
CCTG | C | 82 | a0001c0001t0002g0059a0001c0001t0002g0071a0001c0001t0002g0081others(79): Show | 82 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.220-5218_220-5216d others(5): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183008540 | ||||||
chr2:183008630
|
G | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0050g0033 | 3 | NA18970.hp2 NA18978.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.220-5305C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183008630 | ||||||
chr2:183008630
|
G | T | 11 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.220-5305C>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183008630 | ||||||
chr2:183008911
|
C | A | 4 | a0001c0001t0001g0039a0001c0001t0019g0002a0001c0001t0019g0053others(1): Show | 5 | NA18944.hp2 NA18955.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-5586G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183008911 | ||||||
chr2:183009060
|
T | G | 212 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(209): Show | 215 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(212): Show |
intron_variant | MODIFIER | c.220-5735A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009060 | ||||||
chr2:183009148
|
C | T | 1 | a0001c0001t0025g0027 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.220-5823G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009148 | ||||||
chr2:183009372
|
G | A | 1 | a0002c0008t0024g0135 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.220-6047C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009372 | ||||||
chr2:183009421
|
G | GGGAA | 21 | a0001c0001t0002g0081a0001c0001t0002g0084a0001c0001t0007g0065others(18): Show | 21 | HG01081.hp1 HG01099.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.220-6100_220-6097d others(6): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009421 | ||||||
chr2:183009421
|
G | GGGAAGGA others(1): Show |
9 | a0001c0001t0007g0060a0001c0001t0007g0100a0001c0001t0008g0095others(6): Show | 9 | HG00609.hp1 HG02074.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.220-6104_220-6097d others(10): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009421 | ||||||
chr2:183009421
|
G | GGGAAGGA others(5): Show |
5 | a0001c0001t0002g0099a0001c0001t0002g0124a0001c0001t0010g0188others(2): Show | 5 | HG00438.hp1 HG00597.hp1 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.220-6108_220-6097d others(14): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009421 | ||||||
chr2:183009421
|
GGGAA | G | 26 | a0001c0001t0011g0023a0001c0001t0011g0024a0001c0001t0011g0025others(23): Show | 27 | HG01243.hp1 HG01255.hp2 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.220-6100_220-6097d others(6): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009421 | ||||||
chr2:183009421
|
GGGAAGGA others(5): Show |
G | 6 | a0001c0001t0021g0121a0001c0002t0043g0013a0001c0002t0060g0183others(3): Show | 6 | HG02615.hp2 HG02818.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.220-6108_220-6097d others(14): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009421 | ||||||
chr2:183009467
|
G | C | 1 | a0001c0002t0074g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.220-6142C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009467 | ||||||
chr2:183009468
|
A | T | 1 | a0001c0004t0062g0194 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.220-6143T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009468 | ||||||
chr2:183009469
|
AGGAAGGA others(17): Show |
A | 1 | a0001c0002t0110g0214 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.220-6168_220-6145d others(26): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009469 | ||||||
chr2:183009471
|
G | C | 8 | a0001c0002t0003g0198a0001c0002t0003g0202a0001c0002t0003g0203others(5): Show | 8 | HG00597.hp2 HG01255.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.220-6146C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009471 | ||||||
chr2:183009471
|
G | GAAGC | 8 | a0001c0002t0003g0199a0001c0003t0006g0168a0001c0003t0006g0182others(5): Show | 8 | HG02486.hp2 HG02922.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.220-6147_220-6146i others(6): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009471 | ||||||
chr2:183009475
|
G | C | 65 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(62): Show | 66 | HG00597.hp2 HG00621.hp2 HG01069.hp2 others(63): Show |
intron_variant | MODIFIER | c.220-6150C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009475 | ||||||
chr2:183009475
|
G | GAAGC | 12 | a0001c0001t0005g0031a0001c0001t0010g0094a0001c0001t0010g0132others(9): Show | 12 | HG01071.hp2 HG01261.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.220-6154_220-6151d others(6): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009475 | ||||||
chr2:183009475
|
G | GAAGCAAG others(1): Show |
9 | a0001c0002t0003g0192a0001c0002t0003g0206a0001c0002t0036g0208others(6): Show | 9 | HG02630.hp2 HG02698.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.220-6158_220-6151d others(10): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009475 | ||||||
chr2:183009475
|
G | GAAGGAAG others(1): Show |
26 | a0001c0001t0001g0028a0001c0001t0001g0032a0001c0001t0001g0050others(23): Show | 26 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.220-6151_220-6150i others(10): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009475 | ||||||
chr2:183009475
|
G | GAAGGAAG others(5): Show |
7 | a0001c0002t0003g0201a0001c0002t0106g0143a0001c0002t0107g0207others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.220-6151_220-6150i others(14): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009475 | ||||||
chr2:183009475
|
G | GAAGGAAG others(5): Show |
12 | a0001c0001t0002g0059a0001c0001t0002g0108a0001c0001t0008g0063others(9): Show | 12 | HG01261.hp1 HG02280.hp1 HG03098.hp1 others(9): Show |
intron_variant | MODIFIER | c.220-6151_220-6150i others(14): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009475 | ||||||
chr2:183009475
|
G | GAAGGAAG others(9): Show |
3 | a0001c0001t0014g0134a0001c0001t0080g0062a0002c0008t0024g0135 | 3 | HG01978.hp1 HG02523.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.220-6151_220-6150i others(18): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009475 | ||||||
chr2:183009475
|
G | GAAGGAAG others(9): Show |
2 | a0001c0001t0093g0064a0001c0003t0004g0164 | 2 | HG03225.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.220-6151_220-6150i others(18): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009475 | ||||||
chr2:183009475
|
G | GAAGGAAG others(13): Show |
1 | a0001c0003t0004g0166 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.220-6151_220-6150i others(22): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009475 | ||||||
chr2:183009475
|
G | GAAGGAAG others(13): Show |
1 | a0001c0002t0041g0012 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.220-6151_220-6150i others(22): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009475 | ||||||
chr2:183009475
|
G | GAAGGAAG others(9): Show |
2 | a0001c0004t0028g0056a0001c0004t0066g0055 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.220-6151_220-6150i others(18): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009475 | ||||||
chr2:183009475
|
G | GTAGCAAG others(1): Show |
5 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0004t0016g0001others(2): Show | 6 | HG01099.hp1 HG01109.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.220-6151_220-6150i others(10): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009475 | ||||||
chr2:183009479
|
C | G | 20 | a0001c0001t0002g0071a0001c0001t0002g0081a0001c0001t0002g0084others(17): Show | 20 | HG00438.hp1 HG01069.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.220-6154G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009479 | ||||||
chr2:183009481
|
A | AGCAAGCA others(5): Show |
17 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(14): Show | 18 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.220-6168_220-6157d others(14): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009481 | ||||||
chr2:183009481
|
A | G | 1 | a0001c0002t0074g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.220-6156T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009481 | ||||||
chr2:183009499
|
C | A | 11 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.220-6174G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009499 | ||||||
chr2:183009560
|
G | T | 1 | a0001c0002t0043g0013 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.220-6235C>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009560 | ||||||
chr2:183009636
|
G | A | 11 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.220-6311C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009636 | ||||||
chr2:183009674
|
G | T | 18 | a0001c0002t0003g0198a0001c0002t0003g0199a0001c0002t0003g0201others(15): Show | 18 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.220-6349C>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183009674 | ||||||
chr2:183010001
|
T | C | 21 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(18): Show | 21 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.220-6676A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183010001 | ||||||
chr2:183010426
|
C | T | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.220-7101G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183010426 | ||||||
chr2:183010736
|
C | A | 49 | a0001c0001t0002g0090a0001c0001t0002g0108a0001c0001t0002g0124others(46): Show | 49 | HG00597.hp1 HG00609.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.220-7411G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183010736 | ||||||
chr2:183010738
|
G | A | 18 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(15): Show | 19 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.220-7413C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183010738 | ||||||
chr2:183011190
|
A | G | 13 | a0001c0003t0006g0057a0001c0003t0006g0058a0001c0003t0006g0168others(10): Show | 13 | HG01243.hp2 HG02572.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.220-7865T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183011190 | ||||||
chr2:183011208
|
T | C | 3 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0062g0194 | 4 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-7883A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183011208 | ||||||
chr2:183011486
|
T | G | 85 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(82): Show | 87 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.220-8161A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183011486 | ||||||
chr2:183011612
|
G | A | 2 | a0001c0002t0043g0013a0001c0002t0065g0191 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.220-8287C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183011612 | ||||||
chr2:183011659
|
G | A | 85 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(82): Show | 87 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.220-8334C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183011659 | ||||||
chr2:183011729
|
G | A | 14 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(11): Show | 15 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.220-8404C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183011729 | ||||||
chr2:183011972
|
T | C | 3 | a0001c0001t0022g0110a0001c0001t0022g0111a0001c0001t0095g0112 | 3 | HG02647.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.220-8647A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183011972 | ||||||
chr2:183011995
|
T | C | 7 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0028g0054others(4): Show | 8 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.220-8670A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183011995 | ||||||
chr2:183012004
|
A | G | 11 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.220-8679T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183012004 | ||||||
chr2:183012016
|
A | T | 1 | a0001c0003t0026g0171 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.220-8691T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183012016 | ||||||
chr2:183012098
|
G | A | 1 | a0001c0001t0086g0072 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.220-8773C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183012098 | ||||||
chr2:183012200
|
T | C | 214 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(211): Show | 217 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(214): Show |
intron_variant | MODIFIER | c.220-8875A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183012200 | ||||||
chr2:183012225
|
T | C | 1 | a0001c0002t0104g0193 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.220-8900A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183012225 | ||||||
chr2:183012464
|
T | C | 2 | a0001c0002t0060g0183a0001c0009t0061g0184 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.220-9139A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183012464 | ||||||
chr2:183012570
|
CTCCTA | C | 4 | a0001c0003t0012g0167a0001c0003t0012g0174a0001c0003t0012g0177others(1): Show | 4 | HG00609.hp2 HG00621.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.220-9250_220-9246d others(7): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183012570 | ||||||
chr2:183012613
|
C | T | 11 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.220-9288G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183012613 | ||||||
chr2:183012621
|
C | CT | 16 | a0001c0001t0001g0028a0001c0001t0005g0018a0001c0001t0007g0117others(13): Show | 16 | HG01255.hp1 HG01255.hp2 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.220-9297dupA | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183012621 | ||||||
chr2:183012772
|
C | A | 1 | a0001c0002t0065g0191 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.220-9447G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183012772 | ||||||
chr2:183012779
|
A | AT | 45 | a0001c0001t0002g0090a0001c0001t0007g0117a0001c0001t0022g0119others(42): Show | 46 | HG00597.hp2 HG01109.hp2 HG01169.hp1 others(43): Show |
intron_variant | MODIFIER | c.220-9455dupA | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183012779 | ||||||
chr2:183012779
|
A | ATT | 11 | a0001c0002t0009g0145a0001c0002t0013g0146a0001c0002t0013g0147others(8): Show | 12 | HG01099.hp1 HG01358.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.220-9456_220-9455d others(4): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183012779 | ||||||
chr2:183012779
|
AT | A | 7 | a0001c0001t0007g0060a0001c0001t0021g0113a0001c0001t0092g0137others(4): Show | 7 | HG00609.hp1 HG02056.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.220-9455delA | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183012779 | ||||||
chr2:183012826
|
T | G | 2 | a0001c0002t0003g0192a0001c0002t0104g0193 | 2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.220-9501A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183012826 | ||||||
chr2:183012861
|
G | C | 1 | a0001c0001t0002g0084 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.220-9536C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183012861 | ||||||
chr2:183013365
|
A | C | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.220-10040T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183013365 | ||||||
chr2:183013741
|
T | C | 6 | a0001c0003t0012g0167a0001c0003t0012g0174a0001c0003t0012g0177others(3): Show | 6 | HG00609.hp2 HG00621.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.219+10065A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183013741 | ||||||
chr2:183013787
|
C | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0017 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.219+10019G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183013787 | ||||||
chr2:183013922
|
G | A | 1 | a0001c0011t0109g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.219+9884C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183013922 | ||||||
chr2:183014077
|
T | C | 2 | a0001c0001t0007g0065a0001c0001t0077g0130 | 2 | NA18983.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.219+9729A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183014077 | ||||||
chr2:183014917
|
C | T | 1 | a0001c0002t0003g0201 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.219+8889G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183014917 | ||||||
chr2:183015268
|
G | C | 4 | a0001c0002t0043g0013a0001c0002t0063g0190a0001c0002t0064g0189others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+8538C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183015268 | ||||||
chr2:183015503
|
A | C | 3 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0062g0194 | 4 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.219+8303T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183015503 | ||||||
chr2:183015772
|
T | C | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(38): Show | 42 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.219+8034A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183015772 | ||||||
chr2:183015837
|
GAAGAA | G | 5 | a0001c0002t0003g0206a0001c0002t0036g0197a0001c0002t0036g0208others(2): Show | 5 | HG01261.hp1 HG02145.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+7964_219+7968d others(7): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183015837 | ||||||
chr2:183015902
|
T | G | 20 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(17): Show | 21 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.219+7904A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183015902 | ||||||
chr2:183015988
|
T | C | 2 | a0001c0002t0037g0212a0001c0002t0037g0213 | 2 | HG01109.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.219+7818A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183015988 | ||||||
chr2:183016020
|
T | A | 1 | a0001c0002t0108g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.219+7786A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183016020 | ||||||
chr2:183016287
|
T | A | 1 | a0001c0004t0028g0054 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.219+7519A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183016287 | ||||||
chr2:183016682
|
C | T | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(38): Show | 42 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.219+7124G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183016682 | ||||||
chr2:183016743
|
A | G | 6 | a0001c0002t0003g0192a0001c0002t0043g0013a0001c0002t0063g0190others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.219+7063T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183016743 | ||||||
chr2:183016822
|
G | A | 3 | a0001c0003t0004g0164a0001c0003t0004g0165a0001c0003t0004g0166 | 3 | HG01884.hp2 HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.219+6984C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183016822 | ||||||
chr2:183016841
|
C | A | 208 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(205): Show | 211 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(208): Show |
intron_variant | MODIFIER | c.219+6965G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183016841 | ||||||
chr2:183016885
|
T | C | 2 | a0001c0004t0016g0001a0001c0004t0016g0010 | 3 | HG01099.hp1 HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.219+6921A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183016885 | ||||||
chr2:183016890
|
A | T | 3 | a0001c0005t0071g0155a0001c0005t0072g0157a0001c0005t0073g0156 | 3 | HG02647.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.219+6916T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183016890 | ||||||
chr2:183016943
|
T | G | 1 | a0001c0001t0082g0085 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.219+6863A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183016943 | ||||||
chr2:183017222
|
G | C | 1 | a0001c0002t0063g0190 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.219+6584C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183017222 | ||||||
chr2:183017256
|
C | T | 3 | a0001c0005t0071g0155a0001c0005t0072g0157a0001c0005t0073g0156 | 3 | HG02647.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.219+6550G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183017256 | ||||||
chr2:183017518
|
G | A | 1 | a0001c0002t0013g0146 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.219+6288C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183017518 | ||||||
chr2:183017837
|
A | C | 4 | a0001c0002t0003g0192a0001c0002t0063g0190a0001c0002t0064g0189others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+5969T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183017837 | ||||||
chr2:183017972
|
G | A | 1 | a0001c0001t0007g0114 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.219+5834C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183017972 | ||||||
chr2:183018675
|
C | A | 210 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(207): Show | 213 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(210): Show |
intron_variant | MODIFIER | c.219+5131G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183018675 | ||||||
chr2:183018959
|
T | A | 11 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.219+4847A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183018959 | ||||||
chr2:183018961
|
A | G | 20 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(17): Show | 20 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.219+4845T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183018961 | ||||||
chr2:183019095
|
A | G | 1 | a0001c0001t0096g0073 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.219+4711T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183019095 | ||||||
chr2:183019116
|
T | C | 14 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(11): Show | 15 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.219+4690A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183019116 | ||||||
chr2:183019139
|
T | C | 5 | a0001c0002t0009g0145a0001c0002t0013g0146a0001c0002t0013g0147others(2): Show | 5 | HG02622.hp2 HG02965.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+4667A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183019139 | ||||||
chr2:183019177
|
C | T | 85 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(82): Show | 87 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.219+4629G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183019177 | ||||||
chr2:183019615
|
T | TAA | 42 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(39): Show | 43 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.219+4189_219+4190d others(4): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183019615 | ||||||
chr2:183019779
|
A | C | 1 | a0001c0002t0060g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.219+4027T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183019779 | ||||||
chr2:183019857
|
C | T | 1 | a0001c0001t0080g0062 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.219+3949G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183019857 | ||||||
chr2:183020006
|
G | T | 85 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(82): Show | 87 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.219+3800C>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183020006 | ||||||
chr2:183020079
|
A | C | 9 | a0001c0002t0003g0192a0001c0002t0003g0199a0001c0002t0003g0201others(6): Show | 9 | HG01261.hp1 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.219+3727T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183020079 | ||||||
chr2:183020097
|
A | C | 1 | a0001c0002t0106g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.219+3709T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183020097 | ||||||
chr2:183020201
|
G | T | 1 | a0001c0001t0030g0087 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.219+3605C>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183020201 | ||||||
chr2:183020223
|
G | A | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.219+3583C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183020223 | ||||||
chr2:183020404
|
G | A | 3 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0062g0194 | 4 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.219+3402C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183020404 | ||||||
chr2:183020454
|
G | A | 3 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0062g0194 | 4 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.219+3352C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183020454 | ||||||
chr2:183020464
|
C | CA | 16 | a0001c0001t0002g0090a0001c0001t0008g0115a0001c0001t0011g0025others(13): Show | 17 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.219+3341dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183020464 | ||||||
chr2:183020464
|
C | CAA | 6 | a0001c0002t0009g0153a0001c0002t0068g0154a0001c0002t0103g0144others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.219+3340_219+3341d others(4): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183020464 | ||||||
chr2:183020476
|
AAAAAG | A | 17 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(14): Show | 17 | HG00597.hp2 HG01261.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.219+3325_219+3329d others(7): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183020476 | ||||||
chr2:183020481
|
G | A | 60 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(57): Show | 61 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(58): Show |
intron_variant | MODIFIER | c.219+3325C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183020481 | ||||||
chr2:183020482
|
A | AG | 3 | a0001c0003t0006g0182a0001c0003t0027g0176a0001c0003t0027g0185 | 3 | HG02145.hp2 NA18972.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.219+3323_219+3324i others(3): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183020482 | ||||||
chr2:183020482
|
A | G | 29 | a0001c0002t0060g0183a0001c0003t0004g0160a0001c0003t0004g0161others(26): Show | 29 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.219+3324T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183020482 | ||||||
chr2:183020485
|
A | G | 1 | a0001c0002t0013g0146 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.219+3321T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183020485 | ||||||
chr2:183020530
|
T | C | 2 | a0001c0004t0016g0001a0001c0004t0016g0010 | 3 | HG01099.hp1 HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.219+3276A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183020530 | ||||||
chr2:183020555
|
G | A | 1 | a0001c0002t0064g0189 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.219+3251C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183020555 | ||||||
chr2:183020626
|
G | A | 32 | a0001c0002t0060g0183a0001c0003t0004g0160a0001c0003t0004g0161others(29): Show | 32 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.219+3180C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183020626 | ||||||
chr2:183020819
|
A | G | 2 | a0001c0001t0079g0125a0001c0001t0084g0126 | 2 | NA18939.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.219+2987T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183020819 | ||||||
chr2:183020916
|
CA | C | 14 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(11): Show | 15 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.219+2889delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183020916 | ||||||
chr2:183021452
|
A | T | 3 | a0001c0001t0034g0116a0001c0002t0043g0013a0001c0002t0065g0191 | 3 | HG02818.hp2 HG03453.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.219+2354T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183021452 | ||||||
chr2:183021509
|
G | A | 19 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(16): Show | 19 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.219+2297C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183021509 | ||||||
chr2:183021543
|
C | A | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.219+2263G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183021543 | ||||||
chr2:183021643
|
C | G | 7 | a0001c0003t0004g0160a0001c0003t0004g0161a0001c0003t0004g0162others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.219+2163G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183021643 | ||||||
chr2:183021793
|
G | A | 1 | a0001c0002t0003g0199 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.219+2013C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183021793 | ||||||
chr2:183021799
|
CA | C | 2 | a0001c0003t0006g0168a0001c0003t0006g0169 | 2 | HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.219+2006delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183021799 | ||||||
chr2:183021944
|
T | C | 20 | a0001c0001t0002g0090a0001c0001t0002g0124a0001c0001t0005g0140others(17): Show | 20 | HG00597.hp1 HG01069.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.219+1862A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183021944 | ||||||
chr2:183022120
|
TG | T | 8 | a0001c0001t0010g0094a0001c0001t0011g0015a0001c0001t0011g0023others(5): Show | 8 | NA18942.hp1 NA18973.hp1 NA18975.hp2 others(5): Show |
intron_variant | MODIFIER | c.219+1685delC | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183022120 | ||||||
chr2:183022403
|
A | G | 1 | a0001c0001t0031g0093 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.219+1403T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183022403 | ||||||
chr2:183022845
|
T | C | 3 | a0001c0003t0015g0007a0001c0003t0015g0008a0001c0003t0015g0009 | 3 | HG01081.hp2 HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.219+961A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183022845 | ||||||
chr2:183023250
|
C | T | 210 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(207): Show | 213 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(210): Show |
intron_variant | MODIFIER | c.219+556G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183023250 | ||||||
chr2:183023266
|
T | C | 2 | a0001c0001t0079g0125a0001c0001t0084g0126 | 2 | NA18939.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.219+540A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183023266 | ||||||
chr2:183023543
|
C | G | 7 | a0001c0003t0004g0160a0001c0003t0004g0161a0001c0003t0004g0162others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.219+263G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183023543 | ||||||
chr2:183023654
|
G | C | 2 | a0001c0002t0003g0206a0001c0002t0107g0207 | 2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.219+152C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183023654 | ||||||
chr2:183023669
|
A | T | 1 | a0001c0003t0047g0179 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.219+137T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183023669 | ||||||
chr2:183023695
|
T | C | 7 | a0001c0003t0004g0160a0001c0003t0004g0161a0001c0003t0004g0162others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.219+111A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 2/30 | chr2 | 183023695 | ||||||
chr2:183024721
|
G | C | 1 | a0001c0002t0063g0190 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.109-805C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183024721 | ||||||
chr2:183024737
|
T | C | 4 | a0001c0002t0003g0192a0001c0002t0063g0190a0001c0002t0064g0189others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-821A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183024737 | ||||||
chr2:183024815
|
T | G | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.109-899A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183024815 | ||||||
chr2:183025045
|
T | C | 3 | a0001c0001t0025g0035a0001c0001t0051g0034a0001c0001t0053g0022 | 3 | NA18942.hp1 NA18949.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.109-1129A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183025045 | ||||||
chr2:183025062
|
AC | A | 2 | a0001c0002t0003g0192a0001c0002t0104g0193 | 2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.109-1147delG | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183025062 | ||||||
chr2:183025217
|
C | T | 3 | a0001c0001t0011g0023a0001c0001t0011g0024a0001c0001t0011g0025 | 3 | NA18973.hp1 NA18975.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.109-1301G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183025217 | ||||||
chr2:183025262
|
T | C | 1 | a0001c0001t0031g0127 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.109-1346A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183025262 | ||||||
chr2:183025268
|
A | C | 1 | a0001c0003t0006g0057 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.109-1352T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183025268 | ||||||
chr2:183025446
|
C | G | 1 | a0001c0001t0005g0140 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.109-1530G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183025446 | ||||||
chr2:183025558
|
T | C | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.109-1642A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183025558 | ||||||
chr2:183025638
|
T | C | 1 | a0001c0002t0108g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.109-1722A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183025638 | ||||||
chr2:183025750
|
T | C | 30 | a0001c0003t0004g0160a0001c0003t0004g0161a0001c0003t0004g0162others(27): Show | 30 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.109-1834A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183025750 | ||||||
chr2:183025932
|
T | A | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-2016A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183025932 | ||||||
chr2:183025950
|
A | T | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-2034T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183025950 | ||||||
chr2:183026397
|
A | C | 85 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(82): Show | 87 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.109-2481T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183026397 | ||||||
chr2:183026487
|
TA | T | 5 | a0001c0001t0001g0039a0001c0001t0002g0071a0001c0001t0014g0092others(2): Show | 5 | HG02976.hp2 NA18942.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.109-2572delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183026487 | ||||||
chr2:183026597
|
A | C | 8 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.109-2681T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183026597 | ||||||
chr2:183026735
|
G | T | 1 | a0001c0002t0003g0199 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.109-2819C>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183026735 | ||||||
chr2:183026787
|
G | A | 13 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(10): Show | 14 | HG02257.hp1 HG02559.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.109-2871C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183026787 | ||||||
chr2:183026875
|
T | C | 3 | a0001c0002t0003g0192a0001c0002t0064g0189a0001c0002t0104g0193 | 3 | HG02109.hp1 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.109-2959A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183026875 | ||||||
chr2:183026934
|
T | C | 1 | a0001c0002t0074g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.109-3018A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183026934 | ||||||
chr2:183026937
|
T | C | 23 | a0001c0003t0006g0057a0001c0003t0006g0058a0001c0003t0006g0168others(20): Show | 23 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.109-3021A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183026937 | ||||||
chr2:183027030
|
C | A | 3 | a0001c0005t0071g0155a0001c0005t0072g0157a0001c0005t0073g0156 | 3 | HG02647.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.109-3114G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183027030 | ||||||
chr2:183027043
|
C | T | 84 | a0001c0001t0002g0059a0001c0001t0002g0071a0001c0001t0002g0081others(81): Show | 84 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.109-3127G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183027043 | ||||||
chr2:183027045
|
TCTAAATA others(4): Show |
T | 8 | a0001c0001t0002g0090a0001c0001t0030g0087a0001c0001t0032g0088others(5): Show | 8 | HG01069.hp1 HG01081.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-3140_109-3130d others(13): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183027045 | ||||||
chr2:183027195
|
T | G | 1 | a0001c0001t0005g0036 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.109-3279A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183027195 | ||||||
chr2:183027241
|
A | T | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.109-3325T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183027241 | ||||||
chr2:183027270
|
A | T | 3 | a0001c0003t0015g0007a0001c0003t0015g0008a0001c0003t0015g0009 | 3 | HG01081.hp2 HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.109-3354T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183027270 | ||||||
chr2:183027378
|
C | T | 20 | a0001c0002t0003g0198a0001c0002t0003g0199a0001c0002t0003g0201others(17): Show | 20 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.109-3462G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183027378 | ||||||
chr2:183027501
|
G | A | 4 | a0001c0001t0010g0128a0001c0001t0010g0186a0001c0001t0077g0130others(1): Show | 4 | NA18964.hp2 NA18983.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-3585C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183027501 | ||||||
chr2:183027550
|
C | G | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-3634G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183027550 | ||||||
chr2:183027621
|
C | T | 1 | a0001c0001t0029g0138 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.109-3705G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183027621 | ||||||
chr2:183027691
|
C | A | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.109-3775G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183027691 | ||||||
chr2:183027704
|
A | T | 23 | a0001c0003t0006g0057a0001c0003t0006g0058a0001c0003t0006g0168others(20): Show | 23 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.109-3788T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183027704 | ||||||
chr2:183028000
|
C | A | 3 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0062g0194 | 4 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.109-4084G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183028000 | ||||||
chr2:183028028
|
A | T | 1 | a0001c0001t0005g0140 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.109-4112T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183028028 | ||||||
chr2:183028057
|
G | A | 1 | a0001c0003t0015g0009 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.109-4141C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183028057 | ||||||
chr2:183028071
|
C | T | 1 | a0001c0001t0024g0086 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.109-4155G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183028071 | ||||||
chr2:183028128
|
A | G | 30 | a0001c0003t0004g0160a0001c0003t0004g0161a0001c0003t0004g0162others(27): Show | 30 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.109-4212T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183028128 | ||||||
chr2:183028341
|
T | C | 21 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(18): Show | 21 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.109-4425A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183028341 | ||||||
chr2:183028387
|
T | C | 74 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(71): Show | 75 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.109-4471A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183028387 | ||||||
chr2:183028557
|
T | C | 55 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(52): Show | 55 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.109-4641A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183028557 | ||||||
chr2:183028676
|
A | G | 15 | a0001c0001t0002g0059a0001c0001t0002g0071a0001c0001t0002g0081others(12): Show | 15 | HG00438.hp2 HG02055.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.109-4760T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183028676 | ||||||
chr2:183028769
|
T | C | 6 | a0001c0003t0012g0167a0001c0003t0012g0174a0001c0003t0012g0177others(3): Show | 6 | HG00609.hp2 HG00621.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.109-4853A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183028769 | ||||||
chr2:183028893
|
C | T | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-4977G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183028893 | ||||||
chr2:183028929
|
C | T | 1 | a0001c0003t0012g0167 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.109-5013G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183028929 | ||||||
chr2:183028957
|
C | CA | 193 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(190): Show | 195 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(192): Show |
intron_variant | MODIFIER | c.109-5042dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183028957 | ||||||
chr2:183028957
|
C | CAA | 16 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0010g0132others(13): Show | 17 | HG00621.hp2 HG01071.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.109-5043_109-5042d others(4): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183028957 | ||||||
chr2:183029007
|
C | T | 1 | a0001c0002t0065g0191 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.109-5091G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183029007 | ||||||
chr2:183029049
|
G | A | 17 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(14): Show | 18 | HG02257.hp1 HG02559.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.109-5133C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183029049 | ||||||
chr2:183029127
|
A | C | 1 | a0001c0003t0012g0174 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.109-5211T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183029127 | ||||||
chr2:183029242
|
A | C | 34 | a0001c0002t0043g0013a0001c0002t0063g0190a0001c0002t0064g0189others(31): Show | 34 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.109-5326T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183029242 | ||||||
chr2:183029247
|
A | C | 20 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(17): Show | 20 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.109-5331T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183029247 | ||||||
chr2:183029327
|
A | C | 1 | a0001c0001t0011g0015 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.109-5411T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183029327 | ||||||
chr2:183029438
|
T | C | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-5522A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183029438 | ||||||
chr2:183029658
|
A | C | 2 | a0001c0004t0028g0056a0001c0004t0066g0055 | 2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.109-5742T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183029658 | ||||||
chr2:183029724
|
A | G | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-5808T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183029724 | ||||||
chr2:183029821
|
G | GA | 28 | a0001c0001t0078g0136a0001c0002t0036g0208a0001c0002t0060g0183others(25): Show | 28 | HG01081.hp2 HG01243.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.109-5906dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183029821 | ||||||
chr2:183029821
|
G | GAA | 6 | a0001c0003t0012g0174a0001c0003t0012g0175a0001c0003t0012g0177others(3): Show | 6 | HG00609.hp2 HG00621.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.109-5907_109-5906d others(4): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183029821 | ||||||
chr2:183029821
|
GA | G | 8 | a0001c0001t0001g0038a0001c0002t0003g0198a0001c0002t0009g0145others(5): Show | 8 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-5906delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183029821 | ||||||
chr2:183029822
|
A | G | 1 | a0001c0004t0028g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.109-5906T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183029822 | ||||||
chr2:183029839
|
A | G | 1 | a0001c0002t0108g0014 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.109-5923T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183029839 | ||||||
chr2:183029851
|
GA | G | 7 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0028g0054others(4): Show | 8 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.109-5936delT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183029851 | ||||||
chr2:183029982
|
G | A | 1 | a0001c0001t0092g0137 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.109-6066C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183029982 | ||||||
chr2:183030332
|
TTTTA | T | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.109-6420_109-6417d others(6): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183030332 | ||||||
chr2:183031001
|
T | C | 1 | a0001c0001t0086g0072 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.108+6991A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183031001 | ||||||
chr2:183031191
|
C | T | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+6801G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183031191 | ||||||
chr2:183031203
|
C | T | 4 | a0001c0002t0003g0192a0001c0002t0063g0190a0001c0002t0064g0189others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+6789G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183031203 | ||||||
chr2:183031211
|
A | T | 1 | a0001c0002t0036g0197 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.108+6781T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183031211 | ||||||
chr2:183031222
|
C | CA | 6 | a0001c0002t0003g0192a0001c0002t0043g0013a0001c0002t0063g0190others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+6769dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183031222 | ||||||
chr2:183031440
|
T | C | 32 | a0001c0002t0060g0183a0001c0003t0004g0160a0001c0003t0004g0161others(29): Show | 32 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.108+6552A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183031440 | ||||||
chr2:183031518
|
A | G | 1 | a0001c0003t0015g0009 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.108+6474T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183031518 | ||||||
chr2:183031631
|
A | C | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.108+6361T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183031631 | ||||||
chr2:183031668
|
G | A | 1 | a0001c0003t0047g0179 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.108+6324C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183031668 | ||||||
chr2:183031987
|
A | C | 1 | a0001c0001t0086g0072 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.108+6005T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183031987 | ||||||
chr2:183032283
|
T | C | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.108+5709A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183032283 | ||||||
chr2:183032410
|
A | C | 1 | a0001c0002t0074g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.108+5582T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183032410 | ||||||
chr2:183032410
|
A | G | 4 | a0001c0002t0003g0192a0001c0002t0063g0190a0001c0002t0064g0189others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+5582T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183032410 | ||||||
chr2:183032501
|
C | T | 1 | a0001c0004t0066g0055 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.108+5491G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183032501 | ||||||
chr2:183032503
|
C | T | 18 | a0001c0002t0003g0198a0001c0002t0003g0199a0001c0002t0003g0201others(15): Show | 18 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.108+5489G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183032503 | ||||||
chr2:183032637
|
T | C | 4 | a0001c0002t0003g0192a0001c0002t0063g0190a0001c0002t0064g0189others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+5355A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183032637 | ||||||
chr2:183032640
|
C | A | 84 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(81): Show | 86 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.108+5352G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183032640 | ||||||
chr2:183032755
|
A | G | 14 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(11): Show | 15 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.108+5237T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183032755 | ||||||
chr2:183032803
|
T | G | 11 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.108+5189A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183032803 | ||||||
chr2:183032884
|
C | A | 1 | a0001c0001t0057g0037 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.108+5108G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183032884 | ||||||
chr2:183032884
|
C | CA | 3 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0062g0194 | 4 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.108+5107dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183032884 | ||||||
chr2:183032965
|
G | A | 1 | a0001c0001t0093g0064 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.108+5027C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183032965 | ||||||
chr2:183033076
|
A | C | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.108+4916T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183033076 | ||||||
chr2:183033150
|
T | G | 11 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(8): Show | 12 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.108+4842A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183033150 | ||||||
chr2:183033509
|
C | T | 13 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(10): Show | 14 | HG02257.hp1 HG02559.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.108+4483G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183033509 | ||||||
chr2:183033964
|
G | A | 1 | a0001c0001t0029g0138 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.108+4028C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183033964 | ||||||
chr2:183034004
|
T | C | 17 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0050others(14): Show | 18 | HG00621.hp2 HG02056.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.108+3988A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183034004 | ||||||
chr2:183034079
|
C | CTAAGTGG others(24): Show |
1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+3882_108+3912d others(33): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183034079 | ||||||
chr2:183034170
|
T | C | 7 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0028g0054others(4): Show | 8 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.108+3822A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183034170 | ||||||
chr2:183034216
|
C | T | 13 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(10): Show | 14 | HG02257.hp1 HG02559.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.108+3776G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183034216 | ||||||
chr2:183034250
|
T | C | 1 | a0001c0011t0109g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.108+3742A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183034250 | ||||||
chr2:183034279
|
T | C | 17 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(14): Show | 18 | HG02257.hp1 HG02559.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.108+3713A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183034279 | ||||||
chr2:183034382
|
GTT | G | 81 | a0001c0001t0002g0059a0001c0001t0002g0081a0001c0001t0002g0082others(78): Show | 81 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.108+3608_108+3609d others(4): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183034382 | ||||||
chr2:183034633
|
G | C | 1 | a0001c0001t0014g0139 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.108+3359C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183034633 | ||||||
chr2:183034841
|
G | C | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.108+3151C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183034841 | ||||||
chr2:183035273
|
C | T | 2 | a0001c0002t0063g0190a0001c0002t0064g0189 | 2 | HG02109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.108+2719G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183035273 | ||||||
chr2:183035283
|
T | TA | 17 | a0001c0002t0009g0003a0001c0002t0009g0145a0001c0002t0009g0151others(14): Show | 18 | HG02257.hp1 HG02559.hp2 HG02622.hp2 others(15): Show |
intron_variant | MODIFIER | c.108+2708dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183035283 | ||||||
chr2:183035312
|
T | C | 21 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(18): Show | 21 | HG00597.hp2 HG01261.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.108+2680A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183035312 | ||||||
chr2:183035546
|
G | A | 41 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(38): Show | 42 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.108+2446C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183035546 | ||||||
chr2:183035788
|
G | C | 1 | a0001c0004t0038g0004 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.108+2204C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183035788 | ||||||
chr2:183035862
|
CTAACTGA others(10): Show |
C | 1 | a0001c0002t0074g0159 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.108+2113_108+2129d others(19): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183035862 | ||||||
chr2:183036024
|
A | C | 32 | a0001c0002t0060g0183a0001c0003t0004g0160a0001c0003t0004g0161others(29): Show | 32 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.108+1968T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036024 | ||||||
chr2:183036061
|
T | C | 2 | a0001c0003t0004g0165a0001c0003t0004g0166 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.108+1931A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036061 | ||||||
chr2:183036069
|
A | G | 3 | a0001c0001t0076g0066a0001c0001t0091g0068a0001c0001t0094g0067 | 3 | HG01069.hp1 HG01081.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.108+1923T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036069 | ||||||
chr2:183036176
|
T | A | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1816A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036176 | ||||||
chr2:183036184
|
C | T | 7 | a0001c0003t0004g0160a0001c0003t0004g0161a0001c0003t0004g0162others(4): Show | 7 | HG01884.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.108+1808G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036184 | ||||||
chr2:183036202
|
CTTATTTA others(11): Show |
C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1772_108+1789d others(20): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036202 | ||||||
chr2:183036224
|
T | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1768A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036224 | ||||||
chr2:183036228
|
G | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1764C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036228 | ||||||
chr2:183036229
|
T | A | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1763A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036229 | ||||||
chr2:183036230
|
T | C | 2 | a0001c0001t0010g0186a0001c0002t0065g0191 | 2 | HG02818.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.108+1762A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036230 | ||||||
chr2:183036231
|
T | A | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1761A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036231 | ||||||
chr2:183036232
|
G | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1760C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036232 | ||||||
chr2:183036233
|
A | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1759T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036233 | ||||||
chr2:183036234
|
T | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1758A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036234 | ||||||
chr2:183036235
|
T | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1757A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036235 | ||||||
chr2:183036236
|
G | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1756C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036236 | ||||||
chr2:183036238
|
A | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1754T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036238 | ||||||
chr2:183036239
|
T | A | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1753A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036239 | ||||||
chr2:183036240
|
T | A | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1752A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036240 | ||||||
chr2:183036243
|
T | A | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1749A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036243 | ||||||
chr2:183036244
|
C | A | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1748G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036244 | ||||||
chr2:183036246
|
T | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1746A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036246 | ||||||
chr2:183036247
|
A | G | 1 | a0001c0001t0007g0065 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.108+1745T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036247 | ||||||
chr2:183036249
|
A | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1743T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036249 | ||||||
chr2:183036250
|
A | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1742T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036250 | ||||||
chr2:183036251
|
A | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1741T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036251 | ||||||
chr2:183036254
|
T | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1738A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036254 | ||||||
chr2:183036255
|
G | T | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1737C>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036255 | ||||||
chr2:183036256
|
T | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1736A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036256 | ||||||
chr2:183036311
|
T | C | 2 | a0001c0001t0007g0060a0001c0001t0097g0061 | 2 | HG00609.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.108+1681A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036311 | ||||||
chr2:183036371
|
A | T | 3 | a0001c0001t0008g0063a0001c0001t0080g0062a0001c0001t0093g0064 | 3 | HG02523.hp1 NA18612.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.108+1621T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036371 | ||||||
chr2:183036483
|
T | G | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1509A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036483 | ||||||
chr2:183036596
|
T | A | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1396A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036596 | ||||||
chr2:183036601
|
C | A | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1391G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036601 | ||||||
chr2:183036603
|
T | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1389A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036603 | ||||||
chr2:183036608
|
G | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1384C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036608 | ||||||
chr2:183036610
|
T | G | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1382A>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036610 | ||||||
chr2:183036625
|
G | A | 1 | a0001c0001t0088g0141 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.108+1367C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036625 | ||||||
chr2:183036653
|
C | G | 2 | a0001c0001t0007g0060a0001c0001t0097g0061 | 2 | HG00609.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.108+1339G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036653 | ||||||
chr2:183036665
|
T | A | 2 | a0001c0002t0035g0209a0001c0002t0035g0210 | 2 | HG02486.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.108+1327A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036665 | ||||||
chr2:183036686
|
T | A | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1306A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036686 | ||||||
chr2:183036687
|
G | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1305C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036687 | ||||||
chr2:183036689
|
G | A | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1303C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036689 | ||||||
chr2:183036691
|
A | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1301T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036691 | ||||||
chr2:183036694
|
C | T | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1298G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036694 | ||||||
chr2:183036710
|
C | G | 3 | a0001c0004t0016g0001a0001c0004t0016g0010a0001c0004t0062g0194 | 4 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.108+1282G>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036710 | ||||||
chr2:183036733
|
A | T | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1259T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036733 | ||||||
chr2:183036734
|
G | A | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1258C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036734 | ||||||
chr2:183036735
|
G | A | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1257C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036735 | ||||||
chr2:183036744
|
T | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1248A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036744 | ||||||
chr2:183036748
|
A | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1244T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036748 | ||||||
chr2:183036749
|
T | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1243A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036749 | ||||||
chr2:183036750
|
T | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1242A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036750 | ||||||
chr2:183036751
|
A | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1241T>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036751 | ||||||
chr2:183036752
|
G | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1240C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036752 | ||||||
chr2:183036755
|
T | A | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1237A>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036755 | ||||||
chr2:183036767
|
T | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1225A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036767 | ||||||
chr2:183036815
|
C | CA | 24 | a0001c0002t0003g0192a0001c0002t0009g0003a0001c0002t0009g0145others(21): Show | 25 | HG02257.hp1 HG02451.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.108+1176dupT | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036815 | ||||||
chr2:183036815
|
C | CAA | 23 | a0001c0003t0004g0160a0001c0003t0004g0161a0001c0003t0004g0162others(20): Show | 23 | HG00609.hp2 HG00621.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.108+1175_108+1176d others(4): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036815 | ||||||
chr2:183036815
|
C | CAAA | 6 | a0001c0002t0060g0183a0001c0003t0006g0182a0001c0003t0020g0181others(3): Show | 6 | HG02145.hp2 NA18969.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+1174_108+1176d others(5): Show |
NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036815 | ||||||
chr2:183036819
|
G | A | 84 | a0001c0002t0003g0192a0001c0002t0003g0198a0001c0002t0003g0199others(81): Show | 86 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.108+1173C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036819 | ||||||
chr2:183036820
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.108+1172T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036820 | ||||||
chr2:183036833
|
C | A | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1159G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036833 | ||||||
chr2:183036835
|
T | C | 1 | a0001c0001t0010g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.108+1157A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036835 | ||||||
chr2:183036949
|
C | T | 2 | a0001c0003t0006g0057a0001c0003t0006g0058 | 2 | HG03654.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.108+1043G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183036949 | ||||||
chr2:183037054
|
T | C | 1 | a0001c0002t0035g0210 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.108+938A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183037054 | ||||||
chr2:183037198
|
A | G | 1 | a0001c0011t0109g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.108+794T>C | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183037198 | ||||||
chr2:183037355
|
G | C | 1 | a0001c0001t0029g0187 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.108+637C>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183037355 | ||||||
chr2:183037456
|
T | C | 1 | a0001c0001t0010g0188 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.108+536A>G | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183037456 | ||||||
chr2:183037486
|
AG | A | 6 | a0001c0002t0003g0192a0001c0002t0043g0013a0001c0002t0063g0190others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+505delC | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183037486 | ||||||
chr2:183037599
|
A | T | 3 | a0001c0004t0028g0054a0001c0004t0028g0056a0001c0004t0066g0055 | 3 | HG02109.hp2 HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.108+393T>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183037599 | ||||||
chr2:183037645
|
C | T | 42 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0020others(39): Show | 43 | HG00621.hp2 HG01069.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.108+347G>A | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183037645 | ||||||
chr2:183037675
|
C | A | 8 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(5): Show | 9 | HG01099.hp1 HG01109.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.108+317G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183037675 | ||||||
chr2:183037840
|
C | A | 1 | a0001c0001t0018g0195 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.108+152G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183037840 | ||||||
chr2:183037923
|
G | A | 16 | a0001c0001t0048g0196a0001c0002t0003g0198a0001c0002t0003g0199others(13): Show | 16 | HG00597.hp2 HG01261.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.108+69C>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183037923 | ||||||
chr2:183037928
|
C | A | 4 | a0001c0002t0037g0212a0001c0002t0037g0213a0001c0002t0041g0012others(1): Show | 4 | HG01109.hp1 HG01169.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+64G>T | NCKAP1 | ENSG00000061676.16 | transcript | ENST00000361354.9 | protein_coding | 1/30 | chr2 | 183037928 |