Item | Value |
---|---|
geneid | 4892 |
ensemblid | ENSG00000197893.14 |
hgncid | 7988 |
symbol | NRAP |
name | nebulin related anchoring protein |
refseq_nuc | NM_198060.4 |
refseq_prot | NP_932326.2 |
ensembl_nuc | ENST00000359988.4 |
ensembl_prot | ENSP00000353078.3 |
mane_status | MANE Select |
chr | chr10 |
start | 113588714 |
end | 113664041 |
strand | - |
ver | v1.2 |
region | chr10:113588714-113664041 |
region5000 | chr10:113583714-113669041 |
regionname0 | NRAP_chr10_113588714_113664041 |
regionname5000 | NRAP_chr10_113583714_113669041 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1730 | 56 | 4 | 11 | 34 | 4 | 3 | 27 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0002 | 0/0 | 1730 | 28 | 3 | 1 | 18 | 0 | 6 | 13 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0003 | 0/0 | 1730 | 24 | 8 | 0 | 10 | 1 | 5 | 9 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0004 | 0/0 | 1730 | 20 | 0 | 4 | 13 | 1 | 2 | 11 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0005 | 0/0 | 1730 | 20 | 4 | 2 | 10 | 0 | 4 | 5 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0006 | 0/0 | 1730 | 14 | 5 | 4 | 4 | 1 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0007 | 0/0 | 1730 | 14 | 1 | 8 | 5 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0008 | 0/0 | 1730 | 14 | 0 | 4 | 7 | 2 | 1 | 6 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0009 | 1/0 | 1730 | 13 | 5 | 5 | 2 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0010 | 0/0 | 1730 | 12 | 1 | 9 | 1 | 0 | 1 | 1 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0011 | 0/0 | 1730 | 11 | 7 | 0 | 3 | 0 | 1 | 1 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0012 | 0/0 | 1730 | 10 | 0 | 3 | 5 | 0 | 2 | 5 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0013 | 0/0 | 1730 | 8 | 0 | 0 | 7 | 1 | 0 | 7 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0014 | 0/0 | 1730 | 8 | 0 | 0 | 8 | 0 | 0 | 3 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0015 | 0/0 | 1730 | 8 | 3 | 2 | 3 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0016 | 0/1 | 1730 | 8 | 2 | 2 | 0 | 0 | 3 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0017 | 0/0 | 1730 | 7 | 0 | 5 | 0 | 1 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0018 | 0/0 | 1730 | 7 | 3 | 0 | 3 | 0 | 1 | 2 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0019 | 0/0 | 1730 | 6 | 1 | 4 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0020 | 0/0 | 1730 | 6 | 3 | 0 | 0 | 0 | 3 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0021 | 0/0 | 1730 | 5 | 0 | 0 | 4 | 1 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0022 | 0/0 | 155 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(150): Show |
chr10 | 113583714 | 113669041 |
a0023 | 0/0 | 1730 | 4 | 0 | 1 | 2 | 0 | 1 | 2 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0024 | 0/0 | 1730 | 4 | 0 | 0 | 4 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0025 | 0/0 | 1730 | 3 | 0 | 0 | 2 | 1 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0026 | 0/0 | 1730 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0027 | 0/0 | 1730 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0028 | 0/0 | 1730 | 3 | 2 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0029 | 0/0 | 1730 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0030 | 0/0 | 1730 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0031 | 0/0 | 1730 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0032 | 0/0 | 1730 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0033 | 0/0 | 1730 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0034 | 0/0 | 1730 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0035 | 0/0 | 1730 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0036 | 0/0 | 1730 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0037 | 0/0 | 1730 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0038 | 0/0 | 1730 | 2 | 0 | 0 | 1 | 1 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0039 | 0/0 | 1730 | 2 | 0 | 0 | 1 | 1 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0040 | 0/0 | 1730 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0041 | 0/0 | 1730 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0042 | 0/0 | 1730 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0043 | 0/0 | 1730 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0044 | 0/0 | 1730 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0045 | 0/0 | 1730 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0046 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0047 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0048 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0049 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0050 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0051 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0052 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0053 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0054 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0055 | 0/0 | 1730 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0056 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0057 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0058 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0059 | 0/0 | 1730 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0060 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0061 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0062 | 0/0 | 1730 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0063 | 0/0 | 1730 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0064 | 0/0 | 1730 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0065 | 0/0 | 1730 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0066 | 0/0 | 1730 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0067 | 0/0 | 1730 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0068 | 0/0 | 1730 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0069 | 0/0 | 1730 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0070 | 0/0 | 1730 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0071 | 0/0 | 1730 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0072 | 0/0 | 1730 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0073 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0074 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0075 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0076 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0077 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0078 | 0/0 | 1730 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0079 | 0/0 | 1730 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
a0080 | 0/0 | 1730 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | MNVQP others(1725): Show |
chr10 | 113583714 | 113669041 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 5190 | 53 | 3 | 11 | 32 | 4 | 3 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0001c0099 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0001c0100 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0001c0102 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0002c0002 | 0/0 | 5190 | 26 | 3 | 1 | 18 | 0 | 4 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0002c0037 | 0/0 | 5190 | 2 | 0 | 0 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0003c0003 | 0/0 | 5190 | 20 | 8 | 0 | 7 | 0 | 5 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0003c0023 | 0/0 | 5190 | 4 | 0 | 0 | 3 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0004c0004 | 0/0 | 5190 | 19 | 0 | 4 | 12 | 1 | 2 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0004c0057 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0005c0005 | 0/0 | 5190 | 14 | 3 | 1 | 6 | 0 | 4 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0005c0021 | 0/0 | 5190 | 5 | 0 | 1 | 4 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0005c0075 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0006c0010 | 0/0 | 5190 | 11 | 4 | 3 | 3 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0006c0104 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0006c0105 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0006c0108 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0007c0006 | 0/0 | 5190 | 13 | 1 | 8 | 4 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0007c0056 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0008c0007 | 0/0 | 5190 | 13 | 0 | 3 | 7 | 2 | 1 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0008c0078 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0009c0009 | 1/0 | 5190 | 12 | 5 | 5 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0009c0079 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0010c0008 | 0/0 | 5190 | 12 | 1 | 9 | 1 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0011c0016 | 0/0 | 5190 | 6 | 4 | 0 | 1 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0011c0025 | 0/0 | 5190 | 3 | 1 | 0 | 2 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0011c0039 | 0/0 | 5190 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0012c0011 | 0/0 | 5190 | 10 | 0 | 3 | 5 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0013c0019 | 0/0 | 5190 | 6 | 0 | 0 | 6 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0013c0041 | 0/0 | 5190 | 2 | 0 | 0 | 1 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0014c0012 | 0/0 | 5190 | 8 | 0 | 0 | 8 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0015c0013 | 0/0 | 5190 | 7 | 2 | 2 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0015c0077 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0016c0020 | 0/0 | 5190 | 5 | 1 | 2 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0016c0052 | 0/0 | 5190 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0016c0054 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0016c0084 | 0/1 | 5190 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0017c0014 | 0/0 | 5190 | 7 | 0 | 5 | 0 | 1 | 1 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0018c0015 | 0/0 | 5190 | 6 | 3 | 0 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0018c0076 | 0/0 | 5190 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0019c0017 | 0/0 | 5190 | 6 | 1 | 4 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0020c0018 | 0/0 | 5190 | 6 | 3 | 0 | 0 | 0 | 3 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0021c0022 | 0/0 | 5190 | 4 | 0 | 0 | 4 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0021c0069 | 0/0 | 5190 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0022c0071 | 0/0 | 5173 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5168): Show |
chr10 | 113583714 | 113669041 | ||
a0022c0072 | 0/0 | 5173 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5168): Show |
chr10 | 113583714 | 113669041 | ||
a0022c0073 | 0/0 | 5173 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5168): Show |
chr10 | 113583714 | 113669041 | ||
a0022c0114 | 0/0 | 5173 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5168): Show |
chr10 | 113583714 | 113669041 | ||
a0022c0115 | 0/0 | 5173 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5168): Show |
chr10 | 113583714 | 113669041 | ||
a0023c0030 | 0/0 | 5190 | 3 | 0 | 0 | 2 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0023c0091 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0024c0024 | 0/0 | 5190 | 4 | 0 | 0 | 4 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0025c0027 | 0/0 | 5190 | 3 | 0 | 0 | 2 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0026c0029 | 0/0 | 5190 | 3 | 3 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0027c0034 | 0/0 | 5190 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0027c0063 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0028c0044 | 0/0 | 5190 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0028c0066 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0029c0028 | 0/0 | 5190 | 3 | 3 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0030c0033 | 0/0 | 5190 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0030c0048 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0031c0032 | 0/0 | 5190 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0031c0061 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0032c0026 | 0/0 | 5190 | 3 | 0 | 0 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0033c0031 | 0/0 | 5190 | 3 | 0 | 0 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0034c0035 | 0/0 | 5190 | 2 | 0 | 1 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0035c0086 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0035c0088 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0036c0045 | 0/0 | 5190 | 2 | 0 | 0 | 2 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0037c0036 | 0/0 | 5190 | 2 | 1 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0038c0093 | 0/0 | 5190 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0038c0094 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0039c0042 | 0/0 | 5190 | 2 | 0 | 0 | 1 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0040c0038 | 0/0 | 5190 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0041c0068 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0041c0106 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0042c0047 | 0/0 | 5190 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0043c0040 | 0/0 | 5190 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0044c0046 | 0/0 | 5190 | 2 | 0 | 0 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0045c0043 | 0/0 | 5190 | 2 | 0 | 0 | 2 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0046c0107 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0047c0110 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0048c0101 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0049c0083 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0050c0050 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0051c0111 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0052c0095 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0053c0049 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0054c0096 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0055c0089 | 0/0 | 5190 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0056c0058 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0057c0097 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0058c0053 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0059c0060 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0060c0112 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0061c0070 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0062c0055 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0063c0113 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0064c0059 | 0/0 | 5190 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0065c0087 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0066c0074 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0067c0064 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0068c0090 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0069c0062 | 0/0 | 5190 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0070c0081 | 0/0 | 5190 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0071c0103 | 0/0 | 5190 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0072c0080 | 0/0 | 5190 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0073c0092 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0074c0098 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0075c0082 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0076c0067 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0077c0109 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0078c0065 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0079c0051 | 0/0 | 5190 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 | ||
a0080c0085 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | ATGAA others(5185): Show |
chr10 | 113583714 | 113669041 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5613 | 52 | 3 | 10 | 32 | 4 | 3 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0001c0001t0013 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0001c0099t0001 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0001c0100t0001 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0001c0102t0001 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0002c0002t0004 | 0/0 | 5612 | 26 | 3 | 1 | 18 | 0 | 4 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0002c0037t0007 | 0/0 | 5612 | 2 | 0 | 0 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0003c0003t0003 | 0/0 | 5613 | 20 | 8 | 0 | 7 | 0 | 5 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0003c0023t0003 | 0/0 | 5613 | 4 | 0 | 0 | 3 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0004c0004t0005 | 0/0 | 5613 | 19 | 0 | 4 | 12 | 1 | 2 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0004c0057t0005 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0005c0005t0001 | 0/0 | 5613 | 13 | 3 | 1 | 6 | 0 | 3 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0005c0005t0011 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0005c0021t0001 | 0/0 | 5613 | 4 | 0 | 0 | 4 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0005c0021t0003 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0005c0075t0001 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0006c0010t0003 | 0/0 | 5613 | 10 | 3 | 3 | 3 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0006c0010t0014 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0006c0104t0003 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0006c0105t0003 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0006c0108t0003 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0007c0006t0006 | 0/0 | 5612 | 13 | 1 | 8 | 4 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0007c0056t0006 | 0/0 | 5612 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0008c0007t0002 | 0/0 | 5612 | 12 | 0 | 2 | 7 | 2 | 1 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0008c0007t0009 | 0/0 | 5612 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0008c0078t0002 | 0/0 | 5612 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0009c0009t0001 | 1/0 | 5613 | 12 | 5 | 5 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0009c0079t0001 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0010c0008t0002 | 0/0 | 5612 | 11 | 1 | 8 | 1 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0010c0008t0010 | 0/0 | 5612 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0011c0016t0004 | 0/0 | 5612 | 6 | 4 | 0 | 1 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0011c0025t0002 | 0/0 | 5612 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0011c0025t0006 | 0/0 | 5612 | 2 | 0 | 0 | 2 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0011c0039t0004 | 0/0 | 5612 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0012c0011t0003 | 0/0 | 5613 | 10 | 0 | 3 | 5 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0013c0019t0002 | 0/0 | 5612 | 6 | 0 | 0 | 6 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0013c0041t0002 | 0/0 | 5612 | 2 | 0 | 0 | 1 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0014c0012t0004 | 0/0 | 5612 | 8 | 0 | 0 | 8 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0015c0013t0002 | 0/0 | 5612 | 7 | 2 | 2 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0015c0077t0002 | 0/0 | 5612 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0016c0020t0005 | 0/0 | 5613 | 5 | 1 | 2 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0016c0052t0005 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0016c0054t0005 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0016c0084t0003 | 0/1 | 5613 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0017c0014t0001 | 0/0 | 5613 | 7 | 0 | 5 | 0 | 1 | 1 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0018c0015t0001 | 0/0 | 5613 | 6 | 3 | 0 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0018c0076t0001 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0019c0017t0002 | 0/0 | 5612 | 6 | 1 | 4 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0020c0018t0001 | 0/0 | 5613 | 6 | 3 | 0 | 0 | 0 | 3 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0021c0022t0001 | 0/0 | 5613 | 3 | 0 | 0 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0021c0022t0012 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0021c0069t0001 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0022c0071t0002 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5590): Show |
chr10 | 113583714 | 113669041 |
a0022c0072t0001 | 0/0 | 5596 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5591): Show |
chr10 | 113583714 | 113669041 |
a0022c0073t0001 | 0/0 | 5596 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5591): Show |
chr10 | 113583714 | 113669041 |
a0022c0114t0004 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5590): Show |
chr10 | 113583714 | 113669041 |
a0022c0115t0004 | 0/0 | 5595 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5590): Show |
chr10 | 113583714 | 113669041 |
a0023c0030t0001 | 0/0 | 5613 | 3 | 0 | 0 | 2 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0023c0091t0001 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0024c0024t0003 | 0/0 | 5613 | 4 | 0 | 0 | 4 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0025c0027t0002 | 0/0 | 5612 | 3 | 0 | 0 | 2 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0026c0029t0002 | 0/0 | 5612 | 3 | 3 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0027c0034t0002 | 0/0 | 5612 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0027c0063t0002 | 0/0 | 5612 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0028c0044t0004 | 0/0 | 5612 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0028c0066t0002 | 0/0 | 5612 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0029c0028t0002 | 0/0 | 5612 | 3 | 3 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0030c0033t0001 | 0/0 | 5613 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0030c0048t0001 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0031c0032t0002 | 0/0 | 5612 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0031c0061t0002 | 0/0 | 5612 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0032c0026t0005 | 0/0 | 5613 | 3 | 0 | 0 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0033c0031t0001 | 0/0 | 5613 | 3 | 0 | 0 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0034c0035t0002 | 0/0 | 5612 | 2 | 0 | 1 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0035c0086t0002 | 0/0 | 5612 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0035c0088t0002 | 0/0 | 5612 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0036c0045t0004 | 0/0 | 5612 | 2 | 0 | 0 | 2 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0037c0036t0002 | 0/0 | 5612 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0037c0036t0008 | 0/0 | 5612 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0038c0093t0002 | 0/0 | 5612 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0038c0094t0002 | 0/0 | 5612 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0039c0042t0002 | 0/0 | 5612 | 2 | 0 | 0 | 1 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0040c0038t0003 | 0/0 | 5613 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0041c0068t0005 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0041c0106t0003 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0042c0047t0003 | 0/0 | 5613 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0043c0040t0001 | 0/0 | 5613 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0044c0046t0004 | 0/0 | 5612 | 2 | 0 | 0 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0045c0043t0001 | 0/0 | 5613 | 2 | 0 | 0 | 2 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0046c0107t0003 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0047c0110t0004 | 0/0 | 5612 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0048c0101t0001 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0049c0083t0004 | 0/0 | 5612 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0050c0050t0002 | 0/0 | 5612 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0051c0111t0004 | 0/0 | 5612 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0052c0095t0001 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0053c0049t0005 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0054c0096t0002 | 0/0 | 5612 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0055c0089t0002 | 0/0 | 5612 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0056c0058t0005 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0057c0097t0001 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0058c0053t0005 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0059c0060t0005 | 0/0 | 5613 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0060c0112t0003 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0061c0070t0001 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0062c0055t0005 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0063c0113t0004 | 0/0 | 5612 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0064c0059t0005 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0065c0087t0001 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0066c0074t0001 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0067c0064t0001 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0068c0090t0001 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0069c0062t0006 | 0/0 | 5612 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0070c0081t0001 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0071c0103t0003 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0072c0080t0002 | 0/0 | 5612 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5607): Show |
chr10 | 113583714 | 113669041 |
a0073c0092t0001 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0074c0098t0001 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0075c0082t0003 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0076c0067t0001 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0077c0109t0003 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0078c0065t0001 | 0/0 | 5613 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0079c0051t0005 | 0/0 | 5613 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
a0080c0085t0003 | 0/0 | 5613 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | AGAAG others(5608): Show |
chr10 | 113583714 | 113669041 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0001t0013g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0099t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0100t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0001c0102t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0002t0004g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0037t0007g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0002c0037t0007g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0003t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0003t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0003t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0003t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0003t0003g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0003t0003g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0003t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0003t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0003t0003g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0003t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0003t0003g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0003t0003g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0003t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0003t0003g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0003t0003g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0003t0003g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0003t0003g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0003t0003g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0003t0003g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0003t0003g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0023t0003g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0023t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0023t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0003c0023t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0004c0004t0005g0001 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0004c0004t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0004c0004t0005g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0004c0004t0005g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0004c0004t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0004c0004t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0004c0004t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0004c0004t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0004c0004t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0004c0004t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0004c0004t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0004c0004t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0004c0004t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0004c0004t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0004c0004t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0004c0004t0005g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0004c0057t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0005c0005t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0005c0005t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0005c0005t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0005c0005t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0005c0005t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0005c0005t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0005c0005t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0005c0005t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0005c0005t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0005c0005t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0005c0005t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0005c0005t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0005c0005t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0005c0005t0011g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0005c0021t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0005c0021t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0005c0021t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0005c0021t0003g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0005c0075t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0006c0010t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0006c0010t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0006c0010t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0006c0010t0003g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0006c0010t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0006c0010t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0006c0010t0003g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0006c0010t0003g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0006c0010t0003g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0006c0010t0003g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0006c0010t0014g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0006c0104t0003g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0006c0105t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0006c0108t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0007c0006t0006g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0007c0006t0006g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0007c0006t0006g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0007c0006t0006g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0007c0006t0006g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0007c0006t0006g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0007c0006t0006g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0007c0006t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0007c0006t0006g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0007c0006t0006g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0007c0006t0006g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0007c0006t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0007c0056t0006g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0008c0007t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0008c0007t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0008c0007t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0008c0007t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0008c0007t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0008c0007t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0008c0007t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0008c0007t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0008c0007t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0008c0007t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0008c0007t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0008c0007t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0008c0007t0009g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0008c0078t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0009c0009t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0009c0009t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0009c0009t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0009c0009t0001g0069 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0009c0009t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0009c0009t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0009c0009t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0009c0009t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0009c0009t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0009c0009t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0009c0079t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0010c0008t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0010c0008t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0010c0008t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0010c0008t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0010c0008t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0010c0008t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0010c0008t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0010c0008t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0010c0008t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0010c0008t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0010c0008t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0010c0008t0010g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0011c0016t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0011c0016t0004g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0011c0016t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0011c0016t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0011c0016t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0011c0016t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0011c0025t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0011c0025t0006g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0011c0025t0006g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0011c0039t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0011c0039t0004g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0012c0011t0003g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0012c0011t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0012c0011t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0012c0011t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0012c0011t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0012c0011t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0012c0011t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0012c0011t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0012c0011t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0013c0019t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0013c0019t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0013c0019t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0013c0019t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0013c0019t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0013c0019t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0013c0041t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0013c0041t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0014c0012t0004g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0014c0012t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0014c0012t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0014c0012t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0014c0012t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0014c0012t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0015c0013t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0015c0013t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0015c0013t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0015c0013t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0015c0013t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0015c0013t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0015c0013t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0015c0077t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0016c0020t0005g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0016c0020t0005g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0016c0020t0005g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0016c0020t0005g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0016c0020t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0016c0052t0005g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0016c0054t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0016c0084t0003g0286 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0017c0014t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0017c0014t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0017c0014t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0017c0014t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0017c0014t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0017c0014t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0017c0014t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0018c0015t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0018c0015t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0018c0015t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0018c0015t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0018c0015t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0018c0015t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0018c0076t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0019c0017t0002g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0019c0017t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0019c0017t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0019c0017t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0019c0017t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0020c0018t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0020c0018t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0020c0018t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0020c0018t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0020c0018t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0021c0022t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0021c0022t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0021c0022t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0021c0022t0012g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0021c0069t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0022c0071t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0022c0072t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0022c0073t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0022c0114t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0022c0115t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0023c0030t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0023c0030t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0023c0030t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0023c0091t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0024c0024t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0024c0024t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0024c0024t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0024c0024t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0025c0027t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0025c0027t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0025c0027t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0026c0029t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0026c0029t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0026c0029t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0027c0034t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0027c0034t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0027c0063t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0028c0044t0004g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0028c0044t0004g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0028c0066t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0029c0028t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0029c0028t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0029c0028t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0030c0033t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0030c0033t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0030c0048t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0031c0032t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0031c0032t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0031c0061t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0032c0026t0005g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0032c0026t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0033c0031t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0033c0031t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0033c0031t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0034c0035t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0034c0035t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0035c0086t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0035c0088t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0036c0045t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0036c0045t0004g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0037c0036t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0037c0036t0008g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0038c0093t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0038c0094t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0039c0042t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0039c0042t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0040c0038t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0040c0038t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0041c0068t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0041c0106t0003g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0042c0047t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0042c0047t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0043c0040t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0044c0046t0004g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0044c0046t0004g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0045c0043t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0045c0043t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0046c0107t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0047c0110t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0048c0101t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0049c0083t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0050c0050t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0051c0111t0004g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0052c0095t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0053c0049t0005g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0054c0096t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0055c0089t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0056c0058t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0057c0097t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0058c0053t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0059c0060t0005g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0060c0112t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0061c0070t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0062c0055t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0063c0113t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0064c0059t0005g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0065c0087t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0066c0074t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0067c0064t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0068c0090t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0069c0062t0006g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0070c0081t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0071c0103t0003g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0072c0080t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0073c0092t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0074c0098t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0075c0082t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0076c0067t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0077c0109t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0078c0065t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0079c0051t0005g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
a0080c0085t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | GBR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00099 | hp2 | a0013 | c0041 | t0002 | g0197 | EUR | GBR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | GBR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00140 | hp2 | a0034 | c0035 | t0002 | g0253 | EUR | GBR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00280 | hp1 | a0006 | c0010 | t0003 | g0315 | EUR | FIN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00280 | hp2 | a0021 | c0069 | t0001 | g0247 | EUR | FIN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00323 | hp1 | a0025 | c0027 | t0002 | g0244 | EUR | FIN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00323 | hp2 | a0003 | c0023 | t0003 | g0312 | EUR | FIN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00408 | hp1 | a0002 | c0002 | t0004 | g0337 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00408 | hp2 | a0014 | c0012 | t0004 | g0003 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00423 | hp1 | a0007 | c0006 | t0006 | g0046 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00438 | hp1 | a0046 | c0107 | t0003 | g0329 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00544 | hp1 | a0014 | c0012 | t0004 | g0003 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00544 | hp2 | a0035 | c0088 | t0002 | g0121 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00558 | hp1 | a0002 | c0002 | t0004 | g0359 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00558 | hp2 | a0008 | c0007 | t0002 | g0098 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00597 | hp1 | a0021 | c0022 | t0001 | g0260 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00597 | hp2 | a0002 | c0002 | t0004 | g0370 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00609 | hp1 | a0036 | c0045 | t0004 | g0327 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00609 | hp2 | a0047 | c0110 | t0004 | g0303 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00621 | hp1 | a0007 | c0006 | t0006 | g0045 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00621 | hp2 | a0006 | c0108 | t0003 | g0306 | EAS | CHS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00639 | hp2 | a0004 | c0004 | t0005 | g0001 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00642 | hp1 | a0009 | c0009 | t0001 | g0002 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00642 | hp2 | a0010 | c0008 | t0002 | g0240 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00733 | hp1 | a0034 | c0035 | t0002 | g0261 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00733 | hp2 | a0004 | c0004 | t0005 | g0016 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00735 | hp1 | a0001 | c0001 | t0013 | g0202 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00735 | hp2 | a0010 | c0008 | t0002 | g0238 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00738 | hp1 | a0006 | c0010 | t0003 | g0352 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00738 | hp2 | a0010 | c0008 | t0002 | g0263 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00741 | hp1 | a0007 | c0006 | t0006 | g0026 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG00741 | hp2 | a0002 | c0002 | t0004 | g0320 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01069 | hp1 | a0006 | c0010 | t0003 | g0313 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01069 | hp2 | a0015 | c0013 | t0002 | g0095 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01070 | hp1 | a0017 | c0014 | t0001 | g0190 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01070 | hp2 | a0010 | c0008 | t0002 | g0241 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01071 | hp1 | a0017 | c0014 | t0001 | g0196 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01071 | hp2 | a0015 | c0013 | t0002 | g0096 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01081 | hp1 | a0017 | c0014 | t0001 | g0178 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01081 | hp2 | a0037 | c0036 | t0008 | g0059 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01099 | hp1 | a0048 | c0101 | t0001 | g0206 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01099 | hp2 | a0016 | c0020 | t0005 | g0023 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01106 | hp1 | a0009 | c0009 | t0001 | g0002 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01106 | hp2 | a0049 | c0083 | t0004 | g0279 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01109 | hp1 | a0005 | c0021 | t0003 | g0383 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01109 | hp2 | a0050 | c0050 | t0002 | g0237 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01167 | hp1 | a0019 | c0017 | t0002 | g0128 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01168 | hp1 | a0009 | c0009 | t0001 | g0079 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01168 | hp2 | a0017 | c0014 | t0001 | g0186 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01169 | hp1 | a0009 | c0009 | t0001 | g0083 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01169 | hp2 | a0019 | c0017 | t0002 | g0126 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01175 | hp1 | a0051 | c0111 | t0004 | g0381 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01175 | hp2 | a0008 | c0007 | t0002 | g0090 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01192 | hp1 | a0012 | c0011 | t0003 | g0290 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01192 | hp2 | a0019 | c0017 | t0002 | g0131 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01243 | hp1 | a0009 | c0009 | t0001 | g0002 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01243 | hp2 | a0006 | c0010 | t0003 | g0350 | AMR | PUR | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01255 | hp1 | a0023 | c0091 | t0001 | g0187 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01255 | hp2 | a0005 | c0005 | t0001 | g0115 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01256 | hp1 | a0004 | c0004 | t0005 | g0001 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01257 | hp1 | a0012 | c0011 | t0003 | g0010 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01257 | hp2 | a0052 | c0095 | t0001 | g0213 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01258 | hp1 | a0012 | c0011 | t0003 | g0010 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01258 | hp2 | a0004 | c0004 | t0005 | g0001 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01261 | hp1 | a0010 | c0008 | t0002 | g0242 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01261 | hp2 | a0008 | c0007 | t0009 | g0084 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01346 | hp1 | a0016 | c0020 | t0005 | g0033 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01346 | hp2 | a0008 | c0078 | t0002 | g0065 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01358 | hp1 | a0053 | c0049 | t0005 | g0031 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01358 | hp2 | a0006 | c0104 | t0003 | g0351 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01361 | hp2 | a0007 | c0006 | t0006 | g0027 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01433 | hp1 | a0017 | c0014 | t0001 | g0191 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01433 | hp2 | a0054 | c0096 | t0002 | g0151 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01496 | hp1 | a0019 | c0017 | t0002 | g0007 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01496 | hp2 | a0010 | c0008 | t0010 | g0245 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01515 | hp1 | a0008 | c0007 | t0002 | g0087 | EUR | IBS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | IBS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01516 | hp1 | a0038 | c0093 | t0002 | g0185 | EUR | IBS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01516 | hp2 | a0055 | c0089 | t0002 | g0110 | EUR | IBS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01517 | hp1 | a0039 | c0042 | t0002 | g0160 | EUR | IBS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01517 | hp2 | a0008 | c0007 | t0002 | g0086 | EUR | IBS | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01884 | hp1 | a0040 | c0038 | t0003 | g0277 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01884 | hp2 | a0026 | c0029 | t0002 | g0123 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01891 | hp1 | a0027 | c0063 | t0002 | g0227 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01891 | hp2 | a0022 | c0071 | t0002 | g0267 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01928 | hp1 | a0007 | c0006 | t0006 | g0035 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01943 | hp1 | a0056 | c0058 | t0005 | g0053 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01943 | hp2 | a0057 | c0097 | t0001 | g0204 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01975 | hp1 | a0007 | c0006 | t0006 | g0013 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01978 | hp1 | a0058 | c0053 | t0005 | g0041 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01978 | hp2 | a0007 | c0006 | t0006 | g0004 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01981 | hp1 | a0059 | c0060 | t0005 | g0015 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02004 | hp1 | a0007 | c0006 | t0006 | g0020 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02015 | hp2 | a0014 | c0012 | t0004 | g0293 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02027 | hp2 | a0024 | c0024 | t0003 | g0318 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02040 | hp2 | a0024 | c0024 | t0003 | g0324 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02055 | hp2 | a0003 | c0003 | t0003 | g0338 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02056 | hp1 | a0005 | c0021 | t0001 | g0130 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02056 | hp2 | a0011 | c0016 | t0004 | g0292 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02071 | hp1 | a0007 | c0056 | t0006 | g0043 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02071 | hp2 | a0060 | c0112 | t0003 | g0323 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02074 | hp1 | a0035 | c0086 | t0002 | g0113 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02074 | hp2 | a0003 | c0023 | t0003 | g0322 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02080 | hp1 | a0004 | c0004 | t0005 | g0029 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02080 | hp2 | a0005 | c0021 | t0001 | g0008 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02083 | hp1 | a0024 | c0024 | t0003 | g0325 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02083 | hp2 | a0028 | c0066 | t0002 | g0251 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02129 | hp1 | a0011 | c0025 | t0006 | g0022 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02129 | hp2 | a0018 | c0015 | t0001 | g0092 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02132 | hp1 | a0005 | c0021 | t0001 | g0008 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02132 | hp2 | a0002 | c0002 | t0004 | g0301 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02135 | hp1 | a0061 | c0070 | t0001 | g0243 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02145 | hp1 | a0011 | c0016 | t0004 | g0295 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02145 | hp2 | a0006 | c0105 | t0003 | g0343 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02148 | hp1 | a0010 | c0008 | t0002 | g0249 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02148 | hp2 | a0007 | c0006 | t0006 | g0004 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02155 | hp1 | a0005 | c0005 | t0001 | g0111 | EAS | CDX | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02155 | hp2 | a0014 | c0012 | t0004 | g0288 | EAS | CDX | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02165 | hp1 | a0005 | c0005 | t0001 | g0114 | EAS | CDX | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02165 | hp2 | a0006 | c0010 | t0003 | g0374 | EAS | CDX | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02257 | hp2 | a0018 | c0015 | t0001 | g0072 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02258 | hp1 | a0062 | c0055 | t0005 | g0056 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02258 | hp2 | a0063 | c0113 | t0004 | g0273 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02273 | hp1 | a0010 | c0008 | t0002 | g0246 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02293 | hp1 | a0010 | c0008 | t0002 | g0248 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02293 | hp2 | a0007 | c0006 | t0006 | g0025 | AMR | PEL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02451 | hp1 | a0028 | c0044 | t0004 | g0376 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02451 | hp2 | a0022 | c0072 | t0001 | g0268 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02523 | hp1 | a0014 | c0012 | t0004 | g0291 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02523 | hp2 | a0004 | c0004 | t0005 | g0047 | EAS | KHV | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02572 | hp1 | a0005 | c0005 | t0001 | g0104 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02572 | hp2 | a0030 | c0033 | t0001 | g0062 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02602 | hp1 | a0064 | c0059 | t0005 | g0048 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02602 | hp2 | a0002 | c0002 | t0004 | g0330 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02615 | hp1 | a0005 | c0005 | t0001 | g0106 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02615 | hp2 | a0026 | c0029 | t0002 | g0127 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02622 | hp1 | a0027 | c0034 | t0002 | g0236 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02622 | hp2 | a0065 | c0087 | t0001 | g0105 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02630 | hp1 | a0037 | c0036 | t0002 | g0265 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02630 | hp2 | a0040 | c0038 | t0003 | g0341 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02698 | hp1 | a0012 | c0011 | t0003 | g0280 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02698 | hp2 | a0005 | c0005 | t0011 | g0125 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02717 | hp1 | a0029 | c0028 | t0002 | g0230 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02717 | hp2 | a0018 | c0015 | t0001 | g0102 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02735 | hp1 | a0020 | c0018 | t0001 | g0129 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02735 | hp2 | a0005 | c0005 | t0001 | g0108 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02809 | hp1 | a0005 | c0005 | t0001 | g0161 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02809 | hp2 | a0020 | c0018 | t0001 | g0112 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02886 | hp1 | a0041 | c0106 | t0003 | g0380 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02886 | hp2 | a0030 | c0033 | t0001 | g0061 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02895 | hp1 | a0016 | c0054 | t0005 | g0057 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02895 | hp2 | a0011 | c0039 | t0004 | g0340 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02896 | hp1 | a0003 | c0003 | t0003 | g0375 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02896 | hp2 | a0042 | c0047 | t0003 | g0275 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02897 | hp1 | a0042 | c0047 | t0003 | g0274 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02897 | hp2 | a0011 | c0039 | t0004 | g0339 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02922 | hp1 | a0009 | c0009 | t0001 | g0103 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02922 | hp2 | a0015 | c0013 | t0002 | g0100 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02965 | hp1 | a0006 | c0010 | t0014 | g0347 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02965 | hp2 | a0043 | c0040 | t0001 | g0006 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02970 | hp1 | a0009 | c0009 | t0001 | g0067 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02970 | hp2 | a0026 | c0029 | t0002 | g0120 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02976 | hp1 | a0031 | c0061 | t0002 | g0264 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02976 | hp2 | a0043 | c0040 | t0001 | g0006 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03041 | hp1 | a0015 | c0013 | t0002 | g0088 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03041 | hp2 | a0006 | c0010 | t0003 | g0349 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03098 | hp1 | a0020 | c0018 | t0001 | g0164 | AFR | MSL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03098 | hp2 | a0066 | c0074 | t0001 | g0266 | AFR | MSL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03130 | hp1 | a0009 | c0009 | t0001 | g0075 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03130 | hp2 | a0019 | c0017 | t0002 | g0107 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03139 | hp1 | a0003 | c0003 | t0003 | g0377 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03139 | hp2 | a0015 | c0077 | t0002 | g0066 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03195 | hp1 | a0067 | c0064 | t0001 | g0233 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03195 | hp2 | a0011 | c0016 | t0004 | g0276 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03239 | hp1 | a0016 | c0020 | t0005 | g0024 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03239 | hp2 | a0003 | c0003 | t0003 | g0326 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03453 | hp1 | a0011 | c0016 | t0004 | g0296 | AFR | MSL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03453 | hp2 | a0068 | c0090 | t0001 | g0163 | AFR | MSL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03486 | hp1 | a0011 | c0025 | t0002 | g0235 | AFR | MSL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03486 | hp2 | a0003 | c0003 | t0003 | g0379 | AFR | MSL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03490 | hp1 | a0004 | c0004 | t0005 | g0001 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03490 | hp2 | a0020 | c0018 | t0001 | g0009 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03491 | hp1 | a0044 | c0046 | t0004 | g0372 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03492 | hp1 | a0020 | c0018 | t0001 | g0009 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03492 | hp2 | a0044 | c0046 | t0004 | g0371 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03516 | hp1 | a0011 | c0016 | t0004 | g0297 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03516 | hp2 | a0022 | c0073 | t0001 | g0269 | AFR | ESN | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03540 | hp1 | a0002 | c0002 | t0004 | g0334 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03540 | hp2 | a0009 | c0009 | t0001 | g0073 | AFR | GWD | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03579 | hp1 | a0005 | c0075 | t0001 | g0158 | AFR | MSL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03579 | hp2 | a0003 | c0003 | t0003 | g0382 | AFR | MSL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03654 | hp1 | a0016 | c0020 | t0005 | g0034 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03654 | hp2 | a0008 | c0007 | t0002 | g0085 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03669 | hp1 | a0002 | c0002 | t0004 | g0298 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03669 | hp2 | a0012 | c0011 | t0003 | g0289 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | STU | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03688 | hp2 | a0069 | c0062 | t0006 | g0050 | SAS | STU | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03704 | hp1 | a0018 | c0076 | t0001 | g0101 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03704 | hp2 | a0002 | c0002 | t0004 | g0331 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03710 | hp1 | a0010 | c0008 | t0002 | g0239 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03710 | hp2 | a0005 | c0005 | t0001 | g0124 | SAS | PJL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03831 | hp1 | a0003 | c0003 | t0003 | g0332 | SAS | BEB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03834 | hp1 | a0019 | c0017 | t0002 | g0007 | SAS | BEB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03834 | hp2 | a0002 | c0002 | t0004 | g0321 | SAS | BEB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03927 | hp1 | a0003 | c0003 | t0003 | g0311 | SAS | BEB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03927 | hp2 | a0016 | c0052 | t0005 | g0032 | SAS | BEB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03942 | hp1 | a0070 | c0081 | t0001 | g0078 | SAS | BEB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03942 | hp2 | a0071 | c0103 | t0003 | g0353 | SAS | BEB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG04115 | hp1 | a0017 | c0014 | t0001 | g0170 | SAS | STU | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG04115 | hp2 | a0003 | c0003 | t0003 | g0362 | SAS | STU | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG04184 | hp1 | a0005 | c0005 | t0001 | g0122 | SAS | BEB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG04184 | hp2 | a0002 | c0037 | t0007 | g0355 | SAS | BEB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG04199 | hp1 | a0072 | c0080 | t0002 | g0089 | SAS | STU | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG04199 | hp2 | a0011 | c0016 | t0004 | g0278 | SAS | STU | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG04228 | hp1 | a0002 | c0037 | t0007 | g0354 | SAS | STU | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG04228 | hp2 | a0003 | c0003 | t0003 | g0361 | SAS | STU | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18522 | hp1 | a0002 | c0002 | t0004 | g0342 | AFR | YRI | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18522 | hp2 | a0006 | c0010 | t0003 | g0345 | AFR | YRI | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18612 | hp1 | a0015 | c0013 | t0002 | g0074 | EAS | CHB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18612 | hp2 | a0021 | c0022 | t0001 | g0255 | EAS | CHB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18747 | hp1 | a0002 | c0002 | t0004 | g0308 | EAS | CHB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18906 | hp1 | a0031 | c0032 | t0002 | g0229 | AFR | YRI | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18906 | hp2 | a0028 | c0044 | t0004 | g0378 | AFR | YRI | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18939 | hp1 | a0039 | c0042 | t0002 | g0219 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18939 | hp2 | a0045 | c0043 | t0001 | g0166 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18940 | hp1 | a0002 | c0002 | t0004 | g0305 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18940 | hp2 | a0014 | c0012 | t0004 | g0294 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18942 | hp2 | a0073 | c0092 | t0001 | g0134 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18944 | hp1 | a0074 | c0098 | t0001 | g0132 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18944 | hp2 | a0018 | c0015 | t0001 | g0080 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18948 | hp1 | a0036 | c0045 | t0004 | g0317 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18948 | hp2 | a0012 | c0011 | t0003 | g0284 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18950 | hp1 | a0002 | c0002 | t0004 | g0011 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18950 | hp2 | a0002 | c0002 | t0004 | g0373 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18951 | hp1 | a0003 | c0023 | t0003 | g0316 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18952 | hp1 | a0004 | c0004 | t0005 | g0051 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18952 | hp2 | a0032 | c0026 | t0005 | g0018 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18954 | hp1 | a0075 | c0082 | t0003 | g0285 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18954 | hp2 | a0003 | c0023 | t0003 | g0319 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18956 | hp2 | a0004 | c0004 | t0005 | g0036 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18959 | hp1 | a0002 | c0002 | t0004 | g0357 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18959 | hp2 | a0015 | c0013 | t0002 | g0064 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18960 | hp1 | a0004 | c0004 | t0005 | g0028 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18960 | hp2 | a0008 | c0007 | t0002 | g0093 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18962 | hp1 | a0033 | c0031 | t0001 | g0224 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18962 | hp2 | a0002 | c0002 | t0004 | g0302 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18963 | hp1 | a0004 | c0004 | t0005 | g0037 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18964 | hp1 | a0033 | c0031 | t0001 | g0225 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18964 | hp2 | a0009 | c0079 | t0001 | g0071 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18968 | hp1 | a0033 | c0031 | t0001 | g0226 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18968 | hp2 | a0003 | c0003 | t0003 | g0356 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18970 | hp1 | a0076 | c0067 | t0001 | g0250 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18970 | hp2 | a0004 | c0004 | t0005 | g0049 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18971 | hp1 | a0003 | c0003 | t0003 | g0364 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18971 | hp2 | a0025 | c0027 | t0002 | g0259 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18972 | hp1 | a0005 | c0005 | t0001 | g0162 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18972 | hp2 | a0015 | c0013 | t0002 | g0063 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18973 | hp1 | a0013 | c0041 | t0002 | g0217 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18973 | hp2 | a0003 | c0003 | t0003 | g0365 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18974 | hp1 | a0004 | c0004 | t0005 | g0042 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18974 | hp2 | a0024 | c0024 | t0003 | g0328 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18975 | hp1 | a0007 | c0006 | t0006 | g0039 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18975 | hp2 | a0004 | c0004 | t0005 | g0012 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18981 | hp1 | a0008 | c0007 | t0002 | g0070 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18981 | hp2 | a0077 | c0109 | t0003 | g0309 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18983 | hp1 | a0023 | c0030 | t0001 | g0157 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18983 | hp2 | a0013 | c0019 | t0002 | g0156 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18984 | hp2 | a0002 | c0002 | t0004 | g0367 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18986 | hp1 | a0008 | c0007 | t0002 | g0082 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18988 | hp1 | a0032 | c0026 | t0005 | g0005 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18988 | hp2 | a0002 | c0002 | t0004 | g0369 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18989 | hp2 | a0012 | c0011 | t0003 | g0270 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18990 | hp1 | a0002 | c0002 | t0004 | g0336 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18990 | hp2 | a0008 | c0007 | t0002 | g0097 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18992 | hp2 | a0002 | c0002 | t0004 | g0011 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18993 | hp1 | a0013 | c0019 | t0002 | g0222 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18993 | hp2 | a0078 | c0065 | t0001 | g0252 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18998 | hp1 | a0005 | c0005 | t0001 | g0116 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18998 | hp2 | a0011 | c0025 | t0006 | g0021 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18999 | hp1 | a0007 | c0006 | t0006 | g0044 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA18999 | hp2 | a0013 | c0019 | t0002 | g0198 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19000 | hp1 | a0006 | c0010 | t0003 | g0310 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19000 | hp2 | a0025 | c0027 | t0002 | g0258 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19003 | hp1 | a0002 | c0002 | t0004 | g0335 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19003 | hp2 | a0012 | c0011 | t0003 | g0283 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19004 | hp2 | a0003 | c0003 | t0003 | g0363 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19005 | hp1 | a0001 | c0100 | t0001 | g0179 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19007 | hp1 | a0012 | c0011 | t0003 | g0287 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19007 | hp2 | a0008 | c0007 | t0002 | g0076 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19009 | hp1 | a0003 | c0003 | t0003 | g0366 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19011 | hp1 | a0013 | c0019 | t0002 | g0174 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19012 | hp1 | a0008 | c0007 | t0002 | g0091 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19012 | hp2 | a0004 | c0004 | t0005 | g0019 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19030 | hp1 | a0003 | c0003 | t0003 | g0344 | AFR | LWK | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19030 | hp2 | a0031 | c0032 | t0002 | g0228 | AFR | LWK | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19043 | hp1 | a0022 | c0115 | t0004 | g0271 | AFR | LWK | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19043 | hp2 | a0029 | c0028 | t0002 | g0231 | AFR | LWK | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19056 | hp2 | a0003 | c0003 | t0003 | g0299 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19057 | hp1 | a0023 | c0030 | t0001 | g0173 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19057 | hp2 | a0014 | c0012 | t0004 | g0003 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19062 | hp1 | a0006 | c0010 | t0003 | g0307 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19062 | hp2 | a0004 | c0057 | t0005 | g0052 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19064 | hp1 | a0012 | c0011 | t0003 | g0281 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19064 | hp2 | a0002 | c0002 | t0004 | g0358 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19065 | hp1 | a0003 | c0003 | t0003 | g0304 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19067 | hp1 | a0005 | c0005 | t0001 | g0117 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19067 | hp2 | a0004 | c0004 | t0005 | g0040 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19068 | hp1 | a0013 | c0019 | t0002 | g0201 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19068 | hp2 | a0005 | c0021 | t0001 | g0119 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19072 | hp2 | a0010 | c0008 | t0002 | g0254 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19078 | hp1 | a0014 | c0012 | t0004 | g0282 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19079 | hp1 | a0021 | c0022 | t0001 | g0256 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19080 | hp1 | a0018 | c0015 | t0001 | g0099 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19083 | hp2 | a0002 | c0002 | t0004 | g0360 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19084 | hp2 | a0002 | c0002 | t0004 | g0368 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19085 | hp1 | a0032 | c0026 | t0005 | g0005 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19087 | hp1 | a0001 | c0099 | t0001 | g0153 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19088 | hp1 | a0045 | c0043 | t0001 | g0175 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19088 | hp2 | a0004 | c0004 | t0005 | g0030 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19089 | hp1 | a0009 | c0009 | t0001 | g0094 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19089 | hp2 | a0038 | c0094 | t0002 | g0181 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19090 | hp1 | a0021 | c0022 | t0012 | g0257 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19091 | hp1 | a0005 | c0005 | t0001 | g0118 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19091 | hp2 | a0013 | c0019 | t0002 | g0109 | EAS | JPT | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19240 | hp1 | a0030 | c0048 | t0001 | g0060 | AFR | YRI | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA19240 | hp2 | a0002 | c0002 | t0004 | g0333 | AFR | YRI | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA20129 | hp1 | a0007 | c0006 | t0006 | g0055 | AFR | ASW | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA20129 | hp2 | a0003 | c0003 | t0003 | g0314 | AFR | ASW | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | TSI | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA20752 | hp2 | a0004 | c0004 | t0005 | g0054 | EUR | TSI | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA20805 | hp1 | a0017 | c0014 | t0001 | g0183 | EUR | TSI | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA20805 | hp2 | a0079 | c0051 | t0005 | g0017 | EUR | TSI | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA20905 | hp1 | a0004 | c0004 | t0005 | g0014 | SAS | GIH | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA20905 | hp2 | a0023 | c0030 | t0001 | g0172 | SAS | GIH | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG01123 | hp2 | a0008 | c0007 | t0002 | g0081 | AMR | CLM | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02109 | hp1 | a0006 | c0010 | t0003 | g0348 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02109 | hp2 | a0020 | c0018 | t0001 | g0165 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02486 | hp1 | a0016 | c0020 | t0005 | g0038 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02486 | hp2 | a0027 | c0034 | t0002 | g0234 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02559 | hp1 | a0041 | c0068 | t0005 | g0058 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG02559 | hp2 | a0029 | c0028 | t0002 | g0232 | AFR | ACB | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03471 | hp1 | a0018 | c0015 | t0001 | g0077 | AFR | MSL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG03471 | hp2 | a0022 | c0114 | t0004 | g0272 | AFR | MSL | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG06807 | hp1 | a0009 | c0009 | t0001 | g0068 | AFR | USA | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
HG06807 | hp2 | a0001 | c0102 | t0001 | g0184 | AFR | USA | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA20300 | hp1 | a0010 | c0008 | t0002 | g0262 | AFR | USA | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | USA | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA21309 | hp1 | a0003 | c0003 | t0003 | g0346 | AFR | LWK | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
NA21309 | hp2 | a0080 | c0085 | t0003 | g0300 | AFR | LWK | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
homoSapiens | chm13v2 | a0016 | c0084 | t0003 | g0286 | REF | REF | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
homoSapiens | grch38p0 | a0009 | c0009 | t0001 | g0069 | REF | REF | NRAP_chr10_113583714_113669041 | NRAP | chr10 | 113583714 | 113669041 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:113588715 | C | T | 1 | a0010 | 1 | HG01496.hp2 | splice_region_variant | LOW | c.*260G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 42/42 | chr10 | 113588715 | |||||||
chr10:113589718 | C | G | 1 | a0057 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.5036G>C | p.Arg1679Pro | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 41/42 | 5195/5613 | 5036/5193 | 1679/1730 | chr10 | 113589718 | |||
chr10:113590607 | C | A | 1 | a0031 | 3 | HG02976.hp1 NA18906.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.4927G>T | p.Ala1643Ser | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/42 | 5086/5613 | 4927/5193 | 1643/1730 | chr10 | 113590607 | |||
chr10:113590838 | G | A | 34 | a0002 a0007 a0008 others(31): Show |
158 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(155): Show |
missense_variant | MODERATE | c.4696C>T | p.Arg1566Cys | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/42 | 4855/5613 | 4696/5193 | 1566/1730 | chr10 | 113590838 | |||
chr10:113592246 | A | G | 11 | a0008 a0014 a0019 others(8): Show |
40 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(37): Show |
missense_variant | MODERATE | c.4592T>C | p.Leu1531Pro | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/42 | 4751/5613 | 4592/5193 | 1531/1730 | chr10 | 113592246 | |||
chr10:113595639 | G | A | 1 | a0065 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.4520C>T | p.Ala1507Val | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/42 | 4679/5613 | 4520/5193 | 1507/1730 | chr10 | 113595639 | |||
chr10:113595726 | C | T | 1 | a0046 | 1 | HG00438.hp1 | missense_variant&splice_region_variant | MODERATE | c.4433G>A | p.Arg1478His | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/42 | 4592/5613 | 4433/5193 | 1478/1730 | chr10 | 113595726 | |||
chr10:113597971 | C | T | 1 | a0042 | 2 | HG02896.hp2 HG02897.hp1 |
missense_variant&splice_region_variant | MODERATE | c.4330G>A | p.Glu1444Lys | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/42 | 4489/5613 | 4330/5193 | 1444/1730 | chr10 | 113597971 | |||
chr10:113604826 | A | G | 1 | a0058 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.4010T>C | p.Met1337Thr | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/42 | 4169/5613 | 4010/5193 | 1337/1730 | chr10 | 113604826 | |||
chr10:113604847 | C | T | 1 | a0052 | 1 | HG01257.hp2 | missense_variant | MODERATE | c.3989G>A | p.Arg1330Gln | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/42 | 4148/5613 | 3989/5193 | 1330/1730 | chr10 | 113604847 | |||
chr10:113606247 | G | T | 3 | a0032 a0073 a0077 |
5 | NA18942.hp2 NA18952.hp2 NA18981.hp2 others(2): Show |
missense_variant | MODERATE | c.3738C>A | p.His1246Gln | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 33/42 | 3897/5613 | 3738/5193 | 1246/1730 | chr10 | 113606247 | |||
chr10:113606257 | T | A | 2 | a0041 a0066 |
3 | HG02559.hp1 HG02886.hp1 HG03098.hp2 |
missense_variant | MODERATE | c.3728A>T | p.Asp1243Val | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 33/42 | 3887/5613 | 3728/5193 | 1243/1730 | chr10 | 113606257 | |||
chr10:113610515 | T | C | 39 | a0001 a0003 a0004 others(36): Show |
190 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(187): Show |
missense_variant | MODERATE | c.3547A>G | p.Ile1183Val | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/42 | 3706/5613 | 3547/5193 | 1183/1730 | chr10 | 113610515 | |||
chr10:113612397 | G | A | 1 | a0017 | 7 | HG01070.hp1 HG01071.hp1 HG01081.hp1 others(4): Show |
missense_variant | MODERATE | c.3335C>T | p.Ala1112Val | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/42 | 3494/5613 | 3335/5193 | 1112/1730 | chr10 | 113612397 | |||
chr10:113614241 | C | T | 1 | a0022 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.3242G>A | p.Ser1081Asn | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/42 | 3401/5613 | 3242/5193 | 1081/1730 | chr10 | 113614241 | |||
chr10:113614244 | C | T | 1 | a0046 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.3239G>A | p.Arg1080Gln | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/42 | 3398/5613 | 3239/5193 | 1080/1730 | chr10 | 113614244 | |||
chr10:113614862 | C | T | 1 | a0034 | 2 | HG00140.hp2 HG00733.hp1 |
missense_variant | MODERATE | c.3163G>A | p.Ala1055Thr | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 28/42 | 3322/5613 | 3163/5193 | 1055/1730 | chr10 | 113614862 | |||
chr10:113615726 | T | C | 1 | a0030 | 3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.3064A>G | p.Met1022Val | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 27/42 | 3223/5613 | 3064/5193 | 1022/1730 | chr10 | 113615726 | |||
chr10:113615783 | G | A | 1 | a0056 | 1 | HG01943.hp1 | missense_variant | MODERATE | c.3007C>T | p.His1003Tyr | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 27/42 | 3166/5613 | 3007/5193 | 1003/1730 | chr10 | 113615783 | |||
chr10:113617531 | T | C | 11 | a0004 a0024 a0036 others(8): Show |
34 | HG00609.hp1 HG00639.hp2 HG00733.hp2 others(31): Show |
missense_variant | MODERATE | c.2897A>G | p.Asp966Gly | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/42 | 3056/5613 | 2897/5193 | 966/1730 | chr10 | 113617531 | |||
chr10:113621937 | G | A | 1 | a0072 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.2701C>T | p.His901Tyr | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/42 | 2860/5613 | 2701/5193 | 901/1730 | chr10 | 113621937 | |||
chr10:113621954 | T | C | 1 | a0064 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.2684A>G | p.Tyr895Cys | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/42 | 2843/5613 | 2684/5193 | 895/1730 | chr10 | 113621954 | |||
chr10:113621988 | G | A | 16 | a0004 a0007 a0010 others(13): Show |
76 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(73): Show |
missense_variant | MODERATE | c.2650C>T | p.Arg884Cys | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/42 | 2809/5613 | 2650/5193 | 884/1730 | chr10 | 113621988 | |||
chr10:113622070 | A | T | 1 | a0050 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.2568T>A | p.Ser856Arg | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/42 | 2727/5613 | 2568/5193 | 856/1730 | chr10 | 113622070 | |||
chr10:113623569 | G | C | 1 | a0068 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.2417C>G | p.Thr806Ser | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/42 | 2576/5613 | 2417/5193 | 806/1730 | chr10 | 113623569 | |||
chr10:113629607 | G | A | 21 | a0004 a0007 a0011 others(18): Show |
91 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(88): Show |
missense_variant | MODERATE | c.2021C>T | p.Ala674Val | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/42 | 2180/5613 | 2021/5193 | 674/1730 | chr10 | 113629607 | |||
chr10:113629689 | C | A | 1 | a0045 | 2 | NA18939.hp2 NA19088.hp1 |
missense_variant | MODERATE | c.1939G>T | p.Ala647Ser | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/42 | 2098/5613 | 1939/5193 | 647/1730 | chr10 | 113629689 | |||
chr10:113629731 | C | A | 1 | a0080 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1897G>T | p.Asp633Tyr | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/42 | 2056/5613 | 1897/5193 | 633/1730 | chr10 | 113629731 | |||
chr10:113631886 | C | T | 1 | a0053 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.1711G>A | p.Ala571Thr | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 17/42 | 1870/5613 | 1711/5193 | 571/1730 | chr10 | 113631886 | |||
chr10:113631927 | T | C | 1 | a0059 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.1670A>G | p.Lys557Arg | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 17/42 | 1829/5613 | 1670/5193 | 557/1730 | chr10 | 113631927 | |||
chr10:113633160 | T | A | 20 | a0002 a0003 a0006 others(17): Show |
109 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
missense_variant | MODERATE | c.1556A>T | p.Asn519Ile | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/42 | 1715/5613 | 1556/5193 | 519/1730 | chr10 | 113633160 | |||
chr10:113634170 | G | A | 26 | a0001 a0005 a0013 others(23): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
missense_variant | MODERATE | c.1469C>T | p.Ser490Leu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/42 | 1628/5613 | 1469/5193 | 490/1730 | chr10 | 113634170 | |||
chr10:113634189 | C | T | 16 | a0002 a0003 a0006 others(13): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
missense_variant | MODERATE | c.1450G>A | p.Asp484Asn | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/42 | 1609/5613 | 1450/5193 | 484/1730 | chr10 | 113634189 | |||
chr10:113641423 | C | T | 1 | a0022 | 3 | HG01891.hp2 HG02451.hp2 HG03516.hp2 |
missense_variant | MODERATE | c.1265G>A | p.Gly422Glu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/42 | 1424/5613 | 1265/5193 | 422/1730 | chr10 | 113641423 | |||
chr10:113645856 | T | C | 48 | a0001 a0004 a0005 others(45): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
missense_variant | MODERATE | c.1079A>G | p.Gln360Arg | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/42 | 1238/5613 | 1079/5193 | 360/1730 | chr10 | 113645856 | |||
chr10:113645889 | G | A | 1 | a0048 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.1046C>T | p.Ser349Leu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/42 | 1205/5613 | 1046/5193 | 349/1730 | chr10 | 113645889 | |||
chr10:113645905 | C | T | 48 | a0001 a0004 a0005 others(45): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
missense_variant | MODERATE | c.1030G>A | p.Ala344Thr | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/42 | 1189/5613 | 1030/5193 | 344/1730 | chr10 | 113645905 | |||
chr10:113647020 | G | A | 1 | a0070 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.896C>T | p.Pro299Leu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/42 | 1055/5613 | 896/5193 | 299/1730 | chr10 | 113647020 | |||
chr10:113650081 | C | T | 24 | a0002 a0003 a0006 others(21): Show |
115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
missense_variant | MODERATE | c.844G>A | p.Ala282Thr | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/42 | 1003/5613 | 844/5193 | 282/1730 | chr10 | 113650081 | |||
chr10:113650475 | T | C | 14 | a0001 a0013 a0017 others(11): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
missense_variant | MODERATE | c.746A>G | p.Tyr249Cys | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 8/42 | 905/5613 | 746/5193 | 249/1730 | chr10 | 113650475 | |||
chr10:113650479 | C | T | 1 | a0022 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.742G>A | p.Ala248Thr | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 8/42 | 901/5613 | 742/5193 | 248/1730 | chr10 | 113650479 | |||
chr10:113651855 | A | G | 74 | a0001 a0002 a0003 others(71): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
missense_variant | MODERATE | c.623T>C | p.Val208Ala | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/42 | 782/5613 | 623/5193 | 208/1730 | chr10 | 113651855 | |||
chr10:113651879 | C | A | 1 | a0044 | 2 | HG03491.hp1 HG03492.hp2 |
missense_variant | MODERATE | c.599G>T | p.Arg200Leu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/42 | 758/5613 | 599/5193 | 200/1730 | chr10 | 113651879 | |||
chr10:113652949 | G | C | 2 | a0042 a0063 |
3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
missense_variant | MODERATE | c.556C>G | p.Gln186Glu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/42 | 715/5613 | 556/5193 | 186/1730 | chr10 | 113652949 | |||
chr10:113653022 | ATAGTCTT others(121): Show |
A | 1 | a0022 | 5 | HG01891.hp2 HG02451.hp2 HG03471.hp2 others(2): Show |
frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.466-111_482del | p.Glu156fs | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/42 | 641/5613 | 466/5193 | 156/1730 | chr10 | 113653022 | |||
chr10:113654092 | C | A | 1 | a0029 | 3 | HG02559.hp2 HG02717.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.394G>T | p.Ala132Ser | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/42 | 553/5613 | 394/5193 | 132/1730 | chr10 | 113654092 | |||
chr10:113662689 | G | A | 2 | a0037 a0066 |
3 | HG01081.hp2 HG02630.hp1 HG03098.hp2 |
missense_variant | MODERATE | c.245C>T | p.Ala82Val | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/42 | 404/5613 | 245/5193 | 82/1730 | chr10 | 113662689 | |||
chr10:113663383 | C | A | 1 | a0033 | 3 | NA18962.hp1 NA18964.hp1 NA18968.hp1 |
missense_variant | MODERATE | c.136G>T | p.Val46Leu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 2/42 | 295/5613 | 136/5193 | 46/1730 | chr10 | 113663383 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:113589708 | C | T | 1 | a0062c0055 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.5046G>A | p.Ala1682Ala | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 41/42 | 5205/5613 | 5046/5193 | 1682/1730 | chr10 | 113589708 | |||
chr10:113590629 | C | T | 2 | a0016c0020 a0016c0052 |
6 | HG01099.hp2 HG01346.hp1 HG02486.hp1 others(3): Show |
synonymous_variant | LOW | c.4905G>A | p.Pro1635Pro | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/42 | 5064/5613 | 4905/5193 | 1635/1730 | chr10 | 113590629 | |||
chr10:113610495 | A | G | 49 | a0001c0001 a0001c0099 a0001c0100 others(46): Show |
192 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(189): Show |
synonymous_variant | LOW | c.3567T>C | p.Ile1189Ile | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/42 | 3726/5613 | 3567/5193 | 1189/1730 | chr10 | 113610495 | |||
chr10:113614201 | C | G | 1 | a0016c0052 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.3282G>C | p.Ala1094Ala | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/42 | 3441/5613 | 3282/5193 | 1094/1730 | chr10 | 113614201 | |||
chr10:113614911 | A | G | 14 | a0010c0008 a0015c0077 a0016c0020 others(11): Show |
38 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(35): Show |
synonymous_variant | LOW | c.3114T>C | p.Asp1038Asp | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 28/42 | 3273/5613 | 3114/5193 | 1038/1730 | chr10 | 113614911 | |||
chr10:113615769 | C | A | 29 | a0001c0001 a0001c0100 a0001c0102 others(26): Show |
107 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(104): Show |
synonymous_variant | LOW | c.3021G>T | p.Pro1007Pro | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 27/42 | 3180/5613 | 3021/5193 | 1007/1730 | chr10 | 113615769 | |||
chr10:113626050 | G | A | 2 | a0001c0099 a0001c0100 |
2 | NA19005.hp1 NA19087.hp1 |
synonymous_variant | LOW | c.2241C>T | p.Ser747Ser | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 21/42 | 2400/5613 | 2241/5193 | 747/1730 | chr10 | 113626050 | |||
chr10:113629597 | G | A | 27 | a0004c0004 a0004c0057 a0007c0006 others(24): Show |
91 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(88): Show |
synonymous_variant | LOW | c.2031C>T | p.Leu677Leu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/42 | 2190/5613 | 2031/5193 | 677/1730 | chr10 | 113629597 | |||
chr10:113633138 | G | T | 1 | a0006c0105 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.1578C>A | p.Pro526Pro | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/42 | 1737/5613 | 1578/5193 | 526/1730 | chr10 | 113633138 | |||
chr10:113633141 | C | T | 1 | a0006c0104 | 1 | HG01358.hp2 | synonymous_variant | LOW | c.1575G>A | p.Leu525Leu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/42 | 1734/5613 | 1575/5193 | 525/1730 | chr10 | 113633141 | |||
chr10:113634169 | C | T | 4 | a0022c0071 a0022c0072 a0022c0073 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
synonymous_variant | LOW | c.1470G>A | p.Ser490Ser | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/42 | 1629/5613 | 1470/5193 | 490/1730 | chr10 | 113634169 | |||
chr10:113640317 | A | G | 1 | a0018c0076 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.1338T>C | p.Ala446Ala | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/42 | 1497/5613 | 1338/5193 | 446/1730 | chr10 | 113640317 | |||
chr10:113646932 | G | A | 1 | a0001c0102 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.984C>T | p.Leu328Leu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/42 | 1143/5613 | 984/5193 | 328/1730 | chr10 | 113646932 | |||
chr10:113651839 | C | A | 31 | a0002c0002 a0002c0037 a0003c0003 others(28): Show |
113 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
synonymous_variant | LOW | c.639G>T | p.Leu213Leu | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/42 | 798/5613 | 639/5193 | 213/1730 | chr10 | 113651839 | |||
chr10:113651905 | C | T | 1 | a0002c0037 | 2 | HG04184.hp2 HG04228.hp1 |
splice_region_variant&synonymous_variant | LOW | c.573G>A | p.Val191Val | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/42 | 732/5613 | 573/5193 | 191/1730 | chr10 | 113651905 | |||
chr10:113653034 | A | G | 37 | a0002c0002 a0002c0037 a0003c0003 others(34): Show |
122 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
synonymous_variant | LOW | c.471T>C | p.Tyr157Tyr | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/42 | 630/5613 | 471/5193 | 157/1730 | chr10 | 113653034 | |||
chr10:113657530 | G | A | 103 | a0001c0001 a0001c0099 a0001c0100 others(100): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
synonymous_variant | LOW | c.300C>T | p.His100His | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/42 | 459/5613 | 300/5193 | 100/1730 | chr10 | 113657530 | |||
chr10:113662715 | A | G | 41 | a0004c0004 a0004c0057 a0007c0006 others(38): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
synonymous_variant | LOW | c.219T>C | p.Asn73Asn | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/42 | 378/5613 | 219/5193 | 73/1730 | chr10 | 113662715 | |||
chr10:113663363 | C | T | 1 | a0030c0048 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.156G>A | p.Pro52Pro | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 2/42 | 315/5613 | 156/5193 | 52/1730 | chr10 | 113663363 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:113588734 | A | G | 1 | a0008c0007t0009 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*241T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 42/42 | 241 | chr10 | 113588734 | ||||||
chr10:113588787 | C | T | 1 | a0005c0005t0011 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*188G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 42/42 | 188 | chr10 | 113588787 | ||||||
chr10:113588823 | C | A | 1 | a0021c0022t0012 | 1 | NA19090.hp1 | 3_prime_UTR_variant | MODIFIER | c.*152G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 42/42 | 152 | chr10 | 113588823 | ||||||
chr10:113588844 | T | C | 1 | a0001c0001t0013 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*131A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 42/42 | 131 | chr10 | 113588844 | ||||||
chr10:113588883 | C | T | 1 | a0002c0037t0007 | 2 | HG04184.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*92G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 42/42 | 92 | chr10 | 113588883 | ||||||
chr10:113588934 | A | G | 1 | a0006c0010t0014 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*41T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 42/42 | 41 | chr10 | 113588934 | ||||||
chr10:113588967 | GA | G | 50 | a0002c0002t0004 a0002c0037t0007 a0007c0006t0006 others(47): Show |
153 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*7delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 42/42 | 7 | chr10 | 113588967 | ||||||
chr10:113663891 | C | T | 1 | a0037c0036t0008 | 1 | HG01081.hp2 | 5_prime_UTR_variant | MODIFIER | c.-9G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 1/42 | 9 | chr10 | 113663891 | ||||||
chr10:113663936 | A | C | 18 | a0004c0004t0005 a0004c0057t0005 a0007c0006t0006 others(15): Show |
55 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(52): Show |
5_prime_UTR_variant | MODIFIER | c.-54T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 1/42 | 54 | chr10 | 113663936 | ||||||
chr10:113663988 | G | A | 33 | a0002c0002t0004 a0002c0037t0007 a0003c0003t0003 others(30): Show |
120 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(117): Show |
5_prime_UTR_variant | MODIFIER | c.-106C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 1/42 | 106 | chr10 | 113663988 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:113589157 | G | A | 34 | a0008c0007t0002g0070 a0008c0007t0002g0076 a0008c0007t0002g0081 others(31): Show |
37 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.5089-78C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 41/41 | chr10 | 113589157 | |||||||
chr10:113589238 | T | G | 1 | a0035c0086t0002g0113 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.5089-159A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 41/41 | chr10 | 113589238 | |||||||
chr10:113589357 | C | T | 1 | a0003c0003t0003g0338 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5089-278G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 41/41 | chr10 | 113589357 | |||||||
chr10:113589484 | C | A | 2 | a0004c0004t0005g0054 a0056c0058t0005g0053 |
2 | HG01943.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.5088+182G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 41/41 | chr10 | 113589484 | |||||||
chr10:113589528 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.5088+138G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 41/41 | chr10 | 113589528 | |||||||
chr10:113589529 | G | A | 3 | a0031c0032t0002g0228 a0031c0032t0002g0229 a0031c0061t0002g0264 |
3 | HG02976.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.5088+137C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 41/41 | chr10 | 113589529 | |||||||
chr10:113589638 | AG | A | 377 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(374): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.5088+27delC | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 41/41 | chr10 | 113589638 | |||||||
chr10:113589922 | A | C | 1 | a0022c0072t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4957-125T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113589922 | |||||||
chr10:113589932 | G | A | 3 | a0029c0028t0002g0230 a0029c0028t0002g0231 a0029c0028t0002g0232 |
3 | HG02559.hp2 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4957-135C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113589932 | |||||||
chr10:113589976 | A | C | 4 | a0016c0054t0005g0057 a0022c0072t0001g0268 a0062c0055t0005g0056 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.4957-179T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113589976 | |||||||
chr10:113590010 | T | G | 1 | a0001c0001t0001g0149 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.4957-213A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113590010 | |||||||
chr10:113590049 | G | T | 2 | a0008c0007t0002g0085 a0072c0080t0002g0089 |
2 | HG03654.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.4957-252C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113590049 | |||||||
chr10:113590174 | T | C | 3 | a0016c0020t0005g0023 a0016c0020t0005g0033 a0016c0052t0005g0032 |
3 | HG01099.hp2 HG01346.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.4957-377A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113590174 | |||||||
chr10:113590288 | C | G | 1 | a0062c0055t0005g0056 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4956+290G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113590288 | |||||||
chr10:113590341 | A | G | 122 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(119): Show |
125 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.4956+237T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113590341 | |||||||
chr10:113590384 | G | A | 9 | a0011c0016t0004g0276 a0011c0016t0004g0295 a0011c0016t0004g0297 others(6): Show |
9 | HG02145.hp1 HG02559.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.4956+194C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113590384 | |||||||
chr10:113590410 | AGTG | A | 3 | a0031c0032t0002g0228 a0031c0032t0002g0229 a0031c0061t0002g0264 |
3 | HG02976.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4956+165_4956+167d others(5): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113590410 | |||||||
chr10:113590540 | G | A | 1 | a0050c0050t0002g0237 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4956+38C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 40/41 | chr10 | 113590540 | |||||||
chr10:113590950 | C | T | 1 | a0015c0013t0002g0088 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4645-61G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113590950 | |||||||
chr10:113591030 | T | C | 4 | a0016c0054t0005g0057 a0022c0072t0001g0268 a0062c0055t0005g0056 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.4645-141A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591030 | |||||||
chr10:113591041 | T | C | 279 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(276): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.4645-152A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591041 | |||||||
chr10:113591047 | G | T | 4 | a0016c0054t0005g0057 a0022c0072t0001g0268 a0062c0055t0005g0056 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.4645-158C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591047 | |||||||
chr10:113591096 | T | C | 1 | a0080c0085t0003g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4645-207A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591096 | |||||||
chr10:113591117 | A | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0192 |
2 | HG00140.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.4645-228T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591117 | |||||||
chr10:113591170 | C | A | 96 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(93): Show |
98 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.4645-281G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591170 | |||||||
chr10:113591317 | A | T | 1 | a0023c0091t0001g0187 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4645-428T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591317 | |||||||
chr10:113591346 | T | C | 121 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(118): Show |
123 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.4645-457A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591346 | |||||||
chr10:113591667 | C | T | 4 | a0021c0022t0001g0255 a0021c0022t0001g0256 a0021c0022t0001g0260 others(1): Show |
4 | HG00597.hp1 NA18612.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.4644+527G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591667 | |||||||
chr10:113591740 | G | A | 1 | a0016c0020t0005g0023 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.4644+454C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591740 | |||||||
chr10:113591810 | A | G | 6 | a0016c0020t0005g0023 a0016c0020t0005g0024 a0016c0020t0005g0033 others(3): Show |
6 | HG01099.hp2 HG01346.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.4644+384T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591810 | |||||||
chr10:113591857 | T | G | 3 | a0029c0028t0002g0230 a0029c0028t0002g0231 a0029c0028t0002g0232 |
3 | HG02559.hp2 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4644+337A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591857 | |||||||
chr10:113591933 | T | G | 1 | a0080c0085t0003g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4644+261A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113591933 | |||||||
chr10:113592141 | A | G | 3 | a0031c0032t0002g0228 a0031c0032t0002g0229 a0031c0061t0002g0264 |
3 | HG02976.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4644+53T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113592141 | |||||||
chr10:113592169 | G | A | 1 | a0062c0055t0005g0056 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4644+25C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113592169 | |||||||
chr10:113592181 | A | G | 4 | a0016c0054t0005g0057 a0022c0072t0001g0268 a0062c0055t0005g0056 others(1): Show |
4 | HG02258.hp1 HG02451.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.4644+13T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 39/41 | chr10 | 113592181 | |||||||
chr10:113592398 | G | T | 1 | a0080c0085t0003g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4537-97C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113592398 | |||||||
chr10:113592408 | C | T | 39 | a0008c0007t0002g0070 a0008c0007t0002g0076 a0008c0007t0002g0081 others(36): Show |
43 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.4537-107G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113592408 | |||||||
chr10:113592428 | T | C | 1 | a0050c0050t0002g0237 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4537-127A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113592428 | |||||||
chr10:113592499 | C | T | 3 | a0007c0006t0006g0055 a0011c0016t0004g0296 a0011c0025t0002g0235 |
3 | HG03453.hp1 HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4537-198G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113592499 | |||||||
chr10:113592504 | C | T | 31 | a0001c0001t0001g0141 a0001c0099t0001g0153 a0003c0003t0003g0332 others(28): Show |
31 | HG01884.hp1 HG02055.hp2 HG02129.hp2 others(28): Show |
intron_variant | MODIFIER | c.4537-203G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113592504 | |||||||
chr10:113592704 | T | C | 7 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0001t0001g0189 others(4): Show |
7 | HG00099.hp1 HG00140.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.4537-403A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113592704 | |||||||
chr10:113592750 | C | T | 2 | a0016c0054t0005g0057 a0022c0072t0001g0268 |
2 | HG02451.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.4537-449G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113592750 | |||||||
chr10:113593202 | G | A | 1 | a0024c0024t0003g0325 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4537-901C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593202 | |||||||
chr10:113593213 | C | T | 2 | a0004c0004t0005g0054 a0056c0058t0005g0053 |
2 | HG01943.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.4537-912G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593213 | |||||||
chr10:113593214 | G | A | 118 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(115): Show |
120 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.4537-913C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593214 | |||||||
chr10:113593254 | G | A | 1 | a0018c0015t0001g0092 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.4537-953C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593254 | |||||||
chr10:113593493 | C | T | 100 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(97): Show |
102 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.4537-1192G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593493 | |||||||
chr10:113593552 | C | T | 22 | a0001c0001t0001g0141 a0001c0099t0001g0153 a0003c0003t0003g0332 others(19): Show |
22 | HG02129.hp2 HG02165.hp1 HG02523.hp2 others(19): Show |
intron_variant | MODIFIER | c.4537-1251G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593552 | |||||||
chr10:113593563 | G | T | 4 | a0003c0003t0003g0304 a0003c0003t0003g0363 a0003c0003t0003g0364 others(1): Show |
4 | NA18971.hp1 NA19004.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.4537-1262C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593563 | |||||||
chr10:113593773 | G | A | 79 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(76): Show |
80 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.4537-1472C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593773 | |||||||
chr10:113593828 | G | C | 1 | a0063c0113t0004g0273 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4537-1527C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593828 | |||||||
chr10:113593942 | G | A | 48 | a0008c0007t0002g0070 a0008c0007t0002g0076 a0008c0007t0002g0081 others(45): Show |
51 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.4537-1641C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593942 | |||||||
chr10:113593979 | G | A | 8 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0241 others(5): Show |
8 | HG00735.hp2 HG01070.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.4536+1644C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593979 | |||||||
chr10:113593988 | C | T | 1 | a0018c0076t0001g0101 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4536+1635G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113593988 | |||||||
chr10:113594085 | C | T | 1 | a0041c0068t0005g0058 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4536+1538G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113594085 | |||||||
chr10:113594147 | A | G | 2 | a0042c0047t0003g0274 a0042c0047t0003g0275 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4536+1476T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113594147 | |||||||
chr10:113594185 | C | T | 1 | a0040c0038t0003g0341 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4536+1438G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113594185 | |||||||
chr10:113594270 | T | C | 1 | a0008c0007t0002g0091 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.4536+1353A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113594270 | |||||||
chr10:113594343 | C | G | 1 | a0071c0103t0003g0353 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4536+1280G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113594343 | |||||||
chr10:113594485 | C | T | 1 | a0003c0003t0003g0363 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.4536+1138G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113594485 | |||||||
chr10:113594500 | C | T | 1 | a0005c0005t0001g0108 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4536+1123G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113594500 | |||||||
chr10:113594813 | C | T | 24 | a0006c0010t0003g0313 a0006c0010t0003g0315 a0006c0010t0003g0374 others(21): Show |
28 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.4536+810G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113594813 | |||||||
chr10:113594903 | G | T | 1 | a0016c0020t0005g0023 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.4536+720C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113594903 | |||||||
chr10:113595119 | C | T | 1 | a0008c0007t0002g0085 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4536+504G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113595119 | |||||||
chr10:113595158 | G | A | 1 | a0065c0087t0001g0105 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4536+465C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113595158 | |||||||
chr10:113595187 | T | C | 1 | a0072c0080t0002g0089 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4536+436A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113595187 | |||||||
chr10:113595284 | G | C | 1 | a0005c0005t0001g0111 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4536+339C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113595284 | |||||||
chr10:113595365 | T | A | 1 | a0072c0080t0002g0089 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4536+258A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113595365 | |||||||
chr10:113595412 | G | GC | 273 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(270): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.4536+210dupG | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113595412 | |||||||
chr10:113595436 | A | G | 40 | a0001c0001t0001g0138 a0001c0001t0001g0141 a0001c0001t0001g0150 others(37): Show |
41 | HG01884.hp1 HG01981.hp2 HG02004.hp2 others(38): Show |
intron_variant | MODIFIER | c.4536+187T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113595436 | |||||||
chr10:113595544 | T | A | 1 | a0062c0055t0005g0056 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4536+79A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113595544 | |||||||
chr10:113595566 | G | T | 3 | a0031c0032t0002g0228 a0031c0032t0002g0229 a0031c0061t0002g0264 |
3 | HG02976.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4536+57C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113595566 | |||||||
chr10:113595569 | A | G | 18 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(15): Show |
18 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.4536+54T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 38/41 | chr10 | 113595569 | |||||||
chr10:113595901 | C | A | 1 | a0027c0034t0002g0236 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4432-174G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113595901 | |||||||
chr10:113595991 | A | G | 1 | a0006c0010t0003g0315 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4432-264T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113595991 | |||||||
chr10:113596148 | T | C | 1 | a0005c0021t0001g0119 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.4432-421A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113596148 | |||||||
chr10:113596165 | C | A | 1 | a0006c0105t0003g0343 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4432-438G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113596165 | |||||||
chr10:113596407 | C | T | 5 | a0001c0001t0001g0152 a0001c0001t0001g0205 a0001c0001t0001g0207 others(2): Show |
5 | HG01928.hp2 HG01943.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.4431+679G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113596407 | |||||||
chr10:113596595 | T | C | 2 | a0011c0016t0004g0276 a0011c0016t0004g0295 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.4431+491A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113596595 | |||||||
chr10:113596705 | C | G | 7 | a0011c0039t0004g0339 a0011c0039t0004g0340 a0016c0054t0005g0057 others(4): Show |
7 | HG01891.hp1 HG02451.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.4431+381G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113596705 | |||||||
chr10:113596829 | T | A | 1 | a0005c0005t0001g0118 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.4431+257A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113596829 | |||||||
chr10:113596917 | A | C | 8 | a0002c0002t0004g0333 a0002c0002t0004g0334 a0015c0013t0002g0088 others(5): Show |
8 | HG01891.hp2 HG02486.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.4431+169T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113596917 | |||||||
chr10:113596930 | T | C | 8 | a0011c0039t0004g0339 a0011c0039t0004g0340 a0016c0054t0005g0057 others(5): Show |
8 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.4431+156A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113596930 | |||||||
chr10:113596988 | T | G | 1 | a0022c0114t0004g0272 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4431+98A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 37/41 | chr10 | 113596988 | |||||||
chr10:113597287 | T | C | 1 | a0002c0002t0004g0342 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4333-103A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/41 | chr10 | 113597287 | |||||||
chr10:113597319 | G | A | 114 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(111): Show |
115 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.4333-135C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/41 | chr10 | 113597319 | |||||||
chr10:113597367 | T | C | 1 | a0018c0015t0001g0072 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4333-183A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/41 | chr10 | 113597367 | |||||||
chr10:113597372 | CA | C | 114 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(111): Show |
115 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.4333-189delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/41 | chr10 | 113597372 | |||||||
chr10:113597420 | C | T | 114 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(111): Show |
115 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.4333-236G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/41 | chr10 | 113597420 | |||||||
chr10:113597563 | C | A | 1 | a0002c0002t0004g0321 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4333-379G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/41 | chr10 | 113597563 | |||||||
chr10:113597705 | A | G | 1 | a0040c0038t0003g0341 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4332+264T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/41 | chr10 | 113597705 | |||||||
chr10:113597732 | A | G | 8 | a0011c0039t0004g0339 a0011c0039t0004g0340 a0016c0054t0005g0057 others(5): Show |
8 | HG01891.hp1 HG02258.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.4332+237T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/41 | chr10 | 113597732 | |||||||
chr10:113597815 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4332+154C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/41 | chr10 | 113597815 | |||||||
chr10:113597928 | G | T | 7 | a0001c0001t0001g0148 a0005c0021t0001g0119 a0005c0021t0001g0130 others(4): Show |
7 | HG02040.hp2 HG02056.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.4332+41C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 36/41 | chr10 | 113597928 | |||||||
chr10:113598217 | T | C | 1 | a0027c0034t0002g0236 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4228-144A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113598217 | |||||||
chr10:113598325 | G | A | 1 | a0022c0114t0004g0272 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4228-252C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113598325 | |||||||
chr10:113598338 | T | C | 3 | a0011c0016t0004g0276 a0011c0016t0004g0295 a0011c0016t0004g0297 |
3 | HG02145.hp1 HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4228-265A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113598338 | |||||||
chr10:113598483 | CT | C | 274 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(271): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.4228-411delA | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113598483 | |||||||
chr10:113598725 | C | T | 1 | a0072c0080t0002g0089 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4228-652G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113598725 | |||||||
chr10:113598769 | C | T | 3 | a0010c0008t0002g0238 a0039c0042t0002g0160 a0055c0089t0002g0110 |
3 | HG00735.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.4228-696G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113598769 | |||||||
chr10:113598817 | T | C | 2 | a0036c0045t0004g0317 a0036c0045t0004g0327 |
2 | HG00609.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.4228-744A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113598817 | |||||||
chr10:113599036 | C | T | 1 | a0063c0113t0004g0273 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4228-963G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113599036 | |||||||
chr10:113599061 | C | G | 62 | a0008c0007t0002g0070 a0008c0007t0002g0076 a0008c0007t0002g0081 others(59): Show |
66 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.4228-988G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113599061 | |||||||
chr10:113599138 | G | A | 1 | a0006c0010t0003g0313 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.4228-1065C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113599138 | |||||||
chr10:113599163 | C | T | 1 | a0005c0005t0011g0125 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4228-1090G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113599163 | |||||||
chr10:113599376 | T | G | 2 | a0022c0073t0001g0269 a0050c0050t0002g0237 |
2 | HG01109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4228-1303A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113599376 | |||||||
chr10:113599778 | CGAA | C | 3 | a0030c0033t0001g0061 a0030c0033t0001g0062 a0030c0048t0001g0060 |
3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4228-1708_4228-170 others(7): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113599778 | |||||||
chr10:113599806 | C | T | 1 | a0013c0019t0002g0109 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.4228-1733G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113599806 | |||||||
chr10:113599807 | CT | C | 35 | a0001c0001t0001g0141 a0001c0099t0001g0153 a0003c0003t0003g0332 others(32): Show |
35 | HG01884.hp1 HG02055.hp2 HG02129.hp2 others(32): Show |
intron_variant | MODIFIER | c.4228-1735delA | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113599807 | |||||||
chr10:113599858 | T | C | 1 | a0061c0070t0001g0243 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4228-1785A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113599858 | |||||||
chr10:113599898 | G | C | 1 | a0016c0020t0005g0034 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4228-1825C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113599898 | |||||||
chr10:113600155 | T | TTC | 40 | a0001c0001t0001g0136 a0001c0001t0001g0146 a0001c0001t0001g0168 others(37): Show |
41 | HG00597.hp1 HG01081.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.4228-2084_4228-208 others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | |||||||
chr10:113600155 | T | TTCTC | 74 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(71): Show |
76 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.4228-2086_4228-208 others(8): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | |||||||
chr10:113600155 | T | TTCTCTC | 14 | a0002c0002t0004g0335 a0006c0010t0003g0310 a0006c0104t0003g0351 others(11): Show |
14 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.4228-2088_4228-208 others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | |||||||
chr10:113600155 | T | TTCTCTCT others(1): Show |
3 | a0011c0039t0004g0339 a0011c0039t0004g0340 a0022c0073t0001g0269 |
3 | HG02895.hp2 HG02897.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4228-2090_4228-208 others(12): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | |||||||
chr10:113600155 | T | TTCTCTCT others(3): Show |
14 | a0001c0001t0001g0205 a0006c0010t0003g0313 a0009c0009t0001g0002 others(11): Show |
16 | HG00642.hp1 HG01069.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.4228-2092_4228-208 others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | |||||||
chr10:113600155 | T | TTCTCTCT others(5): Show |
8 | a0006c0010t0003g0315 a0006c0010t0003g0352 a0010c0008t0002g0239 others(5): Show |
8 | HG00280.hp1 HG00738.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.4228-2094_4228-208 others(16): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | |||||||
chr10:113600155 | T | TTCTCTCT others(7): Show |
13 | a0006c0010t0003g0374 a0006c0105t0003g0343 a0010c0008t0002g0246 others(10): Show |
14 | HG00280.hp2 HG00738.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.4228-2096_4228-208 others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | |||||||
chr10:113600155 | T | TTCTCTCT others(9): Show |
4 | a0010c0008t0002g0240 a0010c0008t0002g0254 a0012c0011t0003g0010 others(1): Show |
5 | HG00642.hp2 HG01192.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.4228-2098_4228-208 others(20): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | |||||||
chr10:113600155 | T | TTCTCTCT others(11): Show |
2 | a0058c0053t0005g0041 a0071c0103t0003g0353 |
2 | HG01978.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.4228-2100_4228-208 others(22): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | |||||||
chr10:113600155 | T | TTCTCTCT others(13): Show |
4 | a0006c0010t0003g0345 a0006c0010t0003g0350 a0009c0009t0001g0079 others(1): Show |
4 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.4228-2102_4228-208 others(24): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | |||||||
chr10:113600155 | T | TTCTCTCT others(17): Show |
1 | a0006c0010t0003g0349 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4228-2106_4228-208 others(28): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | |||||||
chr10:113600155 | T | TTCTCTCT others(19): Show |
1 | a0006c0010t0014g0347 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4228-2108_4228-208 others(30): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | |||||||
chr10:113600155 | TTCTC | T | 8 | a0005c0005t0001g0104 a0005c0005t0001g0106 a0005c0005t0001g0161 others(5): Show |
8 | HG02572.hp1 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.4228-2086_4228-208 others(8): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | |||||||
chr10:113600155 | TTCTCTC | T | 110 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(107): Show |
117 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.4228-2088_4228-208 others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | |||||||
chr10:113600155 | TTCTCTCT others(3): Show |
T | 1 | a0052c0095t0001g0213 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4228-2092_4228-208 others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600155 | |||||||
chr10:113600159 | C | CTCTCTCT others(3): Show |
1 | a0010c0008t0002g0238 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4228-2087_4228-208 others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600159 | |||||||
chr10:113600338 | A | AT | 114 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(111): Show |
121 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.4228-2266dupA | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600338 | |||||||
chr10:113600378 | C | G | 1 | a0080c0085t0003g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4228-2305G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600378 | |||||||
chr10:113600380 | A | T | 8 | a0011c0039t0004g0339 a0011c0039t0004g0340 a0016c0054t0005g0057 others(5): Show |
8 | HG01109.hp2 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.4228-2307T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600380 | |||||||
chr10:113600607 | G | C | 1 | a0051c0111t0004g0381 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.4228-2534C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600607 | |||||||
chr10:113600784 | C | T | 1 | a0005c0005t0001g0106 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4228-2711G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600784 | |||||||
chr10:113600928 | A | G | 218 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(215): Show |
226 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.4228-2855T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113600928 | |||||||
chr10:113601037 | A | G | 218 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(215): Show |
226 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.4228-2964T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113601037 | |||||||
chr10:113601196 | C | T | 1 | a0031c0032t0002g0228 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4228-3123G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113601196 | |||||||
chr10:113601266 | T | C | 1 | a0018c0015t0001g0072 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4228-3193A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113601266 | |||||||
chr10:113601301 | A | G | 218 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(215): Show |
226 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.4228-3228T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113601301 | |||||||
chr10:113601302 | G | C | 3 | a0030c0033t0001g0061 a0030c0033t0001g0062 a0030c0048t0001g0060 |
3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4228-3229C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113601302 | |||||||
chr10:113601558 | G | A | 320 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(317): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.4227+3051C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113601558 | |||||||
chr10:113601606 | G | A | 1 | a0011c0016t0004g0292 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4227+3003C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113601606 | |||||||
chr10:113601846 | TG | T | 81 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(78): Show |
84 | HG00438.hp1 HG00639.hp2 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.4227+2762delC | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113601846 | |||||||
chr10:113601935 | A | C | 1 | a0007c0006t0006g0026 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4227+2674T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113601935 | |||||||
chr10:113602006 | C | T | 2 | a0004c0004t0005g0016 a0079c0051t0005g0017 |
2 | HG00733.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.4227+2603G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113602006 | |||||||
chr10:113602042 | C | T | 1 | a0062c0055t0005g0056 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4227+2567G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113602042 | |||||||
chr10:113602092 | A | G | 320 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(317): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.4227+2517T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113602092 | |||||||
chr10:113602331 | G | A | 1 | a0002c0002t0004g0342 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4227+2278C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113602331 | |||||||
chr10:113602427 | G | A | 2 | a0042c0047t0003g0274 a0042c0047t0003g0275 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4227+2182C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113602427 | |||||||
chr10:113602637 | A | T | 1 | a0008c0007t0009g0084 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4227+1972T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113602637 | |||||||
chr10:113602831 | T | C | 1 | a0080c0085t0003g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4227+1778A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113602831 | |||||||
chr10:113603037 | C | T | 1 | a0020c0018t0001g0112 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4227+1572G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603037 | |||||||
chr10:113603319 | A | G | 84 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(81): Show |
85 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.4227+1290T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603319 | |||||||
chr10:113603369 | T | G | 1 | a0022c0072t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4227+1240A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603369 | |||||||
chr10:113603432 | C | G | 1 | a0040c0038t0003g0341 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4227+1177G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603432 | |||||||
chr10:113603432 | C | T | 3 | a0029c0028t0002g0230 a0029c0028t0002g0231 a0029c0028t0002g0232 |
3 | HG02559.hp2 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4227+1177G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603432 | |||||||
chr10:113603504 | C | T | 14 | a0011c0016t0004g0276 a0011c0016t0004g0295 a0011c0016t0004g0297 others(11): Show |
14 | HG01109.hp2 HG01891.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.4227+1105G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603504 | |||||||
chr10:113603585 | G | A | 81 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(78): Show |
83 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.4227+1024C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603585 | |||||||
chr10:113603620 | G | A | 198 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(195): Show |
206 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.4227+989C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603620 | |||||||
chr10:113603785 | G | C | 1 | a0001c0099t0001g0153 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4227+824C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603785 | |||||||
chr10:113603809 | C | T | 14 | a0011c0016t0004g0276 a0011c0016t0004g0295 a0011c0016t0004g0297 others(11): Show |
14 | HG01109.hp2 HG01891.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.4227+800G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603809 | |||||||
chr10:113603890 | A | G | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
225 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.4227+719T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603890 | |||||||
chr10:113603905 | C | T | 99 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(96): Show |
103 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.4227+704G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113603905 | |||||||
chr10:113604122 | C | T | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
225 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.4227+487G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113604122 | |||||||
chr10:113604177 | C | G | 1 | a0063c0113t0004g0273 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4227+432G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113604177 | |||||||
chr10:113604179 | C | T | 1 | a0005c0005t0011g0125 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4227+430G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113604179 | |||||||
chr10:113604358 | G | A | 2 | a0042c0047t0003g0274 a0042c0047t0003g0275 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4227+251C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113604358 | |||||||
chr10:113604549 | C | T | 1 | a0005c0021t0001g0130 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4227+60G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 35/41 | chr10 | 113604549 | |||||||
chr10:113604959 | G | A | 1 | a0014c0012t0004g0288 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3916-39C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 34/41 | chr10 | 113604959 | |||||||
chr10:113604993 | C | T | 1 | a0016c0020t0005g0023 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3916-73G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 34/41 | chr10 | 113604993 | |||||||
chr10:113605039 | G | A | 2 | a0002c0037t0007g0354 a0002c0037t0007g0355 |
2 | HG04184.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3916-119C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 34/41 | chr10 | 113605039 | |||||||
chr10:113605381 | C | T | 1 | a0064c0059t0005g0048 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3915+381G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 34/41 | chr10 | 113605381 | |||||||
chr10:113605577 | T | G | 1 | a0002c0002t0004g0342 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3915+185A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 34/41 | chr10 | 113605577 | |||||||
chr10:113605905 | A | C | 3 | a0004c0004t0005g0019 a0004c0004t0005g0042 a0004c0004t0005g0051 |
3 | NA18952.hp1 NA18974.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.3808-36T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 33/41 | chr10 | 113605905 | |||||||
chr10:113605927 | G | C | 1 | a0006c0104t0003g0351 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3808-58C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 33/41 | chr10 | 113605927 | |||||||
chr10:113605951 | A | G | 1 | a0013c0019t0002g0174 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.3808-82T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 33/41 | chr10 | 113605951 | |||||||
chr10:113605968 | T | C | 5 | a0002c0002t0004g0360 a0011c0025t0006g0021 a0011c0025t0006g0022 others(2): Show |
5 | HG02129.hp1 NA18983.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.3808-99A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 33/41 | chr10 | 113605968 | |||||||
chr10:113606755 | A | C | 1 | a0001c0001t0001g0189 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3703-473T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113606755 | |||||||
chr10:113606850 | C | G | 219 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(216): Show |
227 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.3703-568G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113606850 | |||||||
chr10:113606894 | C | T | 1 | a0063c0113t0004g0273 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3703-612G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113606894 | |||||||
chr10:113606928 | C | T | 6 | a0004c0004t0005g0054 a0029c0028t0002g0230 a0029c0028t0002g0231 others(3): Show |
6 | HG01943.hp1 HG02135.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3703-646G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113606928 | |||||||
chr10:113607134 | G | A | 3 | a0031c0032t0002g0228 a0031c0032t0002g0229 a0031c0061t0002g0264 |
3 | HG02976.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3703-852C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607134 | |||||||
chr10:113607199 | T | TCAAA | 66 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(63): Show |
70 | HG00438.hp1 HG00639.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.3703-921_3703-918d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607199 | |||||||
chr10:113607199 | TCAAACAA others(1): Show |
T | 23 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(20): Show |
23 | HG00438.hp2 HG01981.hp2 HG02004.hp2 others(20): Show |
intron_variant | MODIFIER | c.3703-925_3703-918d others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607199 | |||||||
chr10:113607201 | A | T | 1 | a0015c0013t0002g0074 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3703-919T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607201 | |||||||
chr10:113607243 | C | CA | 44 | a0008c0007t0002g0070 a0008c0007t0002g0076 a0008c0007t0002g0082 others(41): Show |
47 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.3703-962dupT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607243 | |||||||
chr10:113607373 | G | A | 1 | a0022c0071t0002g0267 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3702+1041C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607373 | |||||||
chr10:113607388 | C | T | 82 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(79): Show |
85 | HG00438.hp1 HG00639.hp2 HG00733.hp2 others(82): Show |
intron_variant | MODIFIER | c.3702+1026G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607388 | |||||||
chr10:113607396 | C | T | 2 | a0016c0054t0005g0057 a0022c0072t0001g0268 |
2 | HG02451.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.3702+1018G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607396 | |||||||
chr10:113607399 | C | CA | 15 | a0006c0010t0003g0313 a0006c0010t0003g0315 a0006c0010t0003g0348 others(12): Show |
16 | HG00280.hp1 HG00280.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.3702+1014dupT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | |||||||
chr10:113607399 | C | CAA | 6 | a0006c0010t0003g0350 a0006c0104t0003g0351 a0006c0105t0003g0343 others(3): Show |
8 | HG00642.hp1 HG01106.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.3702+1013_3702+101 others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | |||||||
chr10:113607399 | C | CAAAAAAA others(3): Show |
5 | a0009c0079t0001g0071 a0016c0020t0005g0024 a0023c0030t0001g0173 others(2): Show |
5 | HG02886.hp1 HG03239.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.3702+1005_3702+101 others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | |||||||
chr10:113607399 | C | CAAAAAAA others(4): Show |
2 | a0016c0020t0005g0023 a0016c0020t0005g0034 |
2 | HG01099.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.3702+1004_3702+101 others(15): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | |||||||
chr10:113607399 | C | CAAAAAAA others(6): Show |
2 | a0016c0020t0005g0033 a0041c0068t0005g0058 |
2 | HG01346.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3702+1002_3702+101 others(17): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | |||||||
chr10:113607399 | C | CAAAAAAA others(8): Show |
1 | a0066c0074t0001g0266 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3702+1000_3702+101 others(19): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | |||||||
chr10:113607399 | CAAAAAAA | C | 13 | a0006c0010t0003g0310 a0007c0006t0006g0027 a0010c0008t0002g0240 others(10): Show |
13 | HG00642.hp2 HG00738.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.3702+1008_3702+101 others(11): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | |||||||
chr10:113607399 | CAAAAAAA others(1): Show |
C | 14 | a0002c0002t0004g0358 a0007c0006t0006g0004 a0007c0006t0006g0020 others(11): Show |
15 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.3702+1007_3702+101 others(12): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | |||||||
chr10:113607399 | CAAAAAAA others(2): Show |
C | 60 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(57): Show |
61 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.3702+1006_3702+101 others(13): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | |||||||
chr10:113607399 | CAAAAAAA others(3): Show |
C | 7 | a0002c0002t0004g0302 a0002c0002t0004g0321 a0002c0002t0004g0368 others(4): Show |
7 | HG00140.hp2 HG02896.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.3702+1005_3702+101 others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | |||||||
chr10:113607399 | CAAAAAAA others(4): Show |
C | 1 | a0003c0003t0003g0332 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3702+1004_3702+101 others(15): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | |||||||
chr10:113607399 | CAAAAAAA others(5): Show |
C | 23 | a0003c0003t0003g0382 a0004c0004t0005g0016 a0005c0005t0001g0104 others(20): Show |
23 | HG00558.hp2 HG00733.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.3702+1003_3702+101 others(16): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | |||||||
chr10:113607399 | CAAAAAAA others(6): Show |
C | 91 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(88): Show |
98 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.3702+1002_3702+101 others(17): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | |||||||
chr10:113607399 | CAAAAAAA others(7): Show |
C | 6 | a0003c0003t0003g0326 a0008c0007t0002g0081 a0011c0016t0004g0297 others(3): Show |
6 | HG01123.hp2 HG01943.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.3702+1001_3702+101 others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | |||||||
chr10:113607399 | CAAAAAAA others(8): Show |
C | 14 | a0011c0016t0004g0276 a0011c0016t0004g0295 a0011c0039t0004g0340 others(11): Show |
14 | HG01109.hp2 HG01891.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.3702+1000_3702+101 others(19): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | |||||||
chr10:113607399 | CAAAAAAA others(9): Show |
C | 5 | a0005c0021t0001g0119 a0011c0039t0004g0339 a0024c0024t0003g0324 others(2): Show |
5 | HG02040.hp2 HG02083.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.3702+999_3702+1014 others(19): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | |||||||
chr10:113607399 | CAAAAAAA others(10): Show |
C | 15 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0001g0168 others(12): Show |
16 | HG00639.hp1 HG02027.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.3702+998_3702+1014 others(20): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | |||||||
chr10:113607399 | CAAAAAAA others(11): Show |
C | 62 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(59): Show |
62 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.3702+997_3702+1014 others(21): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | |||||||
chr10:113607399 | CAAAAAAA others(12): Show |
C | 4 | a0010c0008t0002g0239 a0037c0036t0002g0265 a0037c0036t0008g0059 others(1): Show |
4 | HG01081.hp2 HG02258.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.3702+996_3702+1014 others(22): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | |||||||
chr10:113607399 | CAAAAAAA others(17): Show |
C | 3 | a0030c0033t0001g0061 a0030c0033t0001g0062 a0030c0048t0001g0060 |
3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3702+991_3702+1014 others(27): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607399 | |||||||
chr10:113607414 | A | C | 2 | a0011c0016t0004g0297 a0022c0073t0001g0269 |
2 | HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3702+1000T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607414 | |||||||
chr10:113607415 | A | C | 12 | a0011c0016t0004g0276 a0011c0016t0004g0295 a0011c0039t0004g0340 others(9): Show |
12 | HG01109.hp2 HG01891.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.3702+999T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607415 | |||||||
chr10:113607416 | A | C | 1 | a0011c0039t0004g0339 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3702+998T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607416 | |||||||
chr10:113607419 | AAAAAAAA others(11): Show |
A | 1 | a0069c0062t0006g0050 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3702+977_3702+994d others(20): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607419 | |||||||
chr10:113607424 | A | C | 3 | a0030c0033t0001g0061 a0030c0033t0001g0062 a0030c0048t0001g0060 |
3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3702+990T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607424 | |||||||
chr10:113607432 | A | G | 2 | a0031c0032t0002g0228 a0031c0032t0002g0229 |
2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3702+982T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607432 | |||||||
chr10:113607433 | A | G | 8 | a0015c0013t0002g0063 a0015c0013t0002g0088 a0015c0013t0002g0100 others(5): Show |
8 | HG02451.hp1 HG02486.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.3702+981T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607433 | |||||||
chr10:113607437 | G | A | 1 | a0015c0013t0002g0063 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.3702+977C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607437 | |||||||
chr10:113607438 | A | G | 1 | a0015c0013t0002g0063 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.3702+976T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607438 | |||||||
chr10:113607624 | A | T | 219 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(216): Show |
227 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.3702+790T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113607624 | |||||||
chr10:113608054 | T | A | 1 | a0069c0062t0006g0050 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3702+360A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113608054 | |||||||
chr10:113608213 | A | C | 1 | a0002c0002t0004g0367 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.3702+201T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113608213 | |||||||
chr10:113608304 | A | C | 1 | a0024c0024t0003g0318 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3702+110T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 32/41 | chr10 | 113608304 | |||||||
chr10:113608542 | C | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0221 |
2 | NA19087.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3604-30G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113608542 | |||||||
chr10:113608575 | C | T | 1 | a0001c0100t0001g0179 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.3604-63G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113608575 | |||||||
chr10:113608761 | G | A | 1 | a0063c0113t0004g0273 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3604-249C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113608761 | |||||||
chr10:113608987 | T | C | 1 | a0005c0021t0001g0119 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3604-475A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113608987 | |||||||
chr10:113609043 | C | T | 3 | a0031c0032t0002g0228 a0031c0032t0002g0229 a0031c0061t0002g0264 |
3 | HG02976.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3604-531G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113609043 | |||||||
chr10:113609114 | C | T | 1 | a0027c0063t0002g0227 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3604-602G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113609114 | |||||||
chr10:113609328 | T | A | 3 | a0031c0032t0002g0228 a0031c0032t0002g0229 a0031c0061t0002g0264 |
3 | HG02976.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3604-816A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113609328 | |||||||
chr10:113609335 | G | C | 16 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(13): Show |
16 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.3604-823C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113609335 | |||||||
chr10:113609479 | A | G | 34 | a0008c0007t0002g0070 a0008c0007t0002g0076 a0008c0007t0002g0081 others(31): Show |
38 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.3604-967T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113609479 | |||||||
chr10:113609544 | T | C | 2 | a0031c0032t0002g0228 a0031c0032t0002g0229 |
2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3603+915A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113609544 | |||||||
chr10:113609966 | GA | G | 33 | a0002c0002t0004g0305 a0008c0007t0002g0070 a0008c0007t0002g0076 others(30): Show |
36 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.3603+492delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113609966 | |||||||
chr10:113610042 | C | T | 1 | a0013c0019t0002g0109 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.3603+417G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113610042 | |||||||
chr10:113610069 | G | A | 1 | a0015c0077t0002g0066 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3603+390C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113610069 | |||||||
chr10:113610162 | C | A | 68 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(65): Show |
72 | HG00438.hp1 HG00639.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.3603+297G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113610162 | |||||||
chr10:113610176 | C | A | 1 | a0008c0007t0009g0084 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3603+283G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113610176 | |||||||
chr10:113610252 | AG | A | 32 | a0008c0007t0002g0070 a0008c0007t0002g0076 a0008c0007t0002g0081 others(29): Show |
35 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.3603+206delC | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113610252 | |||||||
chr10:113610265 | G | A | 2 | a0003c0003t0003g0375 a0006c0010t0003g0310 |
2 | HG02896.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.3603+194C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113610265 | |||||||
chr10:113610282 | G | A | 1 | a0020c0018t0001g0165 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3603+177C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113610282 | |||||||
chr10:113610354 | T | TA | 34 | a0002c0002t0004g0305 a0008c0007t0002g0070 a0008c0007t0002g0076 others(31): Show |
37 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.3603+104dupT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113610354 | |||||||
chr10:113610354 | TA | T | 28 | a0001c0001t0001g0133 a0001c0001t0001g0177 a0001c0001t0001g0182 others(25): Show |
28 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.3603+104delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 31/41 | chr10 | 113610354 | |||||||
chr10:113610825 | G | A | 1 | a0003c0003t0003g0375 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3499-262C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113610825 | |||||||
chr10:113611026 | G | A | 1 | a0068c0090t0001g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3499-463C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113611026 | |||||||
chr10:113611216 | G | A | 1 | a0020c0018t0001g0112 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3499-653C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113611216 | |||||||
chr10:113611231 | C | G | 7 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0001t0001g0189 others(4): Show |
7 | HG00099.hp1 HG00140.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.3499-668G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113611231 | |||||||
chr10:113611260 | G | A | 4 | a0003c0003t0003g0338 a0018c0015t0001g0077 a0018c0015t0001g0102 others(1): Show |
4 | HG02055.hp2 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.3499-697C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113611260 | |||||||
chr10:113611355 | T | C | 2 | a0039c0042t0002g0160 a0055c0089t0002g0110 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3499-792A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113611355 | |||||||
chr10:113611378 | G | A | 1 | a0058c0053t0005g0041 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3499-815C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113611378 | |||||||
chr10:113611521 | G | T | 1 | a0031c0061t0002g0264 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3498+713C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113611521 | |||||||
chr10:113611676 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.3498+558C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113611676 | |||||||
chr10:113611736 | G | A | 1 | a0005c0005t0001g0108 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3498+498C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113611736 | |||||||
chr10:113611799 | A | T | 1 | a0015c0077t0002g0066 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3498+435T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113611799 | |||||||
chr10:113612062 | G | A | 2 | a0042c0047t0003g0274 a0042c0047t0003g0275 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3498+172C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113612062 | |||||||
chr10:113612096 | GA | G | 3 | a0031c0032t0002g0228 a0031c0032t0002g0229 a0031c0061t0002g0264 |
3 | HG02976.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3498+137delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113612096 | |||||||
chr10:113612114 | G | T | 84 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(81): Show |
85 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.3498+120C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 30/41 | chr10 | 113612114 | |||||||
chr10:113612651 | T | C | 1 | a0003c0003t0003g0338 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3301-220A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113612651 | |||||||
chr10:113612697 | A | G | 1 | a0077c0109t0003g0309 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3301-266T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113612697 | |||||||
chr10:113612700 | G | A | 1 | a0006c0010t0003g0313 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.3301-269C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113612700 | |||||||
chr10:113612776 | C | T | 1 | a0013c0019t0002g0222 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3301-345G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113612776 | |||||||
chr10:113612806 | G | A | 1 | a0063c0113t0004g0273 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3301-375C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113612806 | |||||||
chr10:113612811 | C | T | 17 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(14): Show |
17 | HG00323.hp1 HG00642.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.3301-380G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113612811 | |||||||
chr10:113612826 | G | A | 95 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(92): Show |
96 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.3301-395C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113612826 | |||||||
chr10:113612841 | C | T | 1 | a0002c0002t0004g0330 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3301-410G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113612841 | |||||||
chr10:113612911 | G | C | 3 | a0030c0033t0001g0061 a0030c0033t0001g0062 a0030c0048t0001g0060 |
3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3301-480C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113612911 | |||||||
chr10:113613518 | C | T | 39 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(36): Show |
39 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.3300+665G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113613518 | |||||||
chr10:113613640 | C | G | 2 | a0011c0016t0004g0276 a0011c0016t0004g0295 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3300+543G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113613640 | |||||||
chr10:113613666 | G | T | 1 | a0012c0011t0003g0290 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3300+517C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113613666 | |||||||
chr10:113613773 | T | A | 1 | a0003c0003t0003g0311 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3300+410A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113613773 | |||||||
chr10:113613851 | T | C | 1 | a0002c0002t0004g0368 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3300+332A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113613851 | |||||||
chr10:113613874 | C | T | 2 | a0012c0011t0003g0280 a0020c0018t0001g0129 |
2 | HG02698.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.3300+309G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113613874 | |||||||
chr10:113613921 | A | C | 140 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(137): Show |
151 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.3300+262T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113613921 | |||||||
chr10:113613999 | C | T | 31 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(28): Show |
31 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.3300+184G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113613999 | |||||||
chr10:113614062 | G | A | 8 | a0001c0001t0001g0146 a0001c0001t0001g0168 a0001c0001t0001g0169 others(5): Show |
8 | HG02027.hp1 NA18939.hp2 NA18994.hp2 others(5): Show |
intron_variant | MODIFIER | c.3300+121C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113614062 | |||||||
chr10:113614092 | T | C | 340 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(337): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.3300+91A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 29/41 | chr10 | 113614092 | |||||||
chr10:113614313 | C | T | 1 | a0004c0004t0005g0019 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.3187-17G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 28/41 | chr10 | 113614313 | |||||||
chr10:113614409 | TAAAAG | T | 4 | a0009c0079t0001g0071 a0023c0030t0001g0157 a0023c0030t0001g0173 others(1): Show |
4 | NA18964.hp2 NA18983.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.3187-118_3187-114d others(7): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 28/41 | chr10 | 113614409 | |||||||
chr10:113614467 | A | G | 1 | a0024c0024t0003g0318 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3187-171T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 28/41 | chr10 | 113614467 | |||||||
chr10:113614523 | G | A | 1 | a0031c0061t0002g0264 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3187-227C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 28/41 | chr10 | 113614523 | |||||||
chr10:113614564 | A | G | 1 | a0013c0019t0002g0222 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3187-268T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 28/41 | chr10 | 113614564 | |||||||
chr10:113614976 | C | T | 1 | a0039c0042t0002g0219 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.3079-30G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 27/41 | chr10 | 113614976 | |||||||
chr10:113615472 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.3078+240C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 27/41 | chr10 | 113615472 | |||||||
chr10:113615524 | A | G | 1 | a0010c0008t0002g0254 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.3078+188T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 27/41 | chr10 | 113615524 | |||||||
chr10:113615567 | G | T | 1 | a0015c0077t0002g0066 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3078+145C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 27/41 | chr10 | 113615567 | |||||||
chr10:113615668 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3078+44G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 27/41 | chr10 | 113615668 | |||||||
chr10:113615669 | G | A | 3 | a0030c0033t0001g0061 a0030c0033t0001g0062 a0030c0048t0001g0060 |
3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3078+43C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 27/41 | chr10 | 113615669 | |||||||
chr10:113616188 | T | C | 6 | a0016c0020t0005g0023 a0016c0020t0005g0024 a0016c0020t0005g0033 others(3): Show |
6 | HG01099.hp2 HG01346.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2974-372A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/41 | chr10 | 113616188 | |||||||
chr10:113616229 | C | T | 2 | a0004c0004t0005g0054 a0056c0058t0005g0053 |
2 | HG01943.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2974-413G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/41 | chr10 | 113616229 | |||||||
chr10:113616359 | A | G | 336 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(333): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.2974-543T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/41 | chr10 | 113616359 | |||||||
chr10:113616402 | T | G | 2 | a0005c0005t0001g0114 a0005c0005t0001g0118 |
2 | HG02165.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2974-586A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/41 | chr10 | 113616402 | |||||||
chr10:113616428 | C | T | 14 | a0011c0016t0004g0276 a0011c0016t0004g0295 a0011c0016t0004g0297 others(11): Show |
14 | HG01081.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.2974-612G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/41 | chr10 | 113616428 | |||||||
chr10:113616497 | A | C | 1 | a0027c0063t0002g0227 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2974-681T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/41 | chr10 | 113616497 | |||||||
chr10:113616892 | G | A | 168 | a0001c0001t0001g0203 a0002c0002t0004g0011 a0002c0002t0004g0298 others(165): Show |
179 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.2973+563C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/41 | chr10 | 113616892 | |||||||
chr10:113616939 | G | C | 2 | a0007c0006t0006g0055 a0062c0055t0005g0056 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2973+516C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/41 | chr10 | 113616939 | |||||||
chr10:113616965 | A | C | 2 | a0002c0002t0004g0336 a0002c0002t0004g0337 |
2 | HG00408.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.2973+490T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/41 | chr10 | 113616965 | |||||||
chr10:113617432 | A | G | 3 | a0001c0001t0001g0137 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | NA18963.hp2 NA19078.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2973+23T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 26/41 | chr10 | 113617432 | |||||||
chr10:113617614 | A | G | 1 | a0002c0037t0007g0355 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2875-61T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113617614 | |||||||
chr10:113617744 | A | C | 102 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(99): Show |
103 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.2875-191T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113617744 | |||||||
chr10:113617957 | C | T | 4 | a0003c0003t0003g0311 a0003c0003t0003g0314 a0006c0010t0003g0313 others(1): Show |
4 | HG00280.hp1 HG01069.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.2875-404G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113617957 | |||||||
chr10:113618013 | G | C | 1 | a0016c0054t0005g0057 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2875-460C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618013 | |||||||
chr10:113618018 | C | T | 336 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(333): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.2875-465G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618018 | |||||||
chr10:113618024 | C | G | 1 | a0003c0003t0003g0379 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2875-471G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618024 | |||||||
chr10:113618105 | T | C | 4 | a0022c0071t0002g0267 a0022c0072t0001g0268 a0022c0073t0001g0269 others(1): Show |
4 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2875-552A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618105 | |||||||
chr10:113618148 | C | CA | 48 | a0001c0001t0001g0135 a0001c0001t0001g0159 a0002c0002t0004g0305 others(45): Show |
55 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.2875-596dupT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618148 | |||||||
chr10:113618341 | C | A | 1 | a0002c0002t0004g0342 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2875-788G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618341 | |||||||
chr10:113618481 | C | T | 4 | a0015c0077t0002g0066 a0042c0047t0003g0274 a0042c0047t0003g0275 others(1): Show |
4 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2875-928G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618481 | |||||||
chr10:113618549 | C | G | 1 | a0001c0001t0001g0159 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2875-996G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618549 | |||||||
chr10:113618592 | G | A | 4 | a0001c0001t0001g0176 a0001c0001t0001g0188 a0001c0001t0001g0194 others(1): Show |
4 | HG00639.hp1 HG01123.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.2875-1039C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618592 | |||||||
chr10:113618605 | T | C | 108 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(105): Show |
109 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.2875-1052A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618605 | |||||||
chr10:113618878 | G | A | 2 | a0007c0006t0006g0039 a0007c0006t0006g0044 |
2 | NA18975.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.2875-1325C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113618878 | |||||||
chr10:113619009 | C | T | 5 | a0001c0001t0001g0138 a0001c0001t0001g0150 a0001c0001t0001g0152 others(2): Show |
5 | HG01433.hp2 HG01981.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.2875-1456G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113619009 | |||||||
chr10:113619357 | G | A | 1 | a0031c0061t0002g0264 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2874+1247C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113619357 | |||||||
chr10:113619619 | CA | C | 224 | a0001c0001t0001g0133 a0001c0001t0001g0136 a0001c0001t0001g0138 others(221): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.2874+984delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113619619 | |||||||
chr10:113619619 | CAA | C | 116 | a0001c0001t0001g0203 a0002c0002t0004g0011 a0002c0002t0004g0298 others(113): Show |
121 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.2874+983_2874+984d others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113619619 | |||||||
chr10:113619801 | G | A | 4 | a0022c0071t0002g0267 a0022c0072t0001g0268 a0022c0073t0001g0269 others(1): Show |
4 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2874+803C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113619801 | |||||||
chr10:113619838 | G | C | 7 | a0003c0003t0003g0375 a0003c0003t0003g0377 a0003c0003t0003g0379 others(4): Show |
7 | HG02559.hp1 HG02886.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2874+766C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113619838 | |||||||
chr10:113619933 | C | T | 1 | a0004c0057t0005g0052 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2874+671G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113619933 | |||||||
chr10:113620033 | C | T | 4 | a0022c0071t0002g0267 a0022c0072t0001g0268 a0022c0073t0001g0269 others(1): Show |
4 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2874+571G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113620033 | |||||||
chr10:113620170 | A | G | 3 | a0042c0047t0003g0274 a0042c0047t0003g0275 a0063c0113t0004g0273 |
3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2874+434T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113620170 | |||||||
chr10:113620303 | A | T | 6 | a0011c0039t0004g0339 a0011c0039t0004g0340 a0027c0034t0002g0234 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2874+301T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113620303 | |||||||
chr10:113620433 | G | C | 1 | a0001c0099t0001g0153 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2874+171C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113620433 | |||||||
chr10:113620552 | C | T | 8 | a0008c0007t0002g0081 a0008c0007t0002g0090 a0008c0007t0009g0084 others(5): Show |
8 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2874+52G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 25/41 | chr10 | 113620552 | |||||||
chr10:113620849 | A | C | 341 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(338): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.2770-141T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113620849 | |||||||
chr10:113620948 | T | C | 11 | a0030c0033t0001g0061 a0030c0033t0001g0062 a0030c0048t0001g0060 others(8): Show |
11 | HG01081.hp2 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.2770-240A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113620948 | |||||||
chr10:113621058 | C | T | 4 | a0029c0028t0002g0230 a0029c0028t0002g0231 a0029c0028t0002g0232 others(1): Show |
4 | HG01884.hp1 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2770-350G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621058 | |||||||
chr10:113621301 | G | C | 1 | a0007c0006t0006g0055 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2769+568C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621301 | |||||||
chr10:113621314 | T | TAC | 5 | a0011c0016t0004g0276 a0011c0016t0004g0295 a0011c0016t0004g0297 others(2): Show |
5 | HG02145.hp1 HG03041.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.2769+553_2769+554d others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621314 | |||||||
chr10:113621314 | T | TACAC | 40 | a0003c0003t0003g0344 a0006c0010t0003g0345 a0006c0010t0003g0348 others(37): Show |
43 | HG00408.hp2 HG00544.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.2769+551_2769+554d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621314 | |||||||
chr10:113621314 | T | TACACAC | 54 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(51): Show |
55 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.2769+549_2769+554d others(8): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621314 | |||||||
chr10:113621314 | T | TACACACA others(1): Show |
6 | a0002c0002t0004g0308 a0002c0002t0004g0360 a0002c0002t0004g0367 others(3): Show |
6 | HG02165.hp2 NA18747.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.2769+547_2769+554d others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621314 | |||||||
chr10:113621314 | TAC | T | 98 | a0001c0001t0001g0149 a0001c0001t0001g0180 a0001c0001t0001g0192 others(95): Show |
103 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.2769+553_2769+554d others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621314 | |||||||
chr10:113621314 | TACAC | T | 125 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(122): Show |
129 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.2769+551_2769+554d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621314 | |||||||
chr10:113621350 | G | T | 1 | a0069c0062t0006g0050 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2769+519C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621350 | |||||||
chr10:113621486 | C | G | 1 | a0080c0085t0003g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2769+383G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621486 | |||||||
chr10:113621583 | C | A | 42 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(39): Show |
47 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.2769+286G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621583 | |||||||
chr10:113621587 | C | A | 1 | a0008c0007t0002g0093 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2769+282G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621587 | |||||||
chr10:113621690 | C | T | 2 | a0037c0036t0002g0265 a0037c0036t0008g0059 |
2 | HG01081.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2769+179G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621690 | |||||||
chr10:113621719 | T | C | 1 | a0031c0061t0002g0264 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2769+150A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621719 | |||||||
chr10:113621776 | T | C | 1 | a0015c0077t0002g0066 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2769+93A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 24/41 | chr10 | 113621776 | |||||||
chr10:113622305 | T | C | 2 | a0022c0114t0004g0272 a0022c0115t0004g0271 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2458-125A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/41 | chr10 | 113622305 | |||||||
chr10:113622354 | A | G | 1 | a0037c0036t0002g0265 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2458-174T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/41 | chr10 | 113622354 | |||||||
chr10:113622486 | G | C | 340 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(337): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.2458-306C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/41 | chr10 | 113622486 | |||||||
chr10:113622832 | CAACT | C | 4 | a0027c0034t0002g0234 a0027c0034t0002g0236 a0027c0063t0002g0227 others(1): Show |
4 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2458-656_2458-653d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/41 | chr10 | 113622832 | |||||||
chr10:113622882 | C | A | 1 | a0001c0001t0001g0140 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2457+647G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/41 | chr10 | 113622882 | |||||||
chr10:113622940 | A | G | 127 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(124): Show |
131 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.2457+589T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/41 | chr10 | 113622940 | |||||||
chr10:113623110 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2457+419A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/41 | chr10 | 113623110 | |||||||
chr10:113623210 | C | A | 1 | a0031c0061t0002g0264 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2457+319G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/41 | chr10 | 113623210 | |||||||
chr10:113623387 | G | A | 86 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(83): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.2457+142C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/41 | chr10 | 113623387 | |||||||
chr10:113623475 | G | A | 1 | a0007c0056t0006g0043 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2457+54C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 23/41 | chr10 | 113623475 | |||||||
chr10:113623724 | C | A | 1 | a0010c0008t0002g0238 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2350-88G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113623724 | |||||||
chr10:113623893 | G | A | 2 | a0010c0008t0002g0239 a0010c0008t0002g0262 |
2 | HG03710.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2350-257C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113623893 | |||||||
chr10:113624000 | G | T | 1 | a0058c0053t0005g0041 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2350-364C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113624000 | |||||||
chr10:113624112 | G | T | 3 | a0031c0032t0002g0228 a0031c0032t0002g0229 a0040c0038t0003g0341 |
3 | HG02630.hp2 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2350-476C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113624112 | |||||||
chr10:113624115 | G | A | 339 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(336): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.2350-479C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113624115 | |||||||
chr10:113624315 | T | G | 1 | a0010c0008t0010g0245 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2349+511A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113624315 | |||||||
chr10:113624354 | G | A | 29 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(26): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.2349+472C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113624354 | |||||||
chr10:113624378 | T | A | 1 | a0073c0092t0001g0134 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2349+448A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113624378 | |||||||
chr10:113624520 | T | A | 1 | a0011c0025t0002g0235 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2349+306A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113624520 | |||||||
chr10:113624538 | C | T | 1 | a0041c0068t0005g0058 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2349+288G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113624538 | |||||||
chr10:113624704 | C | T | 1 | a0016c0054t0005g0057 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2349+122G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113624704 | |||||||
chr10:113624708 | C | A | 47 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(44): Show |
52 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.2349+118G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 22/41 | chr10 | 113624708 | |||||||
chr10:113625000 | G | A | 1 | a0009c0009t0001g0073 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2245-70C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 21/41 | chr10 | 113625000 | |||||||
chr10:113625116 | A | G | 1 | a0027c0034t0002g0236 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2245-186T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 21/41 | chr10 | 113625116 | |||||||
chr10:113625148 | G | A | 1 | a0011c0016t0004g0297 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2245-218C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 21/41 | chr10 | 113625148 | |||||||
chr10:113625250 | A | T | 87 | a0003c0023t0003g0319 a0004c0004t0005g0001 a0004c0004t0005g0012 others(84): Show |
95 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.2245-320T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 21/41 | chr10 | 113625250 | |||||||
chr10:113625261 | C | A | 1 | a0016c0054t0005g0057 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2245-331G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 21/41 | chr10 | 113625261 | |||||||
chr10:113625521 | A | G | 3 | a0012c0011t0003g0270 a0012c0011t0003g0283 a0012c0011t0003g0287 |
3 | NA18989.hp2 NA19003.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2244+526T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 21/41 | chr10 | 113625521 | |||||||
chr10:113625891 | C | T | 18 | a0011c0016t0004g0278 a0011c0016t0004g0292 a0012c0011t0003g0010 others(15): Show |
21 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.2244+156G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 21/41 | chr10 | 113625891 | |||||||
chr10:113625968 | G | A | 7 | a0027c0034t0002g0234 a0027c0034t0002g0236 a0027c0063t0002g0227 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2244+79C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 21/41 | chr10 | 113625968 | |||||||
chr10:113626217 | A | C | 89 | a0001c0001t0001g0212 a0002c0002t0004g0011 a0002c0002t0004g0298 others(86): Show |
90 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.2146-72T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113626217 | |||||||
chr10:113626219 | A | C | 2 | a0002c0037t0007g0354 a0046c0107t0003g0329 |
2 | HG00438.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2146-74T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113626219 | |||||||
chr10:113626220 | C | T | 1 | a0006c0105t0003g0343 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2146-75G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113626220 | |||||||
chr10:113626329 | C | G | 85 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(82): Show |
93 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.2146-184G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113626329 | |||||||
chr10:113626344 | A | T | 1 | a0015c0077t0002g0066 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2146-199T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113626344 | |||||||
chr10:113626528 | T | C | 1 | a0054c0096t0002g0151 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2146-383A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113626528 | |||||||
chr10:113626760 | C | T | 7 | a0027c0034t0002g0234 a0027c0034t0002g0236 a0027c0063t0002g0227 others(4): Show |
7 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2146-615G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113626760 | |||||||
chr10:113626821 | C | A | 85 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(82): Show |
93 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.2146-676G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113626821 | |||||||
chr10:113626945 | C | T | 85 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(82): Show |
93 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.2146-800G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113626945 | |||||||
chr10:113626985 | G | A | 2 | a0008c0007t0002g0082 a0009c0079t0001g0071 |
2 | NA18964.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.2146-840C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113626985 | |||||||
chr10:113627123 | A | G | 6 | a0022c0071t0002g0267 a0022c0072t0001g0268 a0022c0073t0001g0269 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2146-978T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113627123 | |||||||
chr10:113627172 | T | A | 85 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(82): Show |
93 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.2146-1027A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113627172 | |||||||
chr10:113627211 | GA | G | 3 | a0022c0071t0002g0267 a0022c0072t0001g0268 a0022c0073t0001g0269 |
3 | HG01891.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2146-1067delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113627211 | |||||||
chr10:113627253 | C | T | 85 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(82): Show |
93 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.2146-1108G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113627253 | |||||||
chr10:113627349 | G | A | 1 | a0031c0061t0002g0264 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2146-1204C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113627349 | |||||||
chr10:113627840 | T | C | 3 | a0030c0033t0001g0061 a0030c0033t0001g0062 a0030c0048t0001g0060 |
3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2145+1077A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113627840 | |||||||
chr10:113627979 | G | A | 82 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(79): Show |
83 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.2145+938C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113627979 | |||||||
chr10:113628200 | C | T | 85 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(82): Show |
93 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.2145+717G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628200 | |||||||
chr10:113628240 | A | T | 85 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(82): Show |
93 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.2145+677T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628240 | |||||||
chr10:113628257 | G | A | 1 | a0050c0050t0002g0237 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2145+660C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628257 | |||||||
chr10:113628378 | C | T | 3 | a0042c0047t0003g0274 a0042c0047t0003g0275 a0063c0113t0004g0273 |
3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2145+539G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628378 | |||||||
chr10:113628379 | G | A | 21 | a0011c0016t0004g0278 a0011c0016t0004g0292 a0011c0025t0002g0235 others(18): Show |
24 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.2145+538C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628379 | |||||||
chr10:113628463 | C | A | 3 | a0022c0071t0002g0267 a0022c0072t0001g0268 a0022c0073t0001g0269 |
3 | HG01891.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2145+454G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628463 | |||||||
chr10:113628487 | C | T | 85 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(82): Show |
93 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.2145+430G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628487 | |||||||
chr10:113628521 | T | G | 85 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(82): Show |
93 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.2145+396A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628521 | |||||||
chr10:113628609 | A | C | 85 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(82): Show |
93 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.2145+308T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628609 | |||||||
chr10:113628639 | A | G | 1 | a0007c0006t0006g0025 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2145+278T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628639 | |||||||
chr10:113628707 | A | G | 3 | a0042c0047t0003g0274 a0042c0047t0003g0275 a0063c0113t0004g0273 |
3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2145+210T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628707 | |||||||
chr10:113628791 | T | C | 1 | a0021c0069t0001g0247 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2145+126A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628791 | |||||||
chr10:113628829 | A | G | 85 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(82): Show |
93 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.2145+88T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628829 | |||||||
chr10:113628862 | T | C | 1 | a0002c0037t0007g0355 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2145+55A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 20/41 | chr10 | 113628862 | |||||||
chr10:113629062 | A | G | 1 | a0016c0054t0005g0057 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2041-41T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/41 | chr10 | 113629062 | |||||||
chr10:113629098 | G | A | 2 | a0009c0009t0001g0079 a0009c0009t0001g0083 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2041-77C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/41 | chr10 | 113629098 | |||||||
chr10:113629123 | T | C | 1 | a0080c0085t0003g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2041-102A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/41 | chr10 | 113629123 | |||||||
chr10:113629185 | C | T | 86 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(83): Show |
94 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2041-164G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/41 | chr10 | 113629185 | |||||||
chr10:113629283 | CT | C | 48 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(45): Show |
53 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.2041-263delA | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/41 | chr10 | 113629283 | |||||||
chr10:113629370 | A | T | 4 | a0008c0007t0002g0086 a0008c0007t0002g0087 a0008c0078t0002g0065 others(1): Show |
6 | HG00642.hp1 HG01106.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.2040+218T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/41 | chr10 | 113629370 | |||||||
chr10:113629421 | A | C | 86 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(83): Show |
94 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2040+167T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/41 | chr10 | 113629421 | |||||||
chr10:113629455 | C | T | 86 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(83): Show |
94 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2040+133G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/41 | chr10 | 113629455 | |||||||
chr10:113629508 | G | A | 86 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(83): Show |
94 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.2040+80C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 19/41 | chr10 | 113629508 | |||||||
chr10:113629809 | C | T | 2 | a0014c0012t0004g0282 a0014c0012t0004g0291 |
2 | HG02523.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1843-24G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113629809 | |||||||
chr10:113629877 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | NA18956.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1843-92G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113629877 | |||||||
chr10:113629892 | C | T | 1 | a0007c0006t0006g0055 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1843-107G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113629892 | |||||||
chr10:113630291 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1843-506C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113630291 | |||||||
chr10:113630332 | T | C | 113 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(110): Show |
114 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1843-547A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113630332 | |||||||
chr10:113630423 | T | C | 113 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(110): Show |
114 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1843-638A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113630423 | |||||||
chr10:113630508 | A | G | 83 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(80): Show |
91 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1843-723T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113630508 | |||||||
chr10:113630526 | T | C | 3 | a0029c0028t0002g0230 a0029c0028t0002g0231 a0029c0028t0002g0232 |
3 | HG02559.hp2 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1843-741A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113630526 | |||||||
chr10:113630569 | C | T | 1 | a0046c0107t0003g0329 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1843-784G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113630569 | |||||||
chr10:113630594 | C | T | 222 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(219): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.1843-809G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113630594 | |||||||
chr10:113630605 | G | A | 2 | a0005c0021t0003g0383 a0005c0075t0001g0158 |
2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1843-820C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113630605 | |||||||
chr10:113630857 | C | G | 18 | a0011c0016t0004g0278 a0011c0016t0004g0292 a0012c0011t0003g0010 others(15): Show |
21 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.1842+652G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113630857 | |||||||
chr10:113630927 | A | G | 83 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(80): Show |
91 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1842+582T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113630927 | |||||||
chr10:113631221 | A | T | 1 | a0003c0003t0003g0356 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1842+288T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113631221 | |||||||
chr10:113631382 | C | A | 1 | a0022c0071t0002g0267 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1842+127G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 18/41 | chr10 | 113631382 | |||||||
chr10:113631663 | A | G | 1 | a0006c0010t0003g0345 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1741-53T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 17/41 | chr10 | 113631663 | |||||||
chr10:113631703 | G | C | 1 | a0008c0007t0002g0070 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1741-93C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 17/41 | chr10 | 113631703 | |||||||
chr10:113631853 | G | A | 4 | a0001c0001t0001g0176 a0001c0001t0001g0188 a0001c0001t0001g0194 others(1): Show |
4 | HG00639.hp1 HG01123.hp1 HG01255.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1740+4C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 17/41 | chr10 | 113631853 | |||||||
chr10:113632076 | C | T | 1 | a0080c0085t0003g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1633-112G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632076 | |||||||
chr10:113632121 | A | G | 4 | a0022c0071t0002g0267 a0022c0072t0001g0268 a0022c0073t0001g0269 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1633-157T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632121 | |||||||
chr10:113632237 | C | A | 1 | a0004c0004t0005g0030 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1633-273G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632237 | |||||||
chr10:113632246 | G | A | 1 | a0018c0015t0001g0099 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1633-282C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632246 | |||||||
chr10:113632352 | A | G | 84 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(81): Show |
92 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.1633-388T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632352 | |||||||
chr10:113632431 | T | G | 2 | a0004c0004t0005g0054 a0056c0058t0005g0053 |
2 | HG01943.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1633-467A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632431 | |||||||
chr10:113632497 | A | C | 1 | a0031c0061t0002g0264 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1633-533T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632497 | |||||||
chr10:113632569 | GTGTCCCT others(41): Show |
G | 6 | a0003c0003t0003g0346 a0006c0010t0003g0345 a0006c0010t0003g0348 others(3): Show |
6 | HG01243.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1632+467_1632+514d others(50): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632569 | |||||||
chr10:113632620 | C | A | 6 | a0003c0003t0003g0346 a0006c0010t0003g0345 a0006c0010t0003g0348 others(3): Show |
6 | HG01243.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1632+464G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632620 | |||||||
chr10:113632622 | G | GT | 6 | a0003c0003t0003g0346 a0006c0010t0003g0345 a0006c0010t0003g0348 others(3): Show |
6 | HG01243.hp2 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1632+461_1632+462i others(3): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632622 | |||||||
chr10:113632631 | T | C | 1 | a0015c0077t0002g0066 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1632+453A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632631 | |||||||
chr10:113632720 | C | A | 1 | a0003c0003t0003g0362 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1632+364G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632720 | |||||||
chr10:113632735 | G | A | 2 | a0002c0002t0004g0342 a0003c0003t0003g0338 |
2 | HG02055.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1632+349C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632735 | |||||||
chr10:113632834 | G | T | 87 | a0001c0001t0001g0176 a0001c0001t0001g0188 a0001c0001t0001g0194 others(84): Show |
95 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.1632+250C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632834 | |||||||
chr10:113632925 | G | A | 87 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(84): Show |
88 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.1632+159C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632925 | |||||||
chr10:113632930 | A | C | 133 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(130): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.1632+154T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 16/41 | chr10 | 113632930 | |||||||
chr10:113633446 | C | T | 1 | a0005c0005t0001g0115 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1528-258G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633446 | |||||||
chr10:113633458 | T | C | 1 | a0050c0050t0002g0237 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1528-270A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633458 | |||||||
chr10:113633470 | A | G | 3 | a0042c0047t0003g0274 a0042c0047t0003g0275 a0063c0113t0004g0273 |
3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1528-282T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633470 | |||||||
chr10:113633499 | G | A | 2 | a0009c0009t0001g0079 a0009c0009t0001g0083 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1528-311C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633499 | |||||||
chr10:113633618 | G | A | 1 | a0002c0002t0004g0342 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1528-430C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633618 | |||||||
chr10:113633627 | C | T | 23 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(20): Show |
23 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.1528-439G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633627 | |||||||
chr10:113633732 | GTT | G | 4 | a0022c0071t0002g0267 a0022c0072t0001g0268 a0022c0073t0001g0269 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1527+378_1527+379d others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633732 | |||||||
chr10:113633766 | G | C | 3 | a0042c0047t0003g0274 a0042c0047t0003g0275 a0063c0113t0004g0273 |
3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1527+346C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633766 | |||||||
chr10:113633820 | G | A | 216 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(213): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1527+292C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633820 | |||||||
chr10:113633865 | T | C | 1 | a0002c0002t0004g0321 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1527+247A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633865 | |||||||
chr10:113633889 | G | C | 18 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0138 others(15): Show |
18 | HG00438.hp2 HG01433.hp2 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.1527+223C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113633889 | |||||||
chr10:113634103 | G | T | 1 | a0015c0013t0002g0100 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1527+9C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 15/41 | chr10 | 113634103 | |||||||
chr10:113634287 | A | G | 6 | a0010c0008t0002g0240 a0010c0008t0002g0246 a0010c0008t0002g0248 others(3): Show |
6 | HG00323.hp1 HG00642.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.1429-77T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113634287 | |||||||
chr10:113634309 | G | A | 1 | a0016c0054t0005g0057 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1429-99C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113634309 | |||||||
chr10:113634310 | C | T | 1 | a0016c0054t0005g0057 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1429-100G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113634310 | |||||||
chr10:113634508 | C | A | 1 | a0014c0012t0004g0293 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1429-298G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113634508 | |||||||
chr10:113634545 | C | G | 3 | a0011c0016t0004g0292 a0014c0012t0004g0293 a0014c0012t0004g0294 |
3 | HG02015.hp2 HG02056.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.1429-335G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113634545 | |||||||
chr10:113634766 | G | C | 1 | a0004c0004t0005g0049 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1429-556C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113634766 | |||||||
chr10:113634792 | C | T | 86 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(83): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1429-582G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113634792 | |||||||
chr10:113634930 | C | T | 1 | a0031c0061t0002g0264 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1429-720G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113634930 | |||||||
chr10:113634931 | G | A | 109 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(106): Show |
110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1429-721C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113634931 | |||||||
chr10:113635096 | A | G | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1429-886T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113635096 | |||||||
chr10:113635139 | G | A | 85 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(82): Show |
86 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1429-929C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113635139 | |||||||
chr10:113635572 | C | T | 9 | a0027c0034t0002g0234 a0027c0034t0002g0236 a0027c0063t0002g0227 others(6): Show |
9 | HG01891.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1429-1362G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113635572 | |||||||
chr10:113635642 | G | T | 2 | a0002c0002t0004g0302 a0047c0110t0004g0303 |
2 | HG00609.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1429-1432C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113635642 | |||||||
chr10:113635877 | G | C | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1429-1667C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113635877 | |||||||
chr10:113636147 | C | T | 1 | a0031c0061t0002g0264 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1429-1937G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636147 | |||||||
chr10:113636304 | G | T | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1429-2094C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636304 | |||||||
chr10:113636446 | C | T | 109 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(106): Show |
110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.1429-2236G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636446 | |||||||
chr10:113636493 | T | A | 9 | a0003c0003t0003g0344 a0003c0003t0003g0346 a0006c0010t0003g0345 others(6): Show |
9 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1429-2283A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636493 | |||||||
chr10:113636537 | G | A | 1 | a0009c0009t0001g0103 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1429-2327C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636537 | |||||||
chr10:113636623 | T | C | 2 | a0044c0046t0004g0371 a0044c0046t0004g0372 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1429-2413A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636623 | |||||||
chr10:113636756 | C | T | 1 | a0021c0069t0001g0247 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1429-2546G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636756 | |||||||
chr10:113636864 | G | A | 1 | a0058c0053t0005g0041 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1429-2654C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636864 | |||||||
chr10:113636891 | G | A | 4 | a0022c0071t0002g0267 a0022c0072t0001g0268 a0022c0073t0001g0269 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1429-2681C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636891 | |||||||
chr10:113636922 | G | A | 19 | a0011c0016t0004g0278 a0011c0016t0004g0292 a0012c0011t0003g0010 others(16): Show |
22 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.1429-2712C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636922 | |||||||
chr10:113636957 | C | A | 339 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(336): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.1429-2747G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113636957 | |||||||
chr10:113637006 | CA | C | 155 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(152): Show |
161 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.1429-2797delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637006 | |||||||
chr10:113637006 | CAA | C | 34 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0001t0001g0192 others(31): Show |
37 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1429-2798_1429-279 others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637006 | |||||||
chr10:113637006 | CAAA | C | 161 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(158): Show |
167 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.1429-2799_1429-279 others(7): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637006 | |||||||
chr10:113637039 | C | G | 1 | a0009c0009t0001g0068 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1429-2829G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637039 | |||||||
chr10:113637121 | G | A | 5 | a0011c0025t0002g0235 a0011c0039t0004g0339 a0011c0039t0004g0340 others(2): Show |
5 | HG02630.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1429-2911C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637121 | |||||||
chr10:113637132 | A | C | 1 | a0011c0016t0004g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1429-2922T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637132 | |||||||
chr10:113637262 | C | T | 4 | a0027c0034t0002g0234 a0027c0034t0002g0236 a0027c0063t0002g0227 others(1): Show |
4 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1428+2965G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637262 | |||||||
chr10:113637320 | T | C | 1 | a0020c0018t0001g0009 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1428+2907A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637320 | |||||||
chr10:113637374 | G | A | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1428+2853C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637374 | |||||||
chr10:113637416 | T | C | 7 | a0002c0002t0004g0305 a0002c0002t0004g0308 a0003c0003t0003g0304 others(4): Show |
7 | HG00621.hp2 NA18747.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.1428+2811A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637416 | |||||||
chr10:113637445 | G | A | 7 | a0021c0022t0001g0255 a0021c0022t0001g0256 a0021c0022t0001g0260 others(4): Show |
7 | HG00597.hp1 HG02135.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.1428+2782C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637445 | |||||||
chr10:113637464 | G | A | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1428+2763C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637464 | |||||||
chr10:113637600 | G | A | 1 | a0016c0054t0005g0057 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1428+2627C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637600 | |||||||
chr10:113637605 | G | A | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1428+2622C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637605 | |||||||
chr10:113637779 | G | T | 16 | a0002c0002t0004g0333 a0002c0002t0004g0334 a0002c0002t0004g0342 others(13): Show |
16 | HG00738.hp1 HG01243.hp2 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.1428+2448C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637779 | |||||||
chr10:113637826 | G | A | 2 | a0004c0004t0005g0054 a0056c0058t0005g0053 |
2 | HG01943.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1428+2401C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637826 | |||||||
chr10:113637863 | T | C | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1428+2364A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637863 | |||||||
chr10:113637917 | T | C | 339 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(336): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.1428+2310A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637917 | |||||||
chr10:113637922 | CA | C | 317 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(314): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.1428+2304delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113637922 | |||||||
chr10:113638015 | A | G | 1 | a0005c0005t0001g0108 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1428+2212T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113638015 | |||||||
chr10:113638167 | T | A | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1428+2060A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113638167 | |||||||
chr10:113638231 | A | G | 3 | a0030c0033t0001g0061 a0030c0033t0001g0062 a0030c0048t0001g0060 |
3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1428+1996T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113638231 | |||||||
chr10:113638825 | G | A | 86 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(83): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1428+1402C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113638825 | |||||||
chr10:113638833 | C | T | 1 | a0003c0003t0003g0344 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1428+1394G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113638833 | |||||||
chr10:113638835 | C | G | 6 | a0027c0034t0002g0234 a0027c0034t0002g0236 a0027c0063t0002g0227 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1428+1392G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113638835 | |||||||
chr10:113638972 | C | T | 61 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(58): Show |
62 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.1428+1255G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113638972 | |||||||
chr10:113639066 | C | T | 1 | a0020c0018t0001g0129 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1428+1161G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639066 | |||||||
chr10:113639091 | C | CA | 25 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0335 others(22): Show |
26 | HG00408.hp1 HG00558.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1428+1135dupT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639091 | |||||||
chr10:113639091 | CA | C | 29 | a0002c0002t0004g0360 a0006c0010t0003g0352 a0006c0105t0003g0343 others(26): Show |
29 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.1428+1135delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639091 | |||||||
chr10:113639091 | CAAAAAA | C | 13 | a0001c0001t0001g0145 a0001c0001t0013g0202 a0005c0005t0001g0162 others(10): Show |
13 | HG00735.hp1 HG02056.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1428+1130_1428+113 others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639091 | |||||||
chr10:113639091 | CAAAAAAA | C | 205 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(202): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1428+1129_1428+113 others(11): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639091 | |||||||
chr10:113639091 | CAAAAAAA others(2): Show |
C | 6 | a0027c0034t0002g0234 a0027c0034t0002g0236 a0027c0063t0002g0227 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1428+1127_1428+113 others(13): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639091 | |||||||
chr10:113639103 | A | T | 4 | a0003c0003t0003g0375 a0003c0003t0003g0377 a0003c0003t0003g0379 others(1): Show |
4 | HG02896.hp1 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1428+1124T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639103 | |||||||
chr10:113639158 | T | TAAGTC | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1428+1064_1428+106 others(9): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639158 | |||||||
chr10:113639234 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1428+993G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639234 | |||||||
chr10:113639350 | T | C | 1 | a0008c0007t0002g0085 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1428+877A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639350 | |||||||
chr10:113639440 | T | C | 133 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(130): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.1428+787A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639440 | |||||||
chr10:113639477 | T | A | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1428+750A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639477 | |||||||
chr10:113639481 | A | G | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1428+746T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639481 | |||||||
chr10:113639535 | T | G | 339 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(336): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.1428+692A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639535 | |||||||
chr10:113639613 | T | G | 28 | a0004c0004t0005g0012 a0004c0004t0005g0014 a0004c0004t0005g0019 others(25): Show |
30 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1428+614A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639613 | |||||||
chr10:113639625 | C | T | 1 | a0030c0033t0001g0061 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1428+602G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639625 | |||||||
chr10:113639666 | C | A | 5 | a0011c0016t0004g0276 a0011c0016t0004g0295 a0011c0016t0004g0296 others(2): Show |
5 | HG01884.hp1 HG02145.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1428+561G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639666 | |||||||
chr10:113639700 | C | T | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1428+527G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639700 | |||||||
chr10:113639770 | C | A | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1428+457G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639770 | |||||||
chr10:113639936 | T | C | 1 | a0049c0083t0004g0279 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1428+291A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639936 | |||||||
chr10:113639953 | G | T | 1 | a0080c0085t0003g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1428+274C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639953 | |||||||
chr10:113639973 | A | G | 1 | a0003c0003t0003g0361 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1428+254T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113639973 | |||||||
chr10:113640029 | T | C | 1 | a0016c0054t0005g0057 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1428+198A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113640029 | |||||||
chr10:113640212 | TG | T | 4 | a0022c0071t0002g0267 a0022c0072t0001g0268 a0022c0073t0001g0269 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1428+14delC | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 14/41 | chr10 | 113640212 | |||||||
chr10:113640387 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1324-56G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113640387 | |||||||
chr10:113640505 | C | A | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1324-174G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113640505 | |||||||
chr10:113640541 | G | A | 1 | a0009c0009t0001g0103 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1324-210C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113640541 | |||||||
chr10:113640626 | G | GAAGA | 19 | a0011c0016t0004g0278 a0011c0016t0004g0292 a0012c0011t0003g0010 others(16): Show |
22 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.1324-299_1324-296d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113640626 | |||||||
chr10:113640735 | C | G | 1 | a0016c0054t0005g0057 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1324-404G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113640735 | |||||||
chr10:113640933 | AG | A | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1323+431delC | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113640933 | |||||||
chr10:113640996 | C | A | 2 | a0002c0002t0004g0333 a0002c0002t0004g0334 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1323+369G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113640996 | |||||||
chr10:113641000 | C | T | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1323+365G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113641000 | |||||||
chr10:113641003 | T | C | 6 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(3): Show |
6 | HG01099.hp1 HG01928.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1323+362A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113641003 | |||||||
chr10:113641123 | T | A | 3 | a0011c0016t0004g0276 a0011c0016t0004g0295 a0040c0038t0003g0277 |
3 | HG01884.hp1 HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1323+242A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113641123 | |||||||
chr10:113641123 | T | C | 23 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(20): Show |
23 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.1323+242A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113641123 | |||||||
chr10:113641199 | C | T | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1323+166G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113641199 | |||||||
chr10:113641213 | G | A | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1323+152C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113641213 | |||||||
chr10:113641272 | AT | A | 339 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(336): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.1323+92delA | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113641272 | |||||||
chr10:113641284 | G | A | 1 | a0008c0007t0002g0098 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1323+81C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113641284 | |||||||
chr10:113641322 | T | C | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1323+43A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113641322 | |||||||
chr10:113641327 | C | G | 1 | a0006c0104t0003g0351 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1323+38G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 13/41 | chr10 | 113641327 | |||||||
chr10:113641505 | A | G | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1216-33T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641505 | |||||||
chr10:113641570 | A | T | 1 | a0080c0085t0003g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1216-98T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641570 | |||||||
chr10:113641592 | A | G | 1 | a0004c0004t0005g0012 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1216-120T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641592 | |||||||
chr10:113641598 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1216-126G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641598 | |||||||
chr10:113641606 | A | G | 339 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(336): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.1216-134T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641606 | |||||||
chr10:113641608 | A | G | 4 | a0002c0002t0004g0321 a0002c0002t0004g0330 a0002c0002t0004g0331 others(1): Show |
4 | HG02602.hp2 HG03704.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1216-136T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641608 | |||||||
chr10:113641666 | T | C | 3 | a0042c0047t0003g0274 a0042c0047t0003g0275 a0063c0113t0004g0273 |
3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1216-194A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641666 | |||||||
chr10:113641695 | T | C | 1 | a0022c0073t0001g0269 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1216-223A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641695 | |||||||
chr10:113641708 | G | A | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1216-236C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641708 | |||||||
chr10:113641805 | G | A | 1 | a0011c0016t0004g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1216-333C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641805 | |||||||
chr10:113641807 | C | T | 216 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(213): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1216-335G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641807 | |||||||
chr10:113641808 | A | G | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1216-336T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641808 | |||||||
chr10:113641833 | G | A | 24 | a0011c0016t0004g0276 a0011c0016t0004g0278 a0011c0016t0004g0292 others(21): Show |
27 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1216-361C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641833 | |||||||
chr10:113641960 | C | T | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1216-488G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113641960 | |||||||
chr10:113642002 | T | C | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1216-530A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642002 | |||||||
chr10:113642028 | A | T | 1 | a0001c0001t0001g0199 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1216-556T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642028 | |||||||
chr10:113642054 | T | C | 133 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(130): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.1216-582A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642054 | |||||||
chr10:113642125 | C | T | 4 | a0022c0071t0002g0267 a0022c0072t0001g0268 a0022c0073t0001g0269 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1216-653G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642125 | |||||||
chr10:113642212 | C | T | 1 | a0005c0005t0001g0124 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1215+722G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642212 | |||||||
chr10:113642243 | G | T | 1 | a0020c0018t0001g0129 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1215+691C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642243 | |||||||
chr10:113642316 | G | A | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1215+618C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642316 | |||||||
chr10:113642385 | T | A | 3 | a0042c0047t0003g0274 a0042c0047t0003g0275 a0063c0113t0004g0273 |
3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1215+549A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642385 | |||||||
chr10:113642393 | G | A | 24 | a0011c0016t0004g0276 a0011c0016t0004g0278 a0011c0016t0004g0292 others(21): Show |
27 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.1215+541C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642393 | |||||||
chr10:113642488 | G | A | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1215+446C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642488 | |||||||
chr10:113642721 | G | A | 1 | a0037c0036t0008g0059 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1215+213C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642721 | |||||||
chr10:113642763 | A | G | 2 | a0038c0093t0002g0185 a0039c0042t0002g0160 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1215+171T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642763 | |||||||
chr10:113642772 | A | G | 1 | a0070c0081t0001g0078 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1215+162T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642772 | |||||||
chr10:113642856 | T | A | 3 | a0042c0047t0003g0274 a0042c0047t0003g0275 a0063c0113t0004g0273 |
3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1215+78A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642856 | |||||||
chr10:113642921 | G | T | 2 | a0038c0093t0002g0185 a0039c0042t0002g0160 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1215+13C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 12/41 | chr10 | 113642921 | |||||||
chr10:113643263 | G | A | 1 | a0010c0008t0002g0249 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1111-225C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113643263 | |||||||
chr10:113643428 | C | T | 1 | a0072c0080t0002g0089 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1111-390G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113643428 | |||||||
chr10:113643522 | C | A | 2 | a0007c0006t0006g0055 a0062c0055t0005g0056 |
2 | HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1111-484G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113643522 | |||||||
chr10:113643534 | G | T | 1 | a0027c0034t0002g0236 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1111-496C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113643534 | |||||||
chr10:113643569 | C | G | 86 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(83): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.1111-531G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113643569 | |||||||
chr10:113643612 | T | C | 5 | a0010c0008t0002g0240 a0010c0008t0002g0246 a0010c0008t0002g0248 others(2): Show |
5 | HG00642.hp2 HG01496.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111-574A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113643612 | |||||||
chr10:113643828 | C | T | 1 | a0050c0050t0002g0237 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1111-790G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113643828 | |||||||
chr10:113644062 | C | A | 1 | a0001c0001t0001g0193 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1111-1024G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644062 | |||||||
chr10:113644062 | C | T | 1 | a0007c0006t0006g0020 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1111-1024G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644062 | |||||||
chr10:113644147 | C | CAAAAA | 75 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(72): Show |
76 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1111-1114_1111-111 others(9): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644147 | |||||||
chr10:113644147 | C | CAAAAAA | 37 | a0001c0001t0001g0133 a0002c0002t0004g0305 a0002c0002t0004g0368 others(34): Show |
37 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.1111-1115_1111-111 others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644147 | |||||||
chr10:113644147 | C | CAAAAAAA | 89 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(86): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.1111-1116_1111-111 others(11): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644147 | |||||||
chr10:113644147 | C | CAAAAAAA others(1): Show |
63 | a0001c0001t0001g0140 a0001c0001t0001g0142 a0001c0001t0001g0143 others(60): Show |
67 | HG01071.hp1 HG01106.hp2 HG01109.hp1 others(64): Show |
intron_variant | MODIFIER | c.1111-1117_1111-111 others(12): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644147 | |||||||
chr10:113644147 | C | CAAAAAAA others(2): Show |
45 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(42): Show |
50 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1111-1118_1111-111 others(13): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644147 | |||||||
chr10:113644147 | C | CAAAAAAA others(3): Show |
15 | a0004c0004t0005g0019 a0004c0004t0005g0036 a0004c0004t0005g0037 others(12): Show |
15 | HG00423.hp1 HG01109.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.1111-1119_1111-111 others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644147 | |||||||
chr10:113644147 | C | CAAAAAAA others(4): Show |
3 | a0016c0020t0005g0038 a0030c0033t0001g0061 a0064c0059t0005g0048 |
3 | HG02486.hp1 HG02602.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1111-1120_1111-111 others(15): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644147 | |||||||
chr10:113644147 | C | CAAAAAAA others(5): Show |
1 | a0007c0006t0006g0039 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1111-1121_1111-111 others(16): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644147 | |||||||
chr10:113644147 | C | CAAAAAAA others(6): Show |
1 | a0004c0004t0005g0040 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1111-1122_1111-111 others(17): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644147 | |||||||
chr10:113644233 | G | C | 1 | a0009c0009t0001g0073 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1111-1195C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644233 | |||||||
chr10:113644259 | C | T | 48 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(45): Show |
53 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1111-1221G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644259 | |||||||
chr10:113644288 | G | A | 2 | a0002c0002t0004g0333 a0002c0002t0004g0334 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1111-1250C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644288 | |||||||
chr10:113644463 | C | T | 1 | a0015c0077t0002g0066 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1110+1362G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644463 | |||||||
chr10:113644486 | G | A | 339 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(336): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.1110+1339C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644486 | |||||||
chr10:113644562 | T | C | 1 | a0040c0038t0003g0277 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1110+1263A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644562 | |||||||
chr10:113644670 | C | T | 1 | a0057c0097t0001g0204 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1110+1155G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644670 | |||||||
chr10:113644872 | C | T | 3 | a0004c0004t0005g0019 a0004c0004t0005g0042 a0032c0026t0005g0018 |
3 | NA18952.hp2 NA18974.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1110+953G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644872 | |||||||
chr10:113644960 | A | G | 339 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(336): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.1110+865T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113644960 | |||||||
chr10:113645186 | A | T | 1 | a0080c0085t0003g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1110+639T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645186 | |||||||
chr10:113645190 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1110+635C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645190 | |||||||
chr10:113645191 | T | G | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1110+634A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645191 | |||||||
chr10:113645296 | A | C | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1110+529T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645296 | |||||||
chr10:113645335 | T | C | 2 | a0004c0004t0005g0047 a0007c0056t0006g0043 |
2 | HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1110+490A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645335 | |||||||
chr10:113645415 | GTTGT | G | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1110+406_1110+409d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645415 | |||||||
chr10:113645494 | C | T | 9 | a0027c0034t0002g0234 a0027c0034t0002g0236 a0027c0063t0002g0227 others(6): Show |
9 | HG01891.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1110+331G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645494 | |||||||
chr10:113645495 | G | A | 3 | a0029c0028t0002g0230 a0029c0028t0002g0231 a0029c0028t0002g0232 |
3 | HG02559.hp2 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1110+330C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645495 | |||||||
chr10:113645496 | C | A | 1 | a0014c0012t0004g0282 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1110+329G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645496 | |||||||
chr10:113645497 | G | A | 1 | a0009c0009t0001g0068 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1110+328C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645497 | |||||||
chr10:113645530 | G | A | 133 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(130): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.1110+295C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645530 | |||||||
chr10:113645650 | C | G | 9 | a0027c0034t0002g0234 a0027c0034t0002g0236 a0027c0063t0002g0227 others(6): Show |
9 | HG01891.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1110+175G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645650 | |||||||
chr10:113645665 | C | T | 1 | a0009c0009t0001g0068 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1110+160G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645665 | |||||||
chr10:113645707 | G | A | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1110+118C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645707 | |||||||
chr10:113645710 | C | A | 1 | a0027c0034t0002g0234 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1110+115G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645710 | |||||||
chr10:113645809 | C | T | 2 | a0004c0004t0005g0016 a0079c0051t0005g0017 |
2 | HG00733.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1110+16G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645809 | |||||||
chr10:113645818 | T | TACGC | 3 | a0030c0033t0001g0061 a0030c0033t0001g0062 a0030c0048t0001g0060 |
3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
splice_region_variant&intron_variant | LOW | c.1110+3_1110+6dupGC others(2): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 11/41 | chr10 | 113645818 | |||||||
chr10:113645944 | G | GAA | 211 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(208): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
splice_region_variant&intron_variant | LOW | c.994-5_994-4dupTT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113645944 | |||||||
chr10:113645944 | G | GAAA | 6 | a0005c0005t0001g0122 a0007c0006t0006g0055 a0016c0054t0005g0057 others(3): Show |
6 | HG02258.hp2 HG02895.hp1 HG02896.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.994-6_994-4dupTTT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113645944 | |||||||
chr10:113646009 | A | C | 1 | a0009c0009t0001g0073 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.994-68T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646009 | |||||||
chr10:113646032 | A | T | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.994-91T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646032 | |||||||
chr10:113646091 | T | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | NA18956.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.994-150A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646091 | |||||||
chr10:113646159 | A | C | 1 | a0029c0028t0002g0230 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.994-218T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646159 | |||||||
chr10:113646164 | A | G | 2 | a0045c0043t0001g0166 a0045c0043t0001g0175 |
2 | NA18939.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.994-223T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646164 | |||||||
chr10:113646179 | G | A | 339 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(336): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.994-238C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646179 | |||||||
chr10:113646301 | C | T | 4 | a0011c0025t0002g0235 a0011c0039t0004g0339 a0011c0039t0004g0340 others(1): Show |
4 | HG02630.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.994-360G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646301 | |||||||
chr10:113646414 | G | A | 1 | a0058c0053t0005g0041 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.994-473C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646414 | |||||||
chr10:113646463 | A | G | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.993+460T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646463 | |||||||
chr10:113646499 | A | G | 1 | a0002c0002t0004g0301 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.993+424T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646499 | |||||||
chr10:113646548 | A | G | 222 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(219): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.993+375T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646548 | |||||||
chr10:113646565 | C | T | 134 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(131): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.993+358G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646565 | |||||||
chr10:113646609 | C | G | 4 | a0011c0025t0002g0235 a0011c0039t0004g0339 a0011c0039t0004g0340 others(1): Show |
4 | HG02630.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.993+314G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646609 | |||||||
chr10:113646702 | A | G | 221 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(218): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.993+221T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646702 | |||||||
chr10:113646726 | C | T | 217 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(214): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.993+197G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646726 | |||||||
chr10:113646731 | C | T | 1 | a0003c0003t0003g0338 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.993+192G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 10/41 | chr10 | 113646731 | |||||||
chr10:113647389 | T | G | 1 | a0002c0002t0004g0369 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.889-362A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647389 | |||||||
chr10:113647451 | C | T | 24 | a0011c0016t0004g0276 a0011c0016t0004g0278 a0011c0016t0004g0292 others(21): Show |
27 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.889-424G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647451 | |||||||
chr10:113647498 | C | T | 9 | a0004c0004t0005g0047 a0004c0004t0005g0051 a0007c0056t0006g0043 others(6): Show |
10 | HG01891.hp2 HG02071.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.889-471G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647498 | |||||||
chr10:113647498 | CCTCCCCA others(11): Show |
C | 1 | a0026c0029t0002g0123 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.889-489_889-472del others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647498 | |||||||
chr10:113647505 | A | C | 9 | a0004c0004t0005g0047 a0004c0004t0005g0051 a0007c0056t0006g0043 others(6): Show |
10 | HG01891.hp2 HG02071.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.889-478T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647505 | |||||||
chr10:113647506 | A | G | 4 | a0022c0071t0002g0267 a0022c0072t0001g0268 a0022c0073t0001g0269 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-479T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647506 | |||||||
chr10:113647516 | T | C | 5 | a0004c0004t0005g0047 a0004c0004t0005g0051 a0007c0056t0006g0043 others(2): Show |
6 | HG02071.hp1 HG02523.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.889-489A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647516 | |||||||
chr10:113647516 | T | TCTCCCCC others(336): Show |
1 | a0016c0054t0005g0057 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.889-490_889-489ins others(343): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647516 | |||||||
chr10:113647523 | C | CAGTGGTA others(29): Show |
1 | a0022c0071t0002g0267 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.889-497_889-496ins others(36): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647523 | |||||||
chr10:113647524 | G | A | 11 | a0004c0004t0005g0042 a0004c0004t0005g0047 a0004c0004t0005g0051 others(8): Show |
12 | HG01884.hp2 HG01891.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.889-497C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647524 | |||||||
chr10:113647534 | T | C | 3 | a0022c0072t0001g0268 a0022c0073t0001g0269 a0031c0061t0002g0264 |
3 | HG02451.hp2 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.889-507A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647534 | |||||||
chr10:113647534 | T | TCTCCCCC others(11): Show |
2 | a0045c0043t0001g0166 a0045c0043t0001g0175 |
2 | NA18939.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.889-508_889-507ins others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647534 | |||||||
chr10:113647536 | T | TCCCCCAG others(246): Show |
1 | a0029c0028t0002g0230 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.889-510_889-509ins others(253): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647536 | |||||||
chr10:113647536 | T | TCCCCTGG others(30): Show |
3 | a0022c0072t0001g0268 a0022c0073t0001g0269 a0031c0061t0002g0264 |
3 | HG02451.hp2 HG02976.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.889-510_889-509ins others(37): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647536 | |||||||
chr10:113647537 | C | T | 1 | a0003c0003t0003g0382 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.889-510G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647537 | |||||||
chr10:113647541 | C | CAGTGGTA others(173): Show |
1 | a0013c0041t0002g0197 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.889-515_889-514ins others(180): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647541 | |||||||
chr10:113647541 | C | T | 7 | a0004c0004t0005g0047 a0004c0004t0005g0051 a0006c0010t0003g0374 others(4): Show |
8 | HG01884.hp2 HG02071.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.889-514G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647541 | |||||||
chr10:113647542 | G | A | 201 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(198): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.889-515C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647542 | |||||||
chr10:113647542 | G | GGTGGTAC others(29): Show |
1 | a0041c0068t0005g0058 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.889-516_889-515ins others(36): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647542 | |||||||
chr10:113647542 | G | GGTGGTAC others(155): Show |
2 | a0045c0043t0001g0166 a0045c0043t0001g0175 |
2 | NA18939.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.889-516_889-515ins others(162): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647542 | |||||||
chr10:113647552 | T | C | 206 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(203): Show |
217 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.889-525A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647552 | |||||||
chr10:113647559 | C | CAGTGGTA others(228): Show |
1 | a0029c0028t0002g0231 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.889-533_889-532ins others(235): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647559 | |||||||
chr10:113647560 | A | AGTGGTAC others(65): Show |
29 | a0001c0001t0001g0207 a0005c0005t0001g0106 a0005c0005t0001g0108 others(26): Show |
33 | HG00544.hp2 HG01167.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.889-534_889-533ins others(72): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647560 | |||||||
chr10:113647560 | A | AGTGGTAC others(83): Show |
1 | a0050c0050t0002g0237 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.889-534_889-533ins others(90): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647560 | |||||||
chr10:113647560 | A | G | 9 | a0013c0041t0002g0197 a0016c0054t0005g0057 a0022c0071t0002g0267 others(6): Show |
9 | HG00099.hp2 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.889-533T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647560 | |||||||
chr10:113647570 | C | CCTCCCCC others(65): Show |
3 | a0042c0047t0003g0274 a0042c0047t0003g0275 a0063c0113t0004g0273 |
3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.889-544_889-543ins others(72): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647570 | |||||||
chr10:113647570 | C | T | 170 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(167): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.889-543G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647570 | |||||||
chr10:113647577 | T | C | 12 | a0004c0004t0005g0047 a0004c0004t0005g0051 a0007c0056t0006g0043 others(9): Show |
13 | HG00099.hp2 HG01884.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.889-550A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647577 | |||||||
chr10:113647577 | T | TGGTGGTA others(283): Show |
1 | a0005c0005t0001g0104 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.889-551_889-550ins others(290): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647577 | |||||||
chr10:113647577 | T | TGGTGGTA others(173): Show |
1 | a0013c0019t0002g0174 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.889-551_889-550ins others(180): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647577 | |||||||
chr10:113647577 | T | TGGTGGTA others(174): Show |
1 | a0005c0005t0001g0114 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.889-551_889-550ins others(181): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647577 | |||||||
chr10:113647577 | T | TGGTGGTA others(173): Show |
88 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(85): Show |
88 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.889-551_889-550ins others(180): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647577 | |||||||
chr10:113647577 | T | TGGTGGTA others(227): Show |
1 | a0017c0014t0001g0170 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.889-551_889-550ins others(234): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647577 | |||||||
chr10:113647577 | T | TGGTGGTA others(318): Show |
2 | a0011c0016t0004g0276 a0040c0038t0003g0277 |
2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.889-551_889-550ins others(325): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647577 | |||||||
chr10:113647577 | TGGTGGTA others(29): Show |
T | 7 | a0021c0022t0001g0255 a0021c0022t0001g0256 a0021c0022t0001g0260 others(4): Show |
7 | HG00597.hp1 HG02135.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.889-586_889-551del others(36): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647577 | |||||||
chr10:113647578 | G | A | 6 | a0004c0004t0005g0047 a0004c0004t0005g0051 a0007c0056t0006g0043 others(3): Show |
7 | HG01884.hp2 HG02071.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.889-551C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647578 | |||||||
chr10:113647578 | GGTGGTAC others(11): Show |
G | 1 | a0029c0028t0002g0231 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.889-569_889-552del others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647578 | |||||||
chr10:113647587 | T | G | 85 | a0001c0001t0001g0208 a0004c0004t0005g0001 a0004c0004t0005g0012 others(82): Show |
93 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.889-560A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647587 | |||||||
chr10:113647588 | C | T | 73 | a0001c0001t0001g0208 a0004c0004t0005g0001 a0004c0004t0005g0012 others(70): Show |
80 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.889-561G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647588 | |||||||
chr10:113647595 | T | C | 85 | a0001c0001t0001g0208 a0004c0004t0005g0001 a0004c0004t0005g0012 others(82): Show |
93 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.889-568A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647595 | |||||||
chr10:113647596 | A | AGTGGTAC others(137): Show |
1 | a0007c0006t0006g0055 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.889-570_889-569ins others(144): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647596 | |||||||
chr10:113647596 | A | AGTGGTAC others(137): Show |
8 | a0001c0001t0001g0208 a0011c0025t0002g0235 a0011c0039t0004g0339 others(5): Show |
8 | HG01975.hp2 HG02559.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.889-570_889-569ins others(144): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647596 | |||||||
chr10:113647596 | A | AGTGGTAC others(533): Show |
1 | a0080c0085t0003g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.889-570_889-569ins others(540): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647596 | |||||||
chr10:113647596 | A | AGTGGTAC others(137): Show |
38 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0016 others(35): Show |
42 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.889-570_889-569ins others(144): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647596 | |||||||
chr10:113647596 | A | AGTGGTAC others(155): Show |
1 | a0007c0006t0006g0044 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.889-570_889-569ins others(162): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647596 | |||||||
chr10:113647596 | A | AGTGGTAC others(371): Show |
2 | a0004c0004t0005g0014 a0059c0060t0005g0015 |
2 | HG01981.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.889-570_889-569ins others(378): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647596 | |||||||
chr10:113647596 | A | AGTGGTAC others(191): Show |
1 | a0011c0016t0004g0297 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.889-570_889-569ins others(198): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647596 | |||||||
chr10:113647596 | A | AGTGGTAC others(11): Show |
30 | a0001c0001t0001g0207 a0005c0005t0001g0106 a0005c0005t0001g0108 others(27): Show |
34 | HG00544.hp2 HG01109.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.889-587_889-570dup others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647596 | |||||||
chr10:113647596 | A | AGTGGTAC others(642): Show |
1 | a0062c0055t0005g0056 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.889-570_889-569ins others(649): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647596 | |||||||
chr10:113647596 | A | G | 12 | a0004c0004t0005g0047 a0004c0004t0005g0051 a0007c0056t0006g0043 others(9): Show |
13 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.889-569T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647596 | |||||||
chr10:113647602 | A | G | 4 | a0022c0071t0002g0267 a0022c0072t0001g0268 a0022c0073t0001g0269 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-575T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647602 | |||||||
chr10:113647606 | T | C | 27 | a0004c0004t0005g0047 a0004c0004t0005g0051 a0007c0006t0006g0044 others(24): Show |
31 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.889-579A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647606 | |||||||
chr10:113647608 | T | TC | 99 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
intron_variant | MODIFIER | c.889-582dupG | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647608 | |||||||
chr10:113647613 | C | T | 5 | a0004c0004t0005g0047 a0004c0004t0005g0051 a0007c0056t0006g0043 others(2): Show |
6 | HG01884.hp2 HG02071.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.889-586G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647613 | |||||||
chr10:113647614 | G | A | 21 | a0011c0016t0004g0278 a0011c0016t0004g0292 a0011c0016t0004g0295 others(18): Show |
24 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.889-587C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647614 | |||||||
chr10:113647623 | T | G | 129 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(126): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.889-596A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647623 | |||||||
chr10:113647624 | C | T | 25 | a0011c0016t0004g0278 a0011c0016t0004g0292 a0011c0016t0004g0295 others(22): Show |
28 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.889-597G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647624 | |||||||
chr10:113647631 | T | A | 1 | a0031c0032t0002g0229 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.889-604A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647631 | |||||||
chr10:113647631 | T | C | 108 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(105): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.889-604A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647631 | |||||||
chr10:113647632 | A | G | 129 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(126): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.889-605T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647632 | |||||||
chr10:113647644 | TC | T | 109 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.889-618delG | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647644 | |||||||
chr10:113647645 | C | CCCCCAGT others(245): Show |
21 | a0011c0016t0004g0278 a0011c0016t0004g0292 a0011c0016t0004g0295 others(18): Show |
24 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.889-619_889-618ins others(252): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | |||||||
chr10:113647645 | C | CCCCCCGG others(47): Show |
45 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(42): Show |
49 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.889-619_889-618ins others(54): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | |||||||
chr10:113647645 | C | CCCCCCGG others(119): Show |
1 | a0011c0025t0002g0235 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.889-619_889-618ins others(126): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | |||||||
chr10:113647645 | C | CCCCCCGG others(65): Show |
1 | a0029c0028t0002g0232 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.889-619_889-618ins others(72): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | |||||||
chr10:113647645 | C | CCCCCCGG others(29): Show |
29 | a0001c0001t0001g0207 a0005c0005t0001g0106 a0005c0005t0001g0108 others(26): Show |
33 | HG00544.hp2 HG01167.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.889-619_889-618ins others(36): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | |||||||
chr10:113647645 | C | CCCCCGGT others(10): Show |
1 | a0031c0061t0002g0264 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.889-619_889-618ins others(17): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | |||||||
chr10:113647645 | C | CCCCCGGT others(28): Show |
1 | a0031c0032t0002g0229 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.889-619_889-618ins others(35): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | |||||||
chr10:113647645 | C | CCCCCGGT others(83): Show |
1 | a0026c0029t0002g0123 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.889-619_889-618ins others(90): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | |||||||
chr10:113647645 | C | CCCCCGGT others(155): Show |
4 | a0004c0004t0005g0047 a0004c0004t0005g0051 a0007c0056t0006g0043 others(1): Show |
5 | HG02071.hp1 HG02523.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.889-619_889-618ins others(162): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | |||||||
chr10:113647645 | C | CCCCCGGT others(64): Show |
9 | a0006c0010t0003g0348 a0027c0034t0002g0234 a0027c0034t0002g0236 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.889-619_889-618ins others(71): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | |||||||
chr10:113647645 | CCCCCCGG others(11): Show |
C | 1 | a0003c0003t0003g0314 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.889-636_889-619del others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647645 | |||||||
chr10:113647650 | C | CGGTGGTA others(47): Show |
1 | a0011c0016t0004g0297 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.889-624_889-623ins others(54): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647650 | |||||||
chr10:113647675 | G | A | 211 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(208): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.889-648C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647675 | |||||||
chr10:113647678 | G | A | 1 | a0027c0034t0002g0236 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.889-651C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647678 | |||||||
chr10:113647696 | G | GCCTCCCC others(29): Show |
1 | a0001c0001t0001g0208 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.889-670_889-669ins others(36): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647696 | |||||||
chr10:113647700 | C | A | 4 | a0027c0034t0002g0234 a0027c0034t0002g0236 a0027c0063t0002g0227 others(1): Show |
4 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-673G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647700 | |||||||
chr10:113647822 | A | C | 4 | a0022c0071t0002g0267 a0022c0072t0001g0268 a0022c0073t0001g0269 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-795T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647822 | |||||||
chr10:113647890 | C | A | 1 | a0050c0050t0002g0237 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.889-863G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113647890 | |||||||
chr10:113648006 | G | A | 127 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(124): Show |
128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.889-979C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648006 | |||||||
chr10:113648071 | C | T | 4 | a0002c0002t0004g0321 a0002c0002t0004g0330 a0002c0002t0004g0331 others(1): Show |
4 | HG02602.hp2 HG03704.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-1044G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648071 | |||||||
chr10:113648136 | T | C | 1 | a0010c0008t0002g0254 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.889-1109A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648136 | |||||||
chr10:113648155 | G | T | 72 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(69): Show |
80 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.889-1128C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648155 | |||||||
chr10:113648249 | C | T | 26 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(23): Show |
26 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.889-1222G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648249 | |||||||
chr10:113648279 | G | A | 1 | a0017c0014t0001g0186 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.889-1252C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648279 | |||||||
chr10:113648309 | G | T | 1 | a0013c0041t0002g0217 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.889-1282C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648309 | |||||||
chr10:113648437 | T | TCTCTCTC others(4): Show |
2 | a0001c0001t0001g0209 a0073c0092t0001g0134 |
2 | HG01928.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.889-1411_889-1410i others(13): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | |||||||
chr10:113648437 | T | TCTCTCTC others(6): Show |
1 | a0019c0017t0002g0128 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.889-1411_889-1410i others(15): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | |||||||
chr10:113648437 | T | TTC | 25 | a0001c0001t0001g0159 a0002c0002t0004g0302 a0002c0002t0004g0334 others(22): Show |
28 | HG00323.hp2 HG00408.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.889-1412_889-1411d others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | |||||||
chr10:113648437 | T | TTCCCTCT others(7): Show |
1 | a0001c0001t0001g0203 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.889-1411_889-1410i others(16): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | |||||||
chr10:113648437 | T | TTCTC | 52 | a0001c0001t0001g0182 a0002c0002t0004g0308 a0002c0002t0004g0321 others(49): Show |
52 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.889-1414_889-1411d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | |||||||
chr10:113648437 | T | TTCTCTC | 33 | a0001c0001t0001g0137 a0001c0001t0001g0141 a0001c0001t0001g0142 others(30): Show |
33 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.889-1416_889-1411d others(8): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | |||||||
chr10:113648437 | T | TTCTCTCT others(1): Show |
18 | a0001c0001t0001g0135 a0001c0001t0001g0146 a0001c0001t0001g0155 others(15): Show |
18 | HG01069.hp2 HG01071.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.889-1418_889-1411d others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | |||||||
chr10:113648437 | T | TTCTCTCT others(3): Show |
35 | a0001c0001t0001g0136 a0001c0001t0001g0147 a0001c0001t0001g0148 others(32): Show |
35 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.889-1420_889-1411d others(12): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | |||||||
chr10:113648437 | T | TTCTCTCT others(5): Show |
19 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0001g0154 others(16): Show |
22 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.889-1422_889-1411d others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | |||||||
chr10:113648437 | T | TTCTCTCT others(7): Show |
2 | a0001c0001t0001g0133 a0001c0001t0001g0200 |
2 | NA18986.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.889-1424_889-1411d others(16): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | |||||||
chr10:113648437 | T | TTCTCTCT others(9): Show |
3 | a0020c0018t0001g0164 a0020c0018t0001g0165 a0062c0055t0005g0056 |
3 | HG02109.hp2 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.889-1426_889-1411d others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | |||||||
chr10:113648437 | T | TTCTCTCT others(15): Show |
1 | a0007c0006t0006g0055 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.889-1432_889-1411d others(24): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | |||||||
chr10:113648437 | TTC | T | 4 | a0006c0010t0003g0310 a0018c0076t0001g0101 a0030c0033t0001g0061 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-1412_889-1411d others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648437 | |||||||
chr10:113648461 | CTCTCTCT others(1): Show |
C | 3 | a0042c0047t0003g0274 a0042c0047t0003g0275 a0063c0113t0004g0273 |
3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.889-1442_889-1435d others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648461 | |||||||
chr10:113648463 | C | A | 1 | a0029c0028t0002g0231 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.889-1436G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648463 | |||||||
chr10:113648465 | C | A | 3 | a0029c0028t0002g0230 a0029c0028t0002g0231 a0029c0028t0002g0232 |
3 | HG02559.hp2 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.889-1438G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648465 | |||||||
chr10:113648465 | CTCTA | C | 3 | a0011c0016t0004g0276 a0011c0016t0004g0295 a0040c0038t0003g0277 |
3 | HG01884.hp1 HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.889-1442_889-1439d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648465 | |||||||
chr10:113648467 | C | A | 7 | a0003c0003t0003g0361 a0006c0105t0003g0343 a0027c0034t0002g0236 others(4): Show |
7 | HG02145.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.889-1440G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTA | 4 | a0011c0016t0004g0278 a0012c0011t0003g0283 a0012c0011t0003g0284 others(1): Show |
4 | HG04199.hp2 NA18948.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-1442_889-1441d others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTATA | 4 | a0001c0099t0001g0153 a0002c0002t0004g0333 a0003c0003t0003g0362 others(1): Show |
4 | HG04115.hp2 NA18970.hp1 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.889-1444_889-1441d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTATATA | 8 | a0003c0003t0003g0346 a0003c0023t0003g0316 a0005c0021t0001g0119 others(5): Show |
8 | HG00597.hp1 HG02273.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.889-1446_889-1441d others(8): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTATATAT others(1): Show |
3 | a0005c0005t0001g0118 a0035c0086t0002g0113 a0035c0088t0002g0121 |
3 | HG00544.hp2 HG02074.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.889-1448_889-1441d others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTA | 14 | a0002c0002t0004g0330 a0002c0002t0004g0342 a0002c0002t0004g0360 others(11): Show |
14 | HG00621.hp2 HG01243.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTATA | 11 | a0003c0003t0003g0344 a0006c0010t0014g0347 a0010c0008t0002g0238 others(8): Show |
11 | HG00733.hp1 HG00735.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(8): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTATAT others(1): Show |
5 | a0004c0004t0005g0037 a0004c0004t0005g0051 a0005c0005t0001g0114 others(2): Show |
5 | HG02132.hp1 HG02165.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTATAT others(3): Show |
1 | a0005c0021t0001g0130 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.889-1441_889-1440i others(12): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTATAT others(5): Show |
2 | a0015c0013t0002g0063 a0065c0087t0001g0105 |
2 | HG02622.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.889-1441_889-1440i others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTCTA | 14 | a0003c0003t0003g0375 a0006c0010t0003g0348 a0006c0010t0003g0374 others(11): Show |
14 | HG00280.hp2 HG00323.hp1 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(8): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTCTAT others(1): Show |
7 | a0004c0004t0005g0014 a0004c0004t0005g0028 a0004c0004t0005g0036 others(4): Show |
8 | HG01981.hp1 HG03579.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTCTAT others(3): Show |
4 | a0008c0007t0009g0084 a0015c0013t0002g0064 a0016c0020t0005g0024 others(1): Show |
4 | HG01261.hp2 HG03239.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(12): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTCTAT others(5): Show |
6 | a0005c0005t0001g0104 a0005c0005t0001g0162 a0007c0006t0006g0020 others(3): Show |
7 | HG02004.hp1 HG02572.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTCTCT others(1): Show |
10 | a0004c0004t0005g0030 a0005c0005t0001g0111 a0005c0021t0001g0008 others(7): Show |
10 | HG01081.hp1 HG01109.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTCTCT others(3): Show |
6 | a0001c0001t0001g0180 a0001c0001t0001g0220 a0011c0025t0006g0021 others(3): Show |
6 | HG01346.hp1 HG02055.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(12): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTCTCT others(5): Show |
6 | a0001c0001t0001g0138 a0003c0003t0003g0338 a0005c0005t0001g0116 others(3): Show |
6 | HG01099.hp2 HG01978.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTCTCT others(9): Show |
4 | a0004c0004t0005g0016 a0004c0057t0005g0052 a0005c0005t0001g0106 others(1): Show |
4 | HG00733.hp2 HG02615.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTCTCT others(3): Show |
7 | a0001c0001t0001g0177 a0001c0001t0001g0210 a0001c0001t0001g0211 others(4): Show |
7 | HG00099.hp1 HG01361.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(12): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTCTCT others(5): Show |
14 | a0001c0001t0001g0216 a0001c0100t0001g0179 a0004c0004t0005g0019 others(11): Show |
14 | HG00423.hp2 HG00741.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTCTCT others(7): Show |
2 | a0001c0001t0001g0218 a0007c0006t0006g0004 |
2 | HG01978.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.889-1441_889-1440i others(16): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTCTCT others(11): Show |
1 | a0031c0032t0002g0229 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.889-1441_889-1440i others(20): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTCTCT others(5): Show |
7 | a0001c0001t0001g0139 a0001c0001t0001g0214 a0001c0001t0001g0215 others(4): Show |
8 | HG01257.hp2 HG01496.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.889-1441_889-1440i others(14): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTCTCT others(7): Show |
3 | a0001c0001t0001g0221 a0007c0006t0006g0013 a0016c0054t0005g0057 |
3 | HG01975.hp1 HG02895.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.889-1441_889-1440i others(16): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTCTCT others(9): Show |
1 | a0004c0004t0005g0042 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.889-1441_889-1440i others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTCTCT others(11): Show |
1 | a0031c0032t0002g0228 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.889-1441_889-1440i others(20): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTCTCT others(7): Show |
2 | a0005c0005t0001g0115 a0016c0052t0005g0032 |
2 | HG01255.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.889-1441_889-1440i others(16): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | C | CTCTCTCT others(9): Show |
2 | a0001c0001t0001g0212 a0019c0017t0002g0131 |
2 | HG01192.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.889-1441_889-1440i others(18): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648467 | CTA | C | 5 | a0001c0001t0001g0140 a0009c0009t0001g0002 a0011c0025t0002g0235 others(2): Show |
7 | HG00642.hp1 HG01106.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.889-1442_889-1441d others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648467 | |||||||
chr10:113648469 | A | C | 130 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(127): Show |
131 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.889-1442T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648469 | |||||||
chr10:113648471 | A | C | 53 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(50): Show |
55 | HG00558.hp1 HG00642.hp1 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.889-1444T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648471 | |||||||
chr10:113648473 | A | C | 21 | a0001c0001t0001g0133 a0001c0001t0001g0136 a0001c0001t0001g0167 others(18): Show |
21 | HG02015.hp2 HG02056.hp2 HG02523.hp1 others(18): Show |
intron_variant | MODIFIER | c.889-1446T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648473 | |||||||
chr10:113648475 | A | C | 5 | a0001c0001t0001g0167 a0011c0039t0004g0339 a0011c0039t0004g0340 others(2): Show |
5 | HG02630.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.889-1448T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648475 | |||||||
chr10:113648477 | A | C | 1 | a0040c0038t0003g0341 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.889-1450T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648477 | |||||||
chr10:113648479 | A | C | 1 | a0040c0038t0003g0341 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.889-1452T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648479 | |||||||
chr10:113648649 | G | A | 127 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(124): Show |
128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.888+1388C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648649 | |||||||
chr10:113648808 | G | A | 2 | a0002c0002t0004g0368 a0002c0002t0004g0369 |
2 | NA18988.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.888+1229C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648808 | |||||||
chr10:113648877 | G | A | 6 | a0027c0034t0002g0234 a0027c0034t0002g0236 a0027c0063t0002g0227 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.888+1160C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648877 | |||||||
chr10:113648920 | G | T | 212 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(209): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.888+1117C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648920 | |||||||
chr10:113648935 | A | G | 1 | a0009c0009t0001g0073 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.888+1102T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113648935 | |||||||
chr10:113649114 | C | A | 1 | a0062c0055t0005g0056 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.888+923G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649114 | |||||||
chr10:113649258 | T | C | 3 | a0008c0007t0002g0097 a0008c0007t0002g0098 a0018c0015t0001g0099 |
3 | HG00558.hp2 NA18990.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.888+779A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649258 | |||||||
chr10:113649278 | T | C | 1 | a0016c0054t0005g0057 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.888+759A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649278 | |||||||
chr10:113649310 | A | T | 212 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(209): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.888+727T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649310 | |||||||
chr10:113649318 | A | C | 2 | a0030c0033t0001g0061 a0030c0033t0001g0062 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.888+719T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649318 | |||||||
chr10:113649474 | T | A | 1 | a0004c0004t0005g0047 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.888+563A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649474 | |||||||
chr10:113649640 | A | C | 340 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(337): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.888+397T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649640 | |||||||
chr10:113649709 | A | T | 128 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(125): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.888+328T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649709 | |||||||
chr10:113649775 | T | C | 4 | a0022c0071t0002g0267 a0022c0072t0001g0268 a0022c0073t0001g0269 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.888+262A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649775 | |||||||
chr10:113649798 | G | A | 9 | a0027c0034t0002g0234 a0027c0034t0002g0236 a0027c0063t0002g0227 others(6): Show |
9 | HG01891.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.888+239C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649798 | |||||||
chr10:113649855 | G | A | 1 | a0013c0019t0002g0201 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.888+182C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649855 | |||||||
chr10:113649915 | T | C | 3 | a0030c0033t0001g0061 a0030c0033t0001g0062 a0030c0048t0001g0060 |
3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.888+122A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649915 | |||||||
chr10:113649927 | G | A | 1 | a0002c0002t0004g0298 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.888+110C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 9/41 | chr10 | 113649927 | |||||||
chr10:113650166 | C | G | 3 | a0011c0016t0004g0276 a0011c0016t0004g0295 a0040c0038t0003g0277 |
3 | HG01884.hp1 HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.784-25G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 8/41 | chr10 | 113650166 | |||||||
chr10:113650166 | C | T | 4 | a0022c0071t0002g0267 a0022c0072t0001g0268 a0022c0073t0001g0269 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.784-25G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 8/41 | chr10 | 113650166 | |||||||
chr10:113650167 | G | A | 2 | a0031c0032t0002g0228 a0031c0032t0002g0229 |
2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.784-26C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 8/41 | chr10 | 113650167 | |||||||
chr10:113650285 | C | T | 1 | a0016c0054t0005g0057 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.784-144G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 8/41 | chr10 | 113650285 | |||||||
chr10:113650812 | G | A | 1 | a0001c0001t0001g0218 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.676-267C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113650812 | |||||||
chr10:113650899 | A | G | 212 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(209): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.676-354T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113650899 | |||||||
chr10:113650948 | T | A | 1 | a0010c0008t0002g0254 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.676-403A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113650948 | |||||||
chr10:113651069 | A | T | 212 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(209): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.676-524T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651069 | |||||||
chr10:113651080 | A | C | 9 | a0027c0034t0002g0234 a0027c0034t0002g0236 a0027c0063t0002g0227 others(6): Show |
9 | HG01891.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.676-535T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651080 | |||||||
chr10:113651304 | T | C | 3 | a0011c0016t0004g0276 a0011c0016t0004g0295 a0040c0038t0003g0277 |
3 | HG01884.hp1 HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.675+499A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651304 | |||||||
chr10:113651318 | T | G | 1 | a0019c0017t0002g0107 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.675+485A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651318 | |||||||
chr10:113651386 | G | T | 6 | a0027c0034t0002g0234 a0027c0034t0002g0236 a0027c0063t0002g0227 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.675+417C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651386 | |||||||
chr10:113651404 | T | C | 1 | a0031c0061t0002g0264 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.675+399A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651404 | |||||||
chr10:113651483 | T | C | 130 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(127): Show |
131 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.675+320A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651483 | |||||||
chr10:113651507 | G | C | 88 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(85): Show |
89 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.675+296C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651507 | |||||||
chr10:113651546 | G | C | 1 | a0002c0002t0004g0370 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.675+257C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651546 | |||||||
chr10:113651609 | G | A | 1 | a0012c0011t0003g0290 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.675+194C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651609 | |||||||
chr10:113651670 | C | T | 3 | a0042c0047t0003g0274 a0042c0047t0003g0275 a0063c0113t0004g0273 |
3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.675+133G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651670 | |||||||
chr10:113651721 | T | C | 1 | a0011c0016t0004g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.675+82A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 7/41 | chr10 | 113651721 | |||||||
chr10:113651914 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA19009.hp2 | splice_region_variant&intron_variant | LOW | c.571-7T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113651914 | |||||||
chr10:113651951 | C | A | 1 | a0001c0001t0013g0202 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.571-44G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113651951 | |||||||
chr10:113652029 | T | G | 3 | a0030c0033t0001g0061 a0030c0033t0001g0062 a0030c0048t0001g0060 |
3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.571-122A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652029 | |||||||
chr10:113652073 | C | A | 6 | a0027c0034t0002g0234 a0027c0034t0002g0236 a0027c0063t0002g0227 others(3): Show |
6 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.571-166G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652073 | |||||||
chr10:113652168 | ATGTTT | A | 214 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(211): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.571-266_571-262del others(5): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652168 | |||||||
chr10:113652201 | A | G | 340 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(337): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.571-294T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652201 | |||||||
chr10:113652438 | A | G | 342 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(339): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.570+497T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652438 | |||||||
chr10:113652455 | C | A | 4 | a0002c0002t0004g0308 a0006c0010t0003g0307 a0006c0010t0003g0310 others(1): Show |
4 | HG00621.hp2 NA18747.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.570+480G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652455 | |||||||
chr10:113652517 | T | TGCCTGTA others(30): Show |
1 | a0001c0099t0001g0153 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.570+381_570+417dup others(37): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652517 | |||||||
chr10:113652668 | G | A | 126 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(123): Show |
127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.570+267C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652668 | |||||||
chr10:113652768 | G | A | 1 | a0018c0015t0001g0099 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.570+167C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652768 | |||||||
chr10:113652793 | G | A | 1 | a0013c0019t0002g0222 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.570+142C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652793 | |||||||
chr10:113652927 | G | A | 340 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(337): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
splice_region_variant&intron_variant | LOW | c.570+8C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652927 | |||||||
chr10:113652928 | C | T | 46 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(43): Show |
51 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(48): Show |
splice_region_variant&intron_variant | LOW | c.570+7G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 6/41 | chr10 | 113652928 | |||||||
chr10:113653082 | T | C | 1 | a0008c0007t0002g0070 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.466-43A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653082 | |||||||
chr10:113653104 | G | A | 2 | a0031c0032t0002g0228 a0031c0032t0002g0229 |
2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.466-65C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653104 | |||||||
chr10:113653194 | T | C | 1 | a0014c0012t0004g0291 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.466-155A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653194 | |||||||
chr10:113653326 | C | T | 126 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(123): Show |
127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.466-287G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653326 | |||||||
chr10:113653359 | C | T | 126 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(123): Show |
127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.466-320G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653359 | |||||||
chr10:113653408 | C | G | 1 | a0018c0015t0001g0072 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.466-369G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653408 | |||||||
chr10:113653461 | A | C | 4 | a0011c0025t0002g0235 a0011c0039t0004g0339 a0011c0039t0004g0340 others(1): Show |
4 | HG02630.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-422T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653461 | |||||||
chr10:113653566 | G | C | 126 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(123): Show |
127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.465+455C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653566 | |||||||
chr10:113653728 | T | C | 340 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(337): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.465+293A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653728 | |||||||
chr10:113653798 | A | C | 340 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(337): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.465+223T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653798 | |||||||
chr10:113653799 | C | T | 214 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(211): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.465+222G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653799 | |||||||
chr10:113653903 | T | G | 1 | a0001c0001t0001g0203 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.465+118A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653903 | |||||||
chr10:113653941 | T | C | 1 | a0027c0034t0002g0236 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.465+80A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 5/41 | chr10 | 113653941 | |||||||
chr10:113654142 | T | C | 126 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(123): Show |
127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.361-17A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654142 | |||||||
chr10:113654198 | A | AAGAAGAT others(335): Show |
1 | a0030c0033t0001g0062 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.361-74_361-73insGG others(340): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654198 | |||||||
chr10:113654198 | A | AAGAAGAT others(336): Show |
1 | a0030c0048t0001g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.361-74_361-73insGG others(341): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654198 | |||||||
chr10:113654198 | A | AAGAAGAT others(337): Show |
1 | a0030c0033t0001g0061 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.361-74_361-73insGG others(342): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654198 | |||||||
chr10:113654241 | T | C | 19 | a0011c0016t0004g0278 a0011c0016t0004g0292 a0012c0011t0003g0010 others(16): Show |
22 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.361-116A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654241 | |||||||
chr10:113654391 | G | A | 126 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(123): Show |
127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.361-266C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654391 | |||||||
chr10:113654408 | A | T | 214 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(211): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.361-283T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654408 | |||||||
chr10:113654412 | T | C | 1 | a0011c0016t0004g0296 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.361-287A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654412 | |||||||
chr10:113654507 | C | CA | 92 | a0002c0002t0004g0011 a0002c0002t0004g0301 a0002c0002t0004g0302 others(89): Show |
93 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.361-383dupT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654507 | |||||||
chr10:113654507 | C | CAA | 30 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(27): Show |
30 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.361-384_361-383dup others(2): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654507 | |||||||
chr10:113654507 | CA | C | 19 | a0011c0016t0004g0278 a0012c0011t0003g0010 a0012c0011t0003g0270 others(16): Show |
22 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.361-383delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654507 | |||||||
chr10:113654507 | CAAA | C | 182 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(179): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.361-385_361-383del others(3): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654507 | |||||||
chr10:113654520 | A | G | 3 | a0029c0028t0002g0230 a0029c0028t0002g0231 a0029c0028t0002g0232 |
3 | HG02559.hp2 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.361-395T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654520 | |||||||
chr10:113654607 | G | A | 1 | a0064c0059t0005g0048 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.361-482C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654607 | |||||||
chr10:113654632 | T | C | 2 | a0002c0002t0004g0373 a0027c0063t0002g0227 |
2 | HG01891.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.361-507A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654632 | |||||||
chr10:113654751 | G | A | 6 | a0001c0001t0001g0205 a0001c0001t0001g0207 a0001c0001t0001g0208 others(3): Show |
6 | HG01099.hp1 HG01928.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.361-626C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654751 | |||||||
chr10:113654779 | T | C | 126 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(123): Show |
127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.361-654A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654779 | |||||||
chr10:113654780 | T | A | 1 | a0001c0001t0001g0154 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.361-655A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654780 | |||||||
chr10:113654832 | A | T | 1 | a0049c0083t0004g0279 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.361-707T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654832 | |||||||
chr10:113654919 | TA | T | 14 | a0002c0002t0004g0333 a0002c0002t0004g0334 a0002c0002t0004g0342 others(11): Show |
14 | HG00738.hp1 HG01243.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.361-795delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654919 | |||||||
chr10:113654925 | C | T | 12 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(9): Show |
12 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.361-800G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113654925 | |||||||
chr10:113655081 | A | C | 126 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(123): Show |
127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.361-956T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655081 | |||||||
chr10:113655152 | A | G | 127 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(124): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.361-1027T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655152 | |||||||
chr10:113655215 | G | T | 7 | a0021c0022t0001g0255 a0021c0022t0001g0256 a0021c0022t0001g0260 others(4): Show |
7 | HG00597.hp1 HG02135.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.361-1090C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655215 | |||||||
chr10:113655234 | G | A | 1 | a0027c0063t0002g0227 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.361-1109C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655234 | |||||||
chr10:113655242 | A | G | 1 | a0080c0085t0003g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.361-1117T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655242 | |||||||
chr10:113655448 | A | ATCCATTC others(1): Show |
6 | a0022c0071t0002g0267 a0022c0072t0001g0268 a0022c0073t0001g0269 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.361-1324_361-1323i others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655448 | |||||||
chr10:113655452 | A | ATTC | 206 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(203): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.361-1328_361-1327i others(5): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655452 | |||||||
chr10:113655452 | AT | A | 87 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(84): Show |
90 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.361-1328delA | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655452 | |||||||
chr10:113655453 | T | TTC | 8 | a0001c0001t0001g0210 a0004c0004t0005g0049 a0011c0025t0002g0235 others(5): Show |
8 | HG01361.hp1 HG02630.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.361-1329_361-1328i others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655453 | |||||||
chr10:113655455 | T | C | 42 | a0006c0105t0003g0343 a0010c0008t0002g0238 a0010c0008t0002g0239 others(39): Show |
42 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.361-1330A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655455 | |||||||
chr10:113655456 | T | C | 83 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(80): Show |
84 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.361-1331A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655456 | |||||||
chr10:113655457 | T | C | 1 | a0006c0010t0003g0374 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.361-1332A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655457 | |||||||
chr10:113655468 | T | C | 1 | a0020c0018t0001g0129 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.361-1343A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655468 | |||||||
chr10:113655505 | G | A | 126 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(123): Show |
127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.361-1380C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655505 | |||||||
chr10:113655790 | T | A | 214 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(211): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.361-1665A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655790 | |||||||
chr10:113655794 | C | T | 127 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(124): Show |
128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.361-1669G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113655794 | |||||||
chr10:113656044 | TCTCATTA others(7): Show |
T | 127 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(124): Show |
128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.360+1412_360+1425d others(16): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656044 | |||||||
chr10:113656230 | C | CT | 127 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(124): Show |
128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.360+1239dupA | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656230 | |||||||
chr10:113656324 | C | T | 1 | a0050c0050t0002g0237 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.360+1146G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656324 | |||||||
chr10:113656347 | G | A | 1 | a0003c0003t0003g0379 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.360+1123C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656347 | |||||||
chr10:113656414 | C | T | 2 | a0011c0039t0004g0339 a0011c0039t0004g0340 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.360+1056G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656414 | |||||||
chr10:113656463 | T | C | 1 | a0001c0001t0001g0211 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.360+1007A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656463 | |||||||
chr10:113656465 | G | A | 1 | a0021c0022t0001g0260 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.360+1005C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656465 | |||||||
chr10:113656559 | T | C | 111 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(108): Show |
112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.360+911A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656559 | |||||||
chr10:113656575 | G | A | 127 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(124): Show |
128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.360+895C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656575 | |||||||
chr10:113656638 | C | G | 3 | a0042c0047t0003g0274 a0042c0047t0003g0275 a0063c0113t0004g0273 |
3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.360+832G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656638 | |||||||
chr10:113656659 | T | C | 1 | a0018c0076t0001g0101 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.360+811A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656659 | |||||||
chr10:113656687 | G | A | 3 | a0022c0071t0002g0267 a0022c0072t0001g0268 a0022c0073t0001g0269 |
3 | HG01891.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.360+783C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656687 | |||||||
chr10:113656698 | T | C | 127 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(124): Show |
128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.360+772A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656698 | |||||||
chr10:113656809 | C | T | 1 | a0003c0023t0003g0316 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.360+661G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656809 | |||||||
chr10:113656841 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.360+629A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656841 | |||||||
chr10:113656925 | A | T | 1 | a0002c0002t0004g0342 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.360+545T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656925 | |||||||
chr10:113656939 | T | C | 3 | a0042c0047t0003g0274 a0042c0047t0003g0275 a0063c0113t0004g0273 |
3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.360+531A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113656939 | |||||||
chr10:113657001 | C | T | 127 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(124): Show |
128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.360+469G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113657001 | |||||||
chr10:113657060 | T | C | 127 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(124): Show |
128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.360+410A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113657060 | |||||||
chr10:113657073 | G | C | 2 | a0037c0036t0002g0265 a0037c0036t0008g0059 |
2 | HG01081.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.360+397C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113657073 | |||||||
chr10:113657078 | G | A | 1 | a0009c0009t0001g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.360+392C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113657078 | |||||||
chr10:113657096 | G | A | 1 | a0003c0003t0003g0299 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.360+374C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113657096 | |||||||
chr10:113657162 | G | T | 1 | a0020c0018t0001g0112 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.360+308C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113657162 | |||||||
chr10:113657318 | G | C | 7 | a0001c0001t0001g0212 a0001c0001t0001g0214 a0001c0001t0001g0215 others(4): Show |
7 | HG00423.hp2 HG01257.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+152C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113657318 | |||||||
chr10:113657469 | C | T | 1 | a0003c0003t0003g0338 | 1 | HG02055.hp2 | splice_donor_variant&intron_variant | HIGH | c.360+1G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 4/41 | chr10 | 113657469 | |||||||
chr10:113657678 | T | C | 6 | a0003c0003t0003g0375 a0003c0003t0003g0377 a0003c0003t0003g0379 others(3): Show |
6 | HG02451.hp1 HG02896.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.256-104A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113657678 | |||||||
chr10:113657891 | T | C | 3 | a0030c0033t0001g0061 a0030c0033t0001g0062 a0030c0048t0001g0060 |
3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.256-317A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113657891 | |||||||
chr10:113658034 | C | T | 48 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(45): Show |
48 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.256-460G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658034 | |||||||
chr10:113658035 | A | G | 340 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(337): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.256-461T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658035 | |||||||
chr10:113658127 | T | C | 5 | a0011c0025t0002g0235 a0027c0034t0002g0234 a0027c0034t0002g0236 others(2): Show |
5 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.256-553A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658127 | |||||||
chr10:113658163 | T | C | 6 | a0021c0022t0001g0255 a0021c0022t0001g0256 a0021c0022t0001g0260 others(3): Show |
6 | HG00597.hp1 NA18612.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.256-589A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658163 | |||||||
chr10:113658190 | T | C | 2 | a0004c0004t0005g0051 a0032c0026t0005g0005 |
3 | NA18952.hp1 NA18988.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.256-616A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658190 | |||||||
chr10:113658214 | T | G | 1 | a0039c0042t0002g0219 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.256-640A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658214 | |||||||
chr10:113658222 | T | C | 2 | a0002c0002t0004g0330 a0002c0002t0004g0331 |
2 | HG02602.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.256-648A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658222 | |||||||
chr10:113658255 | T | A | 84 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(81): Show |
85 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.256-681A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658255 | |||||||
chr10:113658352 | G | A | 3 | a0042c0047t0003g0274 a0042c0047t0003g0275 a0063c0113t0004g0273 |
3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.256-778C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658352 | |||||||
chr10:113658429 | T | C | 48 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(45): Show |
48 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.256-855A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658429 | |||||||
chr10:113658570 | G | A | 2 | a0022c0114t0004g0272 a0022c0115t0004g0271 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.256-996C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658570 | |||||||
chr10:113658607 | G | A | 85 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(82): Show |
86 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.256-1033C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658607 | |||||||
chr10:113658618 | C | T | 51 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(48): Show |
56 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.256-1044G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658618 | |||||||
chr10:113658704 | A | T | 48 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(45): Show |
48 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.256-1130T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658704 | |||||||
chr10:113658706 | T | C | 48 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(45): Show |
48 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.256-1132A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658706 | |||||||
chr10:113658800 | T | C | 1 | a0005c0021t0001g0130 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.256-1226A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658800 | |||||||
chr10:113658881 | C | CA | 11 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0003c0003t0003g0332 others(8): Show |
11 | HG02258.hp2 HG02559.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.256-1308dupT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658881 | |||||||
chr10:113658881 | CA | C | 55 | a0001c0001t0001g0133 a0001c0001t0001g0159 a0002c0002t0004g0335 others(52): Show |
55 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.256-1308delT | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658881 | |||||||
chr10:113658896 | A | G | 3 | a0007c0006t0006g0055 a0027c0063t0002g0227 a0062c0055t0005g0056 |
3 | HG01891.hp1 HG02258.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.256-1322T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658896 | |||||||
chr10:113658960 | A | G | 50 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(47): Show |
55 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.256-1386T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113658960 | |||||||
chr10:113659156 | C | T | 1 | a0050c0050t0002g0237 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.256-1582G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113659156 | |||||||
chr10:113659290 | C | T | 48 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(45): Show |
48 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.256-1716G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113659290 | |||||||
chr10:113659377 | C | G | 3 | a0022c0071t0002g0267 a0022c0072t0001g0268 a0022c0073t0001g0269 |
3 | HG01891.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.256-1803G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113659377 | |||||||
chr10:113659821 | C | G | 2 | a0022c0114t0004g0272 a0022c0115t0004g0271 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.256-2247G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113659821 | |||||||
chr10:113659833 | C | T | 26 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(23): Show |
26 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.256-2259G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113659833 | |||||||
chr10:113659947 | A | G | 10 | a0011c0025t0002g0235 a0027c0034t0002g0234 a0027c0034t0002g0236 others(7): Show |
10 | HG01891.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.256-2373T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113659947 | |||||||
chr10:113660001 | G | A | 48 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(45): Show |
48 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.256-2427C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660001 | |||||||
chr10:113660028 | A | G | 2 | a0002c0002t0004g0333 a0002c0002t0004g0334 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.256-2454T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660028 | |||||||
chr10:113660051 | A | AAC | 8 | a0003c0003t0003g0299 a0013c0019t0002g0156 a0016c0054t0005g0057 others(5): Show |
8 | HG01109.hp2 HG02559.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.256-2479_256-2478d others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660051 | |||||||
chr10:113660051 | A | AACAC | 35 | a0002c0002t0004g0301 a0002c0002t0004g0302 a0002c0002t0004g0305 others(32): Show |
35 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.256-2481_256-2478d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660051 | |||||||
chr10:113660051 | A | AACACAC | 49 | a0003c0003t0003g0314 a0004c0004t0005g0001 a0004c0004t0005g0012 others(46): Show |
54 | HG00280.hp1 HG00423.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.256-2483_256-2478d others(8): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660051 | |||||||
chr10:113660051 | A | AACACACA others(1): Show |
31 | a0003c0003t0003g0311 a0003c0023t0003g0312 a0007c0006t0006g0013 others(28): Show |
31 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.256-2485_256-2478d others(10): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660051 | |||||||
chr10:113660051 | A | AACACACA others(3): Show |
5 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(2): Show |
5 | HG00642.hp2 HG00735.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.256-2487_256-2478d others(12): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660051 | |||||||
chr10:113660051 | A | C | 1 | a0001c0001t0001g0223 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.256-2477T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660051 | |||||||
chr10:113660051 | AAC | A | 55 | a0008c0007t0002g0070 a0008c0007t0002g0076 a0008c0007t0002g0081 others(52): Show |
59 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.256-2479_256-2478d others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660051 | |||||||
chr10:113660051 | AACAC | A | 12 | a0003c0003t0003g0382 a0005c0021t0003g0383 a0011c0016t0004g0276 others(9): Show |
13 | HG01109.hp1 HG01192.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.256-2481_256-2478d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660051 | |||||||
chr10:113660100 | T | C | 3 | a0037c0036t0002g0265 a0037c0036t0008g0059 a0066c0074t0001g0266 |
3 | HG01081.hp2 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.256-2526A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660100 | |||||||
chr10:113660100 | TATAC | T | 127 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(124): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.256-2530_256-2527d others(6): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660100 | |||||||
chr10:113660126 | A | T | 1 | a0001c0001t0001g0223 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.256-2552T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660126 | |||||||
chr10:113660154 | C | T | 10 | a0002c0002t0004g0301 a0002c0002t0004g0302 a0002c0002t0004g0305 others(7): Show |
10 | HG00609.hp2 HG00621.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.255+2525G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660154 | |||||||
chr10:113660196 | C | T | 85 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(82): Show |
86 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.255+2483G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660196 | |||||||
chr10:113660222 | A | C | 1 | a0080c0085t0003g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.255+2457T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660222 | |||||||
chr10:113660360 | C | T | 2 | a0022c0114t0004g0272 a0022c0115t0004g0271 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.255+2319G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660360 | |||||||
chr10:113660376 | T | A | 1 | a0010c0008t0002g0263 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.255+2303A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660376 | |||||||
chr10:113660407 | G | T | 26 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(23): Show |
26 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.255+2272C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660407 | |||||||
chr10:113660498 | C | T | 2 | a0022c0114t0004g0272 a0022c0115t0004g0271 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.255+2181G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660498 | |||||||
chr10:113660562 | C | T | 1 | a0050c0050t0002g0237 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.255+2117G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660562 | |||||||
chr10:113660669 | A | C | 29 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(26): Show |
29 | HG00438.hp2 HG01433.hp2 HG01981.hp2 others(26): Show |
intron_variant | MODIFIER | c.255+2010T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660669 | |||||||
chr10:113660688 | C | G | 46 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(43): Show |
51 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.255+1991G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660688 | |||||||
chr10:113660739 | G | T | 1 | a0008c0078t0002g0065 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.255+1940C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660739 | |||||||
chr10:113660793 | G | T | 1 | a0003c0003t0003g0299 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.255+1886C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660793 | |||||||
chr10:113660898 | C | T | 2 | a0022c0114t0004g0272 a0022c0115t0004g0271 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.255+1781G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660898 | |||||||
chr10:113660976 | G | T | 31 | a0005c0005t0001g0104 a0005c0005t0001g0106 a0005c0005t0001g0108 others(28): Show |
35 | HG00544.hp2 HG01167.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.255+1703C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113660976 | |||||||
chr10:113661017 | T | C | 97 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(94): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.255+1662A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113661017 | |||||||
chr10:113661032 | A | C | 1 | a0001c0001t0001g0223 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.255+1647T>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113661032 | |||||||
chr10:113661301 | T | A | 1 | a0001c0001t0001g0223 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.255+1378A>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113661301 | |||||||
chr10:113661704 | T | G | 1 | a0031c0061t0002g0264 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.255+975A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113661704 | |||||||
chr10:113661724 | T | C | 24 | a0011c0016t0004g0276 a0011c0016t0004g0278 a0011c0016t0004g0292 others(21): Show |
27 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.255+955A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113661724 | |||||||
chr10:113661749 | C | T | 1 | a0002c0002t0004g0298 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.255+930G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113661749 | |||||||
chr10:113661785 | C | A | 2 | a0004c0004t0005g0054 a0056c0058t0005g0053 |
2 | HG01943.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.255+894G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113661785 | |||||||
chr10:113662033 | C | T | 1 | a0013c0019t0002g0109 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.255+646G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662033 | |||||||
chr10:113662059 | A | G | 1 | a0027c0063t0002g0227 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.255+620T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662059 | |||||||
chr10:113662130 | T | C | 47 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(44): Show |
47 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.255+549A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662130 | |||||||
chr10:113662149 | C | T | 46 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(43): Show |
51 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.255+530G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662149 | |||||||
chr10:113662183 | C | T | 6 | a0005c0005t0001g0104 a0005c0005t0001g0106 a0005c0005t0001g0108 others(3): Show |
7 | HG02572.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.255+496G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662183 | |||||||
chr10:113662202 | T | G | 3 | a0030c0033t0001g0061 a0030c0033t0001g0062 a0030c0048t0001g0060 |
3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.255+477A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662202 | |||||||
chr10:113662227 | T | G | 1 | a0031c0061t0002g0264 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.255+452A>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662227 | |||||||
chr10:113662237 | G | A | 213 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(210): Show |
222 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.255+442C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662237 | |||||||
chr10:113662337 | C | T | 2 | a0011c0016t0004g0276 a0040c0038t0003g0277 |
2 | HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.255+342G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662337 | |||||||
chr10:113662338 | G | C | 3 | a0030c0033t0001g0061 a0030c0033t0001g0062 a0030c0048t0001g0060 |
3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.255+341C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662338 | |||||||
chr10:113662408 | CTCTG | C | 47 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(44): Show |
47 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.255+267_255+270del others(4): Show |
NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662408 | |||||||
chr10:113662419 | A | T | 47 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(44): Show |
47 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.255+260T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662419 | |||||||
chr10:113662439 | C | T | 1 | a0004c0004t0005g0012 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.255+240G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662439 | |||||||
chr10:113662500 | C | G | 13 | a0011c0025t0002g0235 a0027c0034t0002g0234 a0027c0034t0002g0236 others(10): Show |
13 | HG01891.hp1 HG02486.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.255+179G>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662500 | |||||||
chr10:113662518 | G | A | 47 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(44): Show |
47 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.255+161C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662518 | |||||||
chr10:113662533 | C | A | 2 | a0009c0009t0001g0103 a0018c0015t0001g0102 |
2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.255+146G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 3/41 | chr10 | 113662533 | |||||||
chr10:113662866 | A | T | 3 | a0042c0047t0003g0274 a0042c0047t0003g0275 a0063c0113t0004g0273 |
3 | HG02258.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.168-100T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 2/41 | chr10 | 113662866 | |||||||
chr10:113662902 | C | A | 47 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(44): Show |
47 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.168-136G>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 2/41 | chr10 | 113662902 | |||||||
chr10:113663129 | T | C | 47 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(44): Show |
47 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.167+223A>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 2/41 | chr10 | 113663129 | |||||||
chr10:113663227 | G | T | 24 | a0011c0016t0004g0276 a0011c0016t0004g0278 a0011c0016t0004g0292 others(21): Show |
27 | HG00408.hp2 HG00544.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.167+125C>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 2/41 | chr10 | 113663227 | |||||||
chr10:113663255 | A | T | 2 | a0015c0013t0002g0063 a0015c0013t0002g0064 |
2 | NA18959.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.167+97T>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 2/41 | chr10 | 113663255 | |||||||
chr10:113663283 | G | A | 3 | a0037c0036t0002g0265 a0037c0036t0008g0059 a0066c0074t0001g0266 |
3 | HG01081.hp2 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.167+69C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 2/41 | chr10 | 113663283 | |||||||
chr10:113663335 | G | C | 130 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0136 others(127): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.167+17C>G | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 2/41 | chr10 | 113663335 | |||||||
chr10:113663501 | G | A | 1 | a0005c0021t0003g0383 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.73-55C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 1/41 | chr10 | 113663501 | |||||||
chr10:113663536 | G | A | 3 | a0022c0071t0002g0267 a0022c0072t0001g0268 a0022c0073t0001g0269 |
3 | HG01891.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.73-90C>T | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 1/41 | chr10 | 113663536 | |||||||
chr10:113663576 | A | G | 47 | a0010c0008t0002g0238 a0010c0008t0002g0239 a0010c0008t0002g0240 others(44): Show |
47 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.73-130T>C | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 1/41 | chr10 | 113663576 | |||||||
chr10:113663616 | CT | C | 157 | a0002c0002t0004g0011 a0002c0002t0004g0298 a0002c0002t0004g0301 others(154): Show |
161 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.73-171delA | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 1/41 | chr10 | 113663616 | |||||||
chr10:113663632 | C | T | 50 | a0004c0004t0005g0001 a0004c0004t0005g0012 a0004c0004t0005g0014 others(47): Show |
55 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.72+179G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 1/41 | chr10 | 113663632 | |||||||
chr10:113663793 | C | T | 3 | a0030c0033t0001g0061 a0030c0033t0001g0062 a0030c0048t0001g0060 |
3 | HG02572.hp2 HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.72+18G>A | NRAP | ENSG00000197893.14 | transcript | ENST00000359988.4 | protein_coding | 1/41 | chr10 | 113663793 |