Item | Value |
---|---|
geneid | 25904 |
ensemblid | ENSG00000182973.20 |
hgncid | 23817 |
symbol | CNOT10 |
name | CCR4-NOT transcription complex subunit 10 |
refseq_nuc | NM_015442.3 |
refseq_prot | NP_056257.1 |
ensembl_nuc | ENST00000328834.10 |
ensembl_prot | ENSP00000330060.5 |
mane_status | MANE Select |
chr | chr3 |
start | 32685188 |
end | 32773875 |
strand | + |
ver | v1.2 |
region | chr3:32685188-32773875 |
region5000 | chr3:32680188-32778875 |
regionname0 | CNOT10_chr3_32685188_32773875 |
regionname5000 | CNOT10_chr3_32680188_32778875 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 744 | 344 | 80 | 69 | 145 | 14 | 34 | 113 | CNOT10_chr3_32680188_32778875 | CNOT10 | MAADK others(739): Show |
chr3 | 32680188 | 32778875 |
a0002 | 0/0 | 744 | 8 | 6 | 2 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | MAADK others(739): Show |
chr3 | 32680188 | 32778875 |
a0003 | 0/0 | 744 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | MAADK others(739): Show |
chr3 | 32680188 | 32778875 |
a0004 | 0/0 | 744 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | MAADK others(739): Show |
chr3 | 32680188 | 32778875 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2232 | 343 | 80 | 69 | 144 | 14 | 34 | CNOT10_chr3_32680188_32778875 | CNOT10 | ATGGC others(2227): Show |
chr3 | 32680188 | 32778875 | ||
a0001c0003 | 0/0 | 2232 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | ATGGC others(2227): Show |
chr3 | 32680188 | 32778875 | ||
a0002c0002 | 0/0 | 2232 | 8 | 6 | 2 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | ATGGC others(2227): Show |
chr3 | 32680188 | 32778875 | ||
a0003c0004 | 0/0 | 2232 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | ATGGC others(2227): Show |
chr3 | 32680188 | 32778875 | ||
a0004c0005 | 0/0 | 2232 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | ATGGC others(2227): Show |
chr3 | 32680188 | 32778875 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2772 | 325 | 65 | 67 | 144 | 14 | 34 | CNOT10_chr3_32680188_32778875 | CNOT10 | AGTGG others(2767): Show |
chr3 | 32680188 | 32778875 |
a0001c0001t0002 | 0/0 | 2772 | 12 | 11 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | AGTGG others(2767): Show |
chr3 | 32680188 | 32778875 |
a0001c0001t0003 | 1/0 | 2772 | 4 | 2 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | AGTGG others(2767): Show |
chr3 | 32680188 | 32778875 |
a0001c0001t0004 | 0/0 | 2772 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | AGTGG others(2767): Show |
chr3 | 32680188 | 32778875 |
a0001c0001t0005 | 0/0 | 2772 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | AGTGG others(2767): Show |
chr3 | 32680188 | 32778875 |
a0001c0003t0001 | 0/0 | 2772 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | AGTGG others(2767): Show |
chr3 | 32680188 | 32778875 |
a0002c0002t0001 | 0/0 | 2772 | 8 | 6 | 2 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | AGTGG others(2767): Show |
chr3 | 32680188 | 32778875 |
a0003c0004t0001 | 0/0 | 2772 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | AGTGG others(2767): Show |
chr3 | 32680188 | 32778875 |
a0004c0005t0001 | 0/0 | 2772 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | AGTGG others(2767): Show |
chr3 | 32680188 | 32778875 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0258 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0003g0006 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0002c0002t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0002c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0002c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0002c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0002c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0003c0004t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
a0004c0005t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | GBR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | GBR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | GBR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | FIN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | FIN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | CHS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0273 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01106 | hp1 | a0003 | c0004 | t0001 | g0340 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0323 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0272 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | IBS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | IBS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | IBS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0346 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02083 | hp1 | a0001 | c0003 | t0001 | g0134 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CDX | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | CDX | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CDX | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CDX | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0348 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0036 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0214 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0321 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0229 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | MSL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0324 | AFR | MSL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | MSL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0270 | AFR | ESN | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0230 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0192 | AFR | GWD | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | MSL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | STU | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | STU | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | STU | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | BEB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | STU | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | STU | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | STU | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | STU | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | YRI | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | YRI | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | CHB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | YRI | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18969 | hp1 | a0004 | c0005 | t0001 | g0286 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | LWK | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0318 | AFR | LWK | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | LWK | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | YRI | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ASW | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ASW | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0331 | EUR | TSI | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0260 | EUR | TSI | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | TSI | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | TSI | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | GIH | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | GIH | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0269 | AFR | MSL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0271 | AFR | MSL | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0347 | AFR | USA | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | USA | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | USA | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | USA | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | LWK | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0258 | REF | REF | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0006 | REF | REF | CNOT10_chr3_32680188_32778875 | CNOT10 | chr3 | 32680188 | 32778875 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:32727697 | A | T | 1 | a0002 | 8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
missense_variant | MODERATE | c.1042A>T | p.Thr348Ser | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/19 | 1315/2772 | 1042/2235 | 348/744 | chr3 | 32727697 | |||
chr3:32727862 | A | C | 1 | a0004 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.1207A>C | p.Asn403His | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/19 | 1480/2772 | 1207/2235 | 403/744 | chr3 | 32727862 | |||
chr3:32759484 | A | T | 1 | a0003 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.1622A>T | p.Tyr541Phe | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/19 | 1895/2772 | 1622/2235 | 541/744 | chr3 | 32759484 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:32727699 | G | A | 1 | a0001c0003 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.1044G>A | p.Thr348Thr | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/19 | 1317/2772 | 1044/2235 | 348/744 | chr3 | 32727699 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:32685223 | T | C | 1 | a0001c0001t0004 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-238T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/19 | 238 | chr3 | 32685223 | ||||||
chr3:32773725 | A | G | 1 | a0001c0001t0002 | 12 | HG00639.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*114A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 19/19 | 114 | chr3 | 32773725 | ||||||
chr3:32773739 | A | T | 8 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(5): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
3_prime_UTR_variant | MODIFIER | c.*128A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 19/19 | 128 | chr3 | 32773739 | ||||||
chr3:32773769 | A | G | 1 | a0001c0001t0005 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*158A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 19/19 | 158 | chr3 | 32773769 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:32685594 | G | C | 1 | a0001c0001t0001g0007 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.22+112G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32685594 | |||||||
chr3:32685624 | C | T | 1 | a0001c0001t0001g0348 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.22+142C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32685624 | |||||||
chr3:32685654 | C | T | 1 | a0001c0001t0001g0347 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.22+172C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32685654 | |||||||
chr3:32685830 | A | G | 1 | a0001c0001t0002g0346 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.22+348A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32685830 | |||||||
chr3:32685939 | C | CT | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.22+467dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32685939 | ||||||
chr3:32686073 | T | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+591T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32686073 | |||||||
chr3:32686085 | A | G | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.22+603A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32686085 | |||||||
chr3:32686160 | T | G | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.22+678T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32686160 | |||||||
chr3:32686304 | C | G | 1 | a0001c0001t0001g0331 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.22+822C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32686304 | |||||||
chr3:32686319 | A | G | 1 | a0001c0001t0001g0007 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.22+837A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32686319 | |||||||
chr3:32686339 | A | G | 3 | a0001c0001t0001g0328 a0001c0001t0001g0329 a0001c0001t0001g0330 |
3 | NA18991.hp2 NA19005.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.22+857A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32686339 | |||||||
chr3:32686399 | G | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+917G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32686399 | |||||||
chr3:32686611 | G | A | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0346 |
3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.22+1129G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32686611 | |||||||
chr3:32686750 | G | T | 1 | a0001c0001t0001g0327 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.22+1268G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32686750 | |||||||
chr3:32686912 | A | G | 1 | a0001c0001t0001g0326 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.22+1430A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32686912 | |||||||
chr3:32686979 | C | CCT | 52 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(49): Show |
52 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.22+1498_22+1499dup others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32686979 | ||||||
chr3:32687103 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.22+1621A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687103 | |||||||
chr3:32687152 | A | G | 1 | a0001c0001t0001g0325 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.22+1670A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687152 | |||||||
chr3:32687286 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+1804G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687286 | |||||||
chr3:32687286 | G | GC | 10 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0085 others(7): Show |
10 | HG01109.hp2 HG01255.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.22+1810dupC | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687286 | ||||||
chr3:32687293 | G | C | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.22+1811G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687293 | |||||||
chr3:32687295 | T | C | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.22+1813T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687295 | |||||||
chr3:32687297 | T | A | 1 | a0001c0001t0001g0092 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.22+1815T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687297 | |||||||
chr3:32687343 | A | G | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.22+1861A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687343 | |||||||
chr3:32687409 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.22+1927G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687409 | |||||||
chr3:32687420 | C | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+1938C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687420 | |||||||
chr3:32687437 | C | G | 53 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0034 others(50): Show |
53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.22+1955C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687437 | |||||||
chr3:32687438 | G | GGTTTTTT others(5): Show |
53 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(50): Show |
53 | HG00323.hp1 HG00438.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.22+1957_22+1968dup others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687438 | ||||||
chr3:32687439 | G | GTTTTTTT others(4): Show |
1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.22+1959_22+1969dup others(11): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687439 | ||||||
chr3:32687439 | G | GTTTTTTT others(6): Show |
33 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0089 others(30): Show |
34 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.22+1968_22+1969ins others(13): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687439 | ||||||
chr3:32687439 | G | GTTTTTTT others(7): Show |
7 | a0001c0001t0001g0005 a0001c0001t0001g0307 a0001c0001t0001g0308 others(4): Show |
8 | HG00735.hp1 HG01175.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.22+1968_22+1969ins others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687439 | ||||||
chr3:32687439 | G | GTTTTTTT others(8): Show |
1 | a0001c0001t0001g0312 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.22+1968_22+1969ins others(15): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687439 | ||||||
chr3:32687439 | G | GTTTTTTT others(9): Show |
1 | a0001c0001t0001g0313 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.22+1968_22+1969ins others(16): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687439 | ||||||
chr3:32687439 | G | T | 53 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0034 others(50): Show |
53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.22+1957G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687439 | |||||||
chr3:32687440 | T | TTTTTTTT others(4): Show |
27 | a0001c0001t0001g0003 a0001c0001t0001g0093 a0001c0001t0001g0187 others(24): Show |
28 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.22+1968_22+1969ins others(11): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687440 | ||||||
chr3:32687440 | T | TTTTTTTT others(5): Show |
1 | a0001c0001t0001g0090 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.22+1970_22+1981dup others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687440 | ||||||
chr3:32687441 | T | TTTTTTTT others(2): Show |
6 | a0001c0001t0001g0034 a0001c0001t0001g0079 a0001c0001t0001g0080 others(3): Show |
6 | HG00673.hp2 HG01255.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.22+1967_22+1968ins others(9): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687441 | ||||||
chr3:32687441 | T | TTTTTTTT others(3): Show |
106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(103): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.22+1968_22+1969ins others(10): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687441 | ||||||
chr3:32687442 | T | TTTTTTTT others(1): Show |
26 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0038 others(23): Show |
26 | HG00140.hp2 HG00438.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.22+1967_22+1968ins others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687442 | ||||||
chr3:32687442 | T | TTTTTTTT others(2): Show |
12 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(9): Show |
12 | HG00639.hp1 HG02258.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.22+1968_22+1969ins others(9): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687442 | ||||||
chr3:32687443 | T | TTTTTTTG | 21 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0041 others(18): Show |
21 | HG00408.hp1 HG00639.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.22+1967_22+1968ins others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687443 | ||||||
chr3:32687443 | T | TTTTTTTT others(5): Show |
1 | a0001c0001t0001g0094 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.22+1968_22+1969ins others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687443 | ||||||
chr3:32687444 | T | TTTTTTG | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.22+1967_22+1968ins others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687444 | ||||||
chr3:32687446 | T | TTTTTGTT others(6): Show |
1 | a0001c0001t0001g0095 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.22+1968_22+1969ins others(13): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687446 | ||||||
chr3:32687450 | T | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+1968T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687450 | |||||||
chr3:32687452 | G | GTTTTTTT others(6): Show |
3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02273.hp1 NA18974.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.22+1975_22+1987dup others(13): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687452 | ||||||
chr3:32687452 | G | T | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(303): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.22+1970G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687452 | |||||||
chr3:32687453 | T | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0033 others(96): Show |
101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.22+1971T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687453 | |||||||
chr3:32687453 | T | TTTTTTTT others(4): Show |
1 | a0001c0001t0001g0314 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.22+1981_22+1982ins others(11): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687453 | ||||||
chr3:32687454 | T | G | 11 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0091 others(8): Show |
11 | HG01928.hp2 HG02004.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.22+1972T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687454 | |||||||
chr3:32687454 | T | TTTTTTG | 11 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(8): Show |
11 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.22+1977_22+1978ins others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687454 | ||||||
chr3:32687458 | T | G | 1 | a0001c0001t0001g0328 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.22+1976T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687458 | |||||||
chr3:32687459 | T | TTTTGTTT others(5): Show |
22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+1980_22+1981ins others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32687459 | ||||||
chr3:32687462 | T | G | 1 | a0001c0001t0001g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.22+1980T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687462 | |||||||
chr3:32687465 | T | G | 1 | a0001c0001t0001g0096 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.22+1983T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687465 | |||||||
chr3:32687471 | A | G | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0346 |
3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.22+1989A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687471 | |||||||
chr3:32687486 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.22+2004C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687486 | |||||||
chr3:32687491 | A | C | 1 | a0001c0001t0001g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.22+2009A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687491 | |||||||
chr3:32687538 | G | A | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.22+2056G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687538 | |||||||
chr3:32687545 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.22+2063G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687545 | |||||||
chr3:32687804 | G | GT | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+2322_22+2323ins others(1): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687804 | |||||||
chr3:32687805 | A | T | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+2323A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687805 | |||||||
chr3:32687931 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.22+2449A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687931 | |||||||
chr3:32687944 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.22+2462C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687944 | |||||||
chr3:32687962 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.22+2480G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32687962 | |||||||
chr3:32688076 | G | T | 1 | a0001c0001t0001g0091 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.22+2594G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688076 | |||||||
chr3:32688200 | T | G | 5 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(2): Show |
5 | NA18947.hp2 NA18950.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+2718T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688200 | |||||||
chr3:32688287 | A | T | 1 | a0001c0001t0001g0078 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.22+2805A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688287 | |||||||
chr3:32688354 | T | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+2872T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688354 | |||||||
chr3:32688393 | G | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0057 |
2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.22+2911G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688393 | |||||||
chr3:32688400 | A | G | 1 | a0001c0001t0001g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.22+2918A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688400 | |||||||
chr3:32688467 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.22+2985C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688467 | |||||||
chr3:32688570 | C | A | 1 | a0001c0001t0001g0307 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.22+3088C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688570 | |||||||
chr3:32688616 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(114): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.22+3134A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688616 | |||||||
chr3:32688623 | A | G | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0346 |
3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.22+3141A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688623 | |||||||
chr3:32688698 | A | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(2): Show |
5 | HG01168.hp1 HG01169.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.22+3216A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688698 | |||||||
chr3:32688858 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.22+3376T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688858 | |||||||
chr3:32688872 | G | A | 1 | a0001c0001t0001g0333 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.22+3390G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688872 | |||||||
chr3:32688927 | C | T | 23 | a0001c0001t0001g0087 a0001c0001t0001g0210 a0001c0001t0001g0213 others(20): Show |
23 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.22+3445C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688927 | |||||||
chr3:32688989 | G | C | 1 | a0001c0001t0003g0323 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.22+3507G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688989 | |||||||
chr3:32688994 | A | G | 346 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(343): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.22+3512A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32688994 | |||||||
chr3:32689312 | C | A | 4 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0209 others(1): Show |
4 | HG02258.hp1 HG06807.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.22+3830C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32689312 | |||||||
chr3:32689318 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.22+3836C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32689318 | |||||||
chr3:32689353 | C | CA | 9 | a0001c0001t0001g0058 a0001c0001t0001g0097 a0001c0001t0001g0103 others(6): Show |
9 | HG01074.hp2 HG01496.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+3886dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32689353 | ||||||
chr3:32689353 | CA | C | 39 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(36): Show |
39 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.22+3886delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32689353 | ||||||
chr3:32689745 | G | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+4263G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32689745 | |||||||
chr3:32689834 | A | C | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.22+4352A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32689834 | |||||||
chr3:32689929 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | NA18946.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.22+4447T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32689929 | |||||||
chr3:32689965 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.22+4483A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32689965 | |||||||
chr3:32689988 | T | A | 1 | a0001c0001t0001g0333 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.22+4506T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32689988 | |||||||
chr3:32690144 | CTGATTTA others(21): Show |
C | 1 | a0001c0001t0001g0091 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.22+4663_22+4690del others(28): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690144 | |||||||
chr3:32690184 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.22+4702G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690184 | |||||||
chr3:32690268 | T | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+4786T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690268 | |||||||
chr3:32690364 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.22+4882G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690364 | |||||||
chr3:32690414 | T | A | 23 | a0001c0001t0001g0087 a0001c0001t0001g0210 a0001c0001t0001g0213 others(20): Show |
23 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.22+4932T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690414 | |||||||
chr3:32690527 | G | T | 8 | a0002c0002t0001g0214 a0002c0002t0001g0229 a0002c0002t0001g0230 others(5): Show |
8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.22+5045G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690527 | |||||||
chr3:32690539 | T | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+5057T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690539 | |||||||
chr3:32690551 | A | AT | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(119): Show |
124 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.22+5082dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32690551 | ||||||
chr3:32690577 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.22+5095C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690577 | |||||||
chr3:32690578 | G | A | 1 | a0001c0001t0001g0011 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.22+5096G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690578 | |||||||
chr3:32690615 | T | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+5133T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690615 | |||||||
chr3:32690639 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.22+5157C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690639 | |||||||
chr3:32690664 | A | C | 7 | a0001c0001t0001g0097 a0001c0001t0001g0181 a0001c0001t0001g0182 others(4): Show |
7 | NA18943.hp2 NA18946.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.22+5182A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690664 | |||||||
chr3:32690708 | G | T | 1 | a0001c0001t0001g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.22+5226G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690708 | |||||||
chr3:32690749 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+5267A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690749 | |||||||
chr3:32690751 | G | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+5269G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690751 | |||||||
chr3:32690754 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+5272G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690754 | |||||||
chr3:32690758 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+5276A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690758 | |||||||
chr3:32690761 | C | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+5279C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690761 | |||||||
chr3:32690783 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+5301A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690783 | |||||||
chr3:32690807 | A | G | 3 | a0001c0001t0001g0201 a0002c0002t0001g0272 a0002c0002t0001g0273 |
3 | HG00735.hp2 HG01081.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.22+5325A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690807 | |||||||
chr3:32690827 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.22+5345A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690827 | |||||||
chr3:32690936 | C | T | 52 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(49): Show |
52 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.22+5454C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690936 | |||||||
chr3:32690952 | A | G | 1 | a0001c0001t0001g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.22+5470A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32690952 | |||||||
chr3:32690997 | C | CT | 248 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(245): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.22+5531dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32690997 | ||||||
chr3:32690997 | C | CTT | 62 | a0001c0001t0001g0007 a0001c0001t0001g0030 a0001c0001t0001g0033 others(59): Show |
62 | HG00140.hp2 HG00408.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.22+5530_22+5531dup others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32690997 | ||||||
chr3:32690997 | C | CTTTT | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+5528_22+5531dup others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32690997 | ||||||
chr3:32691159 | C | CT | 17 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0095 others(14): Show |
19 | HG00735.hp1 HG01071.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.22+5697dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32691159 | ||||||
chr3:32691159 | CT | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(180): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.22+5697delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32691159 | ||||||
chr3:32691161 | T | A | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.22+5679T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32691161 | |||||||
chr3:32691162 | T | A | 34 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(31): Show |
34 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.22+5680T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32691162 | |||||||
chr3:32691168 | T | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+5686T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32691168 | |||||||
chr3:32691230 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG02735.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.22+5748C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32691230 | |||||||
chr3:32691429 | G | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 |
3 | HG02970.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.22+5947G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32691429 | |||||||
chr3:32691512 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.22+6030G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32691512 | |||||||
chr3:32691534 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.22+6052T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32691534 | |||||||
chr3:32691593 | T | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+6111T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32691593 | |||||||
chr3:32691914 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0001g0082 |
2 | NA19068.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.22+6432G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32691914 | |||||||
chr3:32691919 | G | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0018 others(6): Show |
9 | NA18955.hp2 NA18960.hp2 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+6437G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32691919 | |||||||
chr3:32692014 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.22+6532G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32692014 | |||||||
chr3:32692051 | C | CA | 60 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(57): Show |
60 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.22+6586dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32692051 | ||||||
chr3:32692077 | C | T | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.22+6595C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32692077 | |||||||
chr3:32692079 | CG | C | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.22+6598delG | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32692079 | |||||||
chr3:32692080 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.22+6598G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32692080 | |||||||
chr3:32692109 | C | T | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0346 |
3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.22+6627C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32692109 | |||||||
chr3:32692163 | T | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+6681T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32692163 | |||||||
chr3:32692252 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.22+6770A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32692252 | |||||||
chr3:32692429 | T | C | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.22+6947T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32692429 | |||||||
chr3:32692880 | G | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+7398G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32692880 | |||||||
chr3:32693142 | A | T | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.22+7660A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693142 | |||||||
chr3:32693196 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.22+7714A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693196 | |||||||
chr3:32693200 | G | T | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.22+7718G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693200 | |||||||
chr3:32693293 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.22+7811C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693293 | |||||||
chr3:32693310 | G | A | 3 | a0001c0001t0002g0208 a0001c0001t0002g0209 a0001c0001t0002g0318 |
3 | HG02258.hp1 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.22+7828G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693310 | |||||||
chr3:32693312 | A | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+7830A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693312 | |||||||
chr3:32693466 | C | T | 1 | a0001c0001t0001g0347 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.22+7984C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693466 | |||||||
chr3:32693498 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.22+8016G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693498 | |||||||
chr3:32693543 | C | CT | 27 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(24): Show |
27 | HG01168.hp1 HG01169.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.22+8076dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32693543 | ||||||
chr3:32693690 | C | T | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.22+8208C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693690 | |||||||
chr3:32693819 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.22+8337G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693819 | |||||||
chr3:32693822 | G | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.22+8340G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32693822 | |||||||
chr3:32694138 | AT | A | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.22+8670delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32694138 | ||||||
chr3:32694138 | ATT | A | 10 | a0001c0001t0001g0052 a0001c0001t0001g0225 a0001c0001t0001g0237 others(7): Show |
10 | HG01069.hp1 HG01167.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.22+8669_22+8670del others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32694138 | ||||||
chr3:32694264 | C | T | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.22+8782C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694264 | |||||||
chr3:32694373 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | NA18946.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.22+8891G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694373 | |||||||
chr3:32694598 | T | C | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.22+9116T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694598 | |||||||
chr3:32694635 | G | T | 1 | a0001c0001t0001g0333 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.22+9153G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694635 | |||||||
chr3:32694678 | T | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-9190T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694678 | |||||||
chr3:32694734 | T | G | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(98): Show |
104 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.23-9134T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694734 | |||||||
chr3:32694754 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.23-9114T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694754 | |||||||
chr3:32694808 | C | G | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.23-9060C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694808 | |||||||
chr3:32694853 | A | T | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-9015A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694853 | |||||||
chr3:32694887 | C | G | 1 | a0001c0001t0001g0171 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.23-8981C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694887 | |||||||
chr3:32694889 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.23-8979T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694889 | |||||||
chr3:32694960 | G | A | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-8908G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32694960 | |||||||
chr3:32695171 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.23-8697A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32695171 | |||||||
chr3:32695267 | A | G | 1 | a0001c0001t0002g0346 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.23-8601A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32695267 | |||||||
chr3:32695325 | T | G | 1 | a0001c0001t0001g0342 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.23-8543T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32695325 | |||||||
chr3:32695611 | A | G | 1 | a0001c0001t0001g0347 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.23-8257A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32695611 | |||||||
chr3:32695723 | A | T | 1 | a0001c0001t0001g0094 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.23-8145A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32695723 | |||||||
chr3:32695761 | A | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(2): Show |
5 | NA18960.hp2 NA18962.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-8107A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32695761 | |||||||
chr3:32695963 | AAG | A | 5 | a0001c0001t0001g0333 a0002c0002t0001g0214 a0002c0002t0001g0229 others(2): Show |
5 | HG01081.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-7900_23-7899del others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695963 | ||||||
chr3:32695966 | AGAGTGTG others(3): Show |
A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0332 |
2 | HG02132.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.23-7900_23-7891del others(10): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695966 | ||||||
chr3:32695966 | AGAGTGTG others(5): Show |
A | 20 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(17): Show |
20 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.23-7900_23-7889del others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695966 | ||||||
chr3:32695966 | AGAGTGTG others(7): Show |
A | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-7900_23-7887del others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695966 | ||||||
chr3:32695966 | AGAGTGTG others(9): Show |
A | 9 | a0001c0001t0001g0334 a0001c0001t0001g0339 a0001c0001t0001g0341 others(6): Show |
9 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.23-7900_23-7885del others(16): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695966 | ||||||
chr3:32695968 | A | AGT | 39 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(36): Show |
41 | HG00438.hp2 HG00642.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.23-7853_23-7852dup others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | ||||||
chr3:32695968 | A | AGTGT | 25 | a0001c0001t0001g0095 a0001c0001t0001g0106 a0001c0001t0001g0109 others(22): Show |
25 | HG00558.hp1 HG00738.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.23-7855_23-7852dup others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | ||||||
chr3:32695968 | A | AGTGTGT | 18 | a0001c0001t0001g0094 a0001c0001t0001g0102 a0001c0001t0001g0121 others(15): Show |
18 | HG00597.hp2 HG01255.hp1 HG02148.hp1 others(15): Show |
intron_variant | MODIFIER | c.23-7857_23-7852dup others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | ||||||
chr3:32695968 | A | AGTGTGTG others(1): Show |
8 | a0001c0001t0001g0001 a0001c0001t0001g0108 a0001c0001t0001g0125 others(5): Show |
8 | HG02074.hp1 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.23-7859_23-7852dup others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | ||||||
chr3:32695968 | A | AGTGTGTG others(3): Show |
2 | a0001c0001t0001g0153 a0001c0001t0004g0192 |
2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.23-7861_23-7852dup others(10): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | ||||||
chr3:32695968 | A | AGTGTGTG others(5): Show |
1 | a0001c0001t0001g0132 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.23-7863_23-7852dup others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | ||||||
chr3:32695968 | A | T | 3 | a0001c0001t0001g0030 a0002c0002t0001g0269 a0002c0002t0001g0271 |
3 | HG03471.hp1 HG03471.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.23-7900A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32695968 | |||||||
chr3:32695968 | AGT | A | 39 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0099 others(36): Show |
39 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.23-7853_23-7852del others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | ||||||
chr3:32695968 | AGTGT | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0086 a0001c0001t0001g0090 others(30): Show |
33 | HG00408.hp2 HG00733.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.23-7855_23-7852del others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | ||||||
chr3:32695968 | AGTGTGT | A | 9 | a0001c0001t0001g0087 a0001c0001t0001g0096 a0001c0001t0001g0107 others(6): Show |
9 | HG00099.hp1 HG01891.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.23-7857_23-7852del others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | ||||||
chr3:32695968 | AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0001g0319 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.23-7861_23-7852del others(10): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | ||||||
chr3:32695968 | AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0001g0276 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.23-7863_23-7852del others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | ||||||
chr3:32695968 | AGTGTGTG others(7): Show |
A | 1 | a0001c0001t0001g0063 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.23-7865_23-7852del others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | ||||||
chr3:32695968 | AGTGTGTG others(9): Show |
A | 7 | a0001c0001t0001g0050 a0001c0001t0001g0056 a0001c0001t0001g0072 others(4): Show |
7 | HG00408.hp1 HG01433.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-7867_23-7852del others(16): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | ||||||
chr3:32695968 | AGTGTGTG others(11): Show |
A | 46 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(43): Show |
46 | HG00140.hp2 HG00438.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.23-7869_23-7852del others(18): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | ||||||
chr3:32695968 | AGTGTGTG others(13): Show |
A | 6 | a0001c0001t0001g0058 a0001c0001t0001g0084 a0001c0001t0001g0126 others(3): Show |
6 | HG00639.hp2 HG01109.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.23-7871_23-7852del others(20): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32695968 | ||||||
chr3:32696011 | G | T | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.23-7857G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696011 | |||||||
chr3:32696037 | C | T | 1 | a0001c0001t0001g0002 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.23-7831C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696037 | |||||||
chr3:32696068 | C | A | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.23-7800C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696068 | |||||||
chr3:32696144 | T | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.23-7724T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696144 | |||||||
chr3:32696212 | A | G | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.23-7656A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696212 | |||||||
chr3:32696213 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.23-7655G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696213 | |||||||
chr3:32696311 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.23-7557G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696311 | |||||||
chr3:32696315 | C | CA | 21 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(18): Show |
21 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.23-7541dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32696315 | ||||||
chr3:32696325 | AAAG | A | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.23-7528_23-7526del others(3): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32696325 | ||||||
chr3:32696328 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.23-7540G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696328 | |||||||
chr3:32696331 | G | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0332 a0001c0001t0001g0333 others(13): Show |
16 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.23-7537G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696331 | |||||||
chr3:32696333 | A | G | 1 | a0001c0001t0001g0010 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.23-7535A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696333 | |||||||
chr3:32696334 | G | A | 1 | a0001c0001t0001g0010 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.23-7534G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696334 | |||||||
chr3:32696446 | A | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(98): Show |
103 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.23-7422A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696446 | |||||||
chr3:32696498 | T | G | 1 | a0001c0001t0003g0323 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.23-7370T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696498 | |||||||
chr3:32696516 | G | A | 2 | a0001c0001t0001g0235 a0001c0001t0001g0288 |
2 | HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.23-7352G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696516 | |||||||
chr3:32696534 | T | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-7334T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696534 | |||||||
chr3:32696566 | G | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.23-7302G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696566 | |||||||
chr3:32696790 | T | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-7078T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696790 | |||||||
chr3:32696931 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.23-6937G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32696931 | |||||||
chr3:32697255 | C | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.23-6613C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697255 | |||||||
chr3:32697276 | A | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-6592A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697276 | |||||||
chr3:32697336 | A | G | 1 | a0001c0001t0002g0212 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.23-6532A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697336 | |||||||
chr3:32697450 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.23-6418T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697450 | |||||||
chr3:32697450 | T | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(97): Show |
102 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.23-6418T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697450 | |||||||
chr3:32697534 | G | A | 1 | a0001c0001t0001g0239 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.23-6334G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697534 | |||||||
chr3:32697540 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.23-6328G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697540 | |||||||
chr3:32697629 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.23-6239C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697629 | |||||||
chr3:32697645 | A | G | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
134 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.23-6223A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697645 | |||||||
chr3:32697660 | A | G | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0346 |
3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.23-6208A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697660 | |||||||
chr3:32697667 | G | T | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-6201G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697667 | |||||||
chr3:32697691 | T | A | 1 | a0001c0001t0001g0223 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.23-6177T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697691 | |||||||
chr3:32697722 | T | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-6146T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697722 | |||||||
chr3:32697813 | A | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-6055A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697813 | |||||||
chr3:32697894 | A | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-5974A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32697894 | |||||||
chr3:32698489 | T | G | 1 | a0001c0001t0001g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.23-5379T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32698489 | |||||||
chr3:32698611 | T | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-5257T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32698611 | |||||||
chr3:32698749 | A | G | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0282 |
3 | HG00408.hp1 HG02155.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.23-5119A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32698749 | |||||||
chr3:32698768 | T | C | 1 | a0001c0001t0001g0327 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.23-5100T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32698768 | |||||||
chr3:32698842 | T | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-5026T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32698842 | |||||||
chr3:32698850 | A | G | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.23-5018A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32698850 | |||||||
chr3:32699032 | C | T | 23 | a0001c0001t0001g0087 a0001c0001t0001g0210 a0001c0001t0001g0213 others(20): Show |
23 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.23-4836C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32699032 | |||||||
chr3:32699133 | A | G | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-4735A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32699133 | |||||||
chr3:32699274 | A | G | 100 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(97): Show |
103 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.23-4594A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32699274 | |||||||
chr3:32699349 | G | A | 13 | a0001c0001t0001g0087 a0001c0001t0001g0210 a0001c0001t0001g0213 others(10): Show |
13 | HG01515.hp1 HG01517.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.23-4519G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32699349 | |||||||
chr3:32699423 | T | C | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0282 |
3 | HG00408.hp1 HG02155.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.23-4445T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32699423 | |||||||
chr3:32699535 | C | T | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.23-4333C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32699535 | |||||||
chr3:32699721 | C | T | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.23-4147C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32699721 | |||||||
chr3:32699975 | C | CT | 46 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(43): Show |
46 | HG00140.hp1 HG01069.hp1 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.23-3875dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32699975 | ||||||
chr3:32699975 | CT | C | 8 | a0001c0001t0001g0038 a0001c0001t0001g0105 a0001c0001t0001g0133 others(5): Show |
8 | HG01168.hp2 HG01169.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.23-3875delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32699975 | ||||||
chr3:32700020 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.23-3848G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32700020 | |||||||
chr3:32700041 | T | A | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.23-3827T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32700041 | |||||||
chr3:32700107 | C | G | 1 | a0001c0001t0001g0034 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.23-3761C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32700107 | |||||||
chr3:32700112 | A | G | 1 | a0001c0001t0001g0267 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.23-3756A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32700112 | |||||||
chr3:32700255 | C | T | 8 | a0002c0002t0001g0214 a0002c0002t0001g0229 a0002c0002t0001g0230 others(5): Show |
8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.23-3613C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32700255 | |||||||
chr3:32700275 | C | G | 1 | a0001c0001t0001g0038 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.23-3593C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32700275 | |||||||
chr3:32700639 | G | A | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.23-3229G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32700639 | |||||||
chr3:32700826 | A | G | 4 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0215 others(1): Show |
4 | HG00639.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.23-3042A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32700826 | |||||||
chr3:32700962 | G | T | 1 | a0001c0001t0001g0010 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.23-2906G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32700962 | |||||||
chr3:32700999 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.23-2869C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32700999 | |||||||
chr3:32701167 | T | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-2701T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32701167 | |||||||
chr3:32701284 | CTA | C | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.23-2577_23-2576del others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32701284 | ||||||
chr3:32701443 | A | C | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.23-2425A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32701443 | |||||||
chr3:32701622 | C | G | 3 | a0001c0001t0001g0264 a0001c0001t0001g0302 a0001c0001t0001g0303 |
3 | HG00597.hp1 HG02135.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.23-2246C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32701622 | |||||||
chr3:32701792 | G | T | 346 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(343): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.23-2076G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32701792 | |||||||
chr3:32701853 | T | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-2015T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32701853 | |||||||
chr3:32701861 | C | T | 1 | a0001c0001t0002g0346 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.23-2007C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32701861 | |||||||
chr3:32701898 | T | C | 53 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(50): Show |
53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.23-1970T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32701898 | |||||||
chr3:32701932 | A | G | 1 | a0001c0001t0001g0023 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.23-1936A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32701932 | |||||||
chr3:32702073 | C | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
134 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.23-1795C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702073 | |||||||
chr3:32702087 | C | T | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.23-1781C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702087 | |||||||
chr3:32702088 | A | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.23-1780A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702088 | |||||||
chr3:32702097 | C | CT | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(143): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.23-1756dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32702097 | ||||||
chr3:32702097 | C | CTT | 13 | a0001c0001t0001g0120 a0001c0001t0001g0194 a0001c0001t0001g0195 others(10): Show |
13 | HG00438.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.23-1757_23-1756dup others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32702097 | ||||||
chr3:32702257 | A | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(98): Show |
103 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.23-1611A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702257 | |||||||
chr3:32702325 | T | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0116 |
2 | HG00140.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.23-1543T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702325 | |||||||
chr3:32702338 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.23-1530T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702338 | |||||||
chr3:32702359 | AT | A | 55 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0034 others(52): Show |
55 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.23-1504delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32702359 | ||||||
chr3:32702514 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.23-1354A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702514 | |||||||
chr3:32702530 | T | C | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.23-1338T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702530 | |||||||
chr3:32702606 | A | G | 1 | a0001c0001t0001g0263 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.23-1262A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702606 | |||||||
chr3:32702664 | G | A | 2 | a0001c0001t0001g0179 a0001c0003t0001g0134 |
2 | HG02083.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.23-1204G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702664 | |||||||
chr3:32702916 | G | GT | 6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(3): Show |
6 | NA18945.hp1 NA18955.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.23-939dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32702916 | ||||||
chr3:32702916 | GT | G | 39 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(36): Show |
39 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.23-939delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32702916 | ||||||
chr3:32702976 | A | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.23-892A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702976 | |||||||
chr3:32702985 | C | G | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.23-883C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32702985 | |||||||
chr3:32703013 | G | A | 1 | a0001c0001t0001g0238 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.23-855G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703013 | |||||||
chr3:32703078 | A | AT | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(294): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.23-771dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32703078 | ||||||
chr3:32703078 | A | ATT | 23 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0071 others(20): Show |
25 | HG00140.hp2 HG00735.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.23-772_23-771dupTT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr3 | 32703078 | ||||||
chr3:32703096 | T | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0333 |
2 | HG01255.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.23-772T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703096 | |||||||
chr3:32703104 | T | C | 29 | a0001c0001t0001g0087 a0001c0001t0001g0131 a0001c0001t0001g0199 others(26): Show |
29 | HG00639.hp1 HG01081.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.23-764T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703104 | |||||||
chr3:32703147 | A | G | 59 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0023 others(56): Show |
60 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.23-721A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703147 | |||||||
chr3:32703203 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.23-665C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703203 | |||||||
chr3:32703213 | C | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(17): Show |
20 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.23-655C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703213 | |||||||
chr3:32703215 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(168): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.23-653T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703215 | |||||||
chr3:32703219 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(2): Show |
5 | NA18960.hp2 NA18962.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.23-649T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703219 | |||||||
chr3:32703466 | C | T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(96): Show |
102 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.23-402C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703466 | |||||||
chr3:32703579 | A | G | 1 | a0004c0005t0001g0286 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.23-289A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703579 | |||||||
chr3:32703623 | A | G | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.23-245A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 1/18 | chr3 | 32703623 | |||||||
chr3:32703983 | G | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.117+21G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 2/18 | chr3 | 32703983 | |||||||
chr3:32704121 | T | G | 1 | a0001c0001t0001g0333 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.117+159T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 2/18 | chr3 | 32704121 | |||||||
chr3:32704140 | A | G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0059 a0001c0001t0001g0065 others(1): Show |
4 | HG00438.hp1 NA19007.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+178A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 2/18 | chr3 | 32704140 | |||||||
chr3:32704304 | T | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(98): Show |
103 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.117+342T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 2/18 | chr3 | 32704304 | |||||||
chr3:32704470 | T | C | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.118-341T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 2/18 | chr3 | 32704470 | |||||||
chr3:32704545 | A | G | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.118-266A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 2/18 | chr3 | 32704545 | |||||||
chr3:32704796 | G | GT | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
splice_acceptor_variant&intron_variant | HIGH | c.118-3dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr3 | 32704796 | ||||||
chr3:32705030 | A | G | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
111 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.279+58A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32705030 | |||||||
chr3:32705164 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | NA18612.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.279+192T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32705164 | |||||||
chr3:32705267 | A | G | 2 | a0001c0001t0001g0224 a0001c0001t0001g0257 |
2 | HG02080.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.279+295A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32705267 | |||||||
chr3:32705485 | G | C | 1 | a0001c0001t0001g0333 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.279+513G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32705485 | |||||||
chr3:32705566 | T | C | 1 | a0001c0001t0001g0300 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.279+594T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32705566 | |||||||
chr3:32705709 | A | T | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+737A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32705709 | |||||||
chr3:32705762 | C | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(1): Show |
4 | NA18960.hp2 NA18962.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+790C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32705762 | |||||||
chr3:32705783 | T | C | 54 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0034 others(51): Show |
54 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.279+811T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32705783 | |||||||
chr3:32706152 | G | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.279+1180G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32706152 | |||||||
chr3:32706248 | A | G | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.279+1276A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32706248 | |||||||
chr3:32706546 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.279+1574T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32706546 | |||||||
chr3:32706628 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.279+1656A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32706628 | |||||||
chr3:32706803 | C | G | 1 | a0001c0001t0001g0333 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.279+1831C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32706803 | |||||||
chr3:32706925 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.280-1745T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32706925 | |||||||
chr3:32707100 | A | G | 1 | a0001c0001t0002g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.280-1570A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32707100 | |||||||
chr3:32707275 | CT | C | 6 | a0001c0001t0001g0224 a0001c0001t0001g0241 a0001c0001t0001g0257 others(3): Show |
6 | HG00408.hp2 HG02080.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.280-1383delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr3 | 32707275 | ||||||
chr3:32707308 | G | A | 2 | a0001c0001t0001g0179 a0001c0003t0001g0134 |
2 | HG02083.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.280-1362G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32707308 | |||||||
chr3:32707422 | G | A | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.280-1248G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32707422 | |||||||
chr3:32707570 | G | A | 1 | a0001c0001t0003g0324 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.280-1100G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32707570 | |||||||
chr3:32707583 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.280-1087C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32707583 | |||||||
chr3:32707812 | A | G | 1 | a0001c0001t0001g0299 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.280-858A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32707812 | |||||||
chr3:32708031 | A | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.280-639A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32708031 | |||||||
chr3:32708037 | G | C | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.280-633G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32708037 | |||||||
chr3:32708194 | G | A | 8 | a0002c0002t0001g0214 a0002c0002t0001g0229 a0002c0002t0001g0230 others(5): Show |
8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.280-476G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32708194 | |||||||
chr3:32708275 | T | C | 1 | a0001c0001t0001g0311 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.280-395T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32708275 | |||||||
chr3:32708289 | T | G | 1 | a0001c0001t0001g0095 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.280-381T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32708289 | |||||||
chr3:32708451 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.280-219T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32708451 | |||||||
chr3:32708489 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.280-181A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 3/18 | chr3 | 32708489 | |||||||
chr3:32708839 | C | G | 1 | a0001c0001t0001g0092 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.430+19C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32708839 | |||||||
chr3:32708861 | A | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG02647.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.430+41A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32708861 | |||||||
chr3:32709010 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.430+190A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709010 | |||||||
chr3:32709058 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.430+238T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709058 | |||||||
chr3:32709113 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.430+293C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709113 | |||||||
chr3:32709138 | A | G | 1 | a0001c0001t0001g0320 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.430+318A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709138 | |||||||
chr3:32709229 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.430+409G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709229 | |||||||
chr3:32709317 | G | C | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.430+497G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709317 | |||||||
chr3:32709548 | T | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.430+728T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709548 | |||||||
chr3:32709588 | G | C | 1 | a0001c0001t0001g0282 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.430+768G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709588 | |||||||
chr3:32709620 | C | G | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.430+800C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709620 | |||||||
chr3:32709697 | AGT | A | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.430+879_430+880del others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 32709697 | ||||||
chr3:32709738 | A | G | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.430+918A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709738 | |||||||
chr3:32709865 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.430+1045T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32709865 | |||||||
chr3:32710079 | C | T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0072 others(1): Show |
4 | NA18981.hp2 NA18989.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+1259C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710079 | |||||||
chr3:32710086 | G | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.430+1266G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710086 | |||||||
chr3:32710147 | CA | C | 287 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(284): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.430+1349delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 32710147 | ||||||
chr3:32710147 | CAA | C | 13 | a0001c0001t0001g0096 a0001c0001t0001g0102 a0001c0001t0001g0164 others(10): Show |
13 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.430+1348_430+1349d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 32710147 | ||||||
chr3:32710147 | CAAA | C | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.430+1347_430+1349d others(5): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 32710147 | ||||||
chr3:32710147 | CAAAA | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0332 a0001c0001t0001g0335 others(3): Show |
6 | HG01891.hp1 HG02132.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+1346_430+1349d others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 32710147 | ||||||
chr3:32710159 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.430+1339A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710159 | |||||||
chr3:32710236 | A | T | 1 | a0001c0001t0002g0318 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.430+1416A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710236 | |||||||
chr3:32710289 | A | T | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.430+1469A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710289 | |||||||
chr3:32710305 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.430+1485G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710305 | |||||||
chr3:32710322 | G | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0322 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.430+1502G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710322 | |||||||
chr3:32710421 | C | T | 8 | a0002c0002t0001g0214 a0002c0002t0001g0229 a0002c0002t0001g0230 others(5): Show |
8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.430+1601C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710421 | |||||||
chr3:32710652 | T | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(97): Show |
102 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.430+1832T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710652 | |||||||
chr3:32710688 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.430+1868G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710688 | |||||||
chr3:32710779 | G | T | 1 | a0001c0001t0001g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.430+1959G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710779 | |||||||
chr3:32710780 | G | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.430+1960G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710780 | |||||||
chr3:32710870 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.430+2050G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32710870 | |||||||
chr3:32711277 | G | A | 5 | a0001c0001t0001g0332 a0001c0001t0001g0335 a0001c0001t0001g0336 others(2): Show |
5 | HG01891.hp1 HG03130.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-1950G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32711277 | |||||||
chr3:32711617 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.431-1610T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32711617 | |||||||
chr3:32711704 | G | C | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.431-1523G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32711704 | |||||||
chr3:32711862 | G | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0067 |
2 | NA18985.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.431-1365G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32711862 | |||||||
chr3:32711881 | T | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.431-1346T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32711881 | |||||||
chr3:32711934 | A | T | 1 | a0001c0001t0001g0016 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.431-1293A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32711934 | |||||||
chr3:32712032 | CA | C | 17 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0105 others(14): Show |
17 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.431-1194delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712032 | |||||||
chr3:32712133 | G | T | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.431-1094G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712133 | |||||||
chr3:32712134 | C | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(92): Show |
97 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.431-1093C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712134 | |||||||
chr3:32712163 | G | GT | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0033 others(167): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.431-1050dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 32712163 | ||||||
chr3:32712163 | G | GTT | 15 | a0001c0001t0001g0039 a0001c0001t0001g0070 a0001c0001t0001g0072 others(12): Show |
15 | HG00597.hp2 HG00673.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.431-1051_431-1050d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 32712163 | ||||||
chr3:32712163 | G | T | 3 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0216 |
3 | HG00639.hp1 HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.431-1064G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712163 | |||||||
chr3:32712163 | GTT | G | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.431-1051_431-1050d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr3 | 32712163 | ||||||
chr3:32712167 | T | G | 1 | a0001c0001t0001g0283 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.431-1060T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712167 | |||||||
chr3:32712169 | T | G | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.431-1058T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712169 | |||||||
chr3:32712201 | A | C | 1 | a0002c0002t0001g0273 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.431-1026A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712201 | |||||||
chr3:32712379 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.431-848G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712379 | |||||||
chr3:32712399 | T | C | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.431-828T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712399 | |||||||
chr3:32712424 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0322 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.431-803T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712424 | |||||||
chr3:32712524 | T | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.431-703T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712524 | |||||||
chr3:32712550 | A | G | 1 | a0001c0001t0001g0341 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.431-677A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712550 | |||||||
chr3:32712618 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.431-609G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712618 | |||||||
chr3:32712846 | A | G | 1 | a0002c0002t0001g0269 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.431-381A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712846 | |||||||
chr3:32712866 | A | T | 1 | a0001c0001t0001g0176 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.431-361A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712866 | |||||||
chr3:32712995 | G | A | 4 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0274 others(1): Show |
4 | NA18954.hp2 NA18963.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.431-232G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32712995 | |||||||
chr3:32713052 | G | T | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.431-175G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32713052 | |||||||
chr3:32713124 | T | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.431-103T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32713124 | |||||||
chr3:32713162 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.431-65G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32713162 | |||||||
chr3:32713165 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.431-62G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 4/18 | chr3 | 32713165 | |||||||
chr3:32713744 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.573+375A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32713744 | |||||||
chr3:32713824 | A | AT | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.573+460dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr3 | 32713824 | ||||||
chr3:32713830 | G | T | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.573+461G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32713830 | |||||||
chr3:32713897 | T | A | 1 | a0001c0001t0001g0240 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.573+528T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32713897 | |||||||
chr3:32713958 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.573+589A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32713958 | |||||||
chr3:32714044 | C | G | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.573+675C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714044 | |||||||
chr3:32714083 | A | G | 53 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0034 others(50): Show |
53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.573+714A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714083 | |||||||
chr3:32714237 | C | G | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.573+868C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714237 | |||||||
chr3:32714405 | C | CA | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(25): Show |
28 | HG00639.hp1 HG01168.hp1 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.573+1052dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr3 | 32714405 | ||||||
chr3:32714405 | CA | C | 10 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0069 others(7): Show |
10 | HG01257.hp2 HG02155.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.573+1052delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr3 | 32714405 | ||||||
chr3:32714461 | C | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.573+1092C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714461 | |||||||
chr3:32714535 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.573+1166C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714535 | |||||||
chr3:32714554 | C | CA | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.573+1191dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr3 | 32714554 | ||||||
chr3:32714616 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.573+1247C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714616 | |||||||
chr3:32714641 | G | A | 5 | a0001c0001t0001g0235 a0001c0001t0001g0244 a0001c0001t0001g0288 others(2): Show |
5 | HG01167.hp2 HG01169.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+1272G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714641 | |||||||
chr3:32714643 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.573+1274A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714643 | |||||||
chr3:32714656 | C | G | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0346 |
3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.573+1287C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714656 | |||||||
chr3:32714665 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.573+1296C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714665 | |||||||
chr3:32714666 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0322 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.573+1297G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714666 | |||||||
chr3:32714718 | A | C | 1 | a0001c0001t0001g0299 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.573+1349A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714718 | |||||||
chr3:32714895 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.574-1330C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714895 | |||||||
chr3:32714926 | C | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.574-1299C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32714926 | |||||||
chr3:32715291 | G | A | 1 | a0001c0001t0001g0333 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574-934G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32715291 | |||||||
chr3:32715485 | A | G | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0346 |
3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.574-740A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32715485 | |||||||
chr3:32715546 | A | T | 1 | a0001c0001t0002g0321 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.574-679A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32715546 | |||||||
chr3:32715572 | G | T | 53 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0034 others(50): Show |
53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.574-653G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32715572 | |||||||
chr3:32715655 | C | G | 1 | a0001c0001t0001g0076 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.574-570C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32715655 | |||||||
chr3:32715856 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.574-369A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32715856 | |||||||
chr3:32715951 | A | G | 1 | a0001c0001t0001g0007 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.574-274A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32715951 | |||||||
chr3:32715954 | TG | T | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.574-269delG | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr3 | 32715954 | ||||||
chr3:32716049 | C | T | 1 | a0001c0001t0001g0333 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574-176C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 5/18 | chr3 | 32716049 | |||||||
chr3:32716345 | CAT | C | 4 | a0002c0002t0001g0214 a0002c0002t0001g0229 a0002c0002t0001g0230 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.660+39_660+40delAT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr3 | 32716345 | ||||||
chr3:32716370 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.660+59A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716370 | |||||||
chr3:32716405 | A | G | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.660+94A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716405 | |||||||
chr3:32716418 | C | T | 1 | a0001c0001t0001g0011 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.660+107C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716418 | |||||||
chr3:32716674 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.660+363G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716674 | |||||||
chr3:32716703 | A | C | 2 | a0001c0001t0001g0228 a0001c0001t0001g0305 |
2 | HG01243.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.660+392A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716703 | |||||||
chr3:32716739 | C | A | 1 | a0001c0001t0001g0341 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.661-415C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716739 | |||||||
chr3:32716764 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(92): Show |
97 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.661-390C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716764 | |||||||
chr3:32716806 | A | C | 1 | a0001c0001t0001g0252 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.661-348A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716806 | |||||||
chr3:32716886 | G | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.661-268G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716886 | |||||||
chr3:32716899 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.661-255C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716899 | |||||||
chr3:32716965 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.661-189G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716965 | |||||||
chr3:32716991 | C | T | 17 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0105 others(14): Show |
17 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.661-163C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 6/18 | chr3 | 32716991 | |||||||
chr3:32717269 | TTG | T | 33 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0041 others(30): Show |
33 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.744+36_744+37delGT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr3 | 32717269 | ||||||
chr3:32717271 | G | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(103): Show |
109 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.744+34G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32717271 | |||||||
chr3:32717403 | A | AT | 35 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(32): Show |
35 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.744+179dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr3 | 32717403 | ||||||
chr3:32717460 | A | T | 1 | a0001c0001t0001g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.744+223A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32717460 | |||||||
chr3:32717470 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.744+233T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32717470 | |||||||
chr3:32717514 | CACTT | C | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.744+279_744+282del others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr3 | 32717514 | ||||||
chr3:32717659 | A | C | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.744+422A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32717659 | |||||||
chr3:32717660 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.744+423G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32717660 | |||||||
chr3:32717723 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.744+486G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32717723 | |||||||
chr3:32717891 | T | A | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.744+654T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32717891 | |||||||
chr3:32718258 | C | CT | 18 | a0001c0001t0001g0091 a0001c0001t0001g0168 a0001c0001t0001g0187 others(15): Show |
18 | HG01071.hp2 HG01106.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.744+1043dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr3 | 32718258 | ||||||
chr3:32718258 | CT | C | 35 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(32): Show |
35 | HG00099.hp1 HG01099.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.744+1043delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr3 | 32718258 | ||||||
chr3:32718301 | C | G | 9 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0209 others(6): Show |
9 | HG00639.hp1 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.744+1064C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32718301 | |||||||
chr3:32718435 | T | C | 2 | a0001c0001t0001g0344 a0001c0001t0001g0345 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.744+1198T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32718435 | |||||||
chr3:32718440 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.744+1203C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32718440 | |||||||
chr3:32718444 | C | A | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.744+1207C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32718444 | |||||||
chr3:32718509 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.744+1272G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32718509 | |||||||
chr3:32718515 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.744+1278C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32718515 | |||||||
chr3:32718539 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.744+1302G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32718539 | |||||||
chr3:32718583 | C | CA | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
183 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.744+1367dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr3 | 32718583 | ||||||
chr3:32718583 | C | CAA | 18 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0097 others(15): Show |
19 | HG00735.hp1 HG00741.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.744+1366_744+1367d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr3 | 32718583 | ||||||
chr3:32718583 | CA | C | 18 | a0001c0001t0001g0060 a0001c0001t0001g0332 a0001c0001t0001g0333 others(15): Show |
18 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.744+1367delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr3 | 32718583 | ||||||
chr3:32718833 | G | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.745-1281G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32718833 | |||||||
chr3:32718904 | C | G | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.745-1210C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32718904 | |||||||
chr3:32719204 | G | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.745-910G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32719204 | |||||||
chr3:32719228 | A | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.745-886A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32719228 | |||||||
chr3:32719244 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.745-870G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32719244 | |||||||
chr3:32719414 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.745-700C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32719414 | |||||||
chr3:32719429 | A | C | 17 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0105 others(14): Show |
17 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.745-685A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32719429 | |||||||
chr3:32719605 | A | G | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0346 |
3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.745-509A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32719605 | |||||||
chr3:32719642 | T | C | 91 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(88): Show |
91 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.745-472T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32719642 | |||||||
chr3:32719945 | A | G | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.745-169A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32719945 | |||||||
chr3:32719989 | A | G | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.745-125A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32719989 | |||||||
chr3:32719990 | T | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG00408.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.745-124T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32719990 | |||||||
chr3:32720101 | A | G | 1 | a0002c0002t0001g0273 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.745-13A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 7/18 | chr3 | 32720101 | |||||||
chr3:32720257 | CT | C | 53 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0034 others(50): Show |
53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.862+34delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720257 | ||||||
chr3:32720379 | A | G | 5 | a0001c0001t0001g0332 a0001c0001t0001g0335 a0001c0001t0001g0336 others(2): Show |
5 | HG01891.hp1 HG03130.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.862+148A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720379 | |||||||
chr3:32720512 | A | AT | 36 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(33): Show |
36 | HG01071.hp2 HG01106.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.862+285dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720512 | ||||||
chr3:32720517 | A | T | 37 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(34): Show |
37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.862+286A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720517 | |||||||
chr3:32720550 | T | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0020 |
2 | NA19056.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.862+319T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720550 | |||||||
chr3:32720683 | T | G | 1 | a0001c0001t0001g0256 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.862+452T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720683 | |||||||
chr3:32720727 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.862+496C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720727 | |||||||
chr3:32720789 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.862+558T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720789 | |||||||
chr3:32720803 | T | C | 1 | a0001c0001t0001g0339 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.862+572T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720803 | |||||||
chr3:32720822 | G | GCCCTCCC others(1): Show |
15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.862+600_862+607dup others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720822 | ||||||
chr3:32720831 | C | CCCTCCCT others(1): Show |
3 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0082 |
3 | NA18981.hp2 NA18989.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.862+627_862+634dup others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720831 | ||||||
chr3:32720843 | C | G | 1 | a0001c0001t0001g0002 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.862+612C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720843 | |||||||
chr3:32720859 | C | CCCTTCCT others(9): Show |
2 | a0001c0001t0001g0027 a0001c0001t0001g0029 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.862+634_862+635ins others(16): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720859 | ||||||
chr3:32720859 | C | T | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.862+628C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720859 | |||||||
chr3:32720866 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(113): Show |
118 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.862+635C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720866 | |||||||
chr3:32720867 | T | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(93): Show |
98 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.862+636T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720867 | |||||||
chr3:32720874 | T | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(93): Show |
98 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.862+643T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720874 | |||||||
chr3:32720877 | T | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(113): Show |
118 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.862+646T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720877 | |||||||
chr3:32720879 | T | TCCCTC | 12 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(9): Show |
12 | HG02015.hp2 HG02132.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.862+649_862+650ins others(5): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720879 | ||||||
chr3:32720880 | C | CCCT | 8 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(5): Show |
8 | HG02602.hp1 HG04228.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.862+649_862+650ins others(3): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720880 | |||||||
chr3:32720880 | CT | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(93): Show |
98 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.862+653delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720880 | ||||||
chr3:32720881 | T | C | 8 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(5): Show |
8 | HG02602.hp1 HG04228.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.862+650T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720881 | |||||||
chr3:32720882 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(101): Show |
106 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.862+651T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720882 | |||||||
chr3:32720882 | T | TCC | 12 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(9): Show |
12 | HG02015.hp2 HG02132.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.862+651_862+652ins others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720882 | |||||||
chr3:32720886 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(105): Show |
110 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.862+655C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720886 | |||||||
chr3:32720891 | T | TTTCC | 22 | a0001c0001t0001g0064 a0001c0001t0001g0069 a0001c0001t0001g0088 others(19): Show |
22 | HG01168.hp2 HG02083.hp2 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.862+701_862+704dup others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720891 | ||||||
chr3:32720891 | T | TTTCCTTC others(5): Show |
2 | a0001c0001t0001g0231 a0001c0001t0002g0346 |
2 | HG01891.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.862+693_862+704dup others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720891 | ||||||
chr3:32720891 | TTTCC | T | 29 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0029 others(26): Show |
30 | HG00642.hp1 HG00738.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.862+701_862+704del others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720891 | ||||||
chr3:32720891 | TTTCCTTC others(1): Show |
T | 11 | a0001c0001t0001g0007 a0001c0001t0001g0113 a0001c0001t0001g0114 others(8): Show |
11 | HG00140.hp1 HG00639.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.862+697_862+704del others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720891 | ||||||
chr3:32720891 | TTTCCTTC others(5): Show |
T | 17 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0104 others(14): Show |
17 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.862+693_862+704del others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720891 | ||||||
chr3:32720891 | TTTCCTTC others(9): Show |
T | 3 | a0001c0001t0001g0333 a0001c0001t0002g0209 a0001c0001t0002g0318 |
3 | HG06807.hp2 NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.862+689_862+704del others(16): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720891 | ||||||
chr3:32720891 | TTTCCTTC others(13): Show |
T | 1 | a0001c0001t0001g0328 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.862+685_862+704del others(20): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720891 | ||||||
chr3:32720893 | T | C | 8 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(5): Show |
8 | HG02602.hp1 HG04228.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.862+662T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720893 | |||||||
chr3:32720894 | C | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(5): Show |
8 | HG02602.hp1 HG04228.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.862+663C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720894 | |||||||
chr3:32720895 | C | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(5): Show |
8 | HG02602.hp1 HG04228.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.862+664C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720895 | |||||||
chr3:32720898 | C | CT | 15 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(12): Show |
15 | HG00558.hp1 HG02015.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.862+667_862+668ins others(1): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720898 | |||||||
chr3:32720899 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(105): Show |
110 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.862+668C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720899 | |||||||
chr3:32720900 | TTCC | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(88): Show |
93 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.862+671_862+673del others(3): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720900 | ||||||
chr3:32720900 | TTCCTTCC others(4): Show |
T | 1 | a0001c0001t0001g0164 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.862+671_862+681del others(11): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32720900 | ||||||
chr3:32720902 | C | CT | 8 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(5): Show |
8 | HG02602.hp1 HG04228.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.862+671_862+672ins others(1): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720902 | |||||||
chr3:32720903 | C | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0013 others(5): Show |
8 | HG02602.hp1 HG04228.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.862+672C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720903 | |||||||
chr3:32720949 | T | C | 53 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0034 others(50): Show |
53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.862+718T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32720949 | |||||||
chr3:32721003 | G | C | 1 | a0001c0001t0001g0108 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.862+772G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721003 | |||||||
chr3:32721060 | C | CGTT | 12 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0107 others(9): Show |
12 | HG00099.hp1 HG00639.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.862+829_862+830ins others(3): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721060 | |||||||
chr3:32721060 | C | CT | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
110 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.862+848dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721060 | ||||||
chr3:32721060 | C | CTT | 18 | a0001c0001t0001g0088 a0001c0001t0001g0194 a0001c0001t0001g0204 others(15): Show |
18 | HG00323.hp1 HG00741.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.862+847_862+848dup others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721060 | ||||||
chr3:32721060 | CT | C | 69 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(66): Show |
69 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.862+848delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721060 | ||||||
chr3:32721060 | CTT | C | 15 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0333 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.862+847_862+848del others(2): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721060 | ||||||
chr3:32721064 | T | G | 3 | a0001c0001t0001g0106 a0001c0001t0001g0113 a0001c0001t0001g0116 |
3 | HG00140.hp1 HG01175.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.862+833T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721064 | |||||||
chr3:32721091 | G | T | 1 | a0001c0001t0001g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.862+860G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721091 | |||||||
chr3:32721133 | C | T | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.862+902C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721133 | |||||||
chr3:32721210 | C | T | 1 | a0001c0001t0001g0347 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.862+979C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721210 | |||||||
chr3:32721351 | C | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG00408.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.862+1120C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721351 | |||||||
chr3:32721390 | AC | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.862+1160delC | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721390 | |||||||
chr3:32721394 | T | C | 1 | a0001c0001t0003g0324 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.862+1163T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721394 | |||||||
chr3:32721422 | CTTTCATC others(18): Show |
C | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.862+1195_862+1219d others(27): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721422 | ||||||
chr3:32721429 | C | CT | 271 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(268): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.862+1223dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721429 | ||||||
chr3:32721429 | C | CTT | 35 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(32): Show |
36 | HG00438.hp2 HG00735.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.862+1222_862+1223d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721429 | ||||||
chr3:32721429 | CT | C | 7 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(4): Show |
7 | HG01891.hp1 HG03130.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.862+1223delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721429 | ||||||
chr3:32721429 | CTTTTTTT others(5): Show |
C | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.862+1212_862+1223d others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721429 | ||||||
chr3:32721536 | T | G | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.862+1305T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721536 | |||||||
chr3:32721647 | C | CT | 8 | a0001c0001t0001g0071 a0001c0001t0001g0076 a0001c0001t0001g0121 others(5): Show |
8 | HG00140.hp2 HG01109.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.862+1433dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721647 | ||||||
chr3:32721763 | C | G | 1 | a0001c0001t0001g0046 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.862+1532C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721763 | |||||||
chr3:32721771 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.862+1540C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721771 | |||||||
chr3:32721898 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.862+1667C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721898 | |||||||
chr3:32721959 | T | TA | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.862+1729dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32721959 | ||||||
chr3:32721994 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(91): Show |
96 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.862+1763A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32721994 | |||||||
chr3:32722096 | C | G | 1 | a0001c0001t0002g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.862+1865C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32722096 | |||||||
chr3:32722204 | C | T | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.862+1973C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32722204 | |||||||
chr3:32722278 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0322 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.862+2047G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32722278 | |||||||
chr3:32722390 | A | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.862+2159A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32722390 | |||||||
chr3:32722458 | C | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.862+2227C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32722458 | |||||||
chr3:32722668 | G | T | 1 | a0001c0001t0001g0007 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.862+2437G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32722668 | |||||||
chr3:32722740 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.862+2509T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32722740 | |||||||
chr3:32722756 | G | A | 4 | a0001c0001t0001g0237 a0001c0001t0001g0256 a0001c0001t0001g0259 others(1): Show |
4 | HG01099.hp1 HG01168.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.862+2525G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32722756 | |||||||
chr3:32723078 | T | G | 23 | a0001c0001t0001g0087 a0001c0001t0001g0210 a0001c0001t0001g0213 others(20): Show |
23 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.863-2372T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32723078 | |||||||
chr3:32723132 | A | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.863-2318A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32723132 | |||||||
chr3:32723210 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.863-2240G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32723210 | |||||||
chr3:32723220 | C | T | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(93): Show |
98 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.863-2230C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32723220 | |||||||
chr3:32723387 | G | A | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.863-2063G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32723387 | |||||||
chr3:32723625 | AT | A | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.863-1821delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32723625 | ||||||
chr3:32723743 | G | A | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.863-1707G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32723743 | |||||||
chr3:32723924 | T | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.863-1526T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32723924 | |||||||
chr3:32723929 | A | G | 1 | a0001c0001t0001g0322 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.863-1521A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32723929 | |||||||
chr3:32724089 | A | G | 1 | a0001c0001t0001g0002 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.863-1361A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724089 | |||||||
chr3:32724135 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(92): Show |
97 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.863-1315A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724135 | |||||||
chr3:32724171 | A | G | 17 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0105 others(14): Show |
17 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.863-1279A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724171 | |||||||
chr3:32724213 | A | G | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.863-1237A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724213 | |||||||
chr3:32724231 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.863-1219T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724231 | |||||||
chr3:32724239 | G | A | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.863-1211G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724239 | |||||||
chr3:32724243 | C | CT | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(212): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.863-1189dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32724243 | ||||||
chr3:32724243 | C | CTT | 8 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0073 others(5): Show |
8 | HG01981.hp1 HG02559.hp2 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.863-1190_863-1189d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32724243 | ||||||
chr3:32724314 | C | T | 53 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0034 others(50): Show |
53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.863-1136C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724314 | |||||||
chr3:32724326 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.863-1124A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724326 | |||||||
chr3:32724328 | C | G | 1 | a0001c0001t0001g0012 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.863-1122C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724328 | |||||||
chr3:32724412 | A | AT | 29 | a0001c0001t0001g0073 a0001c0001t0001g0080 a0001c0001t0001g0126 others(26): Show |
29 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.863-1020dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32724412 | ||||||
chr3:32724436 | G | A | 53 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0034 others(50): Show |
53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.863-1014G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724436 | |||||||
chr3:32724514 | G | A | 14 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0335 others(11): Show |
14 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.863-936G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724514 | |||||||
chr3:32724574 | G | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.863-876G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724574 | |||||||
chr3:32724687 | C | T | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.863-763C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724687 | |||||||
chr3:32724797 | G | A | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.863-653G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724797 | |||||||
chr3:32724805 | C | T | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.863-645C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724805 | |||||||
chr3:32724839 | A | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.863-611A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724839 | |||||||
chr3:32724844 | C | T | 1 | a0001c0001t0001g0313 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.863-606C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724844 | |||||||
chr3:32724848 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | NA18612.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.863-602C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32724848 | |||||||
chr3:32724869 | CT | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0084 others(109): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.863-577delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr3 | 32724869 | ||||||
chr3:32725140 | G | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.863-310G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32725140 | |||||||
chr3:32725150 | A | G | 1 | a0001c0001t0001g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.863-300A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32725150 | |||||||
chr3:32725283 | T | A | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.863-167T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32725283 | |||||||
chr3:32725368 | G | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.863-82G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32725368 | |||||||
chr3:32725384 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.863-66A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32725384 | |||||||
chr3:32725413 | A | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0084 others(109): Show |
114 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(111): Show |
intron_variant | MODIFIER | c.863-37A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 8/18 | chr3 | 32725413 | |||||||
chr3:32725783 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1012+184G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32725783 | |||||||
chr3:32725885 | T | A | 53 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0034 others(50): Show |
53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1012+286T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32725885 | |||||||
chr3:32725920 | T | G | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1012+321T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32725920 | |||||||
chr3:32725927 | A | AGTTTT | 63 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0009 others(60): Show |
64 | HG00639.hp1 HG01106.hp2 HG01168.hp1 others(61): Show |
intron_variant | MODIFIER | c.1012+360_1012+364d others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32725927 | ||||||
chr3:32725927 | A | AGTTTTGT others(3): Show |
86 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0085 others(83): Show |
87 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1012+355_1012+364d others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32725927 | ||||||
chr3:32725927 | A | AGTTTTGT others(8): Show |
2 | a0001c0001t0001g0141 a0001c0001t0001g0322 |
2 | HG00558.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1012+350_1012+364d others(17): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32725927 | ||||||
chr3:32725927 | A | AGTTTTGT others(13): Show |
2 | a0001c0001t0001g0156 a0001c0001t0001g0190 |
2 | NA18961.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1012+345_1012+364d others(22): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32725927 | ||||||
chr3:32725927 | AGTTTT | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(107): Show |
113 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.1012+360_1012+364d others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32725927 | ||||||
chr3:32725927 | AGTTTTGT others(3): Show |
A | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1012+355_1012+364d others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32725927 | ||||||
chr3:32725927 | AGTTTTGT others(8): Show |
A | 1 | a0001c0001t0001g0106 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1012+350_1012+364d others(17): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32725927 | ||||||
chr3:32726059 | T | C | 1 | a0001c0001t0001g0333 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1012+460T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726059 | |||||||
chr3:32726142 | A | G | 1 | a0001c0001t0003g0324 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1012+543A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726142 | |||||||
chr3:32726248 | A | G | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1012+649A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726248 | |||||||
chr3:32726418 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1012+819G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726418 | |||||||
chr3:32726477 | G | T | 1 | a0001c0001t0001g0347 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1012+878G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726477 | |||||||
chr3:32726578 | C | G | 1 | a0001c0001t0001g0012 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1012+979C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726578 | |||||||
chr3:32726631 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1012+1032G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726631 | |||||||
chr3:32726693 | CCAT | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1013-974_1013-972d others(5): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726693 | |||||||
chr3:32726694 | C | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0161 |
2 | HG01346.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1013-974C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726694 | |||||||
chr3:32726694 | C | CATA | 16 | a0001c0001t0001g0084 a0001c0001t0001g0096 a0001c0001t0001g0100 others(13): Show |
16 | HG00323.hp2 HG00639.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1013-939_1013-937d others(5): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32726694 | ||||||
chr3:32726694 | C | CATAATA | 3 | a0001c0001t0001g0114 a0001c0001t0001g0147 a0001c0001t0003g0323 |
3 | HG01243.hp1 HG01981.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1013-942_1013-937d others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32726694 | ||||||
chr3:32726694 | CATA | C | 66 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0033 others(63): Show |
67 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1013-939_1013-937d others(5): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32726694 | ||||||
chr3:32726694 | CATAATA | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
105 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.1013-942_1013-937d others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32726694 | ||||||
chr3:32726694 | CATAATAA others(2): Show |
C | 23 | a0001c0001t0001g0087 a0001c0001t0001g0210 a0001c0001t0001g0213 others(20): Show |
23 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.1013-945_1013-937d others(11): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32726694 | ||||||
chr3:32726836 | A | AT | 11 | a0001c0001t0001g0333 a0001c0001t0001g0336 a0001c0001t0001g0338 others(8): Show |
11 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1013-807dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32726836 | ||||||
chr3:32726836 | AT | A | 49 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(46): Show |
49 | HG00438.hp2 HG00733.hp1 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.1013-807delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32726836 | ||||||
chr3:32726836 | ATT | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(241): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1013-808_1013-807d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32726836 | ||||||
chr3:32726836 | ATTT | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0060 others(6): Show |
9 | HG01099.hp1 HG01167.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.1013-809_1013-807d others(5): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32726836 | ||||||
chr3:32726836 | ATTTTTTT | A | 19 | a0001c0001t0001g0087 a0001c0001t0001g0210 a0001c0001t0001g0213 others(16): Show |
19 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.1013-813_1013-807d others(9): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr3 | 32726836 | ||||||
chr3:32726880 | C | T | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1013-788C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726880 | |||||||
chr3:32726902 | A | G | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0076 others(98): Show |
103 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1013-766A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726902 | |||||||
chr3:32726972 | G | A | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1013-696G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32726972 | |||||||
chr3:32727005 | C | G | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1013-663C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32727005 | |||||||
chr3:32727021 | A | G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0112 |
2 | HG02145.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1013-647A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32727021 | |||||||
chr3:32727291 | A | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1013-377A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32727291 | |||||||
chr3:32727375 | G | A | 3 | a0002c0002t0001g0269 a0002c0002t0001g0272 a0002c0002t0001g0273 |
3 | HG01081.hp1 HG01361.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1013-293G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32727375 | |||||||
chr3:32727396 | C | G | 1 | a0001c0001t0001g0058 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1013-272C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32727396 | |||||||
chr3:32727406 | C | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1013-262C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 9/18 | chr3 | 32727406 | |||||||
chr3:32727933 | T | TA | 10 | a0001c0001t0001g0061 a0001c0001t0001g0073 a0001c0001t0001g0092 others(7): Show |
10 | HG01175.hp2 HG01243.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.1215+79dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32727933 | ||||||
chr3:32727933 | TA | T | 10 | a0001c0001t0001g0045 a0001c0001t0001g0115 a0001c0001t0001g0243 others(7): Show |
10 | HG01257.hp1 HG01891.hp1 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.1215+79delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32727933 | ||||||
chr3:32727945 | A | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1215+75A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32727945 | |||||||
chr3:32727979 | T | TTTTA | 5 | a0001c0001t0001g0096 a0001c0001t0001g0131 a0001c0001t0001g0159 others(2): Show |
5 | HG02630.hp1 HG03225.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1215+137_1215+140d others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32727979 | ||||||
chr3:32727979 | T | TTTTATTT others(1): Show |
4 | a0001c0001t0001g0332 a0001c0001t0002g0031 a0001c0001t0002g0032 others(1): Show |
4 | HG01891.hp2 HG03130.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+133_1215+140d others(10): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32727979 | ||||||
chr3:32727979 | T | TTTTATTT others(5): Show |
2 | a0001c0001t0001g0030 a0001c0001t0001g0333 |
2 | NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1215+129_1215+140d others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32727979 | ||||||
chr3:32727979 | T | TTTTATTT others(9): Show |
12 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0020 others(9): Show |
12 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.1215+125_1215+140d others(18): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32727979 | ||||||
chr3:32727979 | T | TTTTATTT others(13): Show |
16 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(13): Show |
16 | HG01168.hp1 HG01169.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.1215+121_1215+140d others(22): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32727979 | ||||||
chr3:32727979 | T | TTTTATTT others(17): Show |
3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 |
3 | HG02015.hp2 NA18993.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1215+117_1215+140d others(26): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32727979 | ||||||
chr3:32727979 | TTTTA | T | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+137_1215+140d others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32727979 | ||||||
chr3:32727979 | TTTTATTT others(5): Show |
T | 135 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(132): Show |
138 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.1215+129_1215+140d others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32727979 | ||||||
chr3:32728018 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1215+148C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728018 | |||||||
chr3:32728099 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1215+229C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728099 | |||||||
chr3:32728117 | C | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1215+247C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728117 | |||||||
chr3:32728160 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1215+290C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728160 | |||||||
chr3:32728230 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1215+360A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728230 | |||||||
chr3:32728276 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(89): Show |
94 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1215+406G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728276 | |||||||
chr3:32728361 | C | G | 1 | a0001c0001t0001g0320 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1215+491C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728361 | |||||||
chr3:32728391 | C | T | 1 | a0002c0002t0001g0269 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1215+521C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728391 | |||||||
chr3:32728762 | A | G | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1215+892A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728762 | |||||||
chr3:32728783 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1215+913T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728783 | |||||||
chr3:32728829 | C | T | 1 | a0001c0001t0001g0313 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1215+959C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728829 | |||||||
chr3:32728857 | T | G | 3 | a0001c0001t0001g0250 a0001c0001t0001g0295 a0001c0001t0001g0326 |
3 | HG02132.hp1 NA18943.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1215+987T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728857 | |||||||
chr3:32728866 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(1): Show |
4 | NA18960.hp2 NA18962.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+996C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728866 | |||||||
chr3:32728897 | G | A | 1 | a0001c0001t0001g0005 | 2 | HG00735.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1215+1027G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32728897 | |||||||
chr3:32729012 | C | T | 1 | a0001c0001t0001g0333 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1215+1142C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729012 | |||||||
chr3:32729053 | G | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1215+1183G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729053 | |||||||
chr3:32729148 | A | T | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1215+1278A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729148 | |||||||
chr3:32729425 | G | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0121 a0001c0001t0001g0122 others(8): Show |
12 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1215+1555G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729425 | |||||||
chr3:32729586 | G | A | 5 | a0001c0001t0001g0087 a0001c0001t0001g0210 a0001c0001t0001g0213 others(2): Show |
5 | HG02615.hp2 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1215+1716G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729586 | |||||||
chr3:32729669 | T | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0029 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1215+1799T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729669 | |||||||
chr3:32729744 | G | C | 4 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0348 others(1): Show |
4 | HG01106.hp1 HG01109.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.1215+1874G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729744 | |||||||
chr3:32729760 | C | CT | 18 | a0001c0001t0001g0232 a0001c0001t0001g0319 a0001c0001t0001g0333 others(15): Show |
18 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1215+1916dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32729760 | ||||||
chr3:32729760 | CT | C | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(152): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1215+1916delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32729760 | ||||||
chr3:32729760 | CTT | C | 102 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(99): Show |
104 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.1215+1915_1215+191 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32729760 | ||||||
chr3:32729760 | CTTT | C | 9 | a0001c0001t0001g0204 a0001c0001t0001g0226 a0001c0001t0001g0239 others(6): Show |
9 | HG01928.hp2 HG02015.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.1215+1914_1215+191 others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32729760 | ||||||
chr3:32729760 | CTTTTTTT others(7): Show |
C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0121 a0001c0001t0001g0122 others(7): Show |
11 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1215+1903_1215+191 others(18): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32729760 | ||||||
chr3:32729771 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1215+1901T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729771 | |||||||
chr3:32729808 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1215+1938G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729808 | |||||||
chr3:32729877 | TC | T | 4 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0215 others(1): Show |
4 | HG00639.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215+2009delC | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32729877 | ||||||
chr3:32729908 | A | C | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1215+2038A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729908 | |||||||
chr3:32729918 | G | A | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
132 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.1215+2048G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32729918 | |||||||
chr3:32730064 | G | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0300 a0001c0001t0001g0301 |
3 | HG00558.hp2 NA18949.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1215+2194G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32730064 | |||||||
chr3:32730335 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1215+2465G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32730335 | |||||||
chr3:32730350 | G | A | 10 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0056 others(7): Show |
10 | NA18947.hp1 NA18972.hp2 NA18985.hp2 others(7): Show |
intron_variant | MODIFIER | c.1215+2480G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32730350 | |||||||
chr3:32730381 | G | GT | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1215+2520dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32730381 | ||||||
chr3:32730623 | C | T | 15 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0106 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1215+2753C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32730623 | |||||||
chr3:32730948 | T | C | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1216-2475T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32730948 | |||||||
chr3:32730950 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1216-2473A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32730950 | |||||||
chr3:32731241 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1216-2182G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32731241 | |||||||
chr3:32731278 | C | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1216-2145C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32731278 | |||||||
chr3:32731489 | T | G | 1 | a0001c0001t0001g0147 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1216-1934T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32731489 | |||||||
chr3:32731630 | C | T | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1216-1793C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32731630 | |||||||
chr3:32731731 | C | A | 1 | a0001c0001t0001g0322 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1216-1692C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32731731 | |||||||
chr3:32731815 | A | G | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1216-1608A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32731815 | |||||||
chr3:32732081 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0084 others(113): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.1216-1342A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32732081 | |||||||
chr3:32732117 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1216-1306G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32732117 | |||||||
chr3:32732338 | C | T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0300 a0001c0001t0001g0301 |
3 | HG00558.hp2 NA18949.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1216-1085C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32732338 | |||||||
chr3:32732350 | G | A | 5 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(2): Show |
5 | NA18945.hp1 NA18955.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.1216-1073G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32732350 | |||||||
chr3:32732490 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1216-933G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32732490 | |||||||
chr3:32732606 | G | GA | 17 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0105 others(14): Show |
17 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1216-806dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr3 | 32732606 | ||||||
chr3:32732626 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1216-797C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32732626 | |||||||
chr3:32732938 | T | G | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1216-485T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32732938 | |||||||
chr3:32732980 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1216-443A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32732980 | |||||||
chr3:32733036 | A | G | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1216-387A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32733036 | |||||||
chr3:32733191 | C | G | 3 | a0001c0001t0001g0123 a0001c0001t0001g0161 a0001c0001t0001g0197 |
3 | HG02970.hp1 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1216-232C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32733191 | |||||||
chr3:32733262 | T | C | 140 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
143 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.1216-161T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32733262 | |||||||
chr3:32733290 | A | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1216-133A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32733290 | |||||||
chr3:32733398 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1216-25A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 10/18 | chr3 | 32733398 | |||||||
chr3:32733566 | A | T | 1 | a0001c0001t0001g0058 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1337+22A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 11/18 | chr3 | 32733566 | |||||||
chr3:32733593 | CATA | C | 10 | a0001c0001t0001g0204 a0001c0001t0001g0226 a0001c0001t0001g0239 others(7): Show |
10 | HG01928.hp2 HG02015.hp1 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.1337+52_1337+54del others(3): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr3 | 32733593 | ||||||
chr3:32733675 | A | T | 1 | a0001c0001t0001g0293 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1337+131A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 11/18 | chr3 | 32733675 | |||||||
chr3:32734369 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1338-431T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 11/18 | chr3 | 32734369 | |||||||
chr3:32734507 | G | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1338-293G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 11/18 | chr3 | 32734507 | |||||||
chr3:32734599 | C | CAATCCAT others(6): Show |
1 | a0001c0001t0001g0292 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1338-200_1338-188d others(15): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr3 | 32734599 | ||||||
chr3:32734599 | C | G | 1 | a0001c0001t0001g0077 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1338-201C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 11/18 | chr3 | 32734599 | |||||||
chr3:32734740 | A | G | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1338-60A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 11/18 | chr3 | 32734740 | |||||||
chr3:32735318 | T | C | 23 | a0001c0001t0001g0087 a0001c0001t0001g0210 a0001c0001t0001g0213 others(20): Show |
23 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.1514+342T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735318 | |||||||
chr3:32735320 | T | G | 23 | a0001c0001t0001g0087 a0001c0001t0001g0210 a0001c0001t0001g0213 others(20): Show |
23 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.1514+344T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735320 | |||||||
chr3:32735324 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1514+348G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735324 | |||||||
chr3:32735330 | G | GCGAGACT others(31): Show |
21 | a0001c0001t0001g0087 a0001c0001t0001g0210 a0001c0001t0001g0213 others(18): Show |
21 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(18): Show |
intron_variant | MODIFIER | c.1514+354_1514+355i others(40): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735330 | |||||||
chr3:32735330 | G | GCGAGACT others(32): Show |
2 | a0001c0001t0001g0219 a0001c0001t0001g0222 |
2 | HG03516.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.1514+354_1514+355i others(41): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735330 | |||||||
chr3:32735331 | T | A | 23 | a0001c0001t0001g0087 a0001c0001t0001g0210 a0001c0001t0001g0213 others(20): Show |
23 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.1514+355T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735331 | |||||||
chr3:32735369 | T | C | 3 | a0001c0001t0001g0244 a0001c0001t0001g0291 a0001c0001t0001g0306 |
3 | HG01167.hp2 HG01169.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.1514+393T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735369 | |||||||
chr3:32735581 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1514+605C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735581 | |||||||
chr3:32735589 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1514+613C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735589 | |||||||
chr3:32735658 | G | A | 14 | a0001c0001t0001g0087 a0001c0001t0001g0210 a0001c0001t0001g0213 others(11): Show |
14 | HG01515.hp1 HG01517.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1514+682G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735658 | |||||||
chr3:32735797 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1514+821A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32735797 | |||||||
chr3:32736025 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1514+1049A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736025 | |||||||
chr3:32736082 | T | TTTTG | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1514+1122_1514+112 others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr3 | 32736082 | ||||||
chr3:32736142 | G | A | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1514+1166G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736142 | |||||||
chr3:32736160 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1514+1184A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736160 | |||||||
chr3:32736166 | A | G | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1514+1190A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736166 | |||||||
chr3:32736204 | A | G | 1 | a0001c0001t0001g0292 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1515-1206A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736204 | |||||||
chr3:32736207 | C | G | 1 | a0001c0001t0001g0007 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1515-1203C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736207 | |||||||
chr3:32736339 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0322 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1515-1071G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736339 | |||||||
chr3:32736415 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1515-995G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736415 | |||||||
chr3:32736556 | C | A | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1515-854C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736556 | |||||||
chr3:32736676 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0112 |
2 | HG02145.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1515-734G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736676 | |||||||
chr3:32736724 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1515-686A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736724 | |||||||
chr3:32736831 | C | T | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1515-579C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736831 | |||||||
chr3:32736915 | G | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0203 |
2 | NA18979.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1515-495G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32736915 | |||||||
chr3:32737009 | T | C | 5 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(2): Show |
5 | HG01168.hp1 HG01169.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515-401T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32737009 | |||||||
chr3:32737034 | C | T | 3 | a0002c0002t0001g0269 a0002c0002t0001g0272 a0002c0002t0001g0273 |
3 | HG01081.hp1 HG01361.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1515-376C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32737034 | |||||||
chr3:32737104 | G | A | 340 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(337): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1515-306G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32737104 | |||||||
chr3:32737221 | G | A | 37 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(34): Show |
37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1515-189G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32737221 | |||||||
chr3:32737245 | G | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(2): Show |
5 | HG01168.hp1 HG01169.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515-165G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32737245 | |||||||
chr3:32737270 | G | A | 1 | a0001c0001t0002g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1515-140G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32737270 | |||||||
chr3:32737283 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1515-127C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 12/18 | chr3 | 32737283 | |||||||
chr3:32737795 | A | T | 140 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
143 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.1595+305A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32737795 | |||||||
chr3:32737809 | A | T | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0346 |
3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1595+319A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32737809 | |||||||
chr3:32737951 | T | C | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1595+461T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32737951 | |||||||
chr3:32738003 | A | G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0072 others(1): Show |
4 | NA18981.hp2 NA18989.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+513A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738003 | |||||||
chr3:32738156 | G | A | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+666G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738156 | |||||||
chr3:32738191 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0222 |
2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1595+701G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738191 | |||||||
chr3:32738324 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1595+834A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738324 | |||||||
chr3:32738336 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1595+846T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738336 | |||||||
chr3:32738465 | C | CT | 12 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0024 others(9): Show |
12 | HG01891.hp2 HG01981.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1595+990dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32738465 | ||||||
chr3:32738465 | CT | C | 53 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(50): Show |
53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1595+990delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32738465 | ||||||
chr3:32738493 | C | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG00408.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1595+1003C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738493 | |||||||
chr3:32738590 | G | A | 17 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0105 others(14): Show |
17 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1595+1100G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738590 | |||||||
chr3:32738608 | G | A | 11 | a0001c0001t0001g0210 a0001c0001t0001g0217 a0001c0001t0001g0218 others(8): Show |
11 | HG01515.hp1 HG01517.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1595+1118G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738608 | |||||||
chr3:32738652 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1595+1162C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738652 | |||||||
chr3:32738664 | G | A | 15 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0106 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1595+1174G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738664 | |||||||
chr3:32738684 | G | T | 1 | a0001c0001t0001g0296 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1595+1194G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738684 | |||||||
chr3:32738695 | G | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1595+1205G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738695 | |||||||
chr3:32738757 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1595+1267C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738757 | |||||||
chr3:32738785 | G | A | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+1295G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738785 | |||||||
chr3:32738905 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1595+1415T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738905 | |||||||
chr3:32738951 | G | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1595+1461G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738951 | |||||||
chr3:32738954 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1595+1464G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32738954 | |||||||
chr3:32739125 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1595+1635C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32739125 | |||||||
chr3:32739201 | C | T | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+1711C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32739201 | |||||||
chr3:32739239 | C | G | 1 | a0001c0001t0002g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1595+1749C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32739239 | |||||||
chr3:32739350 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1595+1860T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32739350 | |||||||
chr3:32739404 | A | G | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+1914A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32739404 | |||||||
chr3:32739519 | C | CT | 7 | a0001c0001t0001g0088 a0001c0001t0001g0237 a0001c0001t0001g0249 others(4): Show |
7 | HG01099.hp1 HG01168.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1595+2037dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32739519 | ||||||
chr3:32739519 | CT | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1595+2037delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32739519 | ||||||
chr3:32739533 | T | C | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+2043T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32739533 | |||||||
chr3:32739621 | T | TA | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(100): Show |
105 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1595+2138dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32739621 | ||||||
chr3:32739755 | T | C | 20 | a0001c0001t0001g0210 a0001c0001t0001g0217 a0001c0001t0001g0218 others(17): Show |
20 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.1595+2265T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32739755 | |||||||
chr3:32739777 | T | G | 1 | a0001c0001t0001g0292 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1595+2287T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32739777 | |||||||
chr3:32739894 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1595+2404C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32739894 | |||||||
chr3:32740033 | G | A | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+2543G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740033 | |||||||
chr3:32740058 | T | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1595+2568T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740058 | |||||||
chr3:32740073 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1595+2583G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740073 | |||||||
chr3:32740080 | G | T | 1 | a0001c0001t0001g0092 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1595+2590G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740080 | |||||||
chr3:32740153 | G | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+2663G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740153 | |||||||
chr3:32740227 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1595+2737G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740227 | |||||||
chr3:32740242 | C | T | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+2752C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740242 | |||||||
chr3:32740299 | A | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0084 others(117): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.1595+2809A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740299 | |||||||
chr3:32740304 | C | A | 102 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(99): Show |
105 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.1595+2814C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740304 | |||||||
chr3:32740432 | A | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1595+2942A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740432 | |||||||
chr3:32740463 | A | G | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+2973A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740463 | |||||||
chr3:32740629 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1595+3139G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740629 | |||||||
chr3:32740637 | T | C | 341 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(338): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1595+3147T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740637 | |||||||
chr3:32740643 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1595+3153A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740643 | |||||||
chr3:32740682 | G | A | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1595+3192G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740682 | |||||||
chr3:32740744 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1595+3254C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740744 | |||||||
chr3:32740840 | C | G | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+3350C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740840 | |||||||
chr3:32740841 | G | T | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1595+3351G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32740841 | |||||||
chr3:32740861 | T | TA | 30 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(27): Show |
30 | HG01169.hp1 HG01243.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1595+3391dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32740861 | ||||||
chr3:32740861 | TA | T | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(111): Show |
117 | HG00323.hp1 HG00558.hp2 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.1595+3391delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32740861 | ||||||
chr3:32740861 | TAA | T | 6 | a0001c0001t0001g0224 a0001c0001t0001g0241 a0001c0001t0001g0257 others(3): Show |
6 | HG00408.hp2 HG01169.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.1595+3390_1595+339 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32740861 | ||||||
chr3:32741052 | T | G | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1595+3562T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741052 | |||||||
chr3:32741541 | G | A | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+4051G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741541 | |||||||
chr3:32741544 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1595+4054C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741544 | |||||||
chr3:32741716 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1595+4226C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741716 | |||||||
chr3:32741756 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1595+4266G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741756 | |||||||
chr3:32741768 | C | CA | 22 | a0001c0001t0001g0045 a0001c0001t0001g0073 a0001c0001t0001g0084 others(19): Show |
22 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.1595+4293dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32741768 | ||||||
chr3:32741768 | C | CAAAAAAA | 8 | a0001c0001t0001g0332 a0001c0001t0001g0339 a0001c0001t0001g0341 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1595+4287_1595+429 others(11): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32741768 | ||||||
chr3:32741768 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0333 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1595+4284_1595+429 others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32741768 | ||||||
chr3:32741768 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1595+4283_1595+429 others(15): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32741768 | ||||||
chr3:32741768 | C | CAAAAAAA others(10): Show |
5 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0026 others(2): Show |
5 | HG01168.hp1 HG01169.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1595+4293_1595+429 others(21): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32741768 | ||||||
chr3:32741768 | C | CAAAAAAA others(11): Show |
10 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(7): Show |
10 | HG02015.hp2 HG02602.hp1 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.1595+4293_1595+429 others(22): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32741768 | ||||||
chr3:32741768 | C | CAAAAAAA others(12): Show |
4 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0017 others(1): Show |
4 | HG02132.hp2 NA18963.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+4293_1595+429 others(23): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32741768 | ||||||
chr3:32741768 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0020 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1595+4293_1595+429 others(24): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32741768 | ||||||
chr3:32741768 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0001g0019 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1595+4293_1595+429 others(25): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32741768 | ||||||
chr3:32741852 | G | A | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+4362G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741852 | |||||||
chr3:32741857 | A | C | 5 | a0002c0002t0001g0214 a0002c0002t0001g0229 a0002c0002t0001g0230 others(2): Show |
5 | HG02895.hp1 HG02897.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1595+4367A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741857 | |||||||
chr3:32741860 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1595+4370G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741860 | |||||||
chr3:32741983 | A | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+4493A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741983 | |||||||
chr3:32741984 | T | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+4494T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741984 | |||||||
chr3:32741988 | A | T | 33 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(30): Show |
33 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1595+4498A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741988 | |||||||
chr3:32741990 | T | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1595+4500T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32741990 | |||||||
chr3:32742088 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1595+4598T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32742088 | |||||||
chr3:32742139 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1595+4649A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32742139 | |||||||
chr3:32742196 | C | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+4706C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32742196 | |||||||
chr3:32742301 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1595+4811A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32742301 | |||||||
chr3:32742318 | A | C | 6 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0277 others(3): Show |
6 | HG01074.hp2 HG01496.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1595+4828A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32742318 | |||||||
chr3:32742363 | T | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0189 |
4 | HG00642.hp1 HG01517.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+4873T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32742363 | |||||||
chr3:32742393 | C | T | 91 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(88): Show |
91 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1595+4903C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32742393 | |||||||
chr3:32742483 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1595+4993G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32742483 | |||||||
chr3:32742491 | C | CA | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+5002dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32742491 | ||||||
chr3:32742550 | T | C | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0346 |
3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1595+5060T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32742550 | |||||||
chr3:32742655 | C | T | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1595+5165C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32742655 | |||||||
chr3:32742984 | C | CT | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(134): Show |
139 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.1595+5513dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32742984 | ||||||
chr3:32742984 | CT | C | 6 | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0001g0052 others(3): Show |
6 | HG01074.hp1 HG02897.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1595+5513delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32742984 | ||||||
chr3:32743010 | G | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0121 a0001c0001t0001g0122 others(7): Show |
11 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1595+5520G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743010 | |||||||
chr3:32743019 | C | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+5529C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743019 | |||||||
chr3:32743025 | T | C | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1595+5535T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743025 | |||||||
chr3:32743026 | C | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+5536C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743026 | |||||||
chr3:32743140 | C | T | 4 | a0002c0002t0001g0214 a0002c0002t0001g0229 a0002c0002t0001g0270 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+5650C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743140 | |||||||
chr3:32743294 | A | G | 15 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0106 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1595+5804A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743294 | |||||||
chr3:32743343 | G | T | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+5853G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743343 | |||||||
chr3:32743368 | G | A | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+5878G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743368 | |||||||
chr3:32743410 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1595+5920G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743410 | |||||||
chr3:32743422 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0222 |
2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1595+5932G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743422 | |||||||
chr3:32743427 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1595+5937C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743427 | |||||||
chr3:32743524 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1595+6034C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743524 | |||||||
chr3:32743525 | A | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1595+6035A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743525 | |||||||
chr3:32743526 | C | G | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+6036C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743526 | |||||||
chr3:32743625 | C | G | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1595+6135C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743625 | |||||||
chr3:32743645 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1595+6155C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743645 | |||||||
chr3:32743679 | A | G | 4 | a0001c0001t0001g0237 a0001c0001t0001g0256 a0001c0001t0001g0259 others(1): Show |
4 | HG01099.hp1 HG01168.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+6189A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743679 | |||||||
chr3:32743726 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1595+6236A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743726 | |||||||
chr3:32743752 | G | A | 1 | a0001c0001t0001g0313 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1595+6262G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743752 | |||||||
chr3:32743789 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1595+6299A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743789 | |||||||
chr3:32743806 | A | G | 1 | a0001c0001t0001g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1595+6316A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743806 | |||||||
chr3:32743857 | T | C | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+6367T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743857 | |||||||
chr3:32743863 | T | G | 343 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(340): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.1595+6373T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743863 | |||||||
chr3:32743904 | G | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+6414G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743904 | |||||||
chr3:32743906 | C | T | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG02004.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1595+6416C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32743906 | |||||||
chr3:32743938 | G | GTA | 4 | a0001c0001t0001g0185 a0001c0001t0001g0250 a0001c0001t0001g0295 others(1): Show |
4 | HG02132.hp1 NA18943.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+6458_1595+645 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32743938 | ||||||
chr3:32744036 | A | G | 2 | a0001c0001t0001g0249 a0001c0001t0001g0287 |
2 | HG01258.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1595+6546A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32744036 | |||||||
chr3:32744284 | G | A | 15 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0106 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1595+6794G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32744284 | |||||||
chr3:32744379 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1595+6889A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32744379 | |||||||
chr3:32744556 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1595+7066A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32744556 | |||||||
chr3:32744571 | G | A | 4 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0215 others(1): Show |
4 | HG00639.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+7081G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32744571 | |||||||
chr3:32744771 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0153 |
2 | HG02258.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1595+7281C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32744771 | |||||||
chr3:32744898 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1595+7408G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32744898 | |||||||
chr3:32745068 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1595+7578G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745068 | |||||||
chr3:32745214 | T | C | 1 | a0001c0001t0001g0018 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1595+7724T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745214 | |||||||
chr3:32745264 | T | C | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1595+7774T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745264 | |||||||
chr3:32745266 | G | A | 15 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0106 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1595+7776G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745266 | |||||||
chr3:32745275 | T | G | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1595+7785T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745275 | |||||||
chr3:32745392 | A | G | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1595+7902A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745392 | |||||||
chr3:32745469 | A | AGATAACA others(3): Show |
344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1595+7979_1595+798 others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745469 | |||||||
chr3:32745471 | T | C | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1595+7981T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745471 | |||||||
chr3:32745472 | G | A | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1595+7982G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745472 | |||||||
chr3:32745473 | A | C | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1595+7983A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745473 | |||||||
chr3:32745475 | T | C | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1595+7985T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745475 | |||||||
chr3:32745488 | C | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+7998C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32745488 | |||||||
chr3:32745707 | G | GA | 5 | a0001c0001t0001g0332 a0001c0001t0001g0335 a0001c0001t0001g0336 others(2): Show |
5 | HG01891.hp1 HG03130.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1595+8219dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32745707 | ||||||
chr3:32745830 | CTG | C | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+8342_1595+834 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32745830 | ||||||
chr3:32746038 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0322 |
2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1595+8548A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746038 | |||||||
chr3:32746055 | T | C | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1595+8565T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746055 | |||||||
chr3:32746148 | T | C | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1595+8658T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746148 | |||||||
chr3:32746279 | A | G | 1 | a0001c0001t0001g0289 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1595+8789A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746279 | |||||||
chr3:32746538 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1595+9048G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746538 | |||||||
chr3:32746664 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1595+9174G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746664 | |||||||
chr3:32746698 | G | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+9208G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746698 | |||||||
chr3:32746757 | T | A | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1595+9267T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746757 | |||||||
chr3:32746815 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1595+9325C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746815 | |||||||
chr3:32746832 | G | A | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+9342G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746832 | |||||||
chr3:32746836 | C | CA | 7 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0129 others(4): Show |
7 | HG00735.hp2 HG00738.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1595+9367dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32746836 | ||||||
chr3:32746836 | CA | C | 150 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
153 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.1595+9367delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32746836 | ||||||
chr3:32746836 | CAA | C | 35 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0040 others(32): Show |
35 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.1595+9366_1595+936 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32746836 | ||||||
chr3:32746836 | CAAAAA | C | 37 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(34): Show |
37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1595+9363_1595+936 others(9): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32746836 | ||||||
chr3:32746960 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1595+9470A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32746960 | |||||||
chr3:32747014 | G | T | 53 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0034 others(50): Show |
53 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1595+9524G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747014 | |||||||
chr3:32747093 | G | A | 4 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0215 others(1): Show |
4 | HG00639.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1595+9603G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747093 | |||||||
chr3:32747201 | A | C | 1 | a0001c0001t0001g0119 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1595+9711A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747201 | |||||||
chr3:32747276 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1595+9786G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747276 | |||||||
chr3:32747307 | A | G | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+9817A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747307 | |||||||
chr3:32747355 | G | A | 15 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0106 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1595+9865G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747355 | |||||||
chr3:32747450 | A | T | 1 | a0001c0001t0001g0341 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1595+9960A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747450 | |||||||
chr3:32747451 | T | A | 1 | a0001c0001t0001g0341 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1595+9961T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747451 | |||||||
chr3:32747634 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1595+10144G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747634 | |||||||
chr3:32747694 | A | C | 3 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0005g0036 |
3 | HG02572.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1595+10204A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747694 | |||||||
chr3:32747731 | C | G | 1 | a0001c0001t0001g0289 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1595+10241C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747731 | |||||||
chr3:32747745 | G | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1595+10255G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747745 | |||||||
chr3:32747808 | C | T | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0346 |
3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1595+10318C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747808 | |||||||
chr3:32747854 | G | A | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+10364G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747854 | |||||||
chr3:32747889 | A | G | 1 | a0001c0001t0001g0333 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1595+10399A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747889 | |||||||
chr3:32747905 | G | GCCAC | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595+10416_1595+10 others(10): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32747905 | ||||||
chr3:32747964 | C | CA | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1595+10483dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32747964 | ||||||
chr3:32747990 | C | T | 1 | a0001c0001t0001g0337 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1595+10500C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32747990 | |||||||
chr3:32748027 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1595+10537A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748027 | |||||||
chr3:32748422 | T | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1595+10932T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748422 | |||||||
chr3:32748461 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1595+10971A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748461 | |||||||
chr3:32748485 | A | G | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596-10973A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748485 | |||||||
chr3:32748605 | C | T | 1 | a0001c0001t0001g0333 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1596-10853C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748605 | |||||||
chr3:32748637 | C | T | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-10821C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748637 | |||||||
chr3:32748669 | C | T | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596-10789C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748669 | |||||||
chr3:32748907 | C | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596-10551C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748907 | |||||||
chr3:32748914 | C | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596-10544C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748914 | |||||||
chr3:32748923 | G | T | 1 | a0001c0001t0001g0339 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1596-10535G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748923 | |||||||
chr3:32748968 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(102): Show |
107 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1596-10490T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32748968 | |||||||
chr3:32749008 | G | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(2): Show |
5 | HG01168.hp1 HG01169.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596-10450G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32749008 | |||||||
chr3:32749192 | G | C | 1 | a0001c0001t0001g0248 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1596-10266G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32749192 | |||||||
chr3:32749216 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1596-10242G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32749216 | |||||||
chr3:32749261 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1596-10197T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32749261 | |||||||
chr3:32749278 | C | G | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596-10180C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32749278 | |||||||
chr3:32749405 | A | AT | 17 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0106 others(14): Show |
17 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1596-10032dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32749405 | ||||||
chr3:32749405 | A | ATT | 14 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0026 others(11): Show |
14 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1596-10033_1596-10 others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32749405 | ||||||
chr3:32749405 | A | ATTT | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(19): Show |
22 | HG01109.hp2 HG01168.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.1596-10034_1596-10 others(9): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32749405 | ||||||
chr3:32749405 | AT | A | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(262): Show |
270 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.1596-10032delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32749405 | ||||||
chr3:32749405 | ATT | A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0049 a0001c0001t0001g0053 others(12): Show |
15 | HG00558.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1596-10033_1596-10 others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32749405 | ||||||
chr3:32749446 | A | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1596-10012A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32749446 | |||||||
chr3:32749479 | G | A | 11 | a0001c0001t0001g0210 a0001c0001t0001g0217 a0001c0001t0001g0218 others(8): Show |
11 | HG01515.hp1 HG01517.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.1596-9979G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32749479 | |||||||
chr3:32749645 | G | A | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1596-9813G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32749645 | |||||||
chr3:32749843 | G | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0121 a0001c0001t0001g0122 others(7): Show |
11 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1596-9615G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32749843 | |||||||
chr3:32749994 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1596-9464A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32749994 | |||||||
chr3:32750091 | T | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1596-9367T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750091 | |||||||
chr3:32750235 | C | A | 1 | a0001c0001t0001g0011 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1596-9223C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750235 | |||||||
chr3:32750240 | A | T | 1 | a0001c0001t0001g0011 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1596-9218A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750240 | |||||||
chr3:32750384 | A | T | 5 | a0002c0002t0001g0214 a0002c0002t0001g0229 a0002c0002t0001g0230 others(2): Show |
5 | HG02895.hp1 HG02897.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596-9074A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750384 | |||||||
chr3:32750424 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1596-9034C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750424 | |||||||
chr3:32750467 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1596-8991G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750467 | |||||||
chr3:32750580 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1596-8878T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750580 | |||||||
chr3:32750712 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1596-8746C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750712 | |||||||
chr3:32750738 | G | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG02735.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1596-8720G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750738 | |||||||
chr3:32750757 | G | A | 2 | a0001c0001t0002g0031 a0001c0001t0002g0032 |
2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1596-8701G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750757 | |||||||
chr3:32750768 | T | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0150 |
2 | HG01928.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1596-8690T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750768 | |||||||
chr3:32750786 | G | A | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1596-8672G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750786 | |||||||
chr3:32750839 | C | T | 2 | a0001c0001t0001g0262 a0001c0001t0001g0275 |
2 | HG00738.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1596-8619C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750839 | |||||||
chr3:32750858 | A | G | 1 | a0001c0001t0001g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1596-8600A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750858 | |||||||
chr3:32750900 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1596-8558T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750900 | |||||||
chr3:32750910 | C | G | 34 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(31): Show |
34 | HG01168.hp1 HG01169.hp1 HG01515.hp1 others(31): Show |
intron_variant | MODIFIER | c.1596-8548C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32750910 | |||||||
chr3:32751056 | G | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
38 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(35): Show |
intron_variant | MODIFIER | c.1596-8402G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751056 | |||||||
chr3:32751101 | GA | G | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1596-8348delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32751101 | ||||||
chr3:32751111 | T | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0094 |
2 | NA18951.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1596-8347T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751111 | |||||||
chr3:32751133 | C | T | 2 | a0001c0001t0001g0227 a0001c0001t0001g0298 |
2 | HG00733.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1596-8325C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751133 | |||||||
chr3:32751164 | A | G | 6 | a0001c0001t0001g0040 a0001c0001t0001g0047 a0001c0001t0001g0049 others(3): Show |
6 | HG00642.hp2 HG00741.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1596-8294A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751164 | |||||||
chr3:32751230 | A | G | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0346 |
3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1596-8228A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751230 | |||||||
chr3:32751274 | A | AT | 9 | a0001c0001t0001g0113 a0001c0001t0001g0129 a0001c0001t0001g0267 others(6): Show |
9 | HG00140.hp1 HG01981.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1596-8172dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32751274 | ||||||
chr3:32751294 | CAG | C | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596-8161_1596-816 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32751294 | ||||||
chr3:32751311 | G | A | 1 | a0002c0002t0001g0271 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1596-8147G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751311 | |||||||
chr3:32751341 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1596-8117A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751341 | |||||||
chr3:32751456 | A | G | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1596-8002A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751456 | |||||||
chr3:32751776 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0304 others(2): Show |
7 | HG00735.hp1 HG01071.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1596-7682T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751776 | |||||||
chr3:32751816 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1596-7642G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751816 | |||||||
chr3:32751978 | T | C | 2 | a0001c0001t0001g0294 a0001c0001t0001g0310 |
2 | HG00741.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1596-7480T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32751978 | |||||||
chr3:32752035 | T | C | 1 | a0001c0001t0002g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1596-7423T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32752035 | |||||||
chr3:32752086 | CG | C | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1596-7369delG | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32752086 | ||||||
chr3:32752506 | G | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596-6952G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32752506 | |||||||
chr3:32752561 | A | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
110 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1596-6897A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32752561 | |||||||
chr3:32752591 | A | G | 15 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.1596-6867A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32752591 | |||||||
chr3:32752814 | A | T | 1 | a0001c0001t0001g0292 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1596-6644A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32752814 | |||||||
chr3:32752841 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1596-6617C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32752841 | |||||||
chr3:32752978 | C | T | 1 | a0002c0002t0001g0271 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1596-6480C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32752978 | |||||||
chr3:32753047 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1596-6411A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32753047 | |||||||
chr3:32753106 | T | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(100): Show |
105 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.1596-6352T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32753106 | |||||||
chr3:32753142 | C | T | 10 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0339 others(7): Show |
10 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.1596-6316C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32753142 | |||||||
chr3:32753290 | C | A | 1 | a0001c0001t0001g0333 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1596-6168C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32753290 | |||||||
chr3:32753314 | C | A | 3 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0280 |
3 | HG02004.hp1 HG02109.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1596-6144C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32753314 | |||||||
chr3:32753539 | A | C | 9 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0209 others(6): Show |
9 | HG00639.hp1 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1596-5919A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32753539 | |||||||
chr3:32753667 | G | A | 1 | a0001c0001t0003g0324 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1596-5791G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32753667 | |||||||
chr3:32753725 | C | T | 8 | a0002c0002t0001g0214 a0002c0002t0001g0229 a0002c0002t0001g0230 others(5): Show |
8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-5733C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32753725 | |||||||
chr3:32753873 | CTGA | C | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(11): Show |
14 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1596-5580_1596-557 others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32753873 | ||||||
chr3:32753918 | T | TCA | 18 | a0001c0001t0001g0007 a0001c0001t0001g0092 a0001c0001t0001g0322 others(15): Show |
18 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1596-5523_1596-552 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32753918 | ||||||
chr3:32753918 | T | TCACA | 51 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(48): Show |
51 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1596-5525_1596-552 others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32753918 | ||||||
chr3:32754083 | A | C | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0346 |
3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1596-5375A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754083 | |||||||
chr3:32754086 | G | C | 2 | a0001c0001t0001g0228 a0001c0001t0001g0305 |
2 | HG01243.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.1596-5372G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754086 | |||||||
chr3:32754108 | A | G | 1 | a0001c0001t0001g0347 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1596-5350A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754108 | |||||||
chr3:32754159 | G | C | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1596-5299G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754159 | |||||||
chr3:32754222 | A | G | 1 | a0001c0001t0001g0339 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1596-5236A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754222 | |||||||
chr3:32754260 | G | A | 1 | a0001c0001t0001g0333 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1596-5198G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754260 | |||||||
chr3:32754274 | G | A | 138 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(135): Show |
141 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.1596-5184G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754274 | |||||||
chr3:32754321 | C | T | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1596-5137C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754321 | |||||||
chr3:32754392 | G | A | 1 | a0001c0001t0001g0333 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1596-5066G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754392 | |||||||
chr3:32754406 | G | A | 8 | a0001c0001t0001g0228 a0001c0001t0001g0236 a0001c0001t0001g0253 others(5): Show |
8 | HG00738.hp1 HG01243.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596-5052G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754406 | |||||||
chr3:32754414 | T | G | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(11): Show |
14 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1596-5044T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754414 | |||||||
chr3:32754464 | A | G | 37 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(34): Show |
37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1596-4994A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754464 | |||||||
chr3:32754472 | G | A | 5 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0056 others(2): Show |
5 | NA18972.hp2 NA18985.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.1596-4986G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754472 | |||||||
chr3:32754476 | C | CA | 45 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0035 others(42): Show |
45 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.1596-4968dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754476 | ||||||
chr3:32754476 | C | CAA | 8 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0049 others(5): Show |
8 | HG00741.hp2 HG02572.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-4969_1596-496 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754476 | ||||||
chr3:32754476 | CAA | C | 10 | a0001c0001t0001g0109 a0001c0001t0001g0333 a0001c0001t0001g0339 others(7): Show |
10 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.1596-4969_1596-496 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754476 | ||||||
chr3:32754476 | CAAA | C | 12 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0106 others(9): Show |
12 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.1596-4970_1596-496 others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754476 | ||||||
chr3:32754485 | A | ATAT | 8 | a0001c0001t0001g0128 a0001c0001t0001g0244 a0001c0001t0001g0245 others(5): Show |
8 | HG01361.hp2 HG01433.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-4973_1596-497 others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754485 | |||||||
chr3:32754487 | A | AAT | 12 | a0001c0001t0001g0210 a0001c0001t0001g0213 a0001c0001t0001g0217 others(9): Show |
12 | HG01515.hp1 HG01517.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.1596-4970_1596-496 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754487 | ||||||
chr3:32754487 | A | ATAT | 60 | a0001c0001t0001g0005 a0001c0001t0001g0088 a0001c0001t0001g0089 others(57): Show |
61 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1596-4971_1596-497 others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754487 | |||||||
chr3:32754487 | A | ATATAT | 5 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0240 others(2): Show |
5 | HG00642.hp1 HG01243.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596-4971_1596-497 others(9): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754487 | |||||||
chr3:32754487 | A | ATATATAT | 7 | a0001c0001t0001g0239 a0001c0001t0001g0246 a0001c0001t0001g0282 others(4): Show |
7 | NA18945.hp2 NA18950.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.1596-4971_1596-497 others(11): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754487 | |||||||
chr3:32754487 | A | T | 12 | a0001c0001t0001g0105 a0001c0001t0001g0111 a0001c0001t0001g0128 others(9): Show |
12 | HG01257.hp2 HG01361.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.1596-4971A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754487 | |||||||
chr3:32754489 | A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0092 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(34): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(25): Show |
1 | a0001c0001t0001g0168 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(36): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(16): Show |
1 | a0001c0001t0001g0086 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(27): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(26): Show |
3 | a0001c0001t0001g0120 a0001c0001t0001g0133 a0001c0001t0001g0151 |
3 | HG01943.hp1 HG02027.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(37): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(32): Show |
1 | a0001c0001t0001g0327 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(43): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0175 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(20): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(13): Show |
2 | a0001c0001t0001g0103 a0001c0001t0001g0195 |
2 | HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(24): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(15): Show |
2 | a0001c0001t0001g0090 a0001c0001t0001g0193 |
2 | HG01358.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(26): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(19): Show |
2 | a0001c0001t0001g0174 a0001c0001t0001g0180 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(30): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(23): Show |
3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0198 |
3 | NA18946.hp1 NA18974.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(34): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(29): Show |
1 | a0001c0001t0001g0325 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(40): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0124 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(25): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(18): Show |
1 | a0001c0001t0001g0172 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(29): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(20): Show |
2 | a0001c0001t0001g0085 a0001c0001t0001g0127 |
2 | HG02135.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(31): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(26): Show |
1 | a0001c0001t0001g0191 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(37): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(28): Show |
1 | a0001c0001t0001g0115 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(39): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(15): Show |
5 | a0001c0001t0001g0091 a0001c0001t0001g0125 a0001c0001t0001g0146 others(2): Show |
5 | HG00099.hp2 HG01975.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(26): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(28): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(19): Show |
1 | a0001c0001t0001g0173 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(30): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(21): Show |
3 | a0001c0001t0001g0142 a0001c0001t0001g0147 a0001c0001t0001g0200 |
3 | NA18967.hp2 NA18982.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(32): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(25): Show |
1 | a0001c0001t0001g0153 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(36): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(27): Show |
4 | a0001c0001t0001g0156 a0001c0001t0001g0162 a0001c0001t0001g0190 others(1): Show |
4 | HG00673.hp1 NA18961.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(38): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(29): Show |
2 | a0001c0001t0001g0170 a0001c0001t0001g0194 |
2 | HG02300.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(40): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(31): Show |
3 | a0001c0001t0001g0166 a0001c0001t0001g0177 a0001c0001t0001g0178 |
3 | NA18945.hp1 NA18972.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(42): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(33): Show |
2 | a0001c0001t0001g0102 a0001c0001t0001g0132 |
2 | HG02155.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(44): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAA others(35): Show |
1 | a0001c0001t0001g0167 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(46): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAT others(22): Show |
1 | a0001c0001t0001g0171 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(33): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAT others(24): Show |
1 | a0001c0001t0001g0143 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(35): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAT others(26): Show |
1 | a0001c0001t0001g0164 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(37): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAAAT others(32): Show |
1 | a0001c0001t0001g0002 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(43): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAATA others(13): Show |
1 | a0001c0001t0001g0140 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(24): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAATA others(15): Show |
7 | a0001c0001t0001g0001 a0001c0001t0001g0121 a0001c0001t0001g0122 others(4): Show |
8 | HG02809.hp1 HG02970.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(26): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAATA others(17): Show |
1 | a0001c0001t0001g0161 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(28): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAATA others(19): Show |
1 | a0001c0001t0001g0196 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(30): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAATA others(21): Show |
3 | a0001c0001t0001g0137 a0001c0001t0001g0176 a0001c0001t0001g0331 |
3 | HG01081.hp2 HG02559.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(32): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAATA others(23): Show |
3 | a0001c0001t0001g0159 a0001c0001t0001g0186 a0001c0001t0001g0202 |
3 | HG00438.hp2 HG02630.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(34): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAATA others(25): Show |
2 | a0001c0001t0001g0135 a0001c0001t0001g0139 |
2 | HG03669.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(36): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAATA others(27): Show |
6 | a0001c0001t0001g0093 a0001c0001t0001g0130 a0001c0001t0001g0148 others(3): Show |
6 | HG01433.hp2 NA18979.hp2 NA19066.hp2 others(3): Show |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(38): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAAATA others(33): Show |
2 | a0001c0001t0001g0149 a0001c0001t0001g0165 |
2 | HG00323.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(44): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAATAT others(20): Show |
2 | a0001c0001t0001g0179 a0001c0003t0001g0134 |
2 | HG02083.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(31): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAATAT others(24): Show |
1 | a0001c0001t0001g0131 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(35): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAAATAT others(26): Show |
1 | a0001c0001t0001g0141 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(37): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAATATA others(1): Show |
17 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0013 others(14): Show |
17 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAATATA others(3): Show |
3 | a0001c0001t0002g0211 a0001c0001t0002g0212 a0001c0001t0002g0216 |
3 | HG00639.hp1 HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1596-4968_1596-496 others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAATATA others(5): Show |
1 | a0001c0001t0001g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(16): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAATATA others(13): Show |
1 | a0001c0001t0001g0160 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(24): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAATATA others(15): Show |
1 | a0001c0001t0001g0138 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(26): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAAATATA others(19): Show |
1 | a0001c0001t0001g0154 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(30): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAATATAT others(22): Show |
1 | a0001c0001t0001g0136 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(33): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AAATATAT others(34): Show |
1 | a0001c0001t0001g0150 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(45): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AATATATA others(19): Show |
2 | a0001c0001t0001g0126 a0001c0001t0001g0144 |
2 | HG01109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1596-4966_1596-496 others(30): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | AATATATA others(21): Show |
1 | a0001c0001t0003g0323 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1596-4966_1596-496 others(32): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754489 | ||||||
chr3:32754489 | A | ATAT | 24 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(21): Show |
24 | HG00738.hp1 HG01071.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.1596-4969_1596-496 others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754489 | |||||||
chr3:32754489 | A | ATATAT | 7 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(4): Show |
7 | HG00733.hp2 HG01069.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.1596-4969_1596-496 others(9): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754489 | |||||||
chr3:32754489 | A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1596-4969_1596-496 others(33): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754489 | |||||||
chr3:32754489 | A | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0084 others(109): Show |
113 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.1596-4969A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754489 | |||||||
chr3:32754490 | A | AAAAAAAA others(27): Show |
1 | a0001c0001t0001g0129 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1596-4968_1596-496 others(38): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754490 | |||||||
chr3:32754491 | T | A | 42 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0037 others(39): Show |
42 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.1596-4967T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754491 | |||||||
chr3:32754491 | TAC | T | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596-4965_1596-496 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754491 | ||||||
chr3:32754493 | C | T | 339 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(336): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1596-4965C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754493 | |||||||
chr3:32754495 | T | A | 1 | a0001c0001t0001g0183 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1596-4963T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754495 | |||||||
chr3:32754497 | T | A | 1 | a0001c0001t0001g0183 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1596-4961T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754497 | |||||||
chr3:32754506 | A | T | 13 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(10): Show |
13 | HG01081.hp1 HG01361.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.1596-4952A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754506 | |||||||
chr3:32754518 | C | CT | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(146): Show |
151 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.1596-4921dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754518 | ||||||
chr3:32754518 | C | CTT | 17 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0070 others(14): Show |
17 | HG00673.hp1 HG01358.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.1596-4922_1596-492 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754518 | ||||||
chr3:32754518 | CT | C | 17 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 others(14): Show |
17 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1596-4921delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754518 | ||||||
chr3:32754518 | CTTTTTT | C | 15 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0106 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1596-4926_1596-492 others(10): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754518 | ||||||
chr3:32754565 | G | A | 8 | a0002c0002t0001g0214 a0002c0002t0001g0229 a0002c0002t0001g0230 others(5): Show |
8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-4893G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754565 | |||||||
chr3:32754644 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1596-4814T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754644 | |||||||
chr3:32754673 | T | C | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(342): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1596-4785T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754673 | |||||||
chr3:32754690 | T | C | 2 | a0001c0001t0001g0245 a0001c0001t0001g0293 |
2 | HG02148.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1596-4768T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754690 | |||||||
chr3:32754698 | T | G | 1 | a0001c0001t0001g0171 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1596-4760T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754698 | |||||||
chr3:32754710 | C | G | 1 | a0001c0001t0001g0333 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1596-4748C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754710 | |||||||
chr3:32754710 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0116 |
2 | HG00140.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1596-4748C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754710 | |||||||
chr3:32754752 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1596-4706T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754752 | |||||||
chr3:32754846 | C | T | 17 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0105 others(14): Show |
17 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1596-4612C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754846 | |||||||
chr3:32754897 | C | CA | 17 | a0001c0001t0001g0030 a0001c0001t0001g0097 a0001c0001t0001g0098 others(14): Show |
17 | HG01074.hp2 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1596-4547dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754897 | ||||||
chr3:32754897 | C | CAAA | 9 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0341 others(6): Show |
9 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1596-4549_1596-454 others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754897 | ||||||
chr3:32754897 | C | CAAAA | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01109.hp2 HG01168.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.1596-4550_1596-454 others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32754897 | ||||||
chr3:32754968 | C | T | 1 | a0001c0001t0001g0290 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1596-4490C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754968 | |||||||
chr3:32754969 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1596-4489G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32754969 | |||||||
chr3:32755034 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1596-4424G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755034 | |||||||
chr3:32755126 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(93): Show |
98 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1596-4332G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755126 | |||||||
chr3:32755171 | G | A | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(11): Show |
14 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1596-4287G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755171 | |||||||
chr3:32755248 | A | G | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0346 |
3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1596-4210A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755248 | |||||||
chr3:32755295 | A | T | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596-4163A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755295 | |||||||
chr3:32755319 | C | CT | 13 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0063 others(10): Show |
13 | HG00438.hp2 HG01106.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1596-4123dupT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32755319 | ||||||
chr3:32755319 | C | CTTT | 20 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(17): Show |
20 | HG01168.hp1 HG01169.hp1 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.1596-4125_1596-412 others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32755319 | ||||||
chr3:32755319 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0128 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1596-4132_1596-412 others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32755319 | ||||||
chr3:32755325 | T | C | 20 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0106 others(17): Show |
20 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.1596-4133T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755325 | |||||||
chr3:32755341 | A | G | 37 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(34): Show |
37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1596-4117A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755341 | |||||||
chr3:32755544 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1596-3914A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755544 | |||||||
chr3:32755587 | A | T | 8 | a0002c0002t0001g0214 a0002c0002t0001g0229 a0002c0002t0001g0230 others(5): Show |
8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-3871A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755587 | |||||||
chr3:32755757 | C | CTT | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1596-3688_1596-368 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32755757 | ||||||
chr3:32755757 | CT | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0045 others(112): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.1596-3687delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32755757 | ||||||
chr3:32755803 | G | C | 1 | a0001c0001t0001g0330 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1596-3655G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755803 | |||||||
chr3:32755849 | A | G | 3 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0005g0036 |
3 | HG02572.hp1 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1596-3609A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32755849 | |||||||
chr3:32755851 | TG | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596-3603delG | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32755851 | ||||||
chr3:32756038 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1596-3420G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756038 | |||||||
chr3:32756313 | G | A | 8 | a0002c0002t0001g0214 a0002c0002t0001g0229 a0002c0002t0001g0230 others(5): Show |
8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-3145G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756313 | |||||||
chr3:32756315 | C | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(93): Show |
98 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1596-3143C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756315 | |||||||
chr3:32756332 | T | C | 1 | a0001c0001t0002g0211 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1596-3126T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756332 | |||||||
chr3:32756382 | G | T | 3 | a0001c0001t0001g0228 a0001c0001t0001g0268 a0001c0001t0001g0305 |
3 | HG01243.hp2 HG01515.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1596-3076G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756382 | |||||||
chr3:32756577 | A | G | 37 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(34): Show |
37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1596-2881A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756577 | |||||||
chr3:32756621 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1596-2837C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756621 | |||||||
chr3:32756697 | T | C | 19 | a0001c0001t0001g0085 a0001c0001t0001g0102 a0001c0001t0001g0120 others(16): Show |
19 | HG00558.hp1 HG00597.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.1596-2761T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756697 | |||||||
chr3:32756879 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1596-2579C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756879 | |||||||
chr3:32756904 | T | TGAGA | 37 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(34): Show |
37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1596-2554_1596-255 others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756904 | |||||||
chr3:32756921 | A | T | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0346 |
3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1596-2537A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756921 | |||||||
chr3:32756979 | A | G | 345 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(342): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1596-2479A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32756979 | |||||||
chr3:32757030 | G | T | 1 | a0001c0001t0002g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1596-2428G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757030 | |||||||
chr3:32757048 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1596-2410G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757048 | |||||||
chr3:32757100 | C | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596-2358C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757100 | |||||||
chr3:32757110 | G | GA | 18 | a0001c0001t0001g0030 a0001c0001t0001g0087 a0001c0001t0001g0129 others(15): Show |
18 | HG01515.hp1 HG01517.hp1 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.1596-2332dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32757110 | ||||||
chr3:32757142 | A | G | 8 | a0002c0002t0001g0214 a0002c0002t0001g0229 a0002c0002t0001g0230 others(5): Show |
8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-2316A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757142 | |||||||
chr3:32757170 | A | ATT | 67 | a0001c0001t0001g0001 a0001c0001t0001g0086 a0001c0001t0001g0093 others(64): Show |
68 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1596-2263_1596-226 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32757170 | ||||||
chr3:32757170 | A | ATTT | 136 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0007 others(133): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1596-2264_1596-226 others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32757170 | ||||||
chr3:32757170 | A | ATTTT | 82 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0033 others(79): Show |
84 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1596-2265_1596-226 others(8): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32757170 | ||||||
chr3:32757170 | A | ATTTTT | 17 | a0001c0001t0001g0054 a0001c0001t0001g0072 a0001c0001t0001g0074 others(14): Show |
17 | HG01517.hp1 HG01934.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1596-2266_1596-226 others(9): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32757170 | ||||||
chr3:32757170 | A | ATTTTTTT others(3): Show |
3 | a0001c0001t0002g0212 a0001c0001t0002g0215 a0001c0001t0002g0216 |
3 | HG02630.hp2 HG02818.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1596-2271_1596-226 others(14): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32757170 | ||||||
chr3:32757170 | ATTTTTT | A | 18 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(15): Show |
18 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.1596-2267_1596-226 others(10): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32757170 | ||||||
chr3:32757203 | G | A | 1 | a0001c0001t0001g0333 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1596-2255G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757203 | |||||||
chr3:32757365 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1596-2093G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757365 | |||||||
chr3:32757398 | C | T | 14 | a0001c0001t0001g0087 a0001c0001t0001g0210 a0001c0001t0001g0213 others(11): Show |
14 | HG01515.hp1 HG01517.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1596-2060C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757398 | |||||||
chr3:32757443 | T | C | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-2015T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757443 | |||||||
chr3:32757469 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1596-1989G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757469 | |||||||
chr3:32757479 | A | G | 1 | a0001c0001t0002g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1596-1979A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757479 | |||||||
chr3:32757508 | C | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(2): Show |
5 | HG01168.hp1 HG01169.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1596-1950C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757508 | |||||||
chr3:32757861 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1596-1597C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757861 | |||||||
chr3:32757914 | C | G | 1 | a0001c0001t0001g0073 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1596-1544C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757914 | |||||||
chr3:32757940 | A | G | 37 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(34): Show |
37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1596-1518A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32757940 | |||||||
chr3:32758042 | C | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1596-1416C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32758042 | |||||||
chr3:32758214 | A | G | 23 | a0001c0001t0001g0087 a0001c0001t0001g0210 a0001c0001t0001g0213 others(20): Show |
23 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.1596-1244A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32758214 | |||||||
chr3:32758347 | C | G | 3 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0003c0004t0001g0340 |
3 | HG01106.hp1 HG01109.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.1596-1111C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32758347 | |||||||
chr3:32758626 | G | A | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596-832G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32758626 | |||||||
chr3:32758796 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1596-662C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32758796 | |||||||
chr3:32758811 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1596-647G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32758811 | |||||||
chr3:32758830 | C | T | 37 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(34): Show |
37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1596-628C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32758830 | |||||||
chr3:32759045 | A | G | 54 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0034 others(51): Show |
54 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1596-413A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32759045 | |||||||
chr3:32759130 | A | AGTGT | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1596-307_1596-304d others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32759130 | ||||||
chr3:32759130 | AGT | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1596-305_1596-304d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32759130 | ||||||
chr3:32759130 | AGTGTGTG others(1): Show |
A | 4 | a0001c0001t0001g0224 a0001c0001t0001g0241 a0001c0001t0001g0257 others(1): Show |
4 | HG00408.hp2 HG02080.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1596-311_1596-304d others(10): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32759130 | ||||||
chr3:32759131 | G | T | 1 | a0001c0001t0001g0154 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1596-327G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32759131 | |||||||
chr3:32759132 | T | A | 1 | a0001c0001t0001g0154 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1596-326T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32759132 | |||||||
chr3:32759133 | G | T | 1 | a0001c0001t0003g0323 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1596-325G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32759133 | |||||||
chr3:32759134 | T | A | 1 | a0001c0001t0003g0323 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1596-324T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32759134 | |||||||
chr3:32759170 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1596-288T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32759170 | |||||||
chr3:32759170 | T | TATAC | 8 | a0001c0001t0001g0087 a0001c0001t0001g0172 a0001c0001t0001g0173 others(5): Show |
8 | HG02647.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-270_1596-267d others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr3 | 32759170 | ||||||
chr3:32759173 | AC | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1596-284delC | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32759173 | |||||||
chr3:32759174 | C | T | 8 | a0002c0002t0001g0214 a0002c0002t0001g0229 a0002c0002t0001g0230 others(5): Show |
8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596-284C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32759174 | |||||||
chr3:32759247 | A | C | 1 | a0001c0001t0001g0225 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1596-211A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32759247 | |||||||
chr3:32759266 | G | A | 1 | a0001c0001t0001g0299 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1596-192G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 13/18 | chr3 | 32759266 | |||||||
chr3:32759681 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0084 others(115): Show |
120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.1709+110A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32759681 | |||||||
chr3:32759702 | GAACGTTT others(3): Show |
G | 1 | a0001c0001t0001g0347 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1709+135_1709+144d others(12): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 32759702 | ||||||
chr3:32759899 | G | C | 4 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0001g0231 others(1): Show |
4 | HG02080.hp2 NA18953.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1709+328G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32759899 | |||||||
chr3:32760008 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1709+437C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760008 | |||||||
chr3:32760062 | A | G | 3 | a0001c0001t0001g0123 a0001c0001t0001g0161 a0001c0001t0001g0197 |
3 | HG02970.hp1 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1709+491A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760062 | |||||||
chr3:32760070 | T | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.1709+499T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760070 | |||||||
chr3:32760107 | A | G | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1709+536A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760107 | |||||||
chr3:32760128 | G | GCCA | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1709+557_1709+558i others(5): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760128 | |||||||
chr3:32760130 | T | G | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1709+559T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760130 | |||||||
chr3:32760131 | C | A | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1709+560C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760131 | |||||||
chr3:32760133 | CT | C | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1709+563delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760133 | |||||||
chr3:32760179 | C | CA | 10 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0334 others(7): Show |
10 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.1709+622dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 32760179 | ||||||
chr3:32760179 | CA | C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0030 a0001c0001t0001g0037 others(4): Show |
7 | HG00140.hp1 HG00408.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1709+622delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 32760179 | ||||||
chr3:32760252 | T | G | 1 | a0001c0001t0001g0140 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1709+681T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760252 | |||||||
chr3:32760270 | C | A | 54 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0034 others(51): Show |
54 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1709+699C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760270 | |||||||
chr3:32760305 | C | T | 1 | a0001c0001t0003g0323 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1709+734C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760305 | |||||||
chr3:32760473 | A | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1709+902A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760473 | |||||||
chr3:32760576 | G | A | 1 | a0001c0001t0002g0207 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1709+1005G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760576 | |||||||
chr3:32760609 | G | C | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(11): Show |
14 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1709+1038G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760609 | |||||||
chr3:32760638 | T | A | 1 | a0001c0001t0001g0128 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1709+1067T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760638 | |||||||
chr3:32760669 | G | T | 1 | a0001c0001t0001g0257 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1709+1098G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760669 | |||||||
chr3:32760898 | C | G | 37 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(34): Show |
37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1709+1327C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760898 | |||||||
chr3:32760903 | C | G | 15 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0106 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1709+1332C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32760903 | |||||||
chr3:32761072 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1709+1501T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761072 | |||||||
chr3:32761088 | C | T | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1709+1517C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761088 | |||||||
chr3:32761145 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1709+1574T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761145 | |||||||
chr3:32761184 | T | C | 3 | a0001c0001t0001g0096 a0001c0001t0001g0131 a0001c0001t0001g0159 |
3 | HG02630.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1710-1549T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761184 | |||||||
chr3:32761198 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(98): Show |
103 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1710-1535C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761198 | |||||||
chr3:32761518 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1710-1215G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761518 | |||||||
chr3:32761590 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1710-1143C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761590 | |||||||
chr3:32761604 | G | GGAGTGCA others(39): Show |
1 | a0001c0001t0001g0086 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1710-1127_1710-108 others(50): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 32761604 | ||||||
chr3:32761660 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1710-1073A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761660 | |||||||
chr3:32761682 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1710-1051C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761682 | |||||||
chr3:32761726 | CT | C | 23 | a0001c0001t0001g0030 a0001c0001t0001g0104 a0001c0001t0001g0106 others(20): Show |
23 | HG00099.hp1 HG00140.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1710-991delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 32761726 | ||||||
chr3:32761726 | CTT | C | 35 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(32): Show |
35 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.1710-992_1710-991d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 32761726 | ||||||
chr3:32761758 | A | G | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1710-975A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761758 | |||||||
chr3:32761780 | G | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(98): Show |
103 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1710-953G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761780 | |||||||
chr3:32761791 | CT | C | 10 | a0001c0001t0001g0204 a0001c0001t0001g0226 a0001c0001t0001g0239 others(7): Show |
10 | HG01928.hp2 HG02015.hp1 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.1710-937delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 32761791 | ||||||
chr3:32761818 | G | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(98): Show |
104 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.1710-915G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761818 | |||||||
chr3:32761829 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1710-904A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761829 | |||||||
chr3:32761876 | G | A | 2 | a0001c0001t0001g0236 a0001c0001t0001g0265 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1710-857G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761876 | |||||||
chr3:32761899 | A | G | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1710-834A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761899 | |||||||
chr3:32761901 | T | C | 1 | a0001c0001t0001g0347 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1710-832T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761901 | |||||||
chr3:32761933 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0197 |
2 | HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1710-800C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32761933 | |||||||
chr3:32762018 | A | G | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1710-715A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32762018 | |||||||
chr3:32762166 | T | TA | 7 | a0001c0001t0001g0076 a0001c0001t0001g0100 a0001c0001t0001g0125 others(4): Show |
7 | HG02809.hp2 HG04184.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.1710-551dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 32762166 | ||||||
chr3:32762239 | G | A | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1710-494G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32762239 | |||||||
chr3:32762259 | C | T | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(11): Show |
14 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1710-474C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32762259 | |||||||
chr3:32762644 | ATAATAAC others(16): Show |
A | 1 | a0001c0001t0001g0341 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1710-86_1710-64del others(23): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr3 | 32762644 | ||||||
chr3:32762693 | C | T | 37 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(34): Show |
37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1710-40C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 14/18 | chr3 | 32762693 | |||||||
chr3:32763029 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1840+166G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763029 | |||||||
chr3:32763157 | G | C | 32 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0041 others(29): Show |
32 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.1840+294G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763157 | |||||||
chr3:32763270 | A | G | 37 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(34): Show |
37 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.1840+407A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763270 | |||||||
chr3:32763338 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1840+475G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763338 | |||||||
chr3:32763380 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1840+517G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763380 | |||||||
chr3:32763456 | G | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0316 |
2 | HG01928.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1840+593G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763456 | |||||||
chr3:32763480 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1840+617G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763480 | |||||||
chr3:32763506 | A | G | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(11): Show |
14 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1840+643A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763506 | |||||||
chr3:32763705 | C | T | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.1841-750C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763705 | |||||||
chr3:32763714 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1841-741A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763714 | |||||||
chr3:32763984 | G | T | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1841-471G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32763984 | |||||||
chr3:32764058 | A | C | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1841-397A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32764058 | |||||||
chr3:32764103 | G | A | 2 | a0001c0001t0001g0236 a0001c0001t0001g0265 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1841-352G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32764103 | |||||||
chr3:32764138 | A | C | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(11): Show |
14 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1841-317A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32764138 | |||||||
chr3:32764269 | G | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0300 a0001c0001t0001g0301 |
3 | HG00558.hp2 NA18949.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1841-186G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32764269 | |||||||
chr3:32764336 | C | CA | 9 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(6): Show |
9 | HG01167.hp1 HG01169.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.1841-105dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 32764336 | ||||||
chr3:32764336 | C | CAA | 13 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(10): Show |
13 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1841-106_1841-105d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr3 | 32764336 | ||||||
chr3:32764351 | G | A | 33 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(30): Show |
33 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1841-104G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32764351 | |||||||
chr3:32764351 | G | T | 35 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0041 others(32): Show |
35 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.1841-104G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 15/18 | chr3 | 32764351 | |||||||
chr3:32764815 | T | A | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.2004+6T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32764815 | |||||||
chr3:32765018 | A | G | 24 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(21): Show |
24 | HG00140.hp2 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.2004+209A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32765018 | |||||||
chr3:32765028 | A | T | 26 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(23): Show |
26 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.2004+219A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32765028 | |||||||
chr3:32765036 | T | A | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2004+227T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32765036 | |||||||
chr3:32765037 | T | A | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2004+228T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32765037 | |||||||
chr3:32765243 | G | A | 5 | a0002c0002t0001g0214 a0002c0002t0001g0229 a0002c0002t0001g0230 others(2): Show |
5 | HG02895.hp1 HG02897.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2004+434G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32765243 | |||||||
chr3:32765254 | GTTGCAGT others(1308): Show |
G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(250): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2004+463_2004+1777 others(3): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32765254 | ||||||
chr3:32765317 | C | CA | 14 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(11): Show |
14 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.2004+521dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32765317 | ||||||
chr3:32765518 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | NA18993.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2004+709G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32765518 | |||||||
chr3:32765646 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2004+837C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32765646 | |||||||
chr3:32765657 | C | CA | 21 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(18): Show |
21 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.2004+858dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32765657 | ||||||
chr3:32765658 | A | C | 1 | a0001c0001t0001g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2004+849A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32765658 | |||||||
chr3:32765818 | G | C | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.2004+1009G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32765818 | |||||||
chr3:32766003 | AT | A | 26 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(23): Show |
26 | HG00733.hp1 HG01169.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.2004+1213delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32766003 | ||||||
chr3:32766003 | ATT | A | 13 | a0001c0001t0001g0029 a0001c0001t0001g0333 a0001c0001t0001g0334 others(10): Show |
13 | HG01071.hp2 HG01106.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2004+1212_2004+121 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32766003 | ||||||
chr3:32766024 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2004+1215A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766024 | |||||||
chr3:32766027 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2004+1218C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766027 | |||||||
chr3:32766035 | C | T | 20 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(17): Show |
20 | HG00408.hp1 HG00438.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.2004+1226C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766035 | |||||||
chr3:32766088 | C | G | 1 | a0001c0001t0001g0062 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2004+1279C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766088 | |||||||
chr3:32766118 | G | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.2004+1309G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766118 | |||||||
chr3:32766186 | A | G | 91 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(88): Show |
91 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.2004+1377A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766186 | |||||||
chr3:32766529 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2004+1720C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766529 | |||||||
chr3:32766588 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.2004+1779G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766588 | |||||||
chr3:32766608 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2004+1799G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766608 | |||||||
chr3:32766622 | G | A | 15 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0106 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.2004+1813G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766622 | |||||||
chr3:32766632 | C | CA | 20 | a0001c0001t0001g0065 a0001c0001t0001g0092 a0001c0001t0001g0128 others(17): Show |
20 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.2004+1840dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32766632 | ||||||
chr3:32766677 | G | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.2004+1868G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766677 | |||||||
chr3:32766678 | C | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(20): Show |
23 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.2004+1869C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766678 | |||||||
chr3:32766796 | T | C | 10 | a0001c0001t0001g0204 a0001c0001t0001g0226 a0001c0001t0001g0239 others(7): Show |
10 | HG01928.hp2 HG02015.hp1 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.2004+1987T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766796 | |||||||
chr3:32766824 | A | T | 1 | a0001c0001t0001g0246 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2004+2015A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32766824 | |||||||
chr3:32767028 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(1): Show |
4 | NA18960.hp2 NA18962.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.2004+2219G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767028 | |||||||
chr3:32767316 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2004+2507C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767316 | |||||||
chr3:32767377 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2005-2510G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767377 | |||||||
chr3:32767427 | G | T | 12 | a0001c0001t0001g0142 a0001c0001t0001g0156 a0001c0001t0001g0164 others(9): Show |
12 | NA18943.hp2 NA18946.hp1 NA18954.hp1 others(9): Show |
intron_variant | MODIFIER | c.2005-2460G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767427 | |||||||
chr3:32767442 | G | C | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2005-2445G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767442 | |||||||
chr3:32767506 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2005-2381C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767506 | |||||||
chr3:32767519 | C | CA | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(159): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.2005-2350dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32767519 | ||||||
chr3:32767519 | C | CAA | 166 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(163): Show |
169 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(166): Show |
intron_variant | MODIFIER | c.2005-2351_2005-235 others(6): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32767519 | ||||||
chr3:32767519 | C | CAAA | 8 | a0001c0001t0001g0088 a0001c0001t0001g0098 a0001c0001t0001g0233 others(5): Show |
8 | HG01258.hp1 HG01891.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.2005-2352_2005-235 others(7): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32767519 | ||||||
chr3:32767555 | A | G | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.2005-2332A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767555 | |||||||
chr3:32767616 | G | A | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.2005-2271G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767616 | |||||||
chr3:32767815 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2005-2072C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767815 | |||||||
chr3:32767878 | T | C | 1 | a0001c0001t0002g0318 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2005-2009T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767878 | |||||||
chr3:32767903 | G | A | 47 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(44): Show |
47 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.2005-1984G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32767903 | |||||||
chr3:32768320 | A | G | 54 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(51): Show |
54 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.2005-1567A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32768320 | |||||||
chr3:32768342 | GA | G | 15 | a0001c0001t0001g0322 a0001c0001t0001g0332 a0001c0001t0001g0333 others(12): Show |
15 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.2005-1544delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32768342 | |||||||
chr3:32768537 | C | T | 8 | a0001c0001t0001g0087 a0001c0001t0001g0172 a0001c0001t0001g0173 others(5): Show |
8 | HG02647.hp1 HG02717.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2005-1350C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32768537 | |||||||
chr3:32768583 | C | CA | 54 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(51): Show |
54 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.2005-1292dupA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32768583 | ||||||
chr3:32768583 | CA | C | 131 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
134 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.2005-1292delA | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr3 | 32768583 | ||||||
chr3:32768616 | C | T | 2 | a0001c0001t0001g0297 a0001c0001t0001g0312 |
2 | NA18953.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.2005-1271C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32768616 | |||||||
chr3:32768654 | A | C | 1 | a0001c0001t0001g0161 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2005-1233A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32768654 | |||||||
chr3:32769073 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0116 |
2 | HG00140.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.2005-814T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32769073 | |||||||
chr3:32769162 | G | A | 8 | a0002c0002t0001g0214 a0002c0002t0001g0229 a0002c0002t0001g0230 others(5): Show |
8 | HG01081.hp1 HG01361.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.2005-725G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32769162 | |||||||
chr3:32769167 | G | C | 1 | a0001c0001t0001g0334 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2005-720G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32769167 | |||||||
chr3:32769179 | C | A | 1 | a0001c0001t0003g0324 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2005-708C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32769179 | |||||||
chr3:32769427 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2005-460G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32769427 | |||||||
chr3:32769710 | T | G | 40 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(37): Show |
40 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.2005-177T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32769710 | |||||||
chr3:32769777 | C | T | 17 | a0001c0001t0001g0007 a0001c0001t0001g0322 a0001c0001t0001g0332 others(14): Show |
17 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.2005-110C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32769777 | |||||||
chr3:32769810 | G | T | 1 | a0001c0001t0001g0247 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2005-77G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 17/18 | chr3 | 32769810 | |||||||
chr3:32770067 | A | AC | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 |
3 | NA18961.hp2 NA18986.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.2080+107dupC | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 32770067 | ||||||
chr3:32770194 | G | T | 1 | a0001c0001t0001g0331 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2080+232G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770194 | |||||||
chr3:32770317 | AT | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0093 others(59): Show |
62 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.2080+381delT | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 32770317 | ||||||
chr3:32770317 | ATT | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.2080+380_2080+381d others(4): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 32770317 | ||||||
chr3:32770317 | ATTT | A | 63 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(60): Show |
63 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.2080+379_2080+381d others(5): Show |
CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr3 | 32770317 | ||||||
chr3:32770319 | T | A | 1 | a0001c0001t0001g0092 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2080+357T>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770319 | |||||||
chr3:32770388 | C | T | 2 | a0001c0001t0001g0344 a0001c0001t0001g0345 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2080+426C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770388 | |||||||
chr3:32770418 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2080+456C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770418 | |||||||
chr3:32770537 | C | G | 17 | a0001c0001t0001g0007 a0001c0001t0001g0322 a0001c0001t0001g0332 others(14): Show |
17 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.2080+575C>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770537 | |||||||
chr3:32770547 | G | A | 15 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0106 others(12): Show |
15 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.2080+585G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770547 | |||||||
chr3:32770678 | C | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
22 | HG01168.hp1 HG01169.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.2080+716C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770678 | |||||||
chr3:32770859 | A | G | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2080+897A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770859 | |||||||
chr3:32770901 | A | G | 17 | a0001c0001t0001g0084 a0001c0001t0001g0104 a0001c0001t0001g0105 others(14): Show |
17 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.2080+939A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770901 | |||||||
chr3:32770964 | C | T | 17 | a0001c0001t0001g0007 a0001c0001t0001g0322 a0001c0001t0001g0332 others(14): Show |
17 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.2080+1002C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770964 | |||||||
chr3:32770998 | C | A | 1 | a0001c0001t0001g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2080+1036C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32770998 | |||||||
chr3:32771199 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2080+1237C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771199 | |||||||
chr3:32771248 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2080+1286G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771248 | |||||||
chr3:32771344 | T | G | 1 | a0001c0001t0001g0188 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2080+1382T>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771344 | |||||||
chr3:32771470 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2080+1508G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771470 | |||||||
chr3:32771559 | C | T | 1 | a0001c0001t0001g0333 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2080+1597C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771559 | |||||||
chr3:32771621 | C | A | 1 | a0001c0001t0001g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2080+1659C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771621 | |||||||
chr3:32771625 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0085 others(99): Show |
104 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.2080+1663T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771625 | |||||||
chr3:32771705 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2080+1743C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771705 | |||||||
chr3:32771762 | C | T | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0346 |
3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2081-1695C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771762 | |||||||
chr3:32771793 | C | A | 63 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0090 others(60): Show |
63 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.2081-1664C>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771793 | |||||||
chr3:32771961 | C | T | 1 | a0001c0001t0002g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2081-1496C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32771961 | |||||||
chr3:32772078 | C | T | 31 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(28): Show |
31 | HG01168.hp1 HG01169.hp1 HG01928.hp2 others(28): Show |
intron_variant | MODIFIER | c.2081-1379C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772078 | |||||||
chr3:32772091 | A | C | 1 | a0001c0001t0001g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2081-1366A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772091 | |||||||
chr3:32772096 | A | C | 26 | a0001c0001t0001g0087 a0001c0001t0001g0210 a0001c0001t0001g0213 others(23): Show |
26 | HG00639.hp1 HG01515.hp1 HG01517.hp1 others(23): Show |
intron_variant | MODIFIER | c.2081-1361A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772096 | |||||||
chr3:32772105 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2081-1352C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772105 | |||||||
chr3:32772140 | G | A | 1 | a0001c0001t0002g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2081-1317G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772140 | |||||||
chr3:32772219 | A | G | 2 | a0001c0001t0001g0259 a0001c0001t0001g0260 |
2 | NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2081-1238A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772219 | |||||||
chr3:32772230 | G | C | 1 | a0001c0001t0001g0259 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2081-1227G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772230 | |||||||
chr3:32772292 | T | C | 8 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.2081-1165T>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772292 | |||||||
chr3:32772344 | G | A | 30 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(27): Show |
30 | HG01168.hp1 HG01169.hp1 HG01928.hp2 others(27): Show |
intron_variant | MODIFIER | c.2081-1113G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772344 | |||||||
chr3:32772438 | A | G | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0346 |
3 | HG01891.hp2 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2081-1019A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772438 | |||||||
chr3:32772446 | A | G | 1 | a0001c0001t0001g0347 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2081-1011A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772446 | |||||||
chr3:32772474 | G | A | 4 | a0001c0001t0001g0335 a0001c0001t0001g0336 a0001c0001t0001g0337 others(1): Show |
4 | HG01891.hp1 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2081-983G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772474 | |||||||
chr3:32772641 | G | C | 1 | a0002c0002t0001g0272 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2081-816G>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772641 | |||||||
chr3:32772651 | C | T | 7 | a0001c0001t0001g0339 a0001c0001t0001g0341 a0001c0001t0001g0342 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2081-806C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772651 | |||||||
chr3:32772657 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2081-800A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772657 | |||||||
chr3:32772704 | A | C | 30 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(27): Show |
30 | HG01168.hp1 HG01169.hp1 HG01928.hp2 others(27): Show |
intron_variant | MODIFIER | c.2081-753A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772704 | |||||||
chr3:32772966 | A | T | 35 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(32): Show |
35 | HG00738.hp1 HG01168.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.2081-491A>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772966 | |||||||
chr3:32772969 | A | C | 35 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(32): Show |
35 | HG00738.hp1 HG01168.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.2081-488A>C | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772969 | |||||||
chr3:32772970 | G | A | 35 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(32): Show |
35 | HG00738.hp1 HG01168.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.2081-487G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772970 | |||||||
chr3:32772971 | C | T | 35 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(32): Show |
35 | HG00738.hp1 HG01168.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.2081-486C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772971 | |||||||
chr3:32772972 | C | T | 35 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(32): Show |
35 | HG00738.hp1 HG01168.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.2081-485C>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32772972 | |||||||
chr3:32773011 | A | G | 1 | a0001c0001t0001g0342 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2081-446A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32773011 | |||||||
chr3:32773038 | G | T | 6 | a0001c0001t0001g0086 a0001c0001t0001g0091 a0001c0001t0001g0103 others(3): Show |
6 | HG00099.hp2 HG01975.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.2081-419G>T | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32773038 | |||||||
chr3:32773056 | G | A | 6 | a0001c0001t0001g0085 a0001c0001t0001g0108 a0001c0001t0001g0127 others(3): Show |
6 | HG00558.hp1 HG00673.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.2081-401G>A | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32773056 | |||||||
chr3:32773207 | A | G | 56 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(53): Show |
56 | HG00140.hp2 HG00408.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.2081-250A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32773207 | |||||||
chr3:32773371 | A | G | 2 | a0001c0001t0001g0052 a0001c0001t0001g0053 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2081-86A>G | CNOT10 | ENSG00000182973.20 | transcript | ENST00000328834.10 | protein_coding | 18/18 | chr3 | 32773371 |