Item | Value |
---|---|
geneid | 4850 |
ensemblid | ENSG00000080802.21 |
hgncid | 7880 |
symbol | CNOT4 |
name | CCR4-NOT transcription complex subunit 4 |
refseq_nuc | NM_001190850.2 |
refseq_prot | NP_001177779.1 |
ensembl_nuc | ENST00000541284.6 |
ensembl_prot | ENSP00000445508.1 |
mane_status | MANE Select |
chr | chr7 |
start | 135361795 |
end | 135510102 |
strand | - |
ver | v1.2 |
region | chr7:135361795-135510102 |
region5000 | chr7:135356795-135515102 |
regionname0 | CNOT4_chr7_135361795_135510102 |
regionname5000 | CNOT4_chr7_135356795_135515102 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 713 | 248 | 62 | 48 | 97 | 9 | 30 | 80 | CNOT4_chr7_135356795_135515102 | CNOT4 | MSRSP others(708): Show |
chr7 | 135356795 | 135515102 |
a0002 | 0/0 | 713 | 104 | 11 | 17 | 68 | 2 | 6 | 55 | CNOT4_chr7_135356795_135515102 | CNOT4 | MSRSP others(708): Show |
chr7 | 135356795 | 135515102 |
a0003 | 0/0 | 713 | 4 | 1 | 3 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | MSRSP others(708): Show |
chr7 | 135356795 | 135515102 |
a0004 | 0/0 | 713 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | MSRSP others(708): Show |
chr7 | 135356795 | 135515102 |
a0005 | 0/0 | 713 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | MSRSP others(708): Show |
chr7 | 135356795 | 135515102 |
a0006 | 0/0 | 713 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | MSRSP others(708): Show |
chr7 | 135356795 | 135515102 |
a0007 | 0/0 | 713 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | MSRSP others(708): Show |
chr7 | 135356795 | 135515102 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2139 | 240 | 57 | 47 | 96 | 9 | 30 | CNOT4_chr7_135356795_135515102 | CNOT4 | ATGTC others(2134): Show |
chr7 | 135356795 | 135515102 | ||
a0001c0003 | 1/0 | 2139 | 6 | 5 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | ATGTC others(2134): Show |
chr7 | 135356795 | 135515102 | ||
a0001c0008 | 0/0 | 2139 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | ATGTC others(2134): Show |
chr7 | 135356795 | 135515102 | ||
a0001c0010 | 0/0 | 2139 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | ATGTC others(2134): Show |
chr7 | 135356795 | 135515102 | ||
a0002c0002 | 0/0 | 2139 | 103 | 11 | 17 | 68 | 2 | 5 | CNOT4_chr7_135356795_135515102 | CNOT4 | ATGTC others(2134): Show |
chr7 | 135356795 | 135515102 | ||
a0002c0011 | 0/0 | 2139 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | ATGTC others(2134): Show |
chr7 | 135356795 | 135515102 | ||
a0003c0004 | 0/0 | 2139 | 4 | 1 | 3 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | ATGTC others(2134): Show |
chr7 | 135356795 | 135515102 | ||
a0004c0005 | 0/0 | 2139 | 3 | 0 | 3 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | ATGTC others(2134): Show |
chr7 | 135356795 | 135515102 | ||
a0005c0007 | 0/0 | 2139 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | ATGTC others(2134): Show |
chr7 | 135356795 | 135515102 | ||
a0006c0006 | 0/0 | 2139 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | ATGTC others(2134): Show |
chr7 | 135356795 | 135515102 | ||
a0007c0009 | 0/0 | 2139 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | ATGTC others(2134): Show |
chr7 | 135356795 | 135515102 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3538 | 189 | 30 | 44 | 84 | 6 | 24 | CNOT4_chr7_135356795_135515102 | CNOT4 | GGAGG others(3533): Show |
chr7 | 135356795 | 135515102 |
a0001c0001t0002 | 0/0 | 3538 | 34 | 25 | 3 | 0 | 3 | 3 | CNOT4_chr7_135356795_135515102 | CNOT4 | GGAGG others(3533): Show |
chr7 | 135356795 | 135515102 |
a0001c0001t0003 | 0/0 | 3538 | 12 | 0 | 0 | 12 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | GGAGG others(3533): Show |
chr7 | 135356795 | 135515102 |
a0001c0001t0004 | 0/0 | 3538 | 2 | 0 | 0 | 0 | 0 | 2 | CNOT4_chr7_135356795_135515102 | CNOT4 | GGAGG others(3533): Show |
chr7 | 135356795 | 135515102 |
a0001c0001t0005 | 0/0 | 3538 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | GGAGG others(3533): Show |
chr7 | 135356795 | 135515102 |
a0001c0001t0007 | 0/0 | 3538 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | GGAGG others(3533): Show |
chr7 | 135356795 | 135515102 |
a0001c0001t0008 | 0/0 | 3538 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | GGAGG others(3533): Show |
chr7 | 135356795 | 135515102 |
a0001c0003t0002 | 1/0 | 3538 | 6 | 5 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | GGAGG others(3533): Show |
chr7 | 135356795 | 135515102 |
a0001c0008t0001 | 0/0 | 3538 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | GGAGG others(3533): Show |
chr7 | 135356795 | 135515102 |
a0001c0010t0002 | 0/0 | 3538 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | GGAGG others(3533): Show |
chr7 | 135356795 | 135515102 |
a0002c0002t0001 | 0/0 | 3538 | 102 | 10 | 17 | 68 | 2 | 5 | CNOT4_chr7_135356795_135515102 | CNOT4 | GGAGG others(3533): Show |
chr7 | 135356795 | 135515102 |
a0002c0002t0006 | 0/0 | 3538 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | GGAGG others(3533): Show |
chr7 | 135356795 | 135515102 |
a0002c0011t0001 | 0/0 | 3538 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | GGAGG others(3533): Show |
chr7 | 135356795 | 135515102 |
a0003c0004t0001 | 0/0 | 3538 | 4 | 1 | 3 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | GGAGG others(3533): Show |
chr7 | 135356795 | 135515102 |
a0004c0005t0001 | 0/0 | 3538 | 3 | 0 | 3 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | GGAGG others(3533): Show |
chr7 | 135356795 | 135515102 |
a0005c0007t0001 | 0/0 | 3538 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | GGAGG others(3533): Show |
chr7 | 135356795 | 135515102 |
a0006c0006t0001 | 0/0 | 3538 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | GGAGG others(3533): Show |
chr7 | 135356795 | 135515102 |
a0007c0009t0001 | 0/0 | 3538 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | GGAGG others(3533): Show |
chr7 | 135356795 | 135515102 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0315 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0007g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0001t0008g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0003t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0003t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0003t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0003t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0003t0002g0186 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0003t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0008t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0001c0010t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0002t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0002c0011t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0003c0004t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0003c0004t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0003c0004t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0003c0004t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0004c0005t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0004c0005t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0004c0005t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0005c0007t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0006c0006t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
a0007c0009t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0226 | EUR | GBR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | GBR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0120 | EUR | FIN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0303 | EUR | FIN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0224 | EUR | FIN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00323 | hp2 | a0005 | c0007 | t0001 | g0308 | EUR | FIN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | CHS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | CHS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0347 | EAS | CHS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | CHS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | CHS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | CHS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0358 | EAS | CHS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0082 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01106 | hp1 | a0004 | c0005 | t0001 | g0127 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01167 | hp1 | a0004 | c0005 | t0001 | g0128 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01167 | hp2 | a0003 | c0004 | t0001 | g0196 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01169 | hp1 | a0004 | c0005 | t0001 | g0126 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01175 | hp1 | a0003 | c0004 | t0001 | g0210 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01255 | hp1 | a0006 | c0006 | t0001 | g0194 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0047 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01257 | hp1 | a0003 | c0004 | t0001 | g0222 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0094 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0097 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0343 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01261 | hp1 | a0001 | c0010 | t0002 | g0324 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0079 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0069 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0063 | EUR | IBS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | IBS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0176 | EUR | IBS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0040 | EUR | IBS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | IBS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0174 | EUR | IBS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0288 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0045 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0043 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0068 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0096 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0048 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0044 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0298 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02055 | hp2 | a0003 | c0004 | t0001 | g0193 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02080 | hp1 | a0001 | c0008 | t0001 | g0323 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0352 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0042 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0292 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CDX | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | CDX | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0066 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02258 | hp1 | a0002 | c0002 | t0006 | g0006 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0106 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02280 | hp2 | a0001 | c0003 | t0002 | g0182 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02451 | hp2 | a0001 | c0003 | t0002 | g0183 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0093 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0335 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0287 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0291 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02886 | hp1 | a0001 | c0003 | t0002 | g0184 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0294 | AFR | ESN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ESN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02970 | hp2 | a0001 | c0003 | t0002 | g0185 | AFR | ESN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0300 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0299 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0084 | AFR | ESN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0052 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0054 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | ESN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | ESN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0051 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0129 | SAS | STU | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | STU | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0105 | SAS | BEB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | BEB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | BEB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | BEB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03927 | hp2 | a0002 | c0011 | t0001 | g0059 | SAS | BEB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | BEB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | BEB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | STU | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | STU | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0225 | SAS | BEB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | BEB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | STU | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | STU | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | STU | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0321 | SAS | STU | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | CHB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | CHB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | CHB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0355 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0349 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0356 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0357 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18997 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0350 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | LWK | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0301 | AFR | LWK | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19054 | hp1 | a0007 | c0009 | t0001 | g0022 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19072 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19075 | hp1 | a0001 | c0001 | t0003 | g0348 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19078 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0353 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0351 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0354 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | YRI | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA19240 | hp2 | a0001 | c0003 | t0002 | g0345 | AFR | YRI | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | ASW | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA20129 | hp2 | a0001 | c0001 | t0008 | g0346 | AFR | ASW | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA20905 | hp1 | a0001 | c0001 | t0007 | g0190 | SAS | GIH | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | GIH | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0061 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | USA | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | USA | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | LWK | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0302 | AFR | LWK | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0315 | REF | REF | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
homoSapiens | grch38p0 | a0001 | c0003 | t0002 | g0186 | REF | REF | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:135362941 | G | A | 1 | a0007 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.2086C>T | p.Pro696Ser | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 12/12 | 2392/3538 | 2086/2142 | 696/713 | chr7 | 135362941 | |||
chr7:135364052 | C | T | 3 | a0002 a0004 a0007 |
108 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(105): Show |
missense_variant | MODERATE | c.1642G>A | p.Val548Ile | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 11/12 | 1948/3538 | 1642/2142 | 548/713 | chr7 | 135364052 | |||
chr7:135394272 | C | T | 1 | a0005 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.1273G>A | p.Val425Ile | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/12 | 1579/3538 | 1273/2142 | 425/713 | chr7 | 135394272 | |||
chr7:135398201 | G | C | 1 | a0003 | 4 | HG01167.hp2 HG01175.hp1 HG01257.hp1 others(1): Show |
missense_variant | MODERATE | c.847C>G | p.Leu283Val | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/12 | 1153/3538 | 847/2142 | 283/713 | chr7 | 135398201 | |||
chr7:135410539 | A | G | 1 | a0006 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.797T>C | p.Val266Ala | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/12 | 1103/3538 | 797/2142 | 266/713 | chr7 | 135410539 | |||
chr7:135438312 | G | C | 1 | a0004 | 3 | HG01106.hp1 HG01167.hp1 HG01169.hp1 |
missense_variant | MODERATE | c.20C>G | p.Ala7Gly | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/12 | 326/3538 | 20/2142 | 7/713 | chr7 | 135438312 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:135362951 | T | C | 10 | a0001c0001 a0001c0008 a0001c0010 others(7): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
synonymous_variant | LOW | c.2076A>G | p.Thr692Thr | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 12/12 | 2382/3538 | 2076/2142 | 692/713 | chr7 | 135362951 | |||
chr7:135394093 | C | T | 1 | a0001c0008 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.1452G>A | p.Ala484Ala | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/12 | 1758/3538 | 1452/2142 | 484/713 | chr7 | 135394093 | |||
chr7:135413590 | G | A | 1 | a0001c0010 | 1 | HG01261.hp1 | synonymous_variant | LOW | c.585C>T | p.Tyr195Tyr | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/12 | 891/3538 | 585/2142 | 195/713 | chr7 | 135413590 | |||
chr7:135422168 | T | C | 1 | a0002c0011 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.360A>G | p.Leu120Leu | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/12 | 666/3538 | 360/2142 | 120/713 | chr7 | 135422168 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:135361800 | C | T | 14 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(11): Show |
319 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*1085G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 12/12 | 1085 | chr7 | 135361800 | ||||||
chr7:135362570 | T | C | 1 | a0001c0001t0004 | 2 | HG03490.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*315A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 12/12 | 315 | chr7 | 135362570 | ||||||
chr7:135362703 | T | G | 1 | a0001c0001t0007 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*182A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 12/12 | 182 | chr7 | 135362703 | ||||||
chr7:135509922 | C | T | 1 | a0002c0002t0006 | 1 | HG02258.hp1 | 5_prime_UTR_variant | MODIFIER | c.-126G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/12 | 71591 | chr7 | 135509922 | ||||||
chr7:135509926 | A | T | 1 | a0001c0001t0005 | 1 | HG02897.hp2 | 5_prime_UTR_variant | MODIFIER | c.-130T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/12 | 71595 | chr7 | 135509926 | ||||||
chr7:135509928 | G | A | 1 | a0001c0001t0008 | 1 | NA20129.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-132C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/12 | chr7 | 135509928 | |||||||
chr7:135510069 | G | A | 1 | a0001c0001t0003 | 12 | HG00597.hp2 HG00673.hp2 HG02083.hp2 others(9): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-273C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/12 | chr7 | 135510069 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:135363212 | G | A | 62 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(59): Show |
64 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.1841-26C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 11/11 | chr7 | 135363212 | |||||||
chr7:135363217 | T | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1841-31A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 11/11 | chr7 | 135363217 | |||||||
chr7:135363281 | G | C | 215 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(212): Show |
217 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.1841-95C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 11/11 | chr7 | 135363281 | |||||||
chr7:135363494 | G | A | 106 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0023 others(103): Show |
108 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.1841-308C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 11/11 | chr7 | 135363494 | |||||||
chr7:135363745 | C | T | 315 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(312): Show |
319 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1840+109G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 11/11 | chr7 | 135363745 | |||||||
chr7:135364612 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1628-546T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135364612 | |||||||
chr7:135364677 | T | C | 2 | a0002c0002t0001g0093 a0002c0002t0001g0102 |
2 | HG02523.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1628-611A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135364677 | |||||||
chr7:135364722 | T | C | 1 | a0001c0001t0001g0260 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1628-656A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135364722 | |||||||
chr7:135364935 | T | C | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1628-869A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135364935 | |||||||
chr7:135365202 | C | G | 1 | a0001c0001t0001g0189 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1628-1136G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135365202 | |||||||
chr7:135365325 | GA | G | 59 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(56): Show |
61 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1628-1260delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135365325 | |||||||
chr7:135365507 | G | GATAA | 221 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(218): Show |
225 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.1628-1445_1628-144 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135365507 | |||||||
chr7:135366078 | C | T | 1 | a0002c0002t0006g0006 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1628-2012G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135366078 | |||||||
chr7:135366127 | G | A | 106 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0023 others(103): Show |
108 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.1628-2061C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135366127 | |||||||
chr7:135366242 | A | G | 55 | a0002c0002t0001g0001 a0002c0002t0001g0023 a0002c0002t0001g0024 others(52): Show |
56 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1628-2176T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135366242 | |||||||
chr7:135366285 | T | C | 1 | a0002c0002t0001g0129 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1628-2219A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135366285 | |||||||
chr7:135366407 | TA | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(218): Show |
225 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.1628-2342delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135366407 | |||||||
chr7:135366502 | G | A | 221 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(218): Show |
225 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.1628-2436C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135366502 | |||||||
chr7:135366569 | A | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1628-2503T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135366569 | |||||||
chr7:135366701 | G | A | 95 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(92): Show |
95 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.1628-2635C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135366701 | |||||||
chr7:135366854 | T | C | 1 | a0001c0001t0001g0317 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1628-2788A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135366854 | |||||||
chr7:135366875 | C | T | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1628-2809G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135366875 | |||||||
chr7:135367002 | A | G | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1628-2936T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367002 | |||||||
chr7:135367147 | C | T | 5 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0191 others(2): Show |
5 | HG01243.hp2 HG02257.hp1 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.1628-3081G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367147 | |||||||
chr7:135367150 | T | G | 1 | a0001c0003t0002g0185 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1628-3084A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367150 | |||||||
chr7:135367215 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1628-3149A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367215 | |||||||
chr7:135367227 | C | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(218): Show |
225 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.1628-3161G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367227 | |||||||
chr7:135367292 | A | C | 106 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0023 others(103): Show |
108 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.1628-3226T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367292 | |||||||
chr7:135367448 | G | C | 9 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(6): Show |
9 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1628-3382C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367448 | |||||||
chr7:135367474 | C | T | 100 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0023 others(97): Show |
102 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.1628-3408G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367474 | |||||||
chr7:135367571 | C | A | 1 | a0001c0001t0001g0276 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1628-3505G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367571 | |||||||
chr7:135367596 | C | T | 16 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(13): Show |
16 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1628-3530G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367596 | |||||||
chr7:135367597 | G | A | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1628-3531C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367597 | |||||||
chr7:135367968 | TA | T | 19 | a0001c0001t0001g0119 a0001c0001t0001g0322 a0001c0001t0001g0327 others(16): Show |
19 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1628-3903delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367968 | |||||||
chr7:135368016 | T | C | 315 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(312): Show |
319 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(316): Show |
intron_variant | MODIFIER | c.1628-3950A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368016 | |||||||
chr7:135368148 | C | T | 12 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(9): Show |
12 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1628-4082G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368148 | |||||||
chr7:135368451 | G | A | 2 | a0002c0002t0001g0001 a0002c0002t0001g0023 |
3 | NA18986.hp2 NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1628-4385C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368451 | |||||||
chr7:135368485 | A | T | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1628-4419T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368485 | |||||||
chr7:135368577 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1628-4511T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368577 | |||||||
chr7:135368598 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1628-4532G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368598 | |||||||
chr7:135368655 | C | T | 3 | a0004c0005t0001g0126 a0004c0005t0001g0127 a0004c0005t0001g0128 |
3 | HG01106.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1628-4589G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368655 | |||||||
chr7:135368683 | C | G | 1 | a0002c0002t0001g0061 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1628-4617G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368683 | |||||||
chr7:135368710 | A | G | 124 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(121): Show |
124 | HG00099.hp2 HG00621.hp2 HG00642.hp1 others(121): Show |
intron_variant | MODIFIER | c.1628-4644T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368710 | |||||||
chr7:135368744 | T | C | 1 | a0001c0001t0001g0340 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1628-4678A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368744 | |||||||
chr7:135368886 | C | T | 258 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(255): Show |
260 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(257): Show |
intron_variant | MODIFIER | c.1628-4820G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368886 | |||||||
chr7:135368962 | A | G | 9 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 others(6): Show |
9 | HG01243.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1628-4896T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368962 | |||||||
chr7:135369017 | G | GT | 19 | a0001c0001t0001g0119 a0001c0001t0001g0322 a0001c0001t0001g0327 others(16): Show |
19 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1628-4952dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369017 | |||||||
chr7:135369071 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1628-5005C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369071 | |||||||
chr7:135369134 | G | A | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1628-5068C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369134 | |||||||
chr7:135369280 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG01123.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1628-5214G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369280 | |||||||
chr7:135369319 | G | A | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1628-5253C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369319 | |||||||
chr7:135369331 | C | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1628-5265G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369331 | |||||||
chr7:135369395 | T | C | 43 | a0001c0001t0001g0141 a0001c0001t0001g0147 a0001c0001t0001g0304 others(40): Show |
43 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1628-5329A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369395 | |||||||
chr7:135369406 | C | T | 25 | a0001c0001t0001g0141 a0001c0001t0001g0147 a0001c0001t0001g0304 others(22): Show |
25 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.1628-5340G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369406 | |||||||
chr7:135369435 | C | G | 5 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0124 others(2): Show |
5 | HG01081.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1628-5369G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369435 | |||||||
chr7:135369542 | C | T | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1628-5476G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369542 | |||||||
chr7:135369619 | G | A | 105 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(102): Show |
107 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.1628-5553C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369619 | |||||||
chr7:135369686 | C | T | 46 | a0001c0001t0001g0141 a0001c0001t0001g0145 a0001c0001t0001g0146 others(43): Show |
46 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1628-5620G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369686 | |||||||
chr7:135369746 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1628-5680G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369746 | |||||||
chr7:135370011 | A | T | 3 | a0001c0001t0001g0240 a0001c0001t0001g0259 a0001c0001t0001g0332 |
3 | HG00733.hp2 HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1628-5945T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370011 | |||||||
chr7:135370229 | C | A | 6 | a0002c0002t0001g0298 a0002c0002t0001g0299 a0002c0002t0001g0300 others(3): Show |
6 | HG02055.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1628-6163G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370229 | |||||||
chr7:135370282 | AAAC | A | 17 | a0001c0001t0001g0141 a0001c0001t0001g0295 a0001c0001t0001g0296 others(14): Show |
17 | HG00597.hp2 HG02083.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1628-6219_1628-621 others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370282 | |||||||
chr7:135370295 | A | C | 1 | a0002c0002t0001g0069 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1628-6229T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370295 | |||||||
chr7:135370482 | A | G | 1 | a0002c0002t0001g0058 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1628-6416T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370482 | |||||||
chr7:135370531 | T | C | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1628-6465A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370531 | |||||||
chr7:135370637 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1628-6571T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370637 | |||||||
chr7:135370650 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1628-6584A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370650 | |||||||
chr7:135370739 | C | G | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-6673G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370739 | |||||||
chr7:135370852 | T | C | 63 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(60): Show |
65 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1628-6786A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370852 | |||||||
chr7:135370876 | A | G | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1628-6810T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370876 | |||||||
chr7:135370956 | A | C | 1 | a0001c0001t0001g0331 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1628-6890T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370956 | |||||||
chr7:135370989 | C | T | 209 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(206): Show |
211 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.1628-6923G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370989 | |||||||
chr7:135371000 | G | A | 338 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(335): Show |
342 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(339): Show |
intron_variant | MODIFIER | c.1628-6934C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135371000 | |||||||
chr7:135371363 | A | C | 1 | a0001c0001t0001g0322 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1628-7297T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135371363 | |||||||
chr7:135371589 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1628-7523A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135371589 | |||||||
chr7:135371868 | G | A | 351 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(348): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.1628-7802C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135371868 | |||||||
chr7:135371941 | A | G | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1628-7875T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135371941 | |||||||
chr7:135371985 | G | A | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1628-7919C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135371985 | |||||||
chr7:135372079 | C | G | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-8013G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135372079 | |||||||
chr7:135372394 | A | G | 105 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(102): Show |
107 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.1628-8328T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135372394 | |||||||
chr7:135372554 | TG | T | 8 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1628-8489delC | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135372554 | |||||||
chr7:135372555 | G | GT | 113 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0164 others(110): Show |
115 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1628-8490dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135372555 | |||||||
chr7:135372555 | GTT | G | 24 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(21): Show |
24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.1628-8491_1628-849 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135372555 | |||||||
chr7:135372562 | T | G | 1 | a0001c0001t0001g0278 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1628-8496A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135372562 | |||||||
chr7:135372579 | C | T | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-8513G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135372579 | |||||||
chr7:135372811 | T | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1628-8745A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135372811 | |||||||
chr7:135372844 | C | T | 2 | a0002c0002t0001g0025 a0002c0002t0001g0040 |
2 | HG01081.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1628-8778G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135372844 | |||||||
chr7:135372845 | G | A | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-8779C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135372845 | |||||||
chr7:135373034 | A | T | 1 | a0001c0001t0001g0188 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1628-8968T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135373034 | |||||||
chr7:135373137 | A | G | 5 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0124 others(2): Show |
5 | HG01081.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1628-9071T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135373137 | |||||||
chr7:135373386 | A | G | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-9320T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135373386 | |||||||
chr7:135373464 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1628-9398C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135373464 | |||||||
chr7:135373645 | C | T | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1628-9579G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135373645 | |||||||
chr7:135373743 | A | AT | 103 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 others(100): Show |
105 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.1628-9678dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135373743 | |||||||
chr7:135373802 | G | A | 209 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(206): Show |
211 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.1628-9736C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135373802 | |||||||
chr7:135373816 | G | A | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1628-9750C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135373816 | |||||||
chr7:135373858 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1628-9792C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135373858 | |||||||
chr7:135374013 | G | A | 1 | a0002c0002t0006g0006 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1628-9947C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135374013 | |||||||
chr7:135374173 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1628-10107G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135374173 | |||||||
chr7:135374390 | T | G | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-10324A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135374390 | |||||||
chr7:135374393 | CTGA | C | 191 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(188): Show |
193 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.1628-10330_1628-10 others(9): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135374393 | |||||||
chr7:135374644 | TA | T | 338 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(335): Show |
342 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(339): Show |
intron_variant | MODIFIER | c.1628-10579delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135374644 | |||||||
chr7:135375000 | T | A | 1 | a0001c0001t0002g0294 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1628-10934A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135375000 | |||||||
chr7:135375010 | G | A | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-10944C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135375010 | |||||||
chr7:135375212 | G | A | 1 | a0002c0002t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1628-11146C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135375212 | |||||||
chr7:135375368 | T | A | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-11302A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135375368 | |||||||
chr7:135375476 | T | TACAC | 18 | a0001c0001t0001g0322 a0001c0001t0001g0327 a0001c0001t0001g0328 others(15): Show |
18 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1628-11414_1628-11 others(10): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135375476 | |||||||
chr7:135375483 | A | G | 24 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(21): Show |
24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.1628-11417T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135375483 | |||||||
chr7:135375575 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1628-11509A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135375575 | |||||||
chr7:135375690 | C | T | 6 | a0002c0002t0001g0298 a0002c0002t0001g0299 a0002c0002t0001g0300 others(3): Show |
6 | HG02055.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1628-11624G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135375690 | |||||||
chr7:135375866 | A | G | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-11800T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135375866 | |||||||
chr7:135375912 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1628-11846C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135375912 | |||||||
chr7:135376027 | A | G | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1628-11961T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135376027 | |||||||
chr7:135376075 | C | T | 1 | a0001c0001t0008g0346 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1628-12009G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135376075 | |||||||
chr7:135376321 | C | G | 1 | a0002c0002t0001g0061 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1628-12255G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135376321 | |||||||
chr7:135376352 | C | CT | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-12287dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135376352 | |||||||
chr7:135376380 | T | C | 1 | a0001c0001t0002g0124 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1628-12314A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135376380 | |||||||
chr7:135376577 | C | T | 140 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(137): Show |
140 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(137): Show |
intron_variant | MODIFIER | c.1628-12511G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135376577 | |||||||
chr7:135376684 | T | C | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1628-12618A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135376684 | |||||||
chr7:135376714 | A | G | 24 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(21): Show |
24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.1628-12648T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135376714 | |||||||
chr7:135376972 | T | C | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-12906A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135376972 | |||||||
chr7:135377003 | T | C | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-12937A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377003 | |||||||
chr7:135377161 | T | A | 1 | a0001c0001t0001g0344 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1628-13095A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377161 | |||||||
chr7:135377204 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1628-13138T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377204 | |||||||
chr7:135377217 | T | C | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1628-13151A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377217 | |||||||
chr7:135377304 | C | T | 18 | a0001c0001t0001g0322 a0001c0001t0001g0327 a0001c0001t0001g0328 others(15): Show |
18 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1628-13238G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377304 | |||||||
chr7:135377415 | T | C | 2 | a0001c0001t0002g0224 a0001c0001t0002g0226 |
2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.1628-13349A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377415 | |||||||
chr7:135377646 | A | G | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1628-13580T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377646 | |||||||
chr7:135377795 | T | C | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1628-13729A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377795 | |||||||
chr7:135377804 | A | G | 1 | a0001c0001t0001g0322 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1628-13738T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377804 | |||||||
chr7:135377878 | G | A | 1 | a0001c0008t0001g0323 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1628-13812C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377878 | |||||||
chr7:135377910 | A | G | 339 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(336): Show |
343 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(340): Show |
intron_variant | MODIFIER | c.1628-13844T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377910 | |||||||
chr7:135377977 | T | C | 1 | a0001c0001t0001g0316 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1628-13911A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377977 | |||||||
chr7:135378075 | G | C | 1 | a0001c0001t0003g0350 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1628-14009C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378075 | |||||||
chr7:135378080 | C | T | 12 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(9): Show |
12 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1628-14014G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378080 | |||||||
chr7:135378251 | C | T | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1628-14185G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378251 | |||||||
chr7:135378320 | A | C | 6 | a0002c0002t0001g0298 a0002c0002t0001g0299 a0002c0002t0001g0300 others(3): Show |
6 | HG02055.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1628-14254T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378320 | |||||||
chr7:135378436 | A | G | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-14370T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378436 | |||||||
chr7:135378456 | G | A | 24 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(21): Show |
24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.1628-14390C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378456 | |||||||
chr7:135378482 | C | T | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1628-14416G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378482 | |||||||
chr7:135378518 | G | GA | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-14453dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378518 | |||||||
chr7:135378518 | GA | G | 252 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(249): Show |
254 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(251): Show |
intron_variant | MODIFIER | c.1628-14453delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378518 | |||||||
chr7:135378545 | G | A | 1 | a0002c0002t0001g0080 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1628-14479C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378545 | |||||||
chr7:135378595 | T | C | 2 | a0001c0001t0001g0327 a0001c0001t0001g0328 |
2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1628-14529A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378595 | |||||||
chr7:135378639 | A | G | 95 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(92): Show |
95 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.1628-14573T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378639 | |||||||
chr7:135378714 | G | A | 18 | a0001c0001t0001g0322 a0001c0001t0001g0327 a0001c0001t0001g0328 others(15): Show |
18 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1628-14648C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378714 | |||||||
chr7:135378788 | C | T | 1 | a0001c0001t0002g0294 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1628-14722G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378788 | |||||||
chr7:135378844 | G | A | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1628-14778C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378844 | |||||||
chr7:135378933 | C | T | 18 | a0001c0001t0001g0322 a0001c0001t0001g0327 a0001c0001t0001g0328 others(15): Show |
18 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1628-14867G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378933 | |||||||
chr7:135378941 | C | T | 1 | a0001c0001t0005g0005 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1628-14875G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378941 | |||||||
chr7:135378984 | C | CA | 102 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(99): Show |
102 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.1628-14919dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378984 | |||||||
chr7:135378984 | C | CAA | 9 | a0001c0001t0001g0148 a0001c0001t0001g0152 a0001c0001t0001g0164 others(6): Show |
9 | HG00738.hp1 HG01106.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.1628-14920_1628-14 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378984 | |||||||
chr7:135378984 | C | CAAA | 13 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(10): Show |
13 | HG02083.hp2 NA18939.hp1 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.1628-14921_1628-14 others(9): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378984 | |||||||
chr7:135379047 | A | G | 2 | a0001c0001t0001g0310 a0005c0007t0001g0308 |
2 | HG00323.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.1627+14871T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379047 | |||||||
chr7:135379055 | A | T | 72 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0228 others(69): Show |
74 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1627+14863T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379055 | |||||||
chr7:135379185 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1627+14733G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379185 | |||||||
chr7:135379218 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1627+14700G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379218 | |||||||
chr7:135379564 | C | A | 24 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(21): Show |
24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.1627+14354G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379564 | |||||||
chr7:135379594 | A | G | 18 | a0001c0001t0001g0322 a0001c0001t0001g0327 a0001c0001t0001g0328 others(15): Show |
18 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1627+14324T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379594 | |||||||
chr7:135379770 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+14148A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379770 | |||||||
chr7:135379806 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1627+14112A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379806 | |||||||
chr7:135379822 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1627+14096A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379822 | |||||||
chr7:135379866 | C | T | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+14052G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379866 | |||||||
chr7:135379931 | T | C | 1 | a0001c0001t0002g0294 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1627+13987A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379931 | |||||||
chr7:135379948 | TA | T | 351 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(348): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.1627+13969delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379948 | |||||||
chr7:135379986 | C | A | 351 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(348): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.1627+13932G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379986 | |||||||
chr7:135380108 | A | C | 1 | a0001c0001t0003g0347 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1627+13810T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380108 | |||||||
chr7:135380130 | A | C | 95 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(92): Show |
95 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.1627+13788T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380130 | |||||||
chr7:135380131 | A | C | 2 | a0002c0002t0001g0025 a0002c0002t0001g0040 |
2 | HG01081.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1627+13787T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380131 | |||||||
chr7:135380135 | A | C | 1 | a0001c0001t0001g0311 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1627+13783T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380135 | |||||||
chr7:135380209 | C | T | 10 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(7): Show |
10 | HG01496.hp1 HG01891.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+13709G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380209 | |||||||
chr7:135380211 | G | C | 2 | a0001c0001t0001g0228 a0001c0001t0004g0004 |
3 | HG03490.hp2 HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1627+13707C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380211 | |||||||
chr7:135380420 | A | G | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+13498T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380420 | |||||||
chr7:135380513 | T | A | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1627+13405A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380513 | |||||||
chr7:135380621 | G | A | 1 | a0002c0002t0006g0006 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1627+13297C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380621 | |||||||
chr7:135380637 | A | C | 8 | a0002c0002t0001g0031 a0002c0002t0001g0035 a0002c0002t0001g0036 others(5): Show |
8 | HG02165.hp2 NA18941.hp2 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.1627+13281T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380637 | |||||||
chr7:135380708 | T | A | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+13210A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380708 | |||||||
chr7:135380729 | C | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+13189G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380729 | |||||||
chr7:135380756 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+13162A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380756 | |||||||
chr7:135380791 | C | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+13127G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380791 | |||||||
chr7:135380795 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0158 |
2 | NA18984.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1627+13123G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380795 | |||||||
chr7:135380859 | T | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1627+13059A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380859 | |||||||
chr7:135381271 | A | C | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+12647T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135381271 | |||||||
chr7:135381320 | T | C | 1 | a0001c0001t0002g0286 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1627+12598A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135381320 | |||||||
chr7:135381372 | C | G | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+12546G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135381372 | |||||||
chr7:135381485 | C | T | 3 | a0001c0001t0003g0349 a0001c0001t0003g0350 a0001c0001t0003g0357 |
3 | NA18954.hp1 NA18990.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1627+12433G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135381485 | |||||||
chr7:135381533 | T | A | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627+12385A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135381533 | |||||||
chr7:135381627 | G | A | 2 | a0001c0001t0002g0285 a0001c0001t0002g0287 |
2 | HG01496.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1627+12291C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135381627 | |||||||
chr7:135381728 | G | A | 1 | a0002c0002t0001g0077 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1627+12190C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135381728 | |||||||
chr7:135381733 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1627+12185C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135381733 | |||||||
chr7:135381771 | C | T | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+12147G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135381771 | |||||||
chr7:135381933 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1627+11985A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135381933 | |||||||
chr7:135382059 | G | A | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+11859C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382059 | |||||||
chr7:135382072 | A | G | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1627+11846T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382072 | |||||||
chr7:135382164 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1627+11754A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382164 | |||||||
chr7:135382453 | A | T | 351 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(348): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.1627+11465T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382453 | |||||||
chr7:135382482 | T | C | 207 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(204): Show |
209 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(206): Show |
intron_variant | MODIFIER | c.1627+11436A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382482 | |||||||
chr7:135382505 | G | A | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1627+11413C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382505 | |||||||
chr7:135382583 | G | GA | 107 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(104): Show |
107 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.1627+11334dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382583 | |||||||
chr7:135382583 | G | GAA | 101 | a0001c0001t0001g0011 a0002c0002t0001g0001 a0002c0002t0001g0002 others(98): Show |
103 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.1627+11333_1627+11 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382583 | |||||||
chr7:135382649 | C | T | 1 | a0002c0002t0001g0049 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1627+11269G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382649 | |||||||
chr7:135382704 | C | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+11214G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382704 | |||||||
chr7:135382880 | G | A | 4 | a0001c0001t0001g0236 a0001c0001t0001g0265 a0001c0001t0001g0266 others(1): Show |
4 | NA18948.hp2 NA18951.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627+11038C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382880 | |||||||
chr7:135382978 | A | T | 1 | a0002c0002t0001g0099 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1627+10940T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382978 | |||||||
chr7:135383060 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1627+10858C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135383060 | |||||||
chr7:135383362 | C | A | 1 | a0001c0001t0001g0322 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1627+10556G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135383362 | |||||||
chr7:135383541 | C | G | 1 | a0002c0002t0001g0181 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1627+10377G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135383541 | |||||||
chr7:135383866 | T | C | 1 | a0001c0001t0001g0272 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1627+10052A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135383866 | |||||||
chr7:135383969 | T | TG | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+9948_1627+994 others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135383969 | |||||||
chr7:135384290 | T | C | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+9628A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384290 | |||||||
chr7:135384291 | T | C | 330 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(327): Show |
334 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(331): Show |
intron_variant | MODIFIER | c.1627+9627A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384291 | |||||||
chr7:135384292 | T | C | 1 | a0001c0001t0001g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1627+9626A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384292 | |||||||
chr7:135384297 | T | C | 1 | a0002c0002t0001g0029 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1627+9621A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384297 | |||||||
chr7:135384384 | G | A | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+9534C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384384 | |||||||
chr7:135384385 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1627+9533G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384385 | |||||||
chr7:135384434 | G | A | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+9484C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384434 | |||||||
chr7:135384476 | G | A | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+9442C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384476 | |||||||
chr7:135384498 | G | T | 1 | a0001c0001t0001g0019 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1627+9420C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384498 | |||||||
chr7:135384520 | T | C | 43 | a0001c0001t0001g0141 a0001c0001t0001g0147 a0001c0001t0001g0304 others(40): Show |
43 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1627+9398A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384520 | |||||||
chr7:135384559 | A | G | 18 | a0001c0001t0001g0322 a0001c0001t0001g0327 a0001c0001t0001g0328 others(15): Show |
18 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1627+9359T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384559 | |||||||
chr7:135384648 | C | G | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+9270G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384648 | |||||||
chr7:135384807 | A | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+9111T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384807 | |||||||
chr7:135384952 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1627+8966T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384952 | |||||||
chr7:135385024 | GTTC | G | 63 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(60): Show |
65 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1627+8891_1627+889 others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135385024 | |||||||
chr7:135385110 | C | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+8808G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135385110 | |||||||
chr7:135385197 | T | C | 4 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
4 | HG00673.hp2 HG02083.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627+8721A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135385197 | |||||||
chr7:135385202 | C | G | 1 | a0001c0001t0005g0005 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1627+8716G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135385202 | |||||||
chr7:135385364 | C | T | 6 | a0002c0002t0001g0298 a0002c0002t0001g0299 a0002c0002t0001g0300 others(3): Show |
6 | HG02055.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1627+8554G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135385364 | |||||||
chr7:135385572 | CTAAGAG | C | 39 | a0002c0002t0001g0002 a0002c0002t0001g0031 a0002c0002t0001g0033 others(36): Show |
40 | HG00438.hp1 HG00673.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1627+8340_1627+834 others(10): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135385572 | |||||||
chr7:135385856 | T | C | 1 | a0001c0001t0002g0117 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1627+8062A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135385856 | |||||||
chr7:135386100 | G | GT | 17 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(14): Show |
17 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.1627+7817dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386100 | |||||||
chr7:135386126 | C | T | 1 | a0001c0001t0002g0124 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1627+7792G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386126 | |||||||
chr7:135386153 | C | CT | 18 | a0001c0001t0001g0147 a0001c0001t0001g0200 a0001c0001t0001g0258 others(15): Show |
18 | HG00673.hp1 HG01261.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1627+7764dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386153 | |||||||
chr7:135386153 | CT | C | 22 | a0001c0001t0001g0141 a0001c0001t0001g0188 a0001c0001t0001g0251 others(19): Show |
22 | HG00323.hp2 HG00597.hp2 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.1627+7764delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386153 | |||||||
chr7:135386153 | CTT | C | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+7763_1627+776 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386153 | |||||||
chr7:135386169 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+7749A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386169 | |||||||
chr7:135386184 | G | T | 1 | a0002c0002t0001g0069 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1627+7734C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386184 | |||||||
chr7:135386406 | TAAC | T | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1627+7509_1627+751 others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386406 | |||||||
chr7:135386568 | C | T | 1 | a0001c0010t0002g0324 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1627+7350G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386568 | |||||||
chr7:135386604 | A | G | 13 | a0001c0001t0001g0200 a0001c0001t0002g0285 a0001c0001t0002g0286 others(10): Show |
13 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1627+7314T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386604 | |||||||
chr7:135386629 | A | G | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+7289T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386629 | |||||||
chr7:135386846 | C | T | 6 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0149 others(3): Show |
6 | HG01123.hp2 NA18968.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.1627+7072G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386846 | |||||||
chr7:135386904 | C | T | 1 | a0001c0001t0002g0286 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1627+7014G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386904 | |||||||
chr7:135387070 | A | G | 1 | a0002c0002t0001g0042 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1627+6848T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387070 | |||||||
chr7:135387136 | A | G | 333 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(330): Show |
337 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(334): Show |
intron_variant | MODIFIER | c.1627+6782T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387136 | |||||||
chr7:135387389 | T | C | 100 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0023 others(97): Show |
102 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.1627+6529A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387389 | |||||||
chr7:135387467 | T | G | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+6451A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387467 | |||||||
chr7:135387521 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+6397A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387521 | |||||||
chr7:135387554 | C | CT | 63 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0228 others(60): Show |
65 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1627+6363dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387554 | |||||||
chr7:135387554 | C | CTT | 8 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.1627+6362_1627+636 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387554 | |||||||
chr7:135387697 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1627+6221G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387697 | |||||||
chr7:135387800 | C | T | 16 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(13): Show |
16 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1627+6118G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387800 | |||||||
chr7:135387805 | T | C | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1627+6113A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387805 | |||||||
chr7:135387955 | A | G | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627+5963T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387955 | |||||||
chr7:135388010 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+5908A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135388010 | |||||||
chr7:135388109 | G | A | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1627+5809C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135388109 | |||||||
chr7:135388184 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1627+5734G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135388184 | |||||||
chr7:135388295 | T | C | 93 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(90): Show |
93 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.1627+5623A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135388295 | |||||||
chr7:135388342 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1627+5576A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135388342 | |||||||
chr7:135388395 | C | T | 4 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(1): Show |
4 | NA18941.hp1 NA18953.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627+5523G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135388395 | |||||||
chr7:135389157 | C | CA | 25 | a0001c0001t0001g0249 a0001c0001t0001g0251 a0001c0001t0001g0252 others(22): Show |
25 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.1627+4760dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389157 | |||||||
chr7:135389157 | C | CAA | 8 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0307 others(5): Show |
8 | HG01081.hp2 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1627+4759_1627+476 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389157 | |||||||
chr7:135389157 | CA | C | 139 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(136): Show |
140 | HG00099.hp2 HG00609.hp1 HG00621.hp2 others(137): Show |
intron_variant | MODIFIER | c.1627+4760delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389157 | |||||||
chr7:135389157 | CAA | C | 9 | a0001c0001t0001g0203 a0001c0001t0001g0268 a0001c0001t0001g0335 others(6): Show |
9 | HG01256.hp1 HG02145.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.1627+4759_1627+476 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389157 | |||||||
chr7:135389215 | C | CT | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+4702_1627+470 others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389215 | |||||||
chr7:135389227 | TC | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+4690delG | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389227 | |||||||
chr7:135389338 | C | A | 7 | a0001c0001t0001g0195 a0001c0001t0001g0197 a0001c0001t0001g0202 others(4): Show |
7 | HG01099.hp1 HG01255.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1627+4580G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389338 | |||||||
chr7:135389342 | A | C | 1 | a0001c0001t0008g0346 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1627+4576T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389342 | |||||||
chr7:135389381 | C | CT | 42 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(39): Show |
42 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1627+4536dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389381 | |||||||
chr7:135389497 | AGGTCAGA others(21): Show |
A | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+4393_1627+442 others(32): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389497 | |||||||
chr7:135389554 | T | C | 2 | a0001c0001t0003g0350 a0001c0001t0003g0357 |
2 | NA18990.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1627+4364A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389554 | |||||||
chr7:135389628 | C | T | 2 | a0002c0002t0001g0025 a0002c0002t0001g0040 |
2 | HG01081.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1627+4290G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389628 | |||||||
chr7:135389814 | A | T | 24 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(21): Show |
24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.1627+4104T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389814 | |||||||
chr7:135389868 | G | GA | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+4049dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389868 | |||||||
chr7:135390048 | C | T | 6 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(3): Show |
6 | HG01515.hp2 HG01517.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1627+3870G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390048 | |||||||
chr7:135390081 | C | G | 18 | a0001c0001t0001g0322 a0001c0001t0001g0327 a0001c0001t0001g0328 others(15): Show |
18 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1627+3837G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390081 | |||||||
chr7:135390163 | A | AC | 42 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(39): Show |
42 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1627+3754dupG | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390163 | |||||||
chr7:135390173 | C | T | 1 | a0002c0002t0001g0090 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1627+3745G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390173 | |||||||
chr7:135390304 | A | C | 1 | a0001c0001t0001g0189 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1627+3614T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390304 | |||||||
chr7:135390438 | CAAT | C | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1627+3477_1627+347 others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390438 | |||||||
chr7:135390450 | A | T | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+3468T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390450 | |||||||
chr7:135390471 | T | A | 1 | a0001c0001t0001g0310 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1627+3447A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390471 | |||||||
chr7:135390485 | A | G | 2 | a0002c0002t0001g0087 a0002c0002t0001g0091 |
2 | NA18995.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1627+3433T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390485 | |||||||
chr7:135390606 | C | A | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+3312G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390606 | |||||||
chr7:135390769 | T | A | 1 | a0002c0002t0006g0006 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1627+3149A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390769 | |||||||
chr7:135390985 | G | A | 3 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 |
3 | HG01123.hp1 HG03654.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1627+2933C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390985 | |||||||
chr7:135391052 | G | A | 1 | a0002c0002t0006g0006 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1627+2866C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135391052 | |||||||
chr7:135391069 | A | C | 1 | a0001c0001t0001g0143 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1627+2849T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135391069 | |||||||
chr7:135391078 | C | G | 1 | a0002c0002t0001g0053 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1627+2840G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135391078 | |||||||
chr7:135391081 | C | T | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+2837G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135391081 | |||||||
chr7:135391155 | G | T | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+2763C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135391155 | |||||||
chr7:135391518 | C | T | 1 | a0001c0001t0001g0258 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1627+2400G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135391518 | |||||||
chr7:135391579 | G | T | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+2339C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135391579 | |||||||
chr7:135391899 | C | G | 4 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
4 | HG00673.hp2 HG02083.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627+2019G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135391899 | |||||||
chr7:135391907 | C | T | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1627+2011G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135391907 | |||||||
chr7:135391923 | A | G | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627+1995T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135391923 | |||||||
chr7:135392056 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1627+1862A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392056 | |||||||
chr7:135392240 | C | A | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1627+1678G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392240 | |||||||
chr7:135392268 | T | C | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1627+1650A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392268 | |||||||
chr7:135392456 | T | C | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+1462A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392456 | |||||||
chr7:135392592 | T | A | 1 | a0002c0002t0001g0053 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1627+1326A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392592 | |||||||
chr7:135392621 | C | T | 4 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
4 | HG00673.hp2 HG02083.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627+1297G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392621 | |||||||
chr7:135392700 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1627+1218G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392700 | |||||||
chr7:135392814 | G | A | 5 | a0002c0002t0001g0057 a0002c0002t0001g0098 a0002c0002t0001g0101 others(2): Show |
5 | HG02129.hp1 NA18946.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1627+1104C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392814 | |||||||
chr7:135392834 | T | C | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+1084A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392834 | |||||||
chr7:135392901 | T | C | 339 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(336): Show |
343 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(340): Show |
intron_variant | MODIFIER | c.1627+1017A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392901 | |||||||
chr7:135392931 | CAAT | C | 14 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(11): Show |
14 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1627+984_1627+986d others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392931 | |||||||
chr7:135392940 | T | C | 1 | a0001c0001t0001g0330 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1627+978A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392940 | |||||||
chr7:135393155 | A | C | 1 | a0001c0001t0002g0293 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1627+763T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135393155 | |||||||
chr7:135393282 | A | G | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1627+636T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135393282 | |||||||
chr7:135393537 | AT | A | 42 | a0001c0001t0001g0316 a0002c0002t0001g0002 a0002c0002t0001g0031 others(39): Show |
43 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.1627+380delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135393537 | |||||||
chr7:135393538 | T | A | 23 | a0001c0001t0001g0141 a0001c0001t0001g0295 a0001c0001t0001g0296 others(20): Show |
23 | HG00597.hp2 HG01891.hp2 HG02083.hp2 others(20): Show |
intron_variant | MODIFIER | c.1627+380A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135393538 | |||||||
chr7:135393617 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1627+301C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135393617 | |||||||
chr7:135394485 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1130-70G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 9/11 | chr7 | 135394485 | |||||||
chr7:135394552 | A | C | 1 | a0001c0001t0002g0124 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1130-137T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 9/11 | chr7 | 135394552 | |||||||
chr7:135394576 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1130-161C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 9/11 | chr7 | 135394576 | |||||||
chr7:135394827 | G | GA | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1130-413dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 9/11 | chr7 | 135394827 | |||||||
chr7:135394957 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1130-542T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 9/11 | chr7 | 135394957 | |||||||
chr7:135395001 | A | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1130-586T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 9/11 | chr7 | 135395001 | |||||||
chr7:135395255 | G | A | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1129+379C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 9/11 | chr7 | 135395255 | |||||||
chr7:135395571 | T | G | 1 | a0001c0001t0001g0311 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1129+63A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 9/11 | chr7 | 135395571 | |||||||
chr7:135395980 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.880-97A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135395980 | |||||||
chr7:135396064 | T | C | 63 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(60): Show |
65 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.880-181A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396064 | |||||||
chr7:135396095 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.880-212T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396095 | |||||||
chr7:135396107 | C | CT | 27 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0236 others(24): Show |
27 | HG00280.hp1 HG00438.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.880-225dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | |||||||
chr7:135396107 | C | CTT | 9 | a0001c0001t0001g0340 a0001c0001t0002g0121 a0001c0001t0002g0130 others(6): Show |
9 | HG01361.hp1 HG01496.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.880-226_880-225dup others(2): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | |||||||
chr7:135396107 | C | CTTT | 13 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0330 others(10): Show |
13 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.880-227_880-225dup others(3): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | |||||||
chr7:135396107 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.880-224G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | |||||||
chr7:135396107 | CT | C | 19 | a0001c0001t0001g0141 a0001c0001t0001g0295 a0001c0001t0001g0297 others(16): Show |
19 | HG00597.hp2 HG00639.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.880-225delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | |||||||
chr7:135396107 | CTT | C | 6 | a0001c0001t0001g0304 a0001c0001t0001g0316 a0001c0001t0002g0294 others(3): Show |
6 | HG00323.hp2 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-226_880-225del others(2): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | |||||||
chr7:135396107 | CTTT | C | 8 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0307 others(5): Show |
8 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-227_880-225del others(3): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | |||||||
chr7:135396107 | CTTTTTTT | C | 6 | a0001c0001t0001g0153 a0001c0001t0001g0164 a0001c0001t0001g0170 others(3): Show |
6 | HG01099.hp1 HG02080.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.880-231_880-225del others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | |||||||
chr7:135396107 | CTTTTTTT others(1): Show |
C | 86 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(83): Show |
86 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.880-232_880-225del others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | |||||||
chr7:135396107 | CTTTTTTT others(5): Show |
C | 1 | a0002c0002t0001g0035 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.880-236_880-225del others(12): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | |||||||
chr7:135396107 | CTTTTTTT others(6): Show |
C | 99 | a0001c0001t0001g0320 a0002c0002t0001g0001 a0002c0002t0001g0002 others(96): Show |
101 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.880-237_880-225del others(13): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | |||||||
chr7:135396108 | T | C | 4 | a0001c0001t0003g0349 a0001c0001t0003g0350 a0001c0001t0003g0354 others(1): Show |
4 | NA18954.hp1 NA18990.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.880-225A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396108 | |||||||
chr7:135396109 | T | C | 10 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(7): Show |
10 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.880-226A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396109 | |||||||
chr7:135396187 | G | A | 4 | a0002c0002t0001g0079 a0002c0002t0001g0298 a0002c0002t0001g0299 others(1): Show |
4 | HG01346.hp1 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-304C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396187 | |||||||
chr7:135396265 | G | A | 27 | a0001c0001t0001g0141 a0001c0001t0001g0147 a0001c0001t0001g0304 others(24): Show |
27 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.880-382C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396265 | |||||||
chr7:135396307 | C | T | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.880-424G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396307 | |||||||
chr7:135396321 | A | G | 326 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(323): Show |
329 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(326): Show |
intron_variant | MODIFIER | c.880-438T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396321 | |||||||
chr7:135396415 | C | A | 1 | a0001c0001t0001g0270 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.880-532G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396415 | |||||||
chr7:135396447 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.880-564A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396447 | |||||||
chr7:135396590 | G | C | 1 | a0002c0002t0001g0299 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.880-707C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396590 | |||||||
chr7:135396615 | G | T | 1 | a0001c0010t0002g0324 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.880-732C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396615 | |||||||
chr7:135396714 | CTGATA | C | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.880-836_880-832del others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396714 | |||||||
chr7:135397276 | G | T | 332 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(329): Show |
336 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(333): Show |
intron_variant | MODIFIER | c.879+893C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397276 | |||||||
chr7:135397317 | A | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.879+852T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397317 | |||||||
chr7:135397607 | C | CA | 96 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(93): Show |
96 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.879+561dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397607 | |||||||
chr7:135397635 | T | C | 339 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(336): Show |
343 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(340): Show |
intron_variant | MODIFIER | c.879+534A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397635 | |||||||
chr7:135397666 | G | A | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.879+503C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397666 | |||||||
chr7:135397694 | A | G | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.879+475T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397694 | |||||||
chr7:135397735 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.879+434G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397735 | |||||||
chr7:135397736 | T | C | 1 | a0002c0002t0001g0028 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.879+433A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397736 | |||||||
chr7:135397821 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.879+348C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397821 | |||||||
chr7:135397848 | C | G | 12 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(9): Show |
12 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.879+321G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397848 | |||||||
chr7:135397850 | A | G | 2 | a0001c0001t0003g0347 a0001c0001t0003g0348 |
2 | HG00597.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.879+319T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397850 | |||||||
chr7:135397922 | A | C | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+247T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397922 | |||||||
chr7:135397999 | T | C | 96 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(93): Show |
96 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.879+170A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397999 | |||||||
chr7:135398300 | G | GA | 108 | a0001c0001t0001g0148 a0001c0001t0001g0304 a0001c0001t0001g0305 others(105): Show |
110 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.822-75dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135398300 | |||||||
chr7:135398473 | C | T | 23 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(20): Show |
23 | HG00099.hp2 HG00621.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.822-247G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135398473 | |||||||
chr7:135398727 | C | T | 1 | a0002c0002t0001g0025 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.822-501G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135398727 | |||||||
chr7:135398802 | T | G | 1 | a0001c0001t0001g0197 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.822-576A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135398802 | |||||||
chr7:135399139 | ATAAC | A | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.822-917_822-914del others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135399139 | |||||||
chr7:135399479 | C | G | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.822-1253G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135399479 | |||||||
chr7:135399764 | G | C | 1 | a0001c0001t0001g0328 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.822-1538C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135399764 | |||||||
chr7:135399849 | C | T | 18 | a0001c0001t0001g0322 a0001c0001t0001g0327 a0001c0001t0001g0328 others(15): Show |
18 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.822-1623G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135399849 | |||||||
chr7:135399924 | A | G | 1 | a0001c0001t0003g0357 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.822-1698T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135399924 | |||||||
chr7:135399972 | GTTTAAAC others(8): Show |
G | 1 | a0002c0002t0001g0074 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.822-1761_822-1747d others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135399972 | |||||||
chr7:135400071 | T | C | 1 | a0001c0010t0002g0324 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.822-1845A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400071 | |||||||
chr7:135400229 | GC | G | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.822-2004delG | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400229 | |||||||
chr7:135400305 | T | G | 4 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0331 others(1): Show |
4 | HG00735.hp1 HG00741.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.822-2079A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400305 | |||||||
chr7:135400339 | G | C | 1 | a0001c0001t0001g0317 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.822-2113C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400339 | |||||||
chr7:135400358 | C | T | 1 | a0002c0002t0006g0006 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.822-2132G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400358 | |||||||
chr7:135400407 | C | T | 24 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(21): Show |
24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.822-2181G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400407 | |||||||
chr7:135400423 | G | A | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.822-2197C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400423 | |||||||
chr7:135400464 | C | T | 13 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(10): Show |
13 | HG01106.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.822-2238G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400464 | |||||||
chr7:135400642 | A | G | 1 | a0002c0002t0001g0077 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.822-2416T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400642 | |||||||
chr7:135400773 | A | G | 1 | a0001c0001t0001g0327 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.822-2547T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400773 | |||||||
chr7:135400777 | T | C | 15 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(12): Show |
15 | HG01069.hp1 HG01261.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.822-2551A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400777 | |||||||
chr7:135401086 | A | T | 1 | a0001c0001t0001g0306 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.822-2860T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135401086 | |||||||
chr7:135401087 | A | T | 1 | a0001c0001t0001g0306 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.822-2861T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135401087 | |||||||
chr7:135401088 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.822-2862T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135401088 | |||||||
chr7:135401275 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.822-3049G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135401275 | |||||||
chr7:135401546 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.822-3320A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135401546 | |||||||
chr7:135401586 | T | A | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.822-3360A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135401586 | |||||||
chr7:135401921 | G | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0242 |
2 | HG00438.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.822-3695C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135401921 | |||||||
chr7:135401937 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.822-3711A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135401937 | |||||||
chr7:135402044 | T | TCTCA | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.822-3819_822-3818i others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402044 | |||||||
chr7:135402064 | T | A | 1 | a0002c0002t0001g0026 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.822-3838A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402064 | |||||||
chr7:135402083 | T | G | 8 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.822-3857A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402083 | |||||||
chr7:135402112 | C | CT | 104 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(101): Show |
104 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.822-3887dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402112 | |||||||
chr7:135402112 | C | CTT | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.822-3888_822-3887d others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402112 | |||||||
chr7:135402144 | C | T | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.822-3918G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402144 | |||||||
chr7:135402185 | C | T | 2 | a0001c0001t0001g0334 a0001c0001t0001g0335 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.822-3959G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402185 | |||||||
chr7:135402188 | C | A | 1 | a0001c0001t0001g0275 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.822-3962G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402188 | |||||||
chr7:135402251 | G | A | 1 | a0002c0002t0001g0066 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.822-4025C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402251 | |||||||
chr7:135402283 | T | C | 100 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0023 others(97): Show |
102 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.822-4057A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402283 | |||||||
chr7:135402299 | G | A | 12 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(9): Show |
12 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.822-4073C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402299 | |||||||
chr7:135402343 | C | G | 1 | a0002c0002t0001g0105 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.822-4117G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402343 | |||||||
chr7:135402389 | G | A | 4 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(1): Show |
4 | HG00280.hp1 HG01361.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.822-4163C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402389 | |||||||
chr7:135402433 | A | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0158 |
2 | NA18984.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.822-4207T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402433 | |||||||
chr7:135402455 | A | G | 1 | a0002c0002t0001g0080 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.822-4229T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402455 | |||||||
chr7:135402472 | T | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.822-4246A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402472 | |||||||
chr7:135402645 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.822-4419G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402645 | |||||||
chr7:135402744 | T | C | 1 | a0001c0001t0001g0309 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.822-4518A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402744 | |||||||
chr7:135402842 | C | T | 1 | a0001c0001t0001g0342 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.822-4616G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402842 | |||||||
chr7:135402866 | C | T | 12 | a0002c0002t0001g0001 a0002c0002t0001g0023 a0002c0002t0001g0024 others(9): Show |
13 | NA18947.hp2 NA18948.hp1 NA18951.hp1 others(10): Show |
intron_variant | MODIFIER | c.822-4640G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402866 | |||||||
chr7:135403127 | C | T | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.822-4901G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135403127 | |||||||
chr7:135403263 | G | A | 1 | a0002c0002t0001g0055 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.822-5037C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135403263 | |||||||
chr7:135403489 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.822-5263G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135403489 | |||||||
chr7:135403508 | G | A | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.822-5282C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135403508 | |||||||
chr7:135403554 | G | A | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.822-5328C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135403554 | |||||||
chr7:135403556 | A | C | 141 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(138): Show |
141 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(138): Show |
intron_variant | MODIFIER | c.822-5330T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135403556 | |||||||
chr7:135403557 | C | T | 1 | a0001c0001t0001g0344 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.822-5331G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135403557 | |||||||
chr7:135403862 | T | C | 1 | a0002c0002t0001g0065 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.822-5636A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135403862 | |||||||
chr7:135403912 | T | C | 1 | a0002c0002t0001g0072 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.822-5686A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135403912 | |||||||
chr7:135403969 | A | G | 12 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0120 others(9): Show |
12 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(9): Show |
intron_variant | MODIFIER | c.822-5743T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135403969 | |||||||
chr7:135404013 | C | T | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.822-5787G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135404013 | |||||||
chr7:135404237 | T | C | 24 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(21): Show |
24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.822-6011A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135404237 | |||||||
chr7:135404284 | CACTTA | C | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.822-6063_822-6059d others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135404284 | |||||||
chr7:135404323 | T | C | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.822-6097A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135404323 | |||||||
chr7:135404375 | T | G | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.821+6140A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135404375 | |||||||
chr7:135404667 | T | C | 2 | a0001c0001t0002g0124 a0001c0001t0002g0125 |
2 | HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.821+5848A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135404667 | |||||||
chr7:135404910 | A | G | 42 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(39): Show |
42 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.821+5605T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135404910 | |||||||
chr7:135404959 | T | C | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.821+5556A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135404959 | |||||||
chr7:135405179 | C | T | 1 | a0001c0001t0001g0331 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.821+5336G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405179 | |||||||
chr7:135405218 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.821+5297C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405218 | |||||||
chr7:135405287 | G | A | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.821+5228C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405287 | |||||||
chr7:135405430 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.821+5085A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405430 | |||||||
chr7:135405477 | T | A | 1 | a0002c0002t0001g0074 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.821+5038A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405477 | |||||||
chr7:135405561 | A | T | 1 | a0002c0002t0001g0074 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.821+4954T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405561 | |||||||
chr7:135405634 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.821+4881A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405634 | |||||||
chr7:135405710 | T | G | 5 | a0002c0002t0001g0298 a0002c0002t0001g0299 a0002c0002t0001g0300 others(2): Show |
5 | HG02055.hp1 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.821+4805A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405710 | |||||||
chr7:135405721 | T | C | 1 | a0001c0001t0001g0309 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.821+4794A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405721 | |||||||
chr7:135405793 | T | C | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.821+4722A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405793 | |||||||
chr7:135405863 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.821+4652C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405863 | |||||||
chr7:135405884 | C | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.821+4631G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405884 | |||||||
chr7:135405921 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.821+4594G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405921 | |||||||
chr7:135406299 | C | T | 1 | a0002c0002t0001g0089 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.821+4216G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135406299 | |||||||
chr7:135406334 | A | G | 1 | a0001c0001t0002g0294 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.821+4181T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135406334 | |||||||
chr7:135406403 | T | C | 29 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(26): Show |
29 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.821+4112A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135406403 | |||||||
chr7:135406506 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.821+4009C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135406506 | |||||||
chr7:135406544 | T | C | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.821+3971A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135406544 | |||||||
chr7:135406565 | G | T | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.821+3950C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135406565 | |||||||
chr7:135406576 | G | A | 105 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(102): Show |
107 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.821+3939C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135406576 | |||||||
chr7:135406820 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.821+3695A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135406820 | |||||||
chr7:135406932 | T | C | 2 | a0002c0002t0001g0041 a0002c0002t0001g0064 |
2 | HG00609.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.821+3583A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135406932 | |||||||
chr7:135406999 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.821+3516A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135406999 | |||||||
chr7:135407157 | C | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.821+3358G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135407157 | |||||||
chr7:135407439 | T | G | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.821+3076A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135407439 | |||||||
chr7:135407500 | G | A | 24 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(21): Show |
24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.821+3015C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135407500 | |||||||
chr7:135407768 | C | T | 1 | a0001c0001t0001g0334 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.821+2747G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135407768 | |||||||
chr7:135407769 | G | A | 72 | a0001c0001t0001g0003 a0001c0001t0001g0145 a0001c0001t0001g0146 others(69): Show |
74 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.821+2746C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135407769 | |||||||
chr7:135407806 | A | G | 19 | a0001c0001t0001g0322 a0001c0001t0001g0327 a0001c0001t0001g0328 others(16): Show |
19 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.821+2709T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135407806 | |||||||
chr7:135407807 | T | A | 1 | a0001c0001t0001g0019 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.821+2708A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135407807 | |||||||
chr7:135407888 | C | T | 1 | a0001c0001t0001g0019 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.821+2627G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135407888 | |||||||
chr7:135407990 | A | G | 1 | a0001c0001t0001g0279 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.821+2525T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135407990 | |||||||
chr7:135408404 | G | A | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.821+2111C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135408404 | |||||||
chr7:135408629 | C | G | 6 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(3): Show |
6 | HG01515.hp2 HG01517.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.821+1886G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135408629 | |||||||
chr7:135408673 | T | C | 1 | a0002c0002t0001g0044 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.821+1842A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135408673 | |||||||
chr7:135408695 | C | T | 261 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(258): Show |
265 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.821+1820G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135408695 | |||||||
chr7:135408736 | G | C | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.821+1779C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135408736 | |||||||
chr7:135408795 | C | A | 112 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(109): Show |
114 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.821+1720G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135408795 | |||||||
chr7:135408984 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.821+1531A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135408984 | |||||||
chr7:135409116 | A | G | 5 | a0002c0002t0001g0298 a0002c0002t0001g0299 a0002c0002t0001g0300 others(2): Show |
5 | HG02055.hp1 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.821+1399T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135409116 | |||||||
chr7:135409207 | C | T | 1 | a0002c0002t0006g0006 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.821+1308G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135409207 | |||||||
chr7:135409253 | C | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.821+1262G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135409253 | |||||||
chr7:135409452 | C | A | 24 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(21): Show |
24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.821+1063G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135409452 | |||||||
chr7:135409550 | A | G | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.821+965T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135409550 | |||||||
chr7:135409896 | A | C | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.821+619T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135409896 | |||||||
chr7:135409898 | A | G | 1 | a0001c0001t0002g0294 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.821+617T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135409898 | |||||||
chr7:135409901 | T | A | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.821+614A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135409901 | |||||||
chr7:135409910 | G | C | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.821+605C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135409910 | |||||||
chr7:135410013 | A | G | 43 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(40): Show |
43 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.821+502T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135410013 | |||||||
chr7:135410055 | G | A | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.821+460C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135410055 | |||||||
chr7:135410262 | G | T | 1 | a0002c0002t0001g0053 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.821+253C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135410262 | |||||||
chr7:135410271 | T | C | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.821+244A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135410271 | |||||||
chr7:135410384 | A | G | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.821+131T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135410384 | |||||||
chr7:135410430 | A | C | 24 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(21): Show |
24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.821+85T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135410430 | |||||||
chr7:135410510 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0168 |
2 | HG00642.hp2 HG01074.hp2 |
splice_region_variant&intron_variant | LOW | c.821+5G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135410510 | |||||||
chr7:135410750 | AATAAT | A | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.688-107_688-103del others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135410750 | |||||||
chr7:135410761 | T | A | 2 | a0001c0003t0002g0185 a0001c0003t0002g0345 |
2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.688-113A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135410761 | |||||||
chr7:135410762 | A | T | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.688-114T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135410762 | |||||||
chr7:135411052 | T | A | 1 | a0001c0001t0001g0296 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.688-404A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135411052 | |||||||
chr7:135411062 | T | C | 71 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0228 others(68): Show |
73 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.688-414A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135411062 | |||||||
chr7:135411249 | T | A | 16 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0120 others(13): Show |
16 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.688-601A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135411249 | |||||||
chr7:135411408 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.688-760T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135411408 | |||||||
chr7:135411901 | G | A | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.688-1253C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135411901 | |||||||
chr7:135412115 | A | G | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.687+1373T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135412115 | |||||||
chr7:135412169 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.687+1319C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135412169 | |||||||
chr7:135412185 | G | A | 8 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.687+1303C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135412185 | |||||||
chr7:135412328 | A | C | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG00642.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.687+1160T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135412328 | |||||||
chr7:135413015 | A | G | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.687+473T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135413015 | |||||||
chr7:135413031 | A | G | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.687+457T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135413031 | |||||||
chr7:135413387 | T | C | 3 | a0002c0002t0001g0051 a0002c0002t0001g0052 a0002c0002t0001g0054 |
3 | HG03491.hp1 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.687+101A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135413387 | |||||||
chr7:135413639 | A | C | 5 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0124 others(2): Show |
5 | HG01081.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.562-26T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135413639 | |||||||
chr7:135413696 | A | C | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.562-83T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135413696 | |||||||
chr7:135413922 | A | G | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.562-309T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135413922 | |||||||
chr7:135413930 | G | A | 19 | a0001c0001t0001g0322 a0001c0001t0001g0327 a0001c0001t0001g0328 others(16): Show |
19 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.562-317C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135413930 | |||||||
chr7:135413960 | C | T | 24 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(21): Show |
24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.562-347G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135413960 | |||||||
chr7:135414007 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.561+324G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135414007 | |||||||
chr7:135414097 | G | T | 8 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.561+234C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135414097 | |||||||
chr7:135414187 | C | G | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.561+144G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135414187 | |||||||
chr7:135414295 | TA | T | 8 | a0001c0001t0001g0020 a0001c0001t0001g0192 a0001c0001t0001g0206 others(5): Show |
8 | HG01069.hp2 HG01256.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.561+35delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135414295 | |||||||
chr7:135414311 | A | T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0213 |
2 | NA19066.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.561+20T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135414311 | |||||||
chr7:135414320 | G | A | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.561+11C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135414320 | |||||||
chr7:135414670 | C | T | 19 | a0001c0001t0001g0322 a0001c0001t0001g0327 a0001c0001t0001g0328 others(16): Show |
19 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.460-238G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 4/11 | chr7 | 135414670 | |||||||
chr7:135414818 | C | G | 1 | a0001c0001t0001g0334 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.459+358G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 4/11 | chr7 | 135414818 | |||||||
chr7:135414900 | C | T | 261 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(258): Show |
265 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.459+276G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 4/11 | chr7 | 135414900 | |||||||
chr7:135415015 | A | G | 2 | a0001c0001t0002g0117 a0001c0001t0002g0118 |
2 | HG01081.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.459+161T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 4/11 | chr7 | 135415015 | |||||||
chr7:135415152 | G | A | 23 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(20): Show |
23 | HG00099.hp2 HG00621.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.459+24C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 4/11 | chr7 | 135415152 | |||||||
chr7:135415440 | A | G | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.373-178T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135415440 | |||||||
chr7:135415454 | A | G | 1 | a0002c0002t0001g0081 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.373-192T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135415454 | |||||||
chr7:135415631 | C | T | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-369G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135415631 | |||||||
chr7:135415633 | A | G | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.373-371T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135415633 | |||||||
chr7:135415639 | C | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(67): Show |
72 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.373-377G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135415639 | |||||||
chr7:135415671 | TAA | T | 4 | a0001c0001t0001g0152 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
4 | HG00738.hp1 HG01106.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.373-411_373-410del others(2): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135415671 | |||||||
chr7:135415727 | C | T | 261 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(258): Show |
265 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.373-465G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135415727 | |||||||
chr7:135415881 | T | C | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.373-619A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135415881 | |||||||
chr7:135415987 | A | G | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.373-725T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135415987 | |||||||
chr7:135416081 | C | T | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-819G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416081 | |||||||
chr7:135416091 | T | C | 1 | a0001c0001t0001g0012 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.373-829A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416091 | |||||||
chr7:135416174 | A | T | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.373-912T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416174 | |||||||
chr7:135416208 | C | T | 24 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(21): Show |
24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.373-946G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416208 | |||||||
chr7:135416297 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.373-1035T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416297 | |||||||
chr7:135416305 | T | A | 2 | a0001c0001t0002g0288 a0001c0001t0002g0289 |
2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.373-1043A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416305 | |||||||
chr7:135416353 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.373-1091A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416353 | |||||||
chr7:135416459 | C | T | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-1197G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416459 | |||||||
chr7:135416557 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.373-1295C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416557 | |||||||
chr7:135416882 | A | G | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.373-1620T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416882 | |||||||
chr7:135416911 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.373-1649A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416911 | |||||||
chr7:135417043 | T | C | 4 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(1): Show |
4 | HG00280.hp1 HG01361.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.373-1781A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135417043 | |||||||
chr7:135417076 | C | A | 1 | a0002c0002t0001g0081 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.373-1814G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135417076 | |||||||
chr7:135417123 | ATAGGTGC others(3): Show |
A | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.373-1871_373-1862d others(12): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135417123 | |||||||
chr7:135417426 | G | A | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.373-2164C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135417426 | |||||||
chr7:135417623 | G | C | 1 | a0002c0002t0001g0046 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.373-2361C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135417623 | |||||||
chr7:135417726 | C | T | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-2464G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135417726 | |||||||
chr7:135417727 | G | A | 2 | a0002c0002t0001g0300 a0002c0002t0001g0302 |
2 | HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.373-2465C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135417727 | |||||||
chr7:135418047 | A | G | 1 | a0002c0002t0001g0092 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.373-2785T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418047 | |||||||
chr7:135418173 | C | T | 1 | a0001c0001t0001g0319 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.373-2911G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418173 | |||||||
chr7:135418248 | T | C | 101 | a0001c0001t0001g0239 a0002c0002t0001g0001 a0002c0002t0001g0002 others(98): Show |
103 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.373-2986A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418248 | |||||||
chr7:135418332 | A | G | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-3070T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418332 | |||||||
chr7:135418355 | A | G | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-3093T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418355 | |||||||
chr7:135418359 | C | T | 1 | a0002c0002t0001g0079 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.373-3097G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418359 | |||||||
chr7:135418362 | T | A | 1 | a0001c0010t0002g0324 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.373-3100A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418362 | |||||||
chr7:135418459 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.373-3197A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418459 | |||||||
chr7:135418547 | A | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.373-3285T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418547 | |||||||
chr7:135418628 | A | G | 10 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(7): Show |
10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-3366T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418628 | |||||||
chr7:135418700 | C | T | 264 | a0001c0001t0001g0003 a0001c0001t0001g0113 a0001c0001t0001g0119 others(261): Show |
268 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.373-3438G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418700 | |||||||
chr7:135418770 | T | A | 3 | a0002c0002t0001g0051 a0002c0002t0001g0052 a0002c0002t0001g0054 |
3 | HG03491.hp1 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.372+3386A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418770 | |||||||
chr7:135418911 | T | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0155 others(136): Show |
142 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.372+3245A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418911 | |||||||
chr7:135418987 | G | A | 4 | a0001c0001t0001g0192 a0001c0001t0001g0200 a0001c0001t0001g0203 others(1): Show |
4 | HG02615.hp1 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.372+3169C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418987 | |||||||
chr7:135419029 | G | C | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+3127C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419029 | |||||||
chr7:135419103 | A | AAAT | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.372+3052_372+3053i others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419103 | |||||||
chr7:135419142 | CT | C | 12 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(9): Show |
12 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.372+3013delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419142 | |||||||
chr7:135419255 | CCTATT | C | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.372+2896_372+2900d others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419255 | |||||||
chr7:135419379 | C | T | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.372+2777G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419379 | |||||||
chr7:135419620 | A | G | 1 | a0001c0001t0001g0277 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.372+2536T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419620 | |||||||
chr7:135419685 | T | C | 2 | a0002c0002t0001g0001 a0002c0002t0001g0023 |
3 | NA18986.hp2 NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.372+2471A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419685 | |||||||
chr7:135419888 | C | A | 5 | a0001c0003t0002g0182 a0001c0003t0002g0183 a0001c0003t0002g0184 others(2): Show |
5 | HG02280.hp2 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+2268G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419888 | |||||||
chr7:135419888 | C | CA | 18 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(15): Show |
18 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.372+2267dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419888 | |||||||
chr7:135419888 | CA | C | 6 | a0001c0001t0001g0141 a0001c0001t0001g0188 a0001c0001t0001g0325 others(3): Show |
6 | HG01167.hp2 HG03041.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.372+2267delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419888 | |||||||
chr7:135419920 | G | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.372+2236C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419920 | |||||||
chr7:135419922 | G | A | 1 | a0002c0002t0001g0074 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.372+2234C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419922 | |||||||
chr7:135419942 | C | A | 100 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0023 others(97): Show |
102 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.372+2214G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419942 | |||||||
chr7:135420041 | C | CAAACA | 39 | a0001c0001t0001g0141 a0001c0001t0001g0322 a0001c0001t0001g0325 others(36): Show |
39 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.372+2114_372+2115i others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420041 | |||||||
chr7:135420041 | C | CAAACAAA others(2): Show |
4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.372+2114_372+2115i others(11): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420041 | |||||||
chr7:135420346 | G | A | 1 | a0002c0002t0001g0055 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.372+1810C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420346 | |||||||
chr7:135420394 | T | C | 5 | a0002c0002t0001g0041 a0002c0002t0001g0056 a0002c0002t0001g0064 others(2): Show |
5 | HG00609.hp2 HG02071.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.372+1762A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420394 | |||||||
chr7:135420445 | T | C | 3 | a0004c0005t0001g0126 a0004c0005t0001g0127 a0004c0005t0001g0128 |
3 | HG01106.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.372+1711A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420445 | |||||||
chr7:135420539 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.372+1617A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420539 | |||||||
chr7:135420577 | C | CA | 36 | a0001c0001t0001g0019 a0001c0001t0001g0119 a0001c0001t0001g0145 others(33): Show |
36 | HG00323.hp2 HG00639.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.372+1578dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420577 | |||||||
chr7:135420577 | C | CAA | 94 | a0001c0001t0001g0295 a0001c0001t0002g0130 a0001c0001t0002g0132 others(91): Show |
95 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.372+1577_372+1578d others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420577 | |||||||
chr7:135420577 | C | CAAA | 6 | a0002c0002t0001g0001 a0002c0002t0001g0023 a0002c0002t0001g0061 others(3): Show |
7 | HG02559.hp1 NA18978.hp2 NA18986.hp2 others(4): Show |
intron_variant | MODIFIER | c.372+1576_372+1578d others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420577 | |||||||
chr7:135420577 | CA | C | 12 | a0001c0001t0001g0020 a0001c0001t0001g0113 a0001c0001t0001g0173 others(9): Show |
12 | HG00621.hp2 HG01099.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.372+1578delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420577 | |||||||
chr7:135420621 | T | TAGTA | 5 | a0002c0002t0001g0298 a0002c0002t0001g0299 a0002c0002t0001g0300 others(2): Show |
5 | HG02055.hp1 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+1531_372+1534d others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420621 | |||||||
chr7:135420784 | C | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(67): Show |
72 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.372+1372G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420784 | |||||||
chr7:135421094 | G | A | 11 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(8): Show |
11 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.372+1062C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421094 | |||||||
chr7:135421199 | A | G | 100 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0023 others(97): Show |
102 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.372+957T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421199 | |||||||
chr7:135421418 | A | AT | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.372+737dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421418 | |||||||
chr7:135421566 | T | A | 1 | a0001c0001t0001g0202 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.372+590A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421566 | |||||||
chr7:135421575 | A | T | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.372+581T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421575 | |||||||
chr7:135421577 | G | A | 4 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(1): Show |
4 | HG01515.hp2 HG01517.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.372+579C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421577 | |||||||
chr7:135421579 | T | G | 1 | a0001c0001t0002g0187 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.372+577A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421579 | |||||||
chr7:135421688 | G | T | 25 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(22): Show |
25 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.372+468C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421688 | |||||||
chr7:135421707 | T | A | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0168 others(2): Show |
5 | HG00642.hp2 HG01074.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.372+449A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421707 | |||||||
chr7:135421733 | C | G | 1 | a0001c0001t0001g0334 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.372+423G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421733 | |||||||
chr7:135421808 | C | T | 11 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(8): Show |
11 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.372+348G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421808 | |||||||
chr7:135421899 | T | C | 2 | a0002c0002t0001g0032 a0002c0002t0001g0083 |
2 | NA18991.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.372+257A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421899 | |||||||
chr7:135421982 | G | A | 6 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0179 others(3): Show |
6 | NA18975.hp1 NA19005.hp2 NA19054.hp1 others(3): Show |
intron_variant | MODIFIER | c.372+174C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421982 | |||||||
chr7:135422106 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.372+50C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135422106 | |||||||
chr7:135422116 | C | CAG | 11 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(8): Show |
11 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.372+39_372+40insCT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135422116 | |||||||
chr7:135422379 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-26C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135422379 | |||||||
chr7:135422396 | T | G | 1 | a0001c0001t0003g0349 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.175-43A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135422396 | |||||||
chr7:135422473 | A | G | 2 | a0001c0001t0001g0325 a0001c0001t0001g0326 |
2 | NA18953.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.175-120T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135422473 | |||||||
chr7:135422567 | C | A | 1 | a0002c0002t0001g0086 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.175-214G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135422567 | |||||||
chr7:135422590 | A | G | 11 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(8): Show |
11 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.175-237T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135422590 | |||||||
chr7:135422873 | G | C | 2 | a0002c0002t0001g0032 a0002c0002t0001g0083 |
2 | NA18991.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.175-520C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135422873 | |||||||
chr7:135422980 | A | T | 1 | a0001c0001t0001g0316 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.175-627T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135422980 | |||||||
chr7:135423000 | C | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.175-647G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135423000 | |||||||
chr7:135423339 | A | C | 1 | a0002c0002t0001g0031 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.175-986T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135423339 | |||||||
chr7:135423461 | A | G | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-1108T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135423461 | |||||||
chr7:135423471 | T | TA | 15 | a0001c0001t0001g0281 a0001c0001t0002g0285 a0001c0001t0002g0286 others(12): Show |
15 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.175-1119dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135423471 | |||||||
chr7:135423471 | TA | T | 10 | a0001c0001t0001g0322 a0001c0001t0001g0344 a0001c0001t0002g0130 others(7): Show |
10 | HG01515.hp1 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.175-1119delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135423471 | |||||||
chr7:135423777 | T | A | 1 | a0001c0001t0001g0344 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-1424A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135423777 | |||||||
chr7:135424038 | AAAACACA others(5): Show |
A | 1 | a0001c0001t0002g0292 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.175-1697_175-1686d others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424038 | |||||||
chr7:135424039 | AAACACAC others(4): Show |
A | 1 | a0001c0001t0001g0254 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.175-1697_175-1687d others(13): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424039 | |||||||
chr7:135424039 | AAACACAC others(8): Show |
A | 2 | a0002c0002t0001g0026 a0002c0002t0001g0051 |
2 | HG03669.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.175-1701_175-1687d others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424039 | |||||||
chr7:135424040 | A | AAC | 14 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0143 others(11): Show |
14 | HG00642.hp2 HG00741.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.175-1689_175-1688d others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | |||||||
chr7:135424040 | A | AACAC | 4 | a0001c0001t0001g0010 a0001c0001t0001g0162 a0001c0001t0001g0189 others(1): Show |
4 | HG00733.hp1 HG02451.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-1691_175-1688d others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | |||||||
chr7:135424040 | AAC | A | 29 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0113 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.175-1689_175-1688d others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | |||||||
chr7:135424040 | AACAC | A | 16 | a0001c0001t0001g0142 a0001c0001t0001g0159 a0001c0001t0001g0160 others(13): Show |
16 | HG00323.hp1 HG00673.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.175-1691_175-1688d others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | |||||||
chr7:135424040 | AACACAC | A | 13 | a0001c0001t0001g0151 a0001c0001t0001g0198 a0001c0001t0001g0203 others(10): Show |
13 | HG00280.hp1 HG00733.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.175-1693_175-1688d others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | |||||||
chr7:135424040 | AACACACA others(1): Show |
A | 30 | a0001c0001t0001g0146 a0001c0001t0001g0195 a0001c0001t0001g0197 others(27): Show |
30 | HG00642.hp1 HG00735.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.175-1695_175-1688d others(10): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | |||||||
chr7:135424040 | AACACACA others(3): Show |
A | 28 | a0001c0001t0001g0119 a0001c0001t0001g0154 a0001c0001t0001g0158 others(25): Show |
28 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.175-1697_175-1688d others(12): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | |||||||
chr7:135424040 | AACACACA others(5): Show |
A | 25 | a0001c0001t0001g0141 a0001c0001t0001g0147 a0001c0001t0001g0228 others(22): Show |
26 | HG00597.hp2 HG01081.hp2 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.175-1699_175-1688d others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | |||||||
chr7:135424040 | AACACACA others(7): Show |
A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0229 a0001c0001t0001g0230 others(51): Show |
55 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.175-1701_175-1688d others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | |||||||
chr7:135424040 | AACACACA others(9): Show |
A | 31 | a0001c0001t0001g0231 a0001c0001t0001g0325 a0001c0001t0001g0326 others(28): Show |
31 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.175-1703_175-1688d others(18): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | |||||||
chr7:135424040 | AACACACA others(11): Show |
A | 74 | a0001c0001t0001g0252 a0002c0002t0001g0001 a0002c0002t0001g0002 others(71): Show |
76 | HG00438.hp1 HG00673.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.175-1705_175-1688d others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | |||||||
chr7:135424040 | AACACACA others(13): Show |
A | 7 | a0001c0001t0001g0145 a0001c0001t0002g0130 a0001c0001t0002g0131 others(4): Show |
7 | HG01243.hp2 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.175-1707_175-1688d others(22): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | |||||||
chr7:135424040 | AACACACA others(17): Show |
A | 1 | a0001c0001t0002g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.175-1711_175-1688d others(26): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | |||||||
chr7:135424056 | C | G | 5 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(2): Show |
5 | HG02258.hp2 HG02622.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-1703G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424056 | |||||||
chr7:135424058 | C | G | 6 | a0002c0002t0001g0298 a0002c0002t0001g0299 a0002c0002t0001g0300 others(3): Show |
6 | HG02055.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-1705G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424058 | |||||||
chr7:135424183 | A | G | 11 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(8): Show |
11 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.175-1830T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424183 | |||||||
chr7:135424480 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.175-2127A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424480 | |||||||
chr7:135424814 | C | A | 1 | a0001c0001t0001g0242 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.175-2461G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424814 | |||||||
chr7:135424814 | C | T | 1 | a0002c0002t0001g0064 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.175-2461G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424814 | |||||||
chr7:135424817 | A | AC | 17 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(14): Show |
17 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.175-2465_175-2464i others(3): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424817 | |||||||
chr7:135424818 | A | C | 13 | a0001c0001t0001g0195 a0001c0001t0001g0207 a0001c0001t0002g0285 others(10): Show |
13 | HG01099.hp1 HG01261.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.175-2465T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424818 | |||||||
chr7:135424823 | A | C | 25 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(22): Show |
25 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.175-2470T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424823 | |||||||
chr7:135424870 | C | A | 1 | a0002c0002t0001g0064 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.175-2517G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424870 | |||||||
chr7:135424971 | A | G | 1 | a0002c0002t0001g0068 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.175-2618T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424971 | |||||||
chr7:135425074 | T | C | 1 | a0002c0002t0001g0084 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.175-2721A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135425074 | |||||||
chr7:135425121 | A | C | 1 | a0001c0001t0001g0114 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.175-2768T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135425121 | |||||||
chr7:135425194 | A | C | 11 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(8): Show |
11 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.175-2841T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135425194 | |||||||
chr7:135425195 | G | A | 11 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(8): Show |
11 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.175-2842C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135425195 | |||||||
chr7:135425664 | A | G | 3 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 |
3 | HG01256.hp1 HG01258.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.175-3311T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135425664 | |||||||
chr7:135425815 | A | T | 11 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(8): Show |
11 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.175-3462T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135425815 | |||||||
chr7:135425837 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0158 |
2 | NA18984.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.175-3484G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135425837 | |||||||
chr7:135425865 | C | G | 1 | a0001c0001t0001g0229 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.175-3512G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135425865 | |||||||
chr7:135426023 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.175-3670G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426023 | |||||||
chr7:135426030 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.175-3677C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426030 | |||||||
chr7:135426315 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.175-3962A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426315 | |||||||
chr7:135426323 | C | G | 1 | a0001c0001t0001g0237 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.175-3970G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426323 | |||||||
chr7:135426330 | C | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.175-3977G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426330 | |||||||
chr7:135426460 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.175-4107C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426460 | |||||||
chr7:135426519 | C | T | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.175-4166G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426519 | |||||||
chr7:135426520 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.175-4167C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426520 | |||||||
chr7:135426602 | CA | C | 218 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0145 others(215): Show |
222 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.175-4250delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426602 | |||||||
chr7:135426615 | A | G | 1 | a0002c0002t0001g0106 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.175-4262T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426615 | |||||||
chr7:135426618 | AG | A | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.175-4266delC | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426618 | |||||||
chr7:135426619 | G | A | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-4266C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426619 | |||||||
chr7:135426629 | A | G | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-4276T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426629 | |||||||
chr7:135426837 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.175-4484G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426837 | |||||||
chr7:135426880 | G | A | 1 | a0001c0001t0001g0344 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-4527C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426880 | |||||||
chr7:135426923 | CA | C | 15 | a0001c0001t0001g0020 a0001c0001t0001g0141 a0001c0001t0001g0325 others(12): Show |
15 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(12): Show |
intron_variant | MODIFIER | c.175-4571delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426923 | |||||||
chr7:135427105 | T | G | 2 | a0001c0001t0001g0147 a0001c0001t0008g0346 |
2 | HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.175-4752A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135427105 | |||||||
chr7:135427110 | C | G | 2 | a0001c0001t0002g0224 a0001c0001t0002g0226 |
2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.175-4757G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135427110 | |||||||
chr7:135427265 | C | G | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0168 others(2): Show |
5 | HG00642.hp2 HG01074.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-4912G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135427265 | |||||||
chr7:135427326 | CT | C | 100 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0023 others(97): Show |
102 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.175-4974delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135427326 | |||||||
chr7:135427391 | C | T | 1 | a0001c0001t0001g0312 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.175-5038G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135427391 | |||||||
chr7:135427540 | T | C | 1 | a0001c0001t0001g0344 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-5187A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135427540 | |||||||
chr7:135427757 | T | TA | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.175-5405dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135427757 | |||||||
chr7:135427762 | AT | A | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-5410delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135427762 | |||||||
chr7:135427763 | T | A | 1 | a0001c0001t0003g0357 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.175-5410A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135427763 | |||||||
chr7:135427993 | G | A | 100 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0023 others(97): Show |
102 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.175-5640C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135427993 | |||||||
chr7:135428255 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.175-5902T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135428255 | |||||||
chr7:135428345 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.175-5992T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135428345 | |||||||
chr7:135428446 | T | C | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-6093A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135428446 | |||||||
chr7:135428898 | A | G | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.175-6545T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135428898 | |||||||
chr7:135429175 | T | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.175-6822A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135429175 | |||||||
chr7:135429425 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.175-7072A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135429425 | |||||||
chr7:135429527 | T | C | 1 | a0001c0001t0002g0137 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.175-7174A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135429527 | |||||||
chr7:135429817 | T | C | 1 | a0002c0002t0006g0006 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.175-7464A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135429817 | |||||||
chr7:135429845 | C | A | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-7492G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135429845 | |||||||
chr7:135429879 | T | C | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-7526A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135429879 | |||||||
chr7:135429993 | C | T | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-7640G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135429993 | |||||||
chr7:135430313 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.174+7845C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135430313 | |||||||
chr7:135430329 | A | G | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.174+7829T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135430329 | |||||||
chr7:135430343 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.174+7815T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135430343 | |||||||
chr7:135430389 | G | A | 261 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(258): Show |
265 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.174+7769C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135430389 | |||||||
chr7:135430623 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0309 |
2 | HG01496.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.174+7535G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135430623 | |||||||
chr7:135430752 | C | T | 1 | a0002c0002t0001g0089 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.174+7406G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135430752 | |||||||
chr7:135431008 | A | G | 3 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0187 |
3 | HG01081.hp2 HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.174+7150T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431008 | |||||||
chr7:135431020 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+7138A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431020 | |||||||
chr7:135431072 | C | A | 1 | a0001c0001t0001g0205 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.174+7086G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431072 | |||||||
chr7:135431086 | G | A | 4 | a0002c0002t0001g0049 a0002c0002t0001g0076 a0002c0002t0001g0077 others(1): Show |
4 | HG00673.hp1 NA18747.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+7072C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431086 | |||||||
chr7:135431131 | G | A | 7 | a0001c0001t0001g0336 a0001c0001t0001g0337 a0001c0001t0001g0338 others(4): Show |
7 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.174+7027C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431131 | |||||||
chr7:135431236 | T | C | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.174+6922A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431236 | |||||||
chr7:135431245 | C | T | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+6913G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431245 | |||||||
chr7:135431461 | G | A | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+6697C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431461 | |||||||
chr7:135431480 | A | G | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+6678T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431480 | |||||||
chr7:135431486 | G | C | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+6672C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431486 | |||||||
chr7:135431647 | G | A | 4 | a0002c0002t0001g0051 a0002c0002t0001g0052 a0002c0002t0001g0054 others(1): Show |
4 | HG03491.hp1 HG03492.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+6511C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431647 | |||||||
chr7:135431651 | G | A | 1 | a0002c0002t0001g0065 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.174+6507C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431651 | |||||||
chr7:135431737 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.174+6421G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431737 | |||||||
chr7:135431743 | C | CA | 10 | a0001c0001t0001g0234 a0001c0001t0001g0244 a0001c0001t0001g0246 others(7): Show |
10 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(7): Show |
intron_variant | MODIFIER | c.174+6414dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431743 | |||||||
chr7:135431809 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.174+6349G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431809 | |||||||
chr7:135431979 | T | C | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.174+6179A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431979 | |||||||
chr7:135432111 | CAAT | C | 8 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.174+6044_174+6046d others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135432111 | |||||||
chr7:135432178 | C | T | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.174+5980G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135432178 | |||||||
chr7:135432223 | G | T | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.174+5935C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135432223 | |||||||
chr7:135432304 | A | T | 18 | a0001c0001t0001g0119 a0002c0002t0001g0002 a0002c0002t0001g0033 others(15): Show |
19 | HG00438.hp1 HG01071.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.174+5854T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135432304 | |||||||
chr7:135432471 | T | C | 1 | a0001c0001t0001g0296 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.174+5687A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135432471 | |||||||
chr7:135432732 | G | C | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+5426C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135432732 | |||||||
chr7:135432812 | C | T | 3 | a0002c0002t0001g0030 a0002c0002t0001g0062 a0002c0002t0001g0100 |
3 | NA18957.hp2 NA18971.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.174+5346G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135432812 | |||||||
chr7:135432894 | G | A | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+5264C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135432894 | |||||||
chr7:135432916 | G | A | 1 | a0001c0001t0008g0346 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.174+5242C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135432916 | |||||||
chr7:135433038 | T | C | 1 | a0001c0001t0001g0270 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.174+5120A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433038 | |||||||
chr7:135433082 | T | G | 8 | a0001c0001t0001g0255 a0001c0001t0002g0120 a0001c0001t0002g0121 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(5): Show |
intron_variant | MODIFIER | c.174+5076A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433082 | |||||||
chr7:135433350 | C | CT | 14 | a0001c0001t0001g0019 a0001c0001t0001g0153 a0001c0001t0001g0227 others(11): Show |
14 | HG00280.hp2 HG02257.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.174+4807dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433350 | |||||||
chr7:135433350 | CT | C | 19 | a0001c0001t0001g0157 a0001c0001t0001g0236 a0001c0001t0001g0304 others(16): Show |
19 | HG02258.hp1 HG02258.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.174+4807delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433350 | |||||||
chr7:135433350 | CTT | C | 13 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0003g0347 others(10): Show |
13 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(10): Show |
intron_variant | MODIFIER | c.174+4806_174+4807d others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433350 | |||||||
chr7:135433371 | T | C | 5 | a0001c0001t0001g0152 a0001c0001t0001g0159 a0001c0001t0001g0174 others(2): Show |
5 | HG00738.hp1 HG01106.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+4787A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433371 | |||||||
chr7:135433546 | T | C | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+4612A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433546 | |||||||
chr7:135433715 | T | A | 1 | a0001c0001t0001g0331 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.174+4443A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433715 | |||||||
chr7:135433855 | C | A | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.174+4303G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433855 | |||||||
chr7:135433943 | C | G | 1 | a0001c0001t0001g0267 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.174+4215G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433943 | |||||||
chr7:135433946 | T | C | 2 | a0001c0001t0001g0151 a0001c0001t0001g0168 |
2 | HG00642.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.174+4212A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433946 | |||||||
chr7:135434070 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.174+4088G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135434070 | |||||||
chr7:135434186 | C | G | 1 | a0001c0001t0001g0344 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.174+3972G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135434186 | |||||||
chr7:135434195 | T | C | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+3963A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135434195 | |||||||
chr7:135434314 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.174+3844C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135434314 | |||||||
chr7:135434632 | G | T | 1 | a0001c0001t0001g0344 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.174+3526C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135434632 | |||||||
chr7:135434669 | A | G | 263 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(260): Show |
267 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.174+3489T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135434669 | |||||||
chr7:135434900 | ACT | A | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+3256_174+3257d others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135434900 | |||||||
chr7:135434920 | T | C | 4 | a0001c0001t0001g0149 a0001c0001t0001g0165 a0001c0001t0001g0166 others(1): Show |
4 | NA18980.hp1 NA18994.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+3238A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135434920 | |||||||
chr7:135434951 | A | G | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+3207T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135434951 | |||||||
chr7:135435005 | C | A | 1 | a0001c0001t0001g0008 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.174+3153G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435005 | |||||||
chr7:135435025 | C | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+3133G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435025 | |||||||
chr7:135435026 | A | G | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+3132T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435026 | |||||||
chr7:135435061 | T | C | 17 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(14): Show |
17 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.174+3097A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435061 | |||||||
chr7:135435083 | C | T | 262 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(259): Show |
266 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.174+3075G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435083 | |||||||
chr7:135435084 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.174+3074C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435084 | |||||||
chr7:135435115 | C | T | 8 | a0002c0002t0001g0043 a0002c0002t0001g0044 a0002c0002t0001g0045 others(5): Show |
8 | HG01257.hp2 HG01258.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.174+3043G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435115 | |||||||
chr7:135435448 | A | G | 263 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(260): Show |
267 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.174+2710T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435448 | |||||||
chr7:135435562 | C | T | 13 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0118 others(10): Show |
13 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(10): Show |
intron_variant | MODIFIER | c.174+2596G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435562 | |||||||
chr7:135435711 | A | C | 1 | a0001c0001t0001g0297 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.174+2447T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435711 | |||||||
chr7:135435922 | C | T | 1 | a0001c0001t0002g0294 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.174+2236G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435922 | |||||||
chr7:135436009 | T | G | 18 | a0001c0001t0002g0116 a0001c0001t0002g0117 a0001c0001t0002g0118 others(15): Show |
18 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(15): Show |
intron_variant | MODIFIER | c.174+2149A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436009 | |||||||
chr7:135436017 | C | CT | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+2140dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436017 | |||||||
chr7:135436057 | T | C | 1 | a0002c0002t0006g0006 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.174+2101A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436057 | |||||||
chr7:135436082 | A | G | 1 | a0002c0002t0001g0109 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.174+2076T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436082 | |||||||
chr7:135436154 | C | T | 1 | a0001c0001t0003g0354 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.174+2004G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436154 | |||||||
chr7:135436393 | A | G | 1 | a0001c0001t0001g0278 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.174+1765T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436393 | |||||||
chr7:135436413 | G | C | 1 | a0001c0001t0003g0354 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.174+1745C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436413 | |||||||
chr7:135436507 | A | G | 1 | a0002c0002t0001g0083 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.174+1651T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436507 | |||||||
chr7:135436632 | AT | A | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+1525delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436632 | |||||||
chr7:135436785 | GATAA | G | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.174+1369_174+1372d others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436785 | |||||||
chr7:135436875 | T | C | 2 | a0002c0002t0001g0079 a0002c0002t0001g0082 |
2 | HG00735.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.174+1283A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436875 | |||||||
chr7:135437082 | A | G | 1 | a0001c0001t0002g0116 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.174+1076T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437082 | |||||||
chr7:135437178 | GCTTTT | G | 61 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(58): Show |
63 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.174+975_174+979del others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437178 | |||||||
chr7:135437213 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.174+945C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437213 | |||||||
chr7:135437221 | G | C | 1 | a0002c0002t0001g0302 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.174+937C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437221 | |||||||
chr7:135437222 | C | T | 1 | a0002c0002t0001g0302 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.174+936G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437222 | |||||||
chr7:135437291 | G | C | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.174+867C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437291 | |||||||
chr7:135437372 | G | C | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.174+786C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437372 | |||||||
chr7:135437410 | C | T | 1 | a0001c0001t0002g0124 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.174+748G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437410 | |||||||
chr7:135437495 | G | A | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+663C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437495 | |||||||
chr7:135437694 | T | G | 2 | a0001c0001t0001g0310 a0005c0007t0001g0308 |
2 | HG00323.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.174+464A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437694 | |||||||
chr7:135437881 | T | C | 3 | a0002c0002t0001g0024 a0002c0002t0001g0027 a0002c0002t0001g0028 |
3 | NA18948.hp1 NA19007.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.174+277A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437881 | |||||||
chr7:135437963 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+195A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437963 | |||||||
chr7:135438062 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+96A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135438062 | |||||||
chr7:135438098 | T | C | 2 | a0002c0002t0001g0094 a0002c0002t0001g0097 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.174+60A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135438098 | |||||||
chr7:135438654 | C | T | 3 | a0001c0001t0002g0130 a0001c0001t0002g0132 a0001c0001t0002g0133 |
3 | HG02896.hp1 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-92-231G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135438654 | |||||||
chr7:135438792 | C | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-369G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135438792 | |||||||
chr7:135438897 | C | T | 4 | a0002c0002t0001g0098 a0002c0002t0001g0101 a0002c0002t0001g0103 others(1): Show |
4 | NA18946.hp1 NA18968.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-474G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135438897 | |||||||
chr7:135439170 | C | A | 2 | a0001c0001t0002g0285 a0001c0001t0002g0287 |
2 | HG01496.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-92-747G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135439170 | |||||||
chr7:135439333 | G | T | 5 | a0001c0003t0002g0182 a0001c0003t0002g0183 a0001c0003t0002g0184 others(2): Show |
5 | HG02280.hp2 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-910C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135439333 | |||||||
chr7:135439449 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-92-1026T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135439449 | |||||||
chr7:135439498 | C | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0229 a0001c0001t0001g0234 others(15): Show |
19 | HG00609.hp1 HG02129.hp2 NA18946.hp2 others(16): Show |
intron_variant | MODIFIER | c.-92-1075G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135439498 | |||||||
chr7:135439585 | C | A | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-1162G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135439585 | |||||||
chr7:135439591 | C | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0158 |
2 | NA18984.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-92-1168G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135439591 | |||||||
chr7:135439730 | T | C | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-1307A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135439730 | |||||||
chr7:135440010 | A | T | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-1587T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440010 | |||||||
chr7:135440157 | T | C | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-1734A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440157 | |||||||
chr7:135440221 | T | TA | 53 | a0001c0001t0001g0255 a0001c0010t0002g0324 a0002c0002t0001g0001 others(50): Show |
54 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.-92-1799dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440221 | |||||||
chr7:135440221 | TA | T | 16 | a0001c0001t0001g0009 a0001c0001t0001g0141 a0001c0001t0001g0172 others(13): Show |
16 | HG00639.hp1 HG01069.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.-92-1799delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440221 | |||||||
chr7:135440288 | T | C | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-92-1865A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440288 | |||||||
chr7:135440329 | C | CT | 19 | a0001c0001t0001g0141 a0001c0001t0001g0228 a0001c0001t0001g0295 others(16): Show |
19 | HG00597.hp2 HG02083.hp2 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.-92-1907dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440329 | |||||||
chr7:135440329 | CT | C | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-1907delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440329 | |||||||
chr7:135440331 | T | G | 1 | a0001c0001t0001g0230 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-92-1908A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440331 | |||||||
chr7:135440414 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-92-1991G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440414 | |||||||
chr7:135440780 | G | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(67): Show |
72 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-92-2357C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440780 | |||||||
chr7:135440875 | T | C | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-2452A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440875 | |||||||
chr7:135441118 | G | A | 1 | a0001c0003t0002g0185 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-92-2695C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441118 | |||||||
chr7:135441140 | C | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-2717G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441140 | |||||||
chr7:135441334 | T | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-92-2911A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441334 | |||||||
chr7:135441406 | TA | T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0245 a0001c0001t0001g0281 others(7): Show |
10 | HG01069.hp1 HG01257.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.-92-2984delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441406 | |||||||
chr7:135441460 | T | C | 1 | a0001c0001t0007g0190 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-92-3037A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441460 | |||||||
chr7:135441550 | C | T | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-3127G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441550 | |||||||
chr7:135441775 | T | G | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-92-3352A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441775 | |||||||
chr7:135441914 | T | C | 6 | a0002c0002t0001g0042 a0002c0002t0001g0063 a0002c0002t0001g0066 others(3): Show |
6 | HG01358.hp1 HG01515.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-3491A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441914 | |||||||
chr7:135441937 | G | C | 1 | a0002c0002t0001g0065 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-92-3514C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441937 | |||||||
chr7:135441964 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-3541T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441964 | |||||||
chr7:135441965 | G | T | 1 | a0001c0001t0001g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-3542C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441965 | |||||||
chr7:135442005 | G | A | 1 | a0002c0002t0001g0100 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-92-3582C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135442005 | |||||||
chr7:135442139 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-92-3716A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135442139 | |||||||
chr7:135442294 | T | C | 2 | a0002c0002t0001g0052 a0002c0002t0001g0054 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-92-3871A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135442294 | |||||||
chr7:135442450 | T | A | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-4027A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135442450 | |||||||
chr7:135442456 | G | A | 1 | a0001c0001t0008g0346 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-92-4033C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135442456 | |||||||
chr7:135442509 | G | T | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-4086C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135442509 | |||||||
chr7:135442595 | C | T | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-4172G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135442595 | |||||||
chr7:135442662 | C | T | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-4239G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135442662 | |||||||
chr7:135442901 | T | A | 1 | a0001c0001t0001g0297 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-92-4478A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135442901 | |||||||
chr7:135443009 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-92-4586A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443009 | |||||||
chr7:135443036 | G | T | 1 | a0001c0001t0001g0162 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-92-4613C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443036 | |||||||
chr7:135443127 | G | T | 1 | a0002c0002t0001g0082 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-92-4704C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443127 | |||||||
chr7:135443188 | CA | C | 153 | a0001c0001t0001g0021 a0001c0001t0001g0119 a0001c0001t0001g0295 others(150): Show |
155 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.-92-4766delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443188 | |||||||
chr7:135443190 | A | C | 2 | a0001c0001t0001g0322 a0002c0002t0006g0006 |
2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-92-4767T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443190 | |||||||
chr7:135443244 | A | G | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-92-4821T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443244 | |||||||
chr7:135443354 | C | CA | 28 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0147 others(25): Show |
29 | HG01071.hp1 HG01256.hp2 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-92-4932dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443354 | |||||||
chr7:135443356 | A | C | 33 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(30): Show |
33 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.-92-4933T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443356 | |||||||
chr7:135443358 | A | C | 19 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(16): Show |
19 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.-92-4935T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443358 | |||||||
chr7:135443376 | C | T | 2 | a0002c0002t0001g0033 a0002c0002t0001g0034 |
2 | NA19003.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-92-4953G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443376 | |||||||
chr7:135443701 | C | T | 1 | a0001c0001t0002g0288 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-92-5278G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443701 | |||||||
chr7:135443742 | C | A | 15 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(12): Show |
15 | HG00597.hp2 HG02083.hp2 HG02965.hp1 others(12): Show |
intron_variant | MODIFIER | c.-92-5319G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443742 | |||||||
chr7:135443906 | T | G | 1 | a0001c0001t0001g0310 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-92-5483A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443906 | |||||||
chr7:135443940 | G | T | 1 | a0001c0001t0001g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-5517C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443940 | |||||||
chr7:135444016 | T | A | 1 | a0001c0001t0001g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-5593A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444016 | |||||||
chr7:135444041 | G | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(67): Show |
72 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-92-5618C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444041 | |||||||
chr7:135444057 | C | G | 1 | a0001c0001t0001g0157 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-92-5634G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444057 | |||||||
chr7:135444061 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-92-5638C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444061 | |||||||
chr7:135444144 | A | AAAT | 17 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(14): Show |
17 | HG00597.hp2 HG02083.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.-92-5724_-92-5722d others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444144 | |||||||
chr7:135444144 | A | T | 1 | a0001c0001t0001g0148 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-92-5721T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444144 | |||||||
chr7:135444144 | AAAT | A | 36 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0241 others(33): Show |
36 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-92-5724_-92-5722d others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444144 | |||||||
chr7:135444144 | AAATAATA others(2): Show |
A | 58 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(55): Show |
60 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.-92-5730_-92-5722d others(11): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444144 | |||||||
chr7:135444144 | AAATAATA others(8): Show |
A | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-92-5736_-92-5722d others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444144 | |||||||
chr7:135444179 | G | A | 1 | a0002c0002t0001g0129 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-92-5756C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444179 | |||||||
chr7:135444291 | G | A | 8 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.-92-5868C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444291 | |||||||
chr7:135444305 | A | G | 1 | a0002c0002t0001g0066 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-92-5882T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444305 | |||||||
chr7:135444367 | A | G | 5 | a0001c0001t0001g0234 a0001c0001t0001g0244 a0001c0001t0001g0246 others(2): Show |
5 | NA18946.hp2 NA18962.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-5944T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444367 | |||||||
chr7:135444502 | G | A | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-6079C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444502 | |||||||
chr7:135444520 | C | T | 4 | a0001c0001t0001g0147 a0001c0001t0003g0351 a0001c0001t0003g0352 others(1): Show |
4 | HG02083.hp2 HG03209.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.-92-6097G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444520 | |||||||
chr7:135444695 | G | A | 19 | a0001c0001t0001g0147 a0001c0001t0001g0327 a0001c0001t0001g0328 others(16): Show |
19 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.-92-6272C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444695 | |||||||
chr7:135444738 | G | C | 1 | a0001c0001t0001g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-6315C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444738 | |||||||
chr7:135444826 | A | T | 1 | a0001c0001t0001g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-6403T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444826 | |||||||
chr7:135444838 | T | C | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-6415A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444838 | |||||||
chr7:135445213 | A | G | 62 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(59): Show |
64 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.-92-6790T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135445213 | |||||||
chr7:135445583 | T | G | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-7160A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135445583 | |||||||
chr7:135445591 | T | A | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-7168A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135445591 | |||||||
chr7:135445607 | T | C | 3 | a0001c0001t0001g0160 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | NA18939.hp2 NA18940.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.-92-7184A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135445607 | |||||||
chr7:135445668 | G | A | 19 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(16): Show |
19 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.-92-7245C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135445668 | |||||||
chr7:135445700 | T | A | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-92-7277A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135445700 | |||||||
chr7:135445754 | T | C | 1 | a0001c0001t0001g0282 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-92-7331A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135445754 | |||||||
chr7:135445782 | G | A | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-7359C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135445782 | |||||||
chr7:135445883 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-7460A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135445883 | |||||||
chr7:135445945 | T | C | 1 | a0001c0001t0004g0004 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-92-7522A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135445945 | |||||||
chr7:135446050 | T | G | 1 | a0001c0001t0001g0263 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-92-7627A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446050 | |||||||
chr7:135446085 | T | C | 1 | a0001c0001t0001g0280 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-92-7662A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446085 | |||||||
chr7:135446107 | C | G | 1 | a0001c0001t0001g0241 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-92-7684G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446107 | |||||||
chr7:135446234 | T | C | 58 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(55): Show |
60 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.-92-7811A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446234 | |||||||
chr7:135446271 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0004g0004 |
3 | HG03490.hp2 HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-92-7848C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446271 | |||||||
chr7:135446288 | T | A | 4 | a0001c0001t0001g0236 a0001c0001t0001g0265 a0001c0001t0001g0266 others(1): Show |
4 | NA18948.hp2 NA18951.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-7865A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446288 | |||||||
chr7:135446336 | C | G | 6 | a0001c0001t0001g0239 a0001c0001t0001g0260 a0001c0001t0001g0261 others(3): Show |
6 | HG02071.hp2 HG03834.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.-92-7913G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446336 | |||||||
chr7:135446406 | A | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-7983T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446406 | |||||||
chr7:135446475 | C | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-8052G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446475 | |||||||
chr7:135446601 | G | C | 261 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(258): Show |
265 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.-92-8178C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446601 | |||||||
chr7:135446609 | A | C | 3 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0140 |
3 | HG02572.hp2 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-92-8186T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446609 | |||||||
chr7:135446905 | AACTATAT others(303): Show |
A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(67): Show |
72 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-92-8792_-92-8483d others(2): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446905 | |||||||
chr7:135446950 | T | A | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-8527A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446950 | |||||||
chr7:135447001 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-92-8578C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447001 | |||||||
chr7:135447013 | C | T | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-8590G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447013 | |||||||
chr7:135447097 | C | T | 8 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(5): Show |
8 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(5): Show |
intron_variant | MODIFIER | c.-92-8674G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447097 | |||||||
chr7:135447130 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-8707A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447130 | |||||||
chr7:135447147 | A | G | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-8724T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447147 | |||||||
chr7:135447246 | A | T | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-8823T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447246 | |||||||
chr7:135447266 | A | T | 5 | a0001c0003t0002g0182 a0001c0003t0002g0183 a0001c0003t0002g0184 others(2): Show |
5 | HG02280.hp2 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-8843T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447266 | |||||||
chr7:135447343 | T | C | 1 | a0001c0001t0002g0286 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-92-8920A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447343 | |||||||
chr7:135447504 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-9081A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447504 | |||||||
chr7:135447770 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-92-9347T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447770 | |||||||
chr7:135447903 | GT | G | 4 | a0001c0001t0001g0152 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
4 | HG00738.hp1 HG01106.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-92-9481delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447903 | |||||||
chr7:135448086 | G | A | 1 | a0002c0002t0001g0033 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-92-9663C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448086 | |||||||
chr7:135448209 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0003g0354 |
2 | NA18941.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-92-9786G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448209 | |||||||
chr7:135448341 | G | A | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-9918C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448341 | |||||||
chr7:135448543 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-10120C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448543 | |||||||
chr7:135448546 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-10123T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448546 | |||||||
chr7:135448547 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-10124C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448547 | |||||||
chr7:135448558 | A | G | 1 | a0001c0001t0001g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-10135T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448558 | |||||||
chr7:135448559 | G | A | 1 | a0001c0001t0001g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-10136C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448559 | |||||||
chr7:135448559 | G | GGGAGGGA others(9): Show |
6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-10137_-92-1013 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448559 | |||||||
chr7:135448583 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-92-10160G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448583 | |||||||
chr7:135448722 | T | A | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-92-10299A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448722 | |||||||
chr7:135448772 | A | G | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-10349T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448772 | |||||||
chr7:135448792 | G | A | 2 | a0002c0002t0001g0110 a0002c0002t0001g0111 |
2 | NA18956.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.-92-10369C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448792 | |||||||
chr7:135448883 | T | G | 1 | a0001c0001t0001g0241 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-92-10460A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448883 | |||||||
chr7:135449056 | C | T | 1 | a0001c0001t0008g0346 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-92-10633G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135449056 | |||||||
chr7:135449083 | A | T | 7 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(4): Show |
7 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(4): Show |
intron_variant | MODIFIER | c.-92-10660T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135449083 | |||||||
chr7:135449098 | C | T | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-10675G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135449098 | |||||||
chr7:135449551 | G | A | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-11128C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135449551 | |||||||
chr7:135449828 | G | T | 7 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(4): Show |
7 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(4): Show |
intron_variant | MODIFIER | c.-92-11405C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135449828 | |||||||
chr7:135449828 | GT | G | 201 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(198): Show |
205 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(202): Show |
intron_variant | MODIFIER | c.-92-11406delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135449828 | |||||||
chr7:135450032 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-92-11609A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135450032 | |||||||
chr7:135450054 | A | C | 61 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(58): Show |
63 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-92-11631T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135450054 | |||||||
chr7:135450511 | G | A | 3 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 |
3 | HG01256.hp1 HG01258.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-92-12088C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135450511 | |||||||
chr7:135450579 | C | A | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-12156G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135450579 | |||||||
chr7:135450641 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-92-12218C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135450641 | |||||||
chr7:135450783 | A | G | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-12360T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135450783 | |||||||
chr7:135450914 | G | A | 5 | a0002c0002t0001g0057 a0002c0002t0001g0098 a0002c0002t0001g0101 others(2): Show |
5 | HG02129.hp1 NA18946.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.-92-12491C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135450914 | |||||||
chr7:135451033 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-92-12610G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451033 | |||||||
chr7:135451063 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-92-12640A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451063 | |||||||
chr7:135451085 | A | G | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-12662T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451085 | |||||||
chr7:135451175 | G | A | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-12752C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451175 | |||||||
chr7:135451238 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-92-12815G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451238 | |||||||
chr7:135451392 | C | G | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-92-12969G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451392 | |||||||
chr7:135451750 | C | T | 17 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(14): Show |
17 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-92-13327G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451750 | |||||||
chr7:135451767 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-92-13344C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451767 | |||||||
chr7:135451814 | G | A | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-13391C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451814 | |||||||
chr7:135451890 | T | C | 1 | a0002c0002t0001g0044 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-92-13467A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451890 | |||||||
chr7:135451975 | T | C | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-13552A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451975 | |||||||
chr7:135452065 | T | A | 1 | a0001c0001t0002g0292 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-92-13642A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452065 | |||||||
chr7:135452132 | C | T | 62 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(59): Show |
64 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.-92-13709G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452132 | |||||||
chr7:135452241 | A | C | 1 | a0001c0001t0001g0329 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-92-13818T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452241 | |||||||
chr7:135452280 | T | TAAGAAAA others(314): Show |
1 | a0001c0001t0001g0141 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-92-13858_-92-1385 others(325): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452280 | |||||||
chr7:135452280 | T | TAAGAAAA others(314): Show |
12 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0003g0347 others(9): Show |
12 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(9): Show |
intron_variant | MODIFIER | c.-92-13858_-92-1385 others(325): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452280 | |||||||
chr7:135452280 | T | TAAGAAAA others(315): Show |
1 | a0001c0001t0003g0356 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-92-13858_-92-1385 others(326): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452280 | |||||||
chr7:135452448 | T | A | 1 | a0002c0002t0006g0006 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-92-14025A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452448 | |||||||
chr7:135452616 | G | A | 1 | a0002c0002t0001g0090 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-92-14193C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452616 | |||||||
chr7:135452805 | T | C | 1 | a0002c0002t0001g0025 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-92-14382A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452805 | |||||||
chr7:135452879 | T | C | 1 | a0001c0001t0002g0294 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-92-14456A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452879 | |||||||
chr7:135452954 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-92-14531A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452954 | |||||||
chr7:135452981 | C | T | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-14558G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452981 | |||||||
chr7:135452983 | T | C | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-14560A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452983 | |||||||
chr7:135452987 | T | C | 1 | a0002c0002t0001g0058 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-92-14564A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452987 | |||||||
chr7:135453045 | G | A | 2 | a0001c0001t0001g0334 a0001c0001t0001g0335 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-92-14622C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453045 | |||||||
chr7:135453173 | T | A | 1 | a0001c0001t0001g0311 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-92-14750A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453173 | |||||||
chr7:135453583 | G | A | 125 | a0001c0001t0001g0119 a0001c0001t0001g0322 a0001c0001t0002g0117 others(122): Show |
127 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.-92-15160C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453583 | |||||||
chr7:135453623 | G | T | 1 | a0002c0002t0001g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-92-15200C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453623 | |||||||
chr7:135453767 | CAT | C | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-92-15346_-92-1534 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453767 | |||||||
chr7:135453801 | AATAT | A | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-92-15382_-92-1537 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453801 | |||||||
chr7:135453809 | TAA | T | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-15388_-92-1538 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453809 | |||||||
chr7:135453814 | A | T | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-15391T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453814 | |||||||
chr7:135453824 | T | TTATATAT others(5): Show |
1 | a0001c0001t0001g0340 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-92-15402_-92-1540 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453824 | |||||||
chr7:135453826 | T | A | 1 | a0001c0001t0001g0340 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-92-15403A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | |||||||
chr7:135453826 | T | TTA | 38 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0150 others(35): Show |
38 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.-92-15405_-92-1540 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | |||||||
chr7:135453826 | T | TTATATAT others(3): Show |
29 | a0001c0001t0001g0145 a0001c0001t0001g0328 a0001c0001t0001g0329 others(26): Show |
29 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.-92-15413_-92-1540 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | |||||||
chr7:135453826 | T | TTATATAT others(5): Show |
40 | a0001c0001t0001g0333 a0001c0001t0001g0336 a0001c0001t0001g0337 others(37): Show |
41 | HG00597.hp1 HG00609.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.-92-15415_-92-1540 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | |||||||
chr7:135453826 | T | TTATATAT others(7): Show |
16 | a0001c0001t0001g0327 a0001c0001t0001g0334 a0001c0001t0001g0335 others(13): Show |
16 | HG00642.hp1 HG00735.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.-92-15417_-92-1540 others(18): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | |||||||
chr7:135453826 | T | TTATATAT others(9): Show |
12 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(9): Show |
12 | HG01256.hp1 HG01258.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.-92-15419_-92-1540 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | |||||||
chr7:135453826 | T | TTATATAT others(11): Show |
2 | a0002c0002t0001g0062 a0002c0002t0001g0098 |
2 | NA18946.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.-92-15421_-92-1540 others(22): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | |||||||
chr7:135453826 | T | TTATATAT others(13): Show |
1 | a0002c0002t0001g0101 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-92-15423_-92-1540 others(24): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | |||||||
chr7:135453826 | T | TTATATAT others(15): Show |
2 | a0004c0005t0001g0126 a0004c0005t0001g0128 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-92-15404_-92-1540 others(26): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | |||||||
chr7:135453826 | T | TTATATAT others(17): Show |
1 | a0004c0005t0001g0127 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-92-15404_-92-1540 others(28): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | |||||||
chr7:135453826 | TTA | T | 67 | a0001c0001t0001g0003 a0001c0001t0001g0188 a0001c0001t0001g0228 others(64): Show |
69 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.-92-15405_-92-1540 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | |||||||
chr7:135453826 | TTATATA | T | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-15409_-92-1540 others(10): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | |||||||
chr7:135453847 | T | TATATATA others(3): Show |
1 | a0002c0002t0001g0109 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-92-15425_-92-1542 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453847 | |||||||
chr7:135453847 | T | TATATATA others(4): Show |
1 | a0002c0002t0001g0039 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-92-15425_-92-1542 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453847 | |||||||
chr7:135453847 | T | TATATATA others(5): Show |
8 | a0002c0002t0001g0028 a0002c0002t0001g0086 a0002c0002t0001g0087 others(5): Show |
8 | NA18947.hp2 NA18948.hp1 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.-92-15425_-92-1542 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453847 | |||||||
chr7:135453847 | T | TATATATA others(7): Show |
2 | a0002c0002t0001g0024 a0002c0002t0001g0027 |
2 | NA19007.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.-92-15425_-92-1542 others(18): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453847 | |||||||
chr7:135453847 | T | TATATATA others(9): Show |
2 | a0002c0002t0001g0001 a0002c0002t0001g0023 |
3 | NA18986.hp2 NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-92-15425_-92-1542 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453847 | |||||||
chr7:135453848 | T | A | 123 | a0001c0001t0001g0119 a0001c0001t0002g0117 a0001c0001t0002g0118 others(120): Show |
125 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-92-15425A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453848 | |||||||
chr7:135453955 | T | C | 1 | a0001c0001t0001g0340 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-92-15532A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453955 | |||||||
chr7:135453987 | T | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-92-15564A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453987 | |||||||
chr7:135453989 | C | CAT | 17 | a0001c0001t0001g0254 a0001c0001t0001g0327 a0001c0001t0001g0329 others(14): Show |
17 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-92-15568_-92-1556 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453989 | |||||||
chr7:135453989 | C | CATAT | 3 | a0001c0001t0001g0328 a0001c0001t0001g0344 a0001c0010t0002g0324 |
3 | HG01261.hp1 HG02572.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-92-15570_-92-1556 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453989 | |||||||
chr7:135453989 | C | CATATAT | 15 | a0001c0001t0002g0117 a0001c0001t0002g0122 a0001c0001t0002g0123 others(12): Show |
15 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.-92-15572_-92-1556 others(10): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453989 | |||||||
chr7:135453989 | C | CATATATA others(1): Show |
4 | a0001c0001t0002g0118 a0001c0001t0002g0120 a0001c0001t0002g0121 others(1): Show |
4 | HG00280.hp1 HG01361.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-15574_-92-1556 others(12): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453989 | |||||||
chr7:135453989 | CAT | C | 21 | a0001c0001t0001g0141 a0001c0001t0001g0147 a0001c0001t0001g0269 others(18): Show |
21 | HG02083.hp2 HG02258.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.-92-15568_-92-1556 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453989 | |||||||
chr7:135454115 | A | G | 5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0168 others(2): Show |
5 | HG00642.hp2 HG01074.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-92-15692T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135454115 | |||||||
chr7:135454263 | C | T | 243 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(240): Show |
247 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.-92-15840G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135454263 | |||||||
chr7:135454385 | A | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-15962T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135454385 | |||||||
chr7:135454514 | A | AT | 4 | a0001c0001t0001g0239 a0001c0001t0001g0280 a0001c0001t0001g0282 others(1): Show |
4 | HG02071.hp2 NA18612.hp2 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-16092dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135454514 | |||||||
chr7:135454516 | T | TA | 238 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(235): Show |
242 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.-92-16094dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135454516 | |||||||
chr7:135454611 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-92-16188A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135454611 | |||||||
chr7:135454662 | GTAAA | G | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-16243_-92-1624 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135454662 | |||||||
chr7:135454684 | G | A | 4 | a0001c0001t0002g0130 a0001c0001t0002g0132 a0001c0001t0002g0133 others(1): Show |
4 | HG02818.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-92-16261C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135454684 | |||||||
chr7:135454976 | T | C | 3 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 |
3 | HG02486.hp1 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-92-16553A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135454976 | |||||||
chr7:135455081 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-92-16658G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135455081 | |||||||
chr7:135455215 | A | G | 1 | a0001c0001t0001g0191 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-92-16792T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135455215 | |||||||
chr7:135455298 | C | T | 1 | a0002c0002t0001g0050 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-92-16875G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135455298 | |||||||
chr7:135455299 | G | A | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-92-16876C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135455299 | |||||||
chr7:135455485 | T | C | 1 | a0001c0003t0002g0184 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-92-17062A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135455485 | |||||||
chr7:135455663 | C | T | 5 | a0001c0001t0001g0234 a0001c0001t0001g0244 a0001c0001t0001g0246 others(2): Show |
5 | NA18946.hp2 NA18962.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-17240G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135455663 | |||||||
chr7:135455721 | A | G | 1 | a0002c0002t0001g0049 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-92-17298T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135455721 | |||||||
chr7:135455751 | G | A | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-17328C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135455751 | |||||||
chr7:135456200 | T | G | 2 | a0001c0001t0001g0317 a0001c0001t0001g0318 |
2 | HG01361.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-92-17777A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135456200 | |||||||
chr7:135456263 | TCTACCAT others(3023): Show |
T | 2 | a0001c0001t0001g0270 a0001c0001t0001g0317 |
2 | HG01361.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-92-20870_-92-1784 others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135456263 | |||||||
chr7:135456321 | T | C | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-17898A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135456321 | |||||||
chr7:135456372 | C | T | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-17949G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135456372 | |||||||
chr7:135456607 | T | C | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-18184A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135456607 | |||||||
chr7:135456816 | A | C | 1 | a0003c0004t0001g0196 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-92-18393T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135456816 | |||||||
chr7:135456868 | G | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-18445C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135456868 | |||||||
chr7:135457003 | C | T | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-18580G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457003 | |||||||
chr7:135457018 | C | A | 1 | a0002c0002t0001g0300 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-92-18595G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457018 | |||||||
chr7:135457372 | T | C | 220 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0145 others(217): Show |
224 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.-92-18949A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457372 | |||||||
chr7:135457424 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-92-19001T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457424 | |||||||
chr7:135457513 | T | G | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-19090A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457513 | |||||||
chr7:135457537 | T | C | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-19114A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457537 | |||||||
chr7:135457595 | T | C | 59 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(56): Show |
61 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.-92-19172A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457595 | |||||||
chr7:135457612 | G | A | 1 | a0002c0002t0001g0066 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-92-19189C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457612 | |||||||
chr7:135457654 | T | C | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-19231A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457654 | |||||||
chr7:135457711 | C | T | 258 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(255): Show |
262 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.-92-19288G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457711 | |||||||
chr7:135457779 | A | T | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-19356T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457779 | |||||||
chr7:135457980 | T | C | 2 | a0001c0001t0001g0151 a0001c0001t0001g0168 |
2 | HG00642.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.-92-19557A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457980 | |||||||
chr7:135458018 | C | T | 4 | a0002c0002t0001g0108 a0002c0002t0001g0109 a0002c0002t0001g0110 others(1): Show |
4 | HG00438.hp1 NA18956.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-19595G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135458018 | |||||||
chr7:135458151 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-92-19728A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135458151 | |||||||
chr7:135458235 | T | C | 6 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0149 others(3): Show |
6 | HG01123.hp2 NA18968.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-19812A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135458235 | |||||||
chr7:135458391 | T | C | 32 | a0001c0001t0001g0003 a0001c0001t0001g0229 a0001c0001t0001g0230 others(29): Show |
33 | HG00438.hp2 HG00609.hp1 HG01934.hp2 others(30): Show |
intron_variant | MODIFIER | c.-92-19968A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135458391 | |||||||
chr7:135458540 | G | A | 3 | a0004c0005t0001g0126 a0004c0005t0001g0127 a0004c0005t0001g0128 |
3 | HG01106.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-92-20117C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135458540 | |||||||
chr7:135458546 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-92-20123G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135458546 | |||||||
chr7:135458673 | T | C | 3 | a0002c0002t0001g0051 a0002c0002t0001g0052 a0002c0002t0001g0054 |
3 | HG03491.hp1 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-92-20250A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135458673 | |||||||
chr7:135458762 | T | C | 1 | a0001c0001t0008g0346 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-92-20339A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135458762 | |||||||
chr7:135458921 | C | A | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-20498G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135458921 | |||||||
chr7:135459103 | A | C | 1 | a0001c0001t0007g0190 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-92-20680T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135459103 | |||||||
chr7:135459223 | G | A | 258 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0119 others(255): Show |
262 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.-92-20800C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135459223 | |||||||
chr7:135459270 | CAGAT | C | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-20851_-92-2084 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135459270 | |||||||
chr7:135459680 | T | C | 2 | a0001c0001t0002g0117 a0001c0001t0002g0118 |
2 | HG01081.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-92-21257A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135459680 | |||||||
chr7:135459766 | G | A | 5 | a0001c0003t0002g0182 a0001c0003t0002g0183 a0001c0003t0002g0184 others(2): Show |
5 | HG02280.hp2 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-21343C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135459766 | |||||||
chr7:135459799 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0168 |
2 | HG00642.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.-92-21376C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135459799 | |||||||
chr7:135459886 | C | A | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-21463G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135459886 | |||||||
chr7:135459914 | T | C | 261 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(258): Show |
265 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.-92-21491A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135459914 | |||||||
chr7:135460067 | A | G | 1 | a0001c0001t0005g0005 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-92-21644T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460067 | |||||||
chr7:135460093 | G | T | 2 | a0001c0001t0001g0322 a0002c0002t0006g0006 |
2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-92-21670C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460093 | |||||||
chr7:135460208 | C | T | 1 | a0002c0002t0001g0083 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-92-21785G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460208 | |||||||
chr7:135460209 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-92-21786C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460209 | |||||||
chr7:135460437 | A | C | 17 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(14): Show |
17 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-92-22014T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460437 | |||||||
chr7:135460590 | A | G | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-22167T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460590 | |||||||
chr7:135460633 | A | G | 1 | a0002c0002t0006g0006 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-92-22210T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460633 | |||||||
chr7:135460636 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-92-22213A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460636 | |||||||
chr7:135460789 | T | C | 1 | a0001c0001t0003g0350 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-92-22366A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460789 | |||||||
chr7:135460825 | T | C | 6 | a0001c0001t0001g0148 a0001c0001t0001g0153 a0001c0001t0001g0161 others(3): Show |
6 | NA18944.hp2 NA18967.hp1 NA19006.hp2 others(3): Show |
intron_variant | MODIFIER | c.-92-22402A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460825 | |||||||
chr7:135460828 | C | G | 7 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(4): Show |
7 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(4): Show |
intron_variant | MODIFIER | c.-92-22405G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460828 | |||||||
chr7:135461006 | G | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-92-22583C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135461006 | |||||||
chr7:135461007 | C | G | 1 | a0001c0001t0001g0316 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-92-22584G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135461007 | |||||||
chr7:135461176 | C | T | 17 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(14): Show |
17 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-92-22753G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135461176 | |||||||
chr7:135461182 | T | C | 1 | a0002c0002t0001g0079 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-92-22759A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135461182 | |||||||
chr7:135461555 | G | C | 5 | a0001c0003t0002g0182 a0001c0003t0002g0183 a0001c0003t0002g0184 others(2): Show |
5 | HG02280.hp2 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-23132C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135461555 | |||||||
chr7:135461849 | T | A | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-92-23426A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135461849 | |||||||
chr7:135462006 | T | G | 1 | a0001c0008t0001g0323 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-92-23583A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462006 | |||||||
chr7:135462064 | T | TA | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-23642dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462064 | |||||||
chr7:135462114 | T | TG | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-23692dupC | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462114 | |||||||
chr7:135462145 | A | G | 1 | a0002c0002t0001g0029 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-92-23722T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462145 | |||||||
chr7:135462362 | C | T | 1 | a0002c0011t0001g0059 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-92-23939G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462362 | |||||||
chr7:135462365 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-92-23942C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462365 | |||||||
chr7:135462465 | A | C | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-24042T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462465 | |||||||
chr7:135462478 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-92-24055C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462478 | |||||||
chr7:135462515 | C | T | 2 | a0002c0002t0001g0068 a0002c0002t0001g0069 |
2 | HG01358.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.-92-24092G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462515 | |||||||
chr7:135462517 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-92-24094G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462517 | |||||||
chr7:135462545 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-92-24122C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462545 | |||||||
chr7:135462677 | A | C | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-24254T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462677 | |||||||
chr7:135462766 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-92-24343T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462766 | |||||||
chr7:135462796 | A | G | 1 | a0001c0001t0001g0344 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-92-24373T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462796 | |||||||
chr7:135462874 | T | C | 12 | a0002c0002t0001g0001 a0002c0002t0001g0023 a0002c0002t0001g0024 others(9): Show |
13 | NA18947.hp2 NA18948.hp1 NA18951.hp1 others(10): Show |
intron_variant | MODIFIER | c.-92-24451A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462874 | |||||||
chr7:135463009 | G | A | 3 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0140 |
3 | HG02572.hp2 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-92-24586C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463009 | |||||||
chr7:135463144 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-24721A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463144 | |||||||
chr7:135463266 | G | T | 1 | a0002c0002t0001g0302 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-92-24843C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463266 | |||||||
chr7:135463304 | G | A | 1 | a0002c0002t0001g0029 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-92-24881C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463304 | |||||||
chr7:135463309 | G | A | 16 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(13): Show |
16 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-92-24886C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463309 | |||||||
chr7:135463438 | T | C | 8 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.-92-25015A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463438 | |||||||
chr7:135463544 | C | CA | 17 | a0001c0001t0001g0143 a0001c0001t0001g0157 a0001c0001t0001g0168 others(14): Show |
17 | HG00438.hp1 HG00642.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.-92-25122dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463544 | |||||||
chr7:135463544 | CA | C | 146 | a0001c0001t0001g0003 a0001c0001t0001g0141 a0001c0001t0001g0145 others(143): Show |
148 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.-92-25122delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463544 | |||||||
chr7:135463594 | G | A | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-25171C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463594 | |||||||
chr7:135463622 | G | A | 61 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(58): Show |
63 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-92-25199C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463622 | |||||||
chr7:135463664 | A | C | 2 | a0001c0001t0001g0265 a0001c0001t0001g0266 |
2 | NA18948.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.-92-25241T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463664 | |||||||
chr7:135464024 | C | CAAAA | 24 | a0001c0001t0001g0146 a0001c0001t0001g0268 a0001c0001t0001g0270 others(21): Show |
24 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.-92-25605_-92-2560 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464024 | |||||||
chr7:135464024 | C | CAAAAA | 90 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(87): Show |
91 | HG00280.hp2 HG00438.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.-92-25606_-92-2560 others(9): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464024 | |||||||
chr7:135464024 | C | CAAAAAA | 120 | a0001c0001t0001g0241 a0001c0001t0001g0260 a0001c0001t0001g0304 others(117): Show |
123 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.-92-25607_-92-2560 others(10): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464024 | |||||||
chr7:135464024 | C | CAAAAAAA | 10 | a0001c0001t0001g0147 a0001c0001t0001g0296 a0001c0001t0001g0297 others(7): Show |
10 | HG01099.hp2 HG02602.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-92-25608_-92-2560 others(11): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464024 | |||||||
chr7:135464024 | C | CAAAAAAA others(1): Show |
15 | a0001c0001t0001g0295 a0001c0001t0001g0327 a0001c0001t0001g0328 others(12): Show |
15 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.-92-25609_-92-2560 others(12): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464024 | |||||||
chr7:135464024 | CA | C | 6 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0149 others(3): Show |
6 | HG01123.hp2 NA18968.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-25602delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464024 | |||||||
chr7:135464047 | G | A | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-92-25624C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464047 | |||||||
chr7:135464121 | GCAGTATG others(9): Show |
G | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-92-25714_-92-2569 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464121 | |||||||
chr7:135464465 | T | C | 10 | a0002c0002t0001g0049 a0002c0002t0001g0076 a0002c0002t0001g0077 others(7): Show |
10 | HG00673.hp1 NA18747.hp1 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.-92-26042A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464465 | |||||||
chr7:135464482 | A | G | 2 | a0001c0001t0001g0322 a0002c0002t0006g0006 |
2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-92-26059T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464482 | |||||||
chr7:135464596 | C | T | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-26173G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464596 | |||||||
chr7:135464635 | A | T | 1 | a0001c0001t0002g0120 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-92-26212T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464635 | |||||||
chr7:135464696 | T | C | 1 | a0002c0002t0001g0053 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-92-26273A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464696 | |||||||
chr7:135464764 | A | T | 1 | a0001c0001t0005g0005 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-92-26341T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464764 | |||||||
chr7:135464816 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-92-26393T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464816 | |||||||
chr7:135465010 | C | T | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-92-26587G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135465010 | |||||||
chr7:135465192 | G | T | 1 | a0001c0001t0001g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-92-26769C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135465192 | |||||||
chr7:135465714 | CAT | C | 6 | a0001c0001t0001g0148 a0001c0001t0001g0153 a0001c0001t0001g0161 others(3): Show |
6 | NA18944.hp2 NA18967.hp1 NA19006.hp2 others(3): Show |
intron_variant | MODIFIER | c.-92-27293_-92-2729 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135465714 | |||||||
chr7:135465731 | C | CA | 27 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(24): Show |
27 | HG00099.hp2 HG00621.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.-92-27309dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135465731 | |||||||
chr7:135465875 | C | G | 1 | a0001c0001t0001g0319 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-92-27452G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135465875 | |||||||
chr7:135466036 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-92-27613C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135466036 | |||||||
chr7:135466111 | G | A | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-27688C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135466111 | |||||||
chr7:135466118 | T | TTG | 260 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(257): Show |
264 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.-92-27697_-92-2769 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135466118 | |||||||
chr7:135466125 | T | C | 1 | a0002c0002t0006g0006 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-92-27702A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135466125 | |||||||
chr7:135466391 | C | T | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-27968G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135466391 | |||||||
chr7:135466455 | G | A | 1 | a0002c0002t0001g0098 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-92-28032C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135466455 | |||||||
chr7:135466475 | C | CA | 17 | a0001c0001t0001g0192 a0001c0001t0001g0200 a0001c0001t0001g0214 others(14): Show |
17 | HG01891.hp2 HG02145.hp2 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.-92-28053dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135466475 | |||||||
chr7:135466475 | CA | C | 17 | a0001c0001t0001g0012 a0001c0001t0001g0158 a0001c0001t0001g0234 others(14): Show |
17 | HG01169.hp2 HG01256.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.-92-28053delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135466475 | |||||||
chr7:135466834 | A | G | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-28411T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135466834 | |||||||
chr7:135467134 | A | G | 3 | a0001c0001t0003g0351 a0001c0001t0003g0352 a0001c0001t0003g0353 |
3 | HG02083.hp2 NA19080.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-92-28711T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135467134 | |||||||
chr7:135467298 | C | T | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-92-28875G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135467298 | |||||||
chr7:135467523 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-92-29100G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135467523 | |||||||
chr7:135467949 | C | G | 1 | a0003c0004t0001g0196 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-92-29526G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135467949 | |||||||
chr7:135467998 | G | A | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-92-29575C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135467998 | |||||||
chr7:135468035 | G | A | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-29612C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468035 | |||||||
chr7:135468138 | C | G | 17 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(14): Show |
17 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-92-29715G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468138 | |||||||
chr7:135468202 | C | T | 2 | a0001c0001t0001g0344 a0001c0003t0002g0182 |
2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-92-29779G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468202 | |||||||
chr7:135468209 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-92-29786G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468209 | |||||||
chr7:135468239 | T | A | 1 | a0001c0001t0001g0322 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-92-29816A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468239 | |||||||
chr7:135468338 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-92-29915T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468338 | |||||||
chr7:135468367 | T | C | 1 | a0001c0001t0001g0317 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-92-29944A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468367 | |||||||
chr7:135468443 | G | A | 104 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(101): Show |
106 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.-92-30020C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468443 | |||||||
chr7:135468502 | A | G | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-30079T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468502 | |||||||
chr7:135468684 | C | CA | 196 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0145 others(193): Show |
200 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.-92-30262dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468684 | |||||||
chr7:135468684 | C | CAA | 35 | a0001c0001t0001g0241 a0001c0001t0001g0284 a0001c0001t0001g0295 others(32): Show |
35 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.-92-30263_-92-3026 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468684 | |||||||
chr7:135468684 | CA | C | 7 | a0001c0001t0001g0009 a0001c0001t0001g0148 a0001c0001t0001g0149 others(4): Show |
7 | HG01069.hp1 HG01934.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-92-30262delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468684 | |||||||
chr7:135469021 | G | A | 61 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(58): Show |
63 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-92-30598C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469021 | |||||||
chr7:135469079 | G | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-30656C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469079 | |||||||
chr7:135469102 | T | A | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-30679A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469102 | |||||||
chr7:135469158 | C | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-30735G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469158 | |||||||
chr7:135469168 | T | C | 21 | a0001c0001t0001g0018 a0001c0001t0001g0141 a0001c0001t0001g0304 others(18): Show |
21 | HG00597.hp2 HG01981.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.-92-30745A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469168 | |||||||
chr7:135469194 | A | G | 3 | a0002c0002t0001g0179 a0002c0002t0001g0180 a0002c0002t0001g0181 |
3 | NA18975.hp1 NA19084.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-92-30771T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469194 | |||||||
chr7:135469767 | A | G | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-31344T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469767 | |||||||
chr7:135469818 | TTTTG | T | 19 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(16): Show |
19 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-92-31399_-92-3139 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469818 | |||||||
chr7:135469882 | C | A | 5 | a0001c0003t0002g0182 a0001c0003t0002g0183 a0001c0003t0002g0184 others(2): Show |
5 | HG02280.hp2 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-31459G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469882 | |||||||
chr7:135469882 | C | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-31459G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469882 | |||||||
chr7:135469934 | G | C | 1 | a0001c0001t0001g0019 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-92-31511C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469934 | |||||||
chr7:135469947 | G | A | 5 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0001t0001g0331 others(2): Show |
5 | HG00733.hp2 HG00735.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.-92-31524C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469947 | |||||||
chr7:135469977 | A | T | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-92-31554T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469977 | |||||||
chr7:135470100 | G | C | 1 | a0001c0001t0001g0271 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-92-31677C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470100 | |||||||
chr7:135470116 | C | G | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-92-31693G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470116 | |||||||
chr7:135470139 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-92-31716C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470139 | |||||||
chr7:135470272 | G | A | 1 | a0001c0001t0001g0276 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-92-31849C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470272 | |||||||
chr7:135470295 | T | G | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-31872A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470295 | |||||||
chr7:135470332 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-92-31909C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470332 | |||||||
chr7:135470398 | T | TG | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-31976dupC | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470398 | |||||||
chr7:135470456 | T | C | 3 | a0001c0001t0001g0150 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG01943.hp2 HG03490.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-92-32033A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470456 | |||||||
chr7:135470547 | G | A | 3 | a0002c0002t0001g0051 a0002c0002t0001g0052 a0002c0002t0001g0054 |
3 | HG03491.hp1 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-92-32124C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470547 | |||||||
chr7:135470571 | TA | T | 264 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0119 others(261): Show |
268 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.-92-32149delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470571 | |||||||
chr7:135470618 | T | C | 38 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(35): Show |
38 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.-92-32195A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470618 | |||||||
chr7:135470619 | G | A | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-32196C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470619 | |||||||
chr7:135470706 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-92-32283C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470706 | |||||||
chr7:135470767 | A | G | 16 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(13): Show |
16 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-92-32344T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470767 | |||||||
chr7:135470839 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-92-32416C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470839 | |||||||
chr7:135471003 | C | G | 1 | a0001c0001t0001g0316 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-92-32580G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135471003 | |||||||
chr7:135471034 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0318 |
2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-92-32611G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135471034 | |||||||
chr7:135471250 | C | A | 1 | a0001c0001t0001g0303 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-92-32827G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135471250 | |||||||
chr7:135471325 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-92-32902C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135471325 | |||||||
chr7:135471381 | C | A | 122 | a0001c0001t0001g0119 a0001c0001t0002g0117 a0001c0001t0002g0118 others(119): Show |
124 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-92-32958G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135471381 | |||||||
chr7:135471488 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-92-33065A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135471488 | |||||||
chr7:135471576 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-92-33153A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135471576 | |||||||
chr7:135471754 | G | T | 1 | a0001c0010t0002g0324 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-92-33331C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135471754 | |||||||
chr7:135471788 | C | T | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-33365G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135471788 | |||||||
chr7:135472044 | G | C | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-33621C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472044 | |||||||
chr7:135472116 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-92-33693A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472116 | |||||||
chr7:135472246 | G | C | 1 | a0002c0002t0001g0068 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-92-33823C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472246 | |||||||
chr7:135472257 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0020 |
3 | NA18954.hp2 NA19075.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-92-33834G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472257 | |||||||
chr7:135472338 | G | A | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-33915C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472338 | |||||||
chr7:135472375 | G | T | 1 | a0002c0002t0006g0006 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-92-33952C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472375 | |||||||
chr7:135472409 | G | A | 1 | a0001c0001t0001g0316 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-92-33986C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472409 | |||||||
chr7:135472420 | C | T | 261 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(258): Show |
265 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.-92-33997G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472420 | |||||||
chr7:135472453 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-92-34030C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472453 | |||||||
chr7:135472456 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0318 |
2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-92-34033C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472456 | |||||||
chr7:135472476 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0011 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-92-34063_-92-3405 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472476 | |||||||
chr7:135472476 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0195 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-92-34065_-92-3405 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472476 | |||||||
chr7:135472476 | CAAAA | C | 6 | a0001c0001t0005g0005 a0002c0002t0001g0031 a0002c0002t0001g0044 others(3): Show |
6 | HG01934.hp1 HG02004.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-34057_-92-3405 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472476 | |||||||
chr7:135472476 | CAAAAA | C | 7 | a0002c0002t0001g0048 a0002c0002t0001g0056 a0002c0002t0001g0072 others(4): Show |
7 | HG01257.hp2 HG01258.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.-92-34058_-92-3405 others(9): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472476 | |||||||
chr7:135472476 | CAAAAAAA | C | 7 | a0001c0001t0001g0311 a0001c0001t0002g0224 a0001c0001t0002g0226 others(4): Show |
7 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.-92-34060_-92-3405 others(11): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472476 | |||||||
chr7:135472476 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0113 a0002c0002t0001g0001 a0002c0002t0001g0023 |
4 | HG00621.hp2 NA18986.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-34063_-92-3405 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472476 | |||||||
chr7:135472476 | CAAAAAAA others(11): Show |
C | 1 | a0001c0001t0001g0009 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-92-34071_-92-3405 others(22): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472476 | |||||||
chr7:135472476 | CAAAAAAA others(12): Show |
C | 1 | a0002c0002t0001g0043 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-92-34072_-92-3405 others(23): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472476 | |||||||
chr7:135472498 | AAAAAAAA others(17): Show |
A | 1 | a0001c0001t0003g0354 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-92-34099_-92-3407 others(28): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472498 | |||||||
chr7:135472501 | AAAAAAAA others(36): Show |
A | 1 | a0001c0008t0001g0323 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-92-34121_-92-3407 others(47): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472501 | |||||||
chr7:135472502 | AAAAAAAA others(17): Show |
A | 1 | a0001c0001t0001g0141 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-92-34103_-92-3408 others(28): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472502 | |||||||
chr7:135472502 | AAAAAAAA others(29): Show |
A | 1 | a0001c0003t0002g0184 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-92-34115_-92-3408 others(40): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472502 | |||||||
chr7:135472503 | AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0001g0314 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-92-34093_-92-3408 others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472503 | |||||||
chr7:135472503 | AAAAAAAA others(14): Show |
A | 1 | a0001c0001t0003g0349 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-92-34101_-92-3408 others(25): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472503 | |||||||
chr7:135472503 | AAAAAAAA others(16): Show |
A | 1 | a0001c0001t0001g0208 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-92-34103_-92-3408 others(27): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472503 | |||||||
chr7:135472503 | AAAAAAAA others(22): Show |
A | 1 | a0001c0001t0001g0274 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-92-34109_-92-3408 others(33): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472503 | |||||||
chr7:135472503 | AAAAAAAA others(26): Show |
A | 1 | a0001c0001t0001g0283 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-92-34113_-92-3408 others(37): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472503 | |||||||
chr7:135472503 | AAAAAAAA others(30): Show |
A | 1 | a0001c0003t0002g0183 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-92-34117_-92-3408 others(41): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472503 | |||||||
chr7:135472504 | AAAAAAAA others(9): Show |
A | 3 | a0001c0001t0002g0130 a0001c0001t0002g0132 a0001c0001t0002g0133 |
3 | HG02896.hp1 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-92-34097_-92-3408 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472504 | |||||||
chr7:135472504 | AAAAAAAA others(11): Show |
A | 1 | a0002c0002t0006g0006 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-92-34099_-92-3408 others(22): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472504 | |||||||
chr7:135472504 | AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0003g0357 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-92-34101_-92-3408 others(24): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472504 | |||||||
chr7:135472504 | AAAAAAAA others(23): Show |
A | 1 | a0001c0001t0001g0263 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-92-34111_-92-3408 others(34): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472504 | |||||||
chr7:135472504 | AAAAAAAA others(25): Show |
A | 4 | a0001c0001t0001g0239 a0001c0001t0001g0260 a0001c0001t0001g0280 others(1): Show |
4 | NA18612.hp2 NA18940.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-34113_-92-3408 others(36): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472504 | |||||||
chr7:135472504 | AAAAAAAA others(27): Show |
A | 1 | a0001c0003t0002g0182 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-92-34115_-92-3408 others(38): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472504 | |||||||
chr7:135472504 | AAAAAAAA others(29): Show |
A | 4 | a0001c0001t0001g0119 a0001c0001t0001g0340 a0001c0003t0002g0185 others(1): Show |
4 | HG01255.hp2 HG02523.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-34117_-92-3408 others(40): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472504 | |||||||
chr7:135472505 | AAAAAAAA others(6): Show |
A | 3 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0331 |
3 | HG00741.hp2 HG01123.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-92-34095_-92-3408 others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472505 | |||||||
chr7:135472505 | AAAAAAAA others(10): Show |
A | 2 | a0001c0001t0001g0330 a0001c0001t0001g0333 |
2 | HG00735.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.-92-34099_-92-3408 others(21): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472505 | |||||||
chr7:135472505 | AAAAAAAA others(18): Show |
A | 1 | a0001c0001t0001g0322 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-92-34107_-92-3408 others(29): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472505 | |||||||
chr7:135472505 | AAAAAAAA others(20): Show |
A | 2 | a0001c0001t0001g0296 a0001c0001t0001g0297 |
2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-92-34109_-92-3408 others(31): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472505 | |||||||
chr7:135472505 | AAAAAAAA others(22): Show |
A | 2 | a0001c0001t0001g0281 a0001c0001t0001g0295 |
2 | HG02723.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-92-34111_-92-3408 others(33): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472505 | |||||||
chr7:135472505 | AAAAAAAA others(24): Show |
A | 2 | a0001c0001t0001g0237 a0001c0001t0002g0135 |
2 | HG01175.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-92-34113_-92-3408 others(35): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472505 | |||||||
chr7:135472506 | A | AATATATA others(5): Show |
1 | a0001c0001t0001g0168 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-92-34084_-92-3408 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472506 | |||||||
chr7:135472506 | A | T | 2 | a0001c0001t0001g0309 a0001c0001t0001g0320 |
2 | HG01496.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-92-34083T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472506 | |||||||
chr7:135472506 | AAAAAAAA others(3): Show |
A | 2 | a0002c0002t0001g0046 a0002c0002t0001g0071 |
2 | HG02293.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-92-34093_-92-3408 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472506 | |||||||
chr7:135472506 | AAAAAAAA others(5): Show |
A | 3 | a0001c0001t0001g0326 a0001c0001t0001g0335 a0001c0001t0002g0120 |
3 | HG00280.hp1 HG02602.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.-92-34095_-92-3408 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472506 | |||||||
chr7:135472506 | AAAAAAAA others(13): Show |
A | 2 | a0001c0001t0001g0344 a0001c0001t0003g0350 |
2 | HG02572.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.-92-34103_-92-3408 others(24): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472506 | |||||||
chr7:135472506 | AAAAAAAA others(15): Show |
A | 1 | a0001c0001t0001g0209 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-92-34105_-92-3408 others(26): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472506 | |||||||
chr7:135472506 | AAAAAAAA others(21): Show |
A | 7 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(4): Show |
7 | NA18944.hp1 NA18992.hp1 NA18995.hp2 others(4): Show |
intron_variant | MODIFIER | c.-92-34111_-92-3408 others(32): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472506 | |||||||
chr7:135472506 | AAAAAAAA others(25): Show |
A | 19 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 others(16): Show |
20 | HG00280.hp2 HG01515.hp2 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-34115_-92-3408 others(36): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472506 | |||||||
chr7:135472506 | AAAAAAAA others(29): Show |
A | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-92-34119_-92-3408 others(40): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472506 | |||||||
chr7:135472507 | AAAAAAAA others(4): Show |
A | 5 | a0002c0002t0001g0025 a0002c0002t0001g0030 a0002c0002t0001g0053 others(2): Show |
5 | HG01081.hp1 HG02040.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-34095_-92-3408 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472507 | |||||||
chr7:135472507 | AAAAAAAA others(6): Show |
A | 4 | a0001c0001t0001g0342 a0001c0001t0002g0122 a0001c0001t0002g0123 others(1): Show |
4 | HG01433.hp2 HG03654.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.-92-34097_-92-3408 others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472507 | |||||||
chr7:135472507 | AAAAAAAA others(10): Show |
A | 2 | a0001c0001t0001g0329 a0002c0002t0001g0062 |
2 | HG01169.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-92-34101_-92-3408 others(21): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472507 | |||||||
chr7:135472507 | AAAAAAAA others(12): Show |
A | 1 | a0001c0001t0001g0332 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-92-34103_-92-3408 others(23): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472507 | |||||||
chr7:135472507 | AAAAAAAA others(16): Show |
A | 1 | a0001c0001t0001g0305 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-92-34107_-92-3408 others(27): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472507 | |||||||
chr7:135472507 | AAAAAAAA others(18): Show |
A | 1 | a0001c0001t0001g0327 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-92-34109_-92-3408 others(29): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472507 | |||||||
chr7:135472507 | AAAAAAAA others(20): Show |
A | 1 | a0001c0001t0001g0276 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-92-34111_-92-3408 others(31): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472507 | |||||||
chr7:135472507 | AAAAAAAA others(22): Show |
A | 1 | a0001c0001t0001g0317 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-92-34113_-92-3408 others(33): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472507 | |||||||
chr7:135472507 | AAAAAAAA others(24): Show |
A | 7 | a0001c0001t0001g0228 a0001c0001t0001g0236 a0001c0001t0001g0238 others(4): Show |
7 | HG00639.hp2 HG00738.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.-92-34115_-92-3408 others(35): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472507 | |||||||
chr7:135472508 | A | AATATATA others(3): Show |
2 | a0001c0001t0001g0174 a0001c0001t0001g0176 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-92-34086_-92-3408 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | |||||||
chr7:135472508 | A | AATATATA others(9): Show |
1 | a0001c0001t0001g0152 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-92-34086_-92-3408 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | |||||||
chr7:135472508 | A | ATATATAT | 3 | a0001c0001t0001g0192 a0001c0001t0001g0220 a0002c0002t0001g0092 |
3 | HG02896.hp2 HG02897.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-92-34086_-92-3408 others(11): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | |||||||
chr7:135472508 | A | ATATATAT others(8): Show |
1 | a0002c0002t0001g0026 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-92-34086_-92-3408 others(19): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | |||||||
chr7:135472508 | A | T | 12 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0001g0213 others(9): Show |
12 | HG00323.hp2 HG00642.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.-92-34085T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | |||||||
chr7:135472508 | AAAAAAAA others(3): Show |
A | 7 | a0001c0001t0001g0172 a0001c0001t0002g0121 a0002c0002t0001g0055 others(4): Show |
7 | HG00621.hp1 HG01361.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.-92-34095_-92-3408 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | |||||||
chr7:135472508 | AAAAAAAA others(5): Show |
A | 6 | a0001c0001t0001g0143 a0001c0001t0001g0325 a0001c0001t0001g0341 others(3): Show |
6 | HG01256.hp1 HG01258.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-92-34097_-92-3408 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | |||||||
chr7:135472508 | AAAAAAAA others(7): Show |
A | 2 | a0001c0001t0001g0334 a0001c0001t0001g0339 |
2 | HG00642.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-92-34099_-92-3408 others(18): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | |||||||
chr7:135472508 | AAAAAAAA others(9): Show |
A | 5 | a0001c0001t0001g0175 a0001c0001t0001g0336 a0001c0001t0001g0337 others(2): Show |
5 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-92-34101_-92-3408 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | |||||||
chr7:135472508 | AAAAAAAA others(15): Show |
A | 1 | a0001c0001t0001g0307 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-92-34107_-92-3408 others(26): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | |||||||
chr7:135472508 | AAAAAAAA others(23): Show |
A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0319 |
2 | HG01891.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.-92-34115_-92-3408 others(34): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | |||||||
chr7:135472508 | AAAAAAAA others(25): Show |
A | 13 | a0001c0001t0001g0207 a0001c0001t0001g0229 a0001c0001t0001g0234 others(10): Show |
13 | HG02129.hp2 HG02615.hp2 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.-92-34117_-92-3408 others(36): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | |||||||
chr7:135472508 | AAAAAAAA others(27): Show |
A | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-92-34119_-92-3408 others(38): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | |||||||
chr7:135472509 | AAAAAAAT others(2): Show |
A | 7 | a0001c0001t0001g0219 a0001c0001t0001g0221 a0001c0001t0003g0355 others(4): Show |
7 | HG00673.hp1 HG01516.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.-92-34095_-92-3408 others(13): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472509 | |||||||
chr7:135472509 | AAAAAAAT others(4): Show |
A | 6 | a0001c0001t0002g0118 a0001c0001t0002g0131 a0002c0002t0001g0058 others(3): Show |
6 | HG02486.hp2 HG02723.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-34097_-92-3408 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472509 | |||||||
chr7:135472509 | AAAAAAAT others(6): Show |
A | 2 | a0001c0001t0002g0117 a0002c0002t0001g0070 |
2 | HG01081.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-92-34099_-92-3408 others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472509 | |||||||
chr7:135472509 | AAAAAAAT others(8): Show |
A | 1 | a0001c0001t0002g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-92-34101_-92-3408 others(19): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472509 | |||||||
chr7:135472509 | AAAAAAAT others(14): Show |
A | 1 | a0001c0001t0001g0159 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-92-34107_-92-3408 others(25): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472509 | |||||||
chr7:135472509 | AAAAAAAT others(16): Show |
A | 2 | a0001c0001t0001g0304 a0002c0002t0001g0047 |
2 | HG01256.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-92-34109_-92-3408 others(27): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472509 | |||||||
chr7:135472509 | AAAAAAAT others(22): Show |
A | 2 | a0001c0001t0001g0240 a0002c0002t0001g0302 |
2 | HG03942.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-92-34115_-92-3408 others(33): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472509 | |||||||
chr7:135472509 | AAAAAAAT others(24): Show |
A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0242 a0001c0001t0001g0249 others(3): Show |
7 | HG00438.hp2 HG02572.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-92-34117_-92-3408 others(35): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472509 | |||||||
chr7:135472510 | A | ATAT | 3 | a0001c0001t0001g0191 a0001c0001t0007g0190 a0002c0002t0001g0095 |
3 | HG01943.hp1 NA19074.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-92-34088_-92-3408 others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | |||||||
chr7:135472510 | A | ATATAT | 3 | a0001c0001t0001g0170 a0002c0002t0001g0086 a0002c0002t0001g0112 |
3 | NA18989.hp1 NA19004.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.-92-34088_-92-3408 others(9): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | |||||||
chr7:135472510 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0151 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-92-34088_-92-3408 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | |||||||
chr7:135472510 | A | ATATATAT others(6): Show |
1 | a0002c0002t0001g0089 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-92-34088_-92-3408 others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | |||||||
chr7:135472510 | A | ATATATAT others(10): Show |
1 | a0002c0002t0001g0098 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-92-34088_-92-3408 others(21): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | |||||||
chr7:135472510 | A | T | 26 | a0001c0001t0001g0113 a0001c0001t0001g0152 a0001c0001t0001g0168 others(23): Show |
27 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-92-34087T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | |||||||
chr7:135472510 | AAAAAATA others(3): Show |
A | 6 | a0001c0001t0001g0173 a0001c0001t0002g0225 a0001c0001t0002g0285 others(3): Show |
6 | HG01496.hp1 HG02647.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-34097_-92-3408 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | |||||||
chr7:135472510 | AAAAAATA others(5): Show |
A | 1 | a0002c0002t0001g0106 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-92-34099_-92-3408 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | |||||||
chr7:135472510 | AAAAAATA others(7): Show |
A | 1 | a0001c0001t0001g0328 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-92-34101_-92-3408 others(18): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | |||||||
chr7:135472510 | AAAAAATA others(11): Show |
A | 1 | a0001c0001t0003g0348 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-92-34105_-92-3408 others(22): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | |||||||
chr7:135472510 | AAAAAATA others(15): Show |
A | 1 | a0001c0001t0001g0306 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-92-34109_-92-3408 others(26): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | |||||||
chr7:135472510 | AAAAAATA others(23): Show |
A | 3 | a0001c0001t0001g0230 a0001c0001t0001g0252 a0001c0001t0001g0256 |
3 | HG00609.hp1 HG01934.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-92-34117_-92-3408 others(34): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | |||||||
chr7:135472510 | AAAAAATA others(25): Show |
A | 1 | a0001c0001t0008g0346 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-92-34119_-92-3408 others(36): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | |||||||
chr7:135472510 | AAAAAATA others(27): Show |
A | 1 | a0001c0001t0002g0124 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-92-34121_-92-3408 others(38): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | |||||||
chr7:135472511 | AAAAATAT others(4): Show |
A | 5 | a0001c0001t0002g0293 a0002c0002t0001g0034 a0002c0002t0001g0080 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-92-34099_-92-3408 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472511 | |||||||
chr7:135472511 | AAAAATAT others(8): Show |
A | 1 | a0001c0001t0001g0217 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-92-34103_-92-3408 others(19): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472511 | |||||||
chr7:135472511 | AAAAATAT others(10): Show |
A | 2 | a0002c0002t0001g0079 a0003c0004t0001g0210 |
2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-92-34105_-92-3408 others(21): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472511 | |||||||
chr7:135472512 | A | ATATAT | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0003c0004t0001g0196 |
3 | HG01167.hp2 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-92-34090_-92-3408 others(9): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472512 | |||||||
chr7:135472512 | A | T | 55 | a0001c0001t0001g0113 a0001c0001t0001g0148 a0001c0001t0001g0151 others(52): Show |
56 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.-92-34089T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472512 | |||||||
chr7:135472512 | AAAATATA others(3): Show |
A | 2 | a0002c0002t0001g0063 a0004c0005t0001g0127 |
2 | HG01106.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-92-34099_-92-3409 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472512 | |||||||
chr7:135472512 | AAAATATA others(9): Show |
A | 1 | a0001c0001t0003g0347 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-92-34105_-92-3409 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472512 | |||||||
chr7:135472512 | AAAATATA others(25): Show |
A | 1 | a0001c0001t0001g0115 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-92-34121_-92-3409 others(36): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472512 | |||||||
chr7:135472513 | AAATATAT others(22): Show |
A | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-92-34119_-92-3409 others(33): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472513 | |||||||
chr7:135472514 | A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0218 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(28): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | |||||||
chr7:135472514 | A | AAAAAAAT others(4): Show |
1 | a0001c0001t0001g0155 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | |||||||
chr7:135472514 | A | AAAAAATA others(3): Show |
2 | a0001c0001t0001g0020 a0001c0001t0001g0156 |
2 | NA18945.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.-92-34092_-92-3409 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | |||||||
chr7:135472514 | A | AAAAAATA others(5): Show |
1 | a0001c0001t0001g0007 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | |||||||
chr7:135472514 | A | AAAAAATA others(7): Show |
1 | a0001c0001t0001g0008 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(18): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | |||||||
chr7:135472514 | A | AAAAAATA others(11): Show |
1 | a0001c0001t0001g0206 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(22): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | |||||||
chr7:135472514 | A | AAAAATAT others(6): Show |
1 | a0001c0001t0001g0017 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | |||||||
chr7:135472514 | A | AAAAATAT others(8): Show |
1 | a0001c0001t0001g0019 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(19): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | |||||||
chr7:135472514 | A | AAAATATA others(3): Show |
1 | a0001c0001t0001g0318 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | |||||||
chr7:135472514 | A | AAAATATA others(5): Show |
1 | a0001c0001t0001g0157 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | |||||||
chr7:135472514 | A | AAAATATA others(13): Show |
1 | a0006c0006t0001g0194 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(24): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | |||||||
chr7:135472514 | A | AATATATA others(5): Show |
1 | a0002c0002t0001g0027 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-92-34103_-92-3409 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | |||||||
chr7:135472514 | A | ATATATAT | 3 | a0001c0001t0001g0163 a0001c0001t0001g0188 a0003c0004t0001g0193 |
3 | HG02055.hp2 HG03041.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.-92-34092_-92-3409 others(11): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | |||||||
chr7:135472514 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0164 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | |||||||
chr7:135472514 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0169 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(19): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | |||||||
chr7:135472514 | A | T | 78 | a0001c0001t0001g0009 a0001c0001t0001g0113 a0001c0001t0001g0142 others(75): Show |
79 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-92-34091T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | |||||||
chr7:135472514 | AATATATA others(5): Show |
A | 2 | a0001c0001t0002g0116 a0001c0001t0002g0286 |
2 | HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-92-34103_-92-3409 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | |||||||
chr7:135472515 | ATATATAT others(18): Show |
A | 1 | a0001c0001t0001g0016 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-92-34117_-92-3409 others(29): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472515 | |||||||
chr7:135472520 | T | A | 1 | a0002c0002t0001g0082 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-92-34097A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472520 | |||||||
chr7:135472542 | T | A | 1 | a0001c0001t0001g0016 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-92-34119A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472542 | |||||||
chr7:135472544 | T | A | 1 | a0001c0001t0001g0016 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-92-34121A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472544 | |||||||
chr7:135472558 | T | C | 1 | a0001c0001t0002g0291 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-92-34135A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472558 | |||||||
chr7:135472674 | T | C | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-34251A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472674 | |||||||
chr7:135472680 | T | TATGC | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-34261_-92-3425 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472680 | |||||||
chr7:135472683 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-92-34260C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472683 | |||||||
chr7:135472712 | C | A | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-34289G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472712 | |||||||
chr7:135472884 | C | A | 1 | a0001c0001t0001g0322 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-92-34461G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472884 | |||||||
chr7:135473232 | T | C | 4 | a0001c0001t0001g0152 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
4 | HG00738.hp1 HG01106.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-92-34809A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473232 | |||||||
chr7:135473287 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-92-34864C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473287 | |||||||
chr7:135473312 | T | C | 1 | a0002c0002t0001g0105 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-92-34889A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473312 | |||||||
chr7:135473373 | A | C | 8 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.-92-34950T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473373 | |||||||
chr7:135473425 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-92-35002A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473425 | |||||||
chr7:135473526 | C | T | 1 | a0001c0001t0002g0139 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-92-35103G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473526 | |||||||
chr7:135473591 | A | G | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-35168T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473591 | |||||||
chr7:135473615 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-35192A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473615 | |||||||
chr7:135473685 | C | T | 2 | a0001c0001t0001g0273 a0001c0001t0001g0278 |
2 | NA18944.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-92-35262G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473685 | |||||||
chr7:135473728 | T | C | 1 | a0001c0001t0001g0319 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-92-35305A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473728 | |||||||
chr7:135473833 | A | T | 2 | a0001c0001t0003g0355 a0001c0001t0003g0356 |
2 | NA18939.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.-92-35410T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473833 | |||||||
chr7:135473852 | T | G | 1 | a0002c0002t0001g0079 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-92-35429A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473852 | |||||||
chr7:135473982 | G | GT | 30 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0142 others(27): Show |
30 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.-92-35560dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473982 | |||||||
chr7:135473982 | GT | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(54): Show |
59 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-92-35560delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473982 | |||||||
chr7:135474038 | G | GGTGCAAT others(1): Show |
18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-35623_-92-3561 others(12): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474038 | |||||||
chr7:135474276 | A | AT | 66 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(63): Show |
66 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.-93+35612dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474276 | |||||||
chr7:135474276 | A | ATT | 24 | a0001c0001t0001g0240 a0001c0001t0001g0250 a0001c0001t0001g0329 others(21): Show |
24 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.-93+35611_-93+3561 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474276 | |||||||
chr7:135474276 | A | ATTT | 6 | a0001c0001t0001g0327 a0001c0001t0001g0331 a0001c0001t0001g0332 others(3): Show |
6 | HG00733.hp2 HG00735.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+35610_-93+3561 others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474276 | |||||||
chr7:135474276 | AT | A | 48 | a0001c0001t0001g0007 a0001c0001t0001g0141 a0001c0001t0001g0175 others(45): Show |
48 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.-93+35612delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474276 | |||||||
chr7:135474276 | ATTTTTTT others(3): Show |
A | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+35603_-93+3561 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474276 | |||||||
chr7:135474616 | T | C | 2 | a0001c0001t0003g0347 a0001c0001t0003g0348 |
2 | HG00597.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.-93+35273A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474616 | |||||||
chr7:135474644 | G | A | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+35245C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474644 | |||||||
chr7:135474833 | T | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-93+35056A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474833 | |||||||
chr7:135474844 | T | A | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-93+35045A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474844 | |||||||
chr7:135474892 | T | G | 69 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(66): Show |
71 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.-93+34997A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474892 | |||||||
chr7:135475097 | G | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+34792C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135475097 | |||||||
chr7:135475419 | G | A | 1 | a0001c0001t0007g0190 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-93+34470C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135475419 | |||||||
chr7:135475521 | C | T | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+34368G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135475521 | |||||||
chr7:135475606 | T | C | 1 | a0001c0001t0001g0333 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-93+34283A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135475606 | |||||||
chr7:135475632 | G | A | 1 | a0002c0002t0001g0090 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-93+34257C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135475632 | |||||||
chr7:135475746 | C | A | 2 | a0002c0002t0001g0110 a0002c0002t0001g0111 |
2 | NA18956.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.-93+34143G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135475746 | |||||||
chr7:135475930 | T | C | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG03834.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-93+33959A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135475930 | |||||||
chr7:135475955 | A | G | 1 | a0002c0002t0001g0082 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-93+33934T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135475955 | |||||||
chr7:135476231 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-93+33658C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135476231 | |||||||
chr7:135476232 | A | T | 1 | a0001c0001t0001g0227 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-93+33657T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135476232 | |||||||
chr7:135476520 | G | A | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-93+33369C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135476520 | |||||||
chr7:135476697 | T | C | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+33192A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135476697 | |||||||
chr7:135477089 | C | T | 1 | a0002c0002t0001g0099 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-93+32800G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477089 | |||||||
chr7:135477139 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-93+32750G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477139 | |||||||
chr7:135477217 | C | G | 1 | a0001c0001t0002g0291 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-93+32672G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477217 | |||||||
chr7:135477343 | C | CA | 106 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(103): Show |
108 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.-93+32545dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477343 | |||||||
chr7:135477524 | ATCTTGTA others(6): Show |
A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0242 |
2 | HG00438.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-93+32352_-93+3236 others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477524 | |||||||
chr7:135477594 | A | C | 1 | a0002c0002t0001g0091 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-93+32295T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477594 | |||||||
chr7:135477614 | C | T | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+32275G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477614 | |||||||
chr7:135477631 | T | A | 1 | a0001c0001t0001g0148 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-93+32258A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477631 | |||||||
chr7:135477633 | T | A | 1 | a0001c0001t0001g0148 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-93+32256A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477633 | |||||||
chr7:135477637 | C | G | 1 | a0001c0001t0001g0148 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-93+32252G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477637 | |||||||
chr7:135477638 | T | A | 1 | a0001c0001t0001g0148 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-93+32251A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477638 | |||||||
chr7:135477641 | A | T | 1 | a0001c0001t0001g0148 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-93+32248T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477641 | |||||||
chr7:135477642 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-93+32247A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477642 | |||||||
chr7:135477644 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-93+32245G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477644 | |||||||
chr7:135477875 | T | A | 1 | a0001c0001t0002g0117 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-93+32014A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477875 | |||||||
chr7:135477893 | CCAATATA others(10): Show |
C | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-93+31979_-93+3199 others(21): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477893 | |||||||
chr7:135477960 | TTAATA | T | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+31924_-93+3192 others(9): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477960 | |||||||
chr7:135477964 | T | C | 1 | a0001c0001t0002g0294 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-93+31925A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477964 | |||||||
chr7:135478149 | C | T | 258 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(255): Show |
262 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.-93+31740G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478149 | |||||||
chr7:135478179 | C | T | 122 | a0001c0001t0001g0119 a0001c0001t0002g0117 a0001c0001t0002g0118 others(119): Show |
124 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-93+31710G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478179 | |||||||
chr7:135478187 | A | G | 61 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(58): Show |
63 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-93+31702T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478187 | |||||||
chr7:135478235 | T | G | 1 | a0001c0001t0001g0263 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-93+31654A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478235 | |||||||
chr7:135478314 | A | G | 38 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(35): Show |
38 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.-93+31575T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478314 | |||||||
chr7:135478506 | C | T | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-93+31383G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478506 | |||||||
chr7:135478544 | A | G | 3 | a0001c0001t0002g0224 a0001c0001t0002g0225 a0001c0001t0002g0226 |
3 | HG00099.hp1 HG00323.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-93+31345T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478544 | |||||||
chr7:135478773 | A | C | 1 | a0001c0001t0001g0148 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-93+31116T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478773 | |||||||
chr7:135478787 | G | C | 17 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(14): Show |
17 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-93+31102C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478787 | |||||||
chr7:135478811 | C | T | 2 | a0001c0001t0001g0338 a0001c0001t0001g0339 |
2 | HG00642.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-93+31078G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478811 | |||||||
chr7:135478817 | A | G | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+31072T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478817 | |||||||
chr7:135479003 | C | T | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+30886G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479003 | |||||||
chr7:135479045 | T | C | 2 | a0002c0002t0001g0042 a0002c0002t0001g0063 |
2 | HG01515.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-93+30844A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479045 | |||||||
chr7:135479089 | C | T | 3 | a0002c0002t0001g0179 a0002c0002t0001g0180 a0002c0002t0001g0181 |
3 | NA18975.hp1 NA19084.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-93+30800G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479089 | |||||||
chr7:135479121 | C | T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0259 |
2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-93+30768G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479121 | |||||||
chr7:135479198 | A | AT | 33 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0142 others(30): Show |
33 | HG00639.hp1 HG01069.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.-93+30690dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479198 | |||||||
chr7:135479198 | A | ATT | 63 | a0001c0001t0001g0003 a0001c0001t0001g0141 a0001c0001t0001g0228 others(60): Show |
65 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.-93+30689_-93+3069 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479198 | |||||||
chr7:135479198 | A | ATTT | 17 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0242 others(14): Show |
17 | HG00438.hp2 HG01123.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-93+30688_-93+3069 others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479198 | |||||||
chr7:135479198 | AT | A | 39 | a0001c0001t0001g0017 a0001c0001t0001g0119 a0001c0001t0001g0147 others(36): Show |
39 | HG00642.hp1 HG00733.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.-93+30690delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479198 | |||||||
chr7:135479198 | ATT | A | 14 | a0001c0001t0001g0344 a0001c0001t0002g0286 a0001c0001t0002g0287 others(11): Show |
14 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-93+30689_-93+3069 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479198 | |||||||
chr7:135479198 | ATTTTTTT others(3): Show |
A | 1 | a0002c0002t0001g0069 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-93+30681_-93+3069 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479198 | |||||||
chr7:135479198 | ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0316 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-93+30677_-93+3069 others(18): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479198 | |||||||
chr7:135479333 | C | G | 2 | a0001c0001t0001g0240 a0001c0001t0001g0259 |
2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-93+30556G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479333 | |||||||
chr7:135479431 | G | A | 3 | a0001c0001t0001g0229 a0001c0001t0001g0248 a0001c0001t0001g0257 |
3 | NA18957.hp1 NA18975.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-93+30458C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479431 | |||||||
chr7:135479451 | C | T | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+30438G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479451 | |||||||
chr7:135479501 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-93+30388C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479501 | |||||||
chr7:135479556 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-93+30333C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479556 | |||||||
chr7:135479575 | A | AT | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+30313dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479575 | |||||||
chr7:135479590 | T | C | 1 | a0001c0001t0001g0344 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-93+30299A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479590 | |||||||
chr7:135479672 | A | G | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-93+30217T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479672 | |||||||
chr7:135479753 | C | T | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+30136G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479753 | |||||||
chr7:135479918 | T | C | 1 | a0001c0001t0001g0344 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-93+29971A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479918 | |||||||
chr7:135479960 | CTAAT | C | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+29925_-93+2992 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479960 | |||||||
chr7:135480202 | C | T | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+29687G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135480202 | |||||||
chr7:135480368 | T | C | 1 | a0001c0001t0001g0019 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-93+29521A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135480368 | |||||||
chr7:135480527 | G | A | 38 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(35): Show |
38 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.-93+29362C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135480527 | |||||||
chr7:135480672 | C | A | 1 | a0002c0002t0001g0084 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-93+29217G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135480672 | |||||||
chr7:135480739 | C | T | 1 | a0002c0002t0001g0041 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-93+29150G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135480739 | |||||||
chr7:135480888 | C | CA | 21 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0171 others(18): Show |
21 | HG01099.hp1 HG01243.hp2 HG01981.hp1 others(18): Show |
intron_variant | MODIFIER | c.-93+29000dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135480888 | |||||||
chr7:135480888 | C | CAA | 30 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(27): Show |
30 | HG00597.hp2 HG00733.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.-93+28999_-93+2900 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135480888 | |||||||
chr7:135480906 | T | A | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+28983A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135480906 | |||||||
chr7:135480995 | GA | G | 22 | a0001c0001t0001g0141 a0001c0001t0001g0208 a0001c0001t0001g0209 others(19): Show |
22 | HG00597.hp2 HG01358.hp2 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.-93+28893delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135480995 | |||||||
chr7:135481007 | A | C | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+28882T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135481007 | |||||||
chr7:135481073 | A | C | 1 | a0001c0001t0001g0020 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-93+28816T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135481073 | |||||||
chr7:135481076 | A | G | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+28813T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135481076 | |||||||
chr7:135481211 | A | G | 1 | a0005c0007t0001g0308 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-93+28678T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135481211 | |||||||
chr7:135481219 | C | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+28670G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135481219 | |||||||
chr7:135481280 | T | C | 1 | a0001c0001t0002g0294 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-93+28609A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135481280 | |||||||
chr7:135481321 | T | C | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+28568A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135481321 | |||||||
chr7:135481773 | C | T | 122 | a0001c0001t0001g0119 a0001c0001t0002g0117 a0001c0001t0002g0118 others(119): Show |
124 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-93+28116G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135481773 | |||||||
chr7:135481910 | A | T | 1 | a0001c0001t0001g0195 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-93+27979T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135481910 | |||||||
chr7:135481956 | G | C | 61 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(58): Show |
63 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-93+27933C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135481956 | |||||||
chr7:135482039 | T | C | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+27850A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482039 | |||||||
chr7:135482251 | T | C | 186 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0147 others(183): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.-93+27638A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482251 | |||||||
chr7:135482443 | C | A | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-93+27446G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482443 | |||||||
chr7:135482482 | G | C | 1 | a0002c0002t0001g0084 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-93+27407C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482482 | |||||||
chr7:135482543 | C | A | 1 | a0006c0006t0001g0194 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-93+27346G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482543 | |||||||
chr7:135482612 | T | C | 1 | a0001c0001t0001g0344 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-93+27277A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482612 | |||||||
chr7:135482678 | C | T | 1 | a0006c0006t0001g0194 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-93+27211G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482678 | |||||||
chr7:135482702 | C | T | 2 | a0001c0001t0001g0325 a0001c0001t0001g0326 |
2 | NA18953.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-93+27187G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482702 | |||||||
chr7:135482986 | C | CA | 24 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0278 others(21): Show |
24 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.-93+26902dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482986 | |||||||
chr7:135482986 | CA | C | 30 | a0001c0001t0001g0141 a0001c0001t0001g0272 a0001c0001t0001g0295 others(27): Show |
30 | HG00280.hp1 HG00597.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.-93+26902delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482986 | |||||||
chr7:135482986 | CAA | C | 8 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93+26901_-93+2690 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482986 | |||||||
chr7:135482986 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0271 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-93+26893_-93+2690 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482986 | |||||||
chr7:135483152 | T | C | 101 | a0001c0001t0001g0241 a0002c0002t0001g0001 a0002c0002t0001g0002 others(98): Show |
103 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.-93+26737A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483152 | |||||||
chr7:135483171 | CA | C | 13 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(10): Show |
13 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(10): Show |
intron_variant | MODIFIER | c.-93+26717delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483171 | |||||||
chr7:135483178 | A | T | 1 | a0001c0001t0003g0348 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-93+26711T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483178 | |||||||
chr7:135483180 | T | A | 1 | a0001c0001t0003g0348 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-93+26709A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483180 | |||||||
chr7:135483180 | T | TA | 3 | a0001c0001t0001g0240 a0001c0001t0001g0260 a0001c0001t0001g0261 |
3 | HG03834.hp2 HG03942.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-93+26708_-93+2670 others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483180 | |||||||
chr7:135483181 | T | A | 30 | a0001c0001t0001g0141 a0001c0001t0001g0145 a0001c0001t0001g0146 others(27): Show |
30 | HG00597.hp2 HG01243.hp2 HG02083.hp2 others(27): Show |
intron_variant | MODIFIER | c.-93+26708A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483181 | |||||||
chr7:135483181 | T | TA | 52 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(49): Show |
54 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-93+26707dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483181 | |||||||
chr7:135483181 | TA | T | 23 | a0001c0001t0001g0147 a0001c0001t0001g0327 a0001c0001t0001g0328 others(20): Show |
23 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.-93+26707delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483181 | |||||||
chr7:135483182 | A | T | 1 | a0002c0002t0001g0082 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-93+26707T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483182 | |||||||
chr7:135483199 | C | T | 261 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(258): Show |
265 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.-93+26690G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483199 | |||||||
chr7:135483251 | T | C | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+26638A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483251 | |||||||
chr7:135483252 | T | C | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+26637A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483252 | |||||||
chr7:135483337 | C | CAA | 17 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(14): Show |
17 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-93+26550_-93+2655 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483337 | |||||||
chr7:135483349 | T | A | 2 | a0002c0002t0001g0068 a0002c0002t0001g0069 |
2 | HG01358.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.-93+26540A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483349 | |||||||
chr7:135483387 | A | T | 1 | a0001c0001t0001g0223 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-93+26502T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483387 | |||||||
chr7:135483592 | G | C | 1 | a0001c0001t0001g0267 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-93+26297C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483592 | |||||||
chr7:135483653 | G | A | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+26236C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483653 | |||||||
chr7:135483719 | G | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+26170C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483719 | |||||||
chr7:135483759 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-93+26130A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483759 | |||||||
chr7:135483893 | A | G | 3 | a0002c0002t0001g0298 a0002c0002t0001g0299 a0002c0002t0001g0301 |
3 | HG02055.hp1 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-93+25996T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483893 | |||||||
chr7:135483941 | A | G | 1 | a0001c0001t0001g0322 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-93+25948T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483941 | |||||||
chr7:135483991 | C | T | 6 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0149 others(3): Show |
6 | HG01123.hp2 NA18968.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+25898G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483991 | |||||||
chr7:135484503 | T | A | 1 | a0001c0001t0001g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-93+25386A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135484503 | |||||||
chr7:135484666 | C | T | 122 | a0001c0001t0001g0119 a0001c0001t0002g0117 a0001c0001t0002g0118 others(119): Show |
124 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-93+25223G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135484666 | |||||||
chr7:135484754 | C | CA | 13 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0269 others(10): Show |
13 | HG00735.hp1 HG02071.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.-93+25134dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135484754 | |||||||
chr7:135484893 | A | G | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+24996T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135484893 | |||||||
chr7:135484942 | C | T | 2 | a0002c0002t0001g0025 a0002c0002t0001g0040 |
2 | HG01081.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-93+24947G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135484942 | |||||||
chr7:135485134 | A | G | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+24755T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485134 | |||||||
chr7:135485139 | C | T | 16 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(13): Show |
16 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-93+24750G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485139 | |||||||
chr7:135485175 | C | T | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+24714G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485175 | |||||||
chr7:135485198 | G | A | 3 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0292 |
3 | HG02145.hp2 HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-93+24691C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485198 | |||||||
chr7:135485225 | G | A | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-93+24664C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485225 | |||||||
chr7:135485361 | C | T | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-93+24528G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485361 | |||||||
chr7:135485368 | C | T | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+24521G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485368 | |||||||
chr7:135485454 | T | TAAAAACA others(3): Show |
6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+24434_-93+2443 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485454 | |||||||
chr7:135485700 | A | G | 261 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0141 others(258): Show |
265 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.-93+24189T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485700 | |||||||
chr7:135485722 | C | T | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+24167G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485722 | |||||||
chr7:135485776 | C | T | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-93+24113G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485776 | |||||||
chr7:135485911 | CA | C | 2 | a0002c0002t0001g0001 a0002c0002t0001g0023 |
3 | NA18986.hp2 NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-93+23977delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485911 | |||||||
chr7:135486007 | G | A | 17 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(14): Show |
17 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-93+23882C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135486007 | |||||||
chr7:135486055 | G | T | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+23834C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135486055 | |||||||
chr7:135486100 | A | T | 2 | a0001c0001t0001g0336 a0001c0001t0001g0337 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-93+23789T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135486100 | |||||||
chr7:135486350 | A | G | 105 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(102): Show |
107 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.-93+23539T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135486350 | |||||||
chr7:135486485 | A | G | 3 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 |
3 | HG02486.hp1 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-93+23404T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135486485 | |||||||
chr7:135486754 | AACTCAGA others(4): Show |
A | 2 | a0002c0002t0001g0030 a0002c0002t0001g0100 |
2 | NA18957.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.-93+23124_-93+2313 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135486754 | |||||||
chr7:135486829 | A | G | 8 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93+23060T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135486829 | |||||||
chr7:135486887 | C | A | 1 | a0002c0002t0001g0080 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-93+23002G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135486887 | |||||||
chr7:135486902 | T | G | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-93+22987A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135486902 | |||||||
chr7:135486963 | C | T | 16 | a0001c0001t0001g0141 a0001c0001t0001g0322 a0001c0001t0001g0325 others(13): Show |
16 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-93+22926G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135486963 | |||||||
chr7:135487042 | T | G | 3 | a0001c0001t0002g0224 a0001c0001t0002g0225 a0001c0001t0002g0226 |
3 | HG00099.hp1 HG00323.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-93+22847A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487042 | |||||||
chr7:135487110 | T | C | 4 | a0001c0001t0001g0149 a0001c0001t0001g0165 a0001c0001t0001g0166 others(1): Show |
4 | NA18980.hp1 NA18994.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93+22779A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487110 | |||||||
chr7:135487161 | A | G | 16 | a0001c0001t0001g0141 a0001c0001t0001g0322 a0001c0001t0001g0325 others(13): Show |
16 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-93+22728T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487161 | |||||||
chr7:135487189 | C | CT | 25 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(22): Show |
25 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.-93+22699dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487189 | |||||||
chr7:135487290 | T | C | 1 | a0001c0001t0001g0319 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-93+22599A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487290 | |||||||
chr7:135487319 | C | A | 1 | a0001c0001t0002g0293 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-93+22570G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487319 | |||||||
chr7:135487384 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-93+22505G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487384 | |||||||
chr7:135487468 | A | G | 128 | a0001c0001t0001g0119 a0001c0001t0001g0304 a0001c0001t0001g0305 others(125): Show |
130 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.-93+22421T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487468 | |||||||
chr7:135487478 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-93+22411C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487478 | |||||||
chr7:135487643 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-93+22246T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487643 | |||||||
chr7:135487698 | A | G | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-93+22191T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487698 | |||||||
chr7:135487744 | C | T | 1 | a0003c0004t0001g0193 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-93+22145G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487744 | |||||||
chr7:135487781 | C | T | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
5 | NA18945.hp1 NA18963.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.-93+22108G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487781 | |||||||
chr7:135487792 | G | A | 1 | a0001c0001t0001g0344 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-93+22097C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487792 | |||||||
chr7:135487981 | C | A | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+21908G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487981 | |||||||
chr7:135488072 | G | A | 287 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(284): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-93+21817C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135488072 | |||||||
chr7:135488296 | G | A | 1 | a0001c0001t0002g0225 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-93+21593C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135488296 | |||||||
chr7:135488522 | A | C | 1 | a0002c0002t0001g0051 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-93+21367T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135488522 | |||||||
chr7:135488540 | C | G | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+21349G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135488540 | |||||||
chr7:135488549 | G | A | 4 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(1): Show |
4 | NA18941.hp1 NA18953.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+21340C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135488549 | |||||||
chr7:135488796 | C | T | 34 | a0001c0001t0001g0141 a0001c0001t0001g0322 a0001c0001t0001g0325 others(31): Show |
34 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.-93+21093G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135488796 | |||||||
chr7:135488981 | G | A | 99 | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0023 others(96): Show |
101 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.-93+20908C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135488981 | |||||||
chr7:135489214 | G | A | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+20675C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489214 | |||||||
chr7:135489384 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-93+20505G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489384 | |||||||
chr7:135489391 | C | CT | 22 | a0001c0001t0001g0142 a0001c0001t0001g0149 a0001c0001t0001g0153 others(19): Show |
22 | HG00438.hp2 HG00738.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.-93+20497dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489391 | |||||||
chr7:135489391 | CT | C | 117 | a0001c0001t0001g0204 a0001c0001t0001g0264 a0001c0001t0001g0265 others(114): Show |
119 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(116): Show |
intron_variant | MODIFIER | c.-93+20497delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489391 | |||||||
chr7:135489391 | CTTTTTTT others(1): Show |
C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+20490_-93+2049 others(12): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489391 | |||||||
chr7:135489391 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-93+20486_-93+2049 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489391 | |||||||
chr7:135489427 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-93+20462C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489427 | |||||||
chr7:135489685 | T | C | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+20204A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489685 | |||||||
chr7:135489693 | G | A | 1 | a0001c0001t0002g0293 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-93+20196C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489693 | |||||||
chr7:135489738 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-93+20151A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489738 | |||||||
chr7:135489747 | T | C | 2 | a0001c0001t0003g0355 a0001c0001t0003g0356 |
2 | NA18939.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.-93+20142A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489747 | |||||||
chr7:135489939 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-93+19950A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489939 | |||||||
chr7:135490120 | G | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+19769C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135490120 | |||||||
chr7:135490144 | T | C | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+19745A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135490144 | |||||||
chr7:135490176 | T | G | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+19713A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135490176 | |||||||
chr7:135490238 | C | T | 17 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(14): Show |
17 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-93+19651G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135490238 | |||||||
chr7:135490298 | C | T | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG00738.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-93+19591G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135490298 | |||||||
chr7:135490551 | AAT | A | 17 | a0001c0001t0002g0285 a0001c0001t0002g0286 a0001c0001t0002g0287 others(14): Show |
17 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-93+19336_-93+1933 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135490551 | |||||||
chr7:135490578 | A | G | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+19311T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135490578 | |||||||
chr7:135491452 | A | C | 2 | a0001c0001t0001g0145 a0001c0001t0008g0346 |
2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-93+18437T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135491452 | |||||||
chr7:135491723 | G | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+18166C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135491723 | |||||||
chr7:135491800 | G | A | 1 | a0002c0002t0001g0106 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-93+18089C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135491800 | |||||||
chr7:135491940 | T | C | 1 | a0001c0001t0001g0319 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-93+17949A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135491940 | |||||||
chr7:135492004 | G | A | 1 | a0002c0002t0001g0081 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-93+17885C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492004 | |||||||
chr7:135492204 | T | C | 1 | a0001c0001t0001g0239 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-93+17685A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492204 | |||||||
chr7:135492243 | T | A | 1 | a0001c0001t0001g0018 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-93+17646A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492243 | |||||||
chr7:135492271 | T | G | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+17618A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492271 | |||||||
chr7:135492468 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-93+17421G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492468 | |||||||
chr7:135492491 | C | G | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+17398G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492491 | |||||||
chr7:135492504 | G | A | 1 | a0002c0002t0001g0070 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-93+17385C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492504 | |||||||
chr7:135492523 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0217 |
2 | NA18942.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-93+17366G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492523 | |||||||
chr7:135492588 | C | G | 1 | a0002c0002t0001g0043 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-93+17301G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492588 | |||||||
chr7:135492632 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-93+17257A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492632 | |||||||
chr7:135492947 | A | G | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+16942T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492947 | |||||||
chr7:135493001 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-93+16888A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135493001 | |||||||
chr7:135493011 | C | G | 1 | a0001c0001t0001g0240 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-93+16878G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135493011 | |||||||
chr7:135493195 | T | G | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+16694A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135493195 | |||||||
chr7:135493279 | T | C | 234 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(231): Show |
236 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.-93+16610A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135493279 | |||||||
chr7:135493312 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-93+16577G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135493312 | |||||||
chr7:135493726 | T | C | 1 | a0001c0001t0001g0317 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-93+16163A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135493726 | |||||||
chr7:135493862 | G | A | 1 | a0002c0002t0001g0300 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-93+16027C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135493862 | |||||||
chr7:135494065 | C | CA | 25 | a0001c0001t0001g0141 a0001c0001t0001g0147 a0001c0001t0001g0167 others(22): Show |
25 | HG00597.hp2 HG00733.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.-93+15823dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494065 | |||||||
chr7:135494065 | CA | C | 118 | a0001c0001t0001g0119 a0001c0001t0001g0334 a0001c0001t0002g0117 others(115): Show |
120 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.-93+15823delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494065 | |||||||
chr7:135494083 | C | T | 1 | a0001c0001t0004g0004 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-93+15806G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494083 | |||||||
chr7:135494195 | C | CGCAGTGG others(26): Show |
1 | a0002c0002t0001g0098 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-93+15661_-93+1569 others(37): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494195 | |||||||
chr7:135494448 | C | T | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+15441G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494448 | |||||||
chr7:135494470 | CA | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(204): Show |
209 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.-93+15418delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494470 | |||||||
chr7:135494470 | CAA | C | 109 | a0001c0001t0001g0232 a0001c0001t0001g0236 a0001c0001t0001g0239 others(106): Show |
111 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.-93+15417_-93+1541 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494470 | |||||||
chr7:135494677 | A | G | 1 | a0002c0002t0001g0086 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-93+15212T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494677 | |||||||
chr7:135494717 | G | C | 1 | a0001c0001t0002g0226 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-93+15172C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494717 | |||||||
chr7:135494737 | A | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(66): Show |
71 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.-93+15152T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494737 | |||||||
chr7:135494758 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-93+15131C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494758 | |||||||
chr7:135494890 | T | C | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+14999A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494890 | |||||||
chr7:135495038 | G | A | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+14851C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495038 | |||||||
chr7:135495181 | G | C | 16 | a0001c0001t0001g0141 a0001c0001t0001g0322 a0001c0001t0001g0325 others(13): Show |
16 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-93+14708C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495181 | |||||||
chr7:135495242 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-93+14647G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495242 | |||||||
chr7:135495323 | G | A | 1 | a0001c0001t0003g0356 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-93+14566C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495323 | |||||||
chr7:135495347 | A | C | 2 | a0002c0002t0001g0024 a0002c0002t0001g0027 |
2 | NA19007.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.-93+14542T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495347 | |||||||
chr7:135495488 | G | A | 39 | a0002c0002t0001g0002 a0002c0002t0001g0031 a0002c0002t0001g0033 others(36): Show |
40 | HG00438.hp1 HG00673.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-93+14401C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495488 | |||||||
chr7:135495492 | G | A | 3 | a0002c0002t0001g0179 a0002c0002t0001g0180 a0002c0002t0001g0181 |
3 | NA18975.hp1 NA19084.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-93+14397C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495492 | |||||||
chr7:135495504 | C | CA | 32 | a0001c0001t0001g0019 a0001c0001t0001g0119 a0001c0001t0001g0148 others(29): Show |
32 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.-93+14384dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495504 | |||||||
chr7:135495504 | CA | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0141 a0001c0001t0001g0147 others(181): Show |
188 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(185): Show |
intron_variant | MODIFIER | c.-93+14384delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495504 | |||||||
chr7:135495504 | CAA | C | 8 | a0001c0001t0001g0279 a0001c0001t0001g0304 a0001c0001t0001g0305 others(5): Show |
8 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93+14383_-93+1438 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495504 | |||||||
chr7:135495662 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-93+14227G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495662 | |||||||
chr7:135495669 | CAAAAAAA others(5): Show |
C | 1 | a0002c0002t0001g0049 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-93+14208_-93+1421 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495669 | |||||||
chr7:135495678 | AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0001g0219 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-93+14195_-93+1421 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495678 | |||||||
chr7:135495678 | AAAAAAAA others(13): Show |
A | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG02015.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-93+14191_-93+1421 others(24): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495678 | |||||||
chr7:135495678 | AAAAAAAA others(25): Show |
A | 1 | a0003c0004t0001g0222 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-93+14179_-93+1421 others(36): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495678 | |||||||
chr7:135495679 | AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0200 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-93+14195_-93+1420 others(19): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495679 | |||||||
chr7:135495679 | AAAAAAAA others(16): Show |
A | 1 | a0001c0001t0001g0192 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-93+14187_-93+1420 others(27): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495679 | |||||||
chr7:135495683 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0002g0225 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-93+14195_-93+1420 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495683 | |||||||
chr7:135495683 | AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0255 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-93+14191_-93+1420 others(19): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495683 | |||||||
chr7:135495683 | AAAAAAAA others(12): Show |
A | 3 | a0001c0001t0003g0349 a0002c0002t0001g0028 a0002c0002t0001g0069 |
3 | HG01358.hp1 NA18948.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.-93+14187_-93+1420 others(23): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495683 | |||||||
chr7:135495683 | AAAAAAAA others(16): Show |
A | 2 | a0002c0002t0001g0066 a0002c0002t0001g0073 |
2 | HG02257.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.-93+14183_-93+1420 others(27): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495683 | |||||||
chr7:135495683 | AAAAAAAA others(24): Show |
A | 1 | a0002c0002t0001g0070 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-93+14175_-93+1420 others(35): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495683 | |||||||
chr7:135495684 | AAAAAAAA others(7): Show |
A | 5 | a0001c0001t0001g0147 a0001c0001t0001g0325 a0001c0001t0001g0326 others(2): Show |
5 | HG01081.hp2 HG03209.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.-93+14191_-93+1420 others(18): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495684 | |||||||
chr7:135495684 | AAAAAAAA others(11): Show |
A | 12 | a0001c0001t0001g0141 a0001c0001t0003g0347 a0001c0001t0003g0348 others(9): Show |
12 | HG00597.hp2 HG02083.hp2 HG03490.hp2 others(9): Show |
intron_variant | MODIFIER | c.-93+14187_-93+1420 others(22): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495684 | |||||||
chr7:135495684 | AAAAAAAA others(15): Show |
A | 3 | a0002c0002t0001g0023 a0002c0002t0001g0092 a0002c0002t0001g0101 |
3 | NA18998.hp2 NA19079.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-93+14183_-93+1420 others(26): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495684 | |||||||
chr7:135495684 | AAAAAAAA others(19): Show |
A | 1 | a0002c0002t0001g0087 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-93+14179_-93+1420 others(30): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495684 | |||||||
chr7:135495684 | AAAAAAAA others(23): Show |
A | 1 | a0002c0002t0001g0071 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-93+14175_-93+1420 others(34): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495684 | |||||||
chr7:135495685 | AAAAAAAA others(6): Show |
A | 1 | a0002c0002t0001g0089 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-93+14191_-93+1420 others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495685 | |||||||
chr7:135495685 | AAAAAAAA others(10): Show |
A | 3 | a0001c0001t0001g0231 a0001c0001t0003g0350 a0001c0010t0002g0324 |
3 | HG01261.hp1 HG02683.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.-93+14187_-93+1420 others(21): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495685 | |||||||
chr7:135495685 | AAAAAAAA others(14): Show |
A | 6 | a0001c0001t0001g0256 a0001c0001t0001g0269 a0001c0001t0001g0278 others(3): Show |
6 | HG00609.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+14183_-93+1420 others(25): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495685 | |||||||
chr7:135495685 | AAAAAAAA others(18): Show |
A | 2 | a0001c0001t0001g0249 a0001c0001t0001g0282 |
2 | NA18940.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-93+14179_-93+1420 others(29): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495685 | |||||||
chr7:135495685 | AAAAAAAA others(22): Show |
A | 1 | a0001c0001t0001g0243 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-93+14175_-93+1420 others(33): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495685 | |||||||
chr7:135495685 | AAAAAAAA others(46): Show |
A | 1 | a0001c0001t0001g0329 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-93+14151_-93+1420 others(57): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495685 | |||||||
chr7:135495686 | AAAAAAAA others(1): Show |
A | 14 | a0001c0001t0002g0120 a0001c0001t0002g0224 a0001c0001t0002g0226 others(11): Show |
14 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+14195_-93+1420 others(12): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495686 | |||||||
chr7:135495686 | AAAAAAAA others(5): Show |
A | 11 | a0001c0001t0002g0285 a0002c0002t0001g0026 a0002c0002t0001g0033 others(8): Show |
11 | HG01496.hp1 HG03491.hp1 HG03669.hp2 others(8): Show |
intron_variant | MODIFIER | c.-93+14191_-93+1420 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495686 | |||||||
chr7:135495686 | AAAAAAAA others(9): Show |
A | 2 | a0001c0001t0002g0288 a0002c0002t0001g0079 |
2 | HG01346.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.-93+14187_-93+1420 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495686 | |||||||
chr7:135495686 | AAAAAAAA others(13): Show |
A | 5 | a0002c0002t0001g0024 a0002c0002t0001g0027 a0002c0002t0001g0030 others(2): Show |
5 | NA18941.hp2 NA18947.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.-93+14183_-93+1420 others(24): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495686 | |||||||
chr7:135495686 | AAAAAAAA others(17): Show |
A | 14 | a0001c0001t0001g0246 a0002c0002t0001g0001 a0002c0002t0001g0041 others(11): Show |
14 | HG00609.hp2 HG01515.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+14179_-93+1420 others(28): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495686 | |||||||
chr7:135495686 | AAAAAAAA others(21): Show |
A | 18 | a0001c0001t0001g0316 a0001c0001t0002g0125 a0002c0002t0001g0001 others(15): Show |
18 | HG00597.hp1 HG00621.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+14175_-93+1420 others(32): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495686 | |||||||
chr7:135495686 | AAAAAAAA others(25): Show |
A | 3 | a0001c0001t0002g0131 a0002c0002t0001g0053 a0002c0002t0001g0086 |
3 | HG02486.hp2 NA19004.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-93+14171_-93+1420 others(36): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495686 | |||||||
chr7:135495686 | AAAAAAAA others(29): Show |
A | 1 | a0002c0002t0001g0129 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-93+14167_-93+1420 others(40): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495686 | |||||||
chr7:135495686 | AAAAAAAA others(33): Show |
A | 4 | a0001c0001t0002g0130 a0001c0001t0002g0132 a0001c0001t0002g0133 others(1): Show |
4 | HG02818.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93+14163_-93+1420 others(44): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495686 | |||||||
chr7:135495686 | AAAAAAAA others(45): Show |
A | 17 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0330 others(14): Show |
17 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-93+14151_-93+1420 others(56): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495686 | |||||||
chr7:135495687 | AAAAAAAG | A | 11 | a0001c0001t0001g0214 a0001c0001t0001g0241 a0001c0001t0002g0118 others(8): Show |
11 | HG00438.hp1 HG01071.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-93+14195_-93+1420 others(11): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495687 | |||||||
chr7:135495687 | AAAAAAAG others(4): Show |
A | 7 | a0001c0001t0001g0267 a0001c0001t0001g0297 a0002c0002t0001g0054 others(4): Show |
7 | HG02965.hp2 HG03492.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.-93+14191_-93+1420 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495687 | |||||||
chr7:135495687 | AAAAAAAG others(12): Show |
A | 6 | a0001c0001t0001g0154 a0001c0001t0004g0004 a0002c0002t0001g0036 others(3): Show |
6 | HG02165.hp2 HG03492.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+14183_-93+1420 others(23): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495687 | |||||||
chr7:135495687 | AAAAAAAG others(16): Show |
A | 11 | a0001c0001t0001g0242 a0001c0001t0001g0252 a0001c0001t0001g0253 others(8): Show |
11 | HG00280.hp2 HG00438.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.-93+14179_-93+1420 others(27): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495687 | |||||||
chr7:135495687 | AAAAAAAG others(20): Show |
A | 21 | a0001c0001t0001g0003 a0001c0001t0001g0230 a0001c0001t0001g0234 others(18): Show |
21 | HG01106.hp1 HG01361.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.-93+14175_-93+1420 others(31): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495687 | |||||||
chr7:135495687 | AAAAAAAG others(24): Show |
A | 1 | a0001c0001t0001g0238 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-93+14171_-93+1420 others(35): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495687 | |||||||
chr7:135495687 | AAAAAAAG others(28): Show |
A | 1 | a0001c0001t0001g0259 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-93+14167_-93+1420 others(39): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495687 | |||||||
chr7:135495687 | AAAAAAAG others(36): Show |
A | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+14159_-93+1420 others(47): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495687 | |||||||
chr7:135495688 | A | G | 2 | a0001c0001t0001g0322 a0002c0002t0006g0006 |
2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-93+14201T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495688 | |||||||
chr7:135495688 | AAAAAAG | A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG01891.hp1 HG01943.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+14195_-93+1420 others(10): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495688 | |||||||
chr7:135495688 | AAAAAAGA others(3): Show |
A | 5 | a0001c0001t0001g0145 a0001c0001t0001g0295 a0002c0002t0001g0111 others(2): Show |
5 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+14191_-93+1420 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495688 | |||||||
chr7:135495688 | AAAAAAGA others(7): Show |
A | 7 | a0001c0001t0001g0151 a0001c0001t0001g0168 a0001c0001t0001g0233 others(4): Show |
7 | HG00642.hp2 HG01074.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.-93+14187_-93+1420 others(18): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495688 | |||||||
chr7:135495688 | AAAAAAGA others(11): Show |
A | 8 | a0001c0001t0001g0272 a0001c0001t0001g0275 a0001c0001t0001g0296 others(5): Show |
8 | HG02145.hp2 HG02622.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-93+14183_-93+1420 others(22): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495688 | |||||||
chr7:135495688 | AAAAAAGA others(15): Show |
A | 7 | a0001c0001t0001g0229 a0001c0001t0001g0248 a0001c0001t0001g0250 others(4): Show |
7 | HG01993.hp1 HG06807.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.-93+14179_-93+1420 others(26): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495688 | |||||||
chr7:135495688 | AAAAAAGA others(19): Show |
A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0244 others(5): Show |
8 | HG02071.hp2 HG02080.hp2 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.-93+14175_-93+1420 others(30): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495688 | |||||||
chr7:135495688 | AAAAAAGA others(23): Show |
A | 8 | a0001c0001t0001g0237 a0001c0001t0001g0240 a0001c0001t0001g0309 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93+14171_-93+1420 others(34): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495688 | |||||||
chr7:135495689 | A | G | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+14200T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495689 | |||||||
chr7:135495689 | AAAAAGAA others(10): Show |
A | 1 | a0001c0001t0001g0232 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-93+14183_-93+1419 others(21): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495689 | |||||||
chr7:135495689 | AAAAAGAA others(18): Show |
A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0310 |
2 | HG01074.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-93+14175_-93+1419 others(29): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495689 | |||||||
chr7:135495689 | AAAAAGAA others(30): Show |
A | 1 | a0001c0001t0001g0239 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-93+14163_-93+1419 others(41): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495689 | |||||||
chr7:135495690 | A | G | 9 | a0001c0001t0001g0119 a0001c0001t0002g0121 a0001c0001t0002g0124 others(6): Show |
9 | HG00735.hp2 HG01255.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.-93+14199T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495690 | |||||||
chr7:135495690 | AAAAG | A | 6 | a0001c0001t0001g0144 a0001c0001t0001g0162 a0001c0001t0001g0169 others(3): Show |
6 | HG01123.hp2 HG01167.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+14195_-93+1419 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495690 | |||||||
chr7:135495690 | AAAAGAAA others(1): Show |
A | 13 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0012 others(10): Show |
13 | HG01069.hp1 HG01346.hp2 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.-93+14191_-93+1419 others(12): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495690 | |||||||
chr7:135495690 | AAAAGAAA others(5): Show |
A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0115 a0001c0001t0001g0156 others(2): Show |
5 | HG00673.hp2 HG01261.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+14187_-93+1419 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495690 | |||||||
chr7:135495690 | AAAAGAAA others(9): Show |
A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0208 a0001c0001t0001g0212 others(1): Show |
4 | HG00099.hp2 HG02293.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93+14183_-93+1419 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495690 | |||||||
chr7:135495690 | AAAAGAAA others(13): Show |
A | 1 | a0001c0001t0001g0158 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-93+14179_-93+1419 others(24): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495690 | |||||||
chr7:135495690 | AAAAGAAA others(17): Show |
A | 1 | a0001c0001t0001g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-93+14175_-93+1419 others(28): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495690 | |||||||
chr7:135495691 | AAAGAAAG | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0001g0114 others(4): Show |
7 | HG00621.hp2 HG00733.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.-93+14191_-93+1419 others(11): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495691 | |||||||
chr7:135495691 | AAAGAAAG others(4): Show |
A | 8 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0001g0164 others(5): Show |
8 | HG02258.hp2 HG02717.hp1 HG03471.hp2 others(5): Show |
intron_variant | MODIFIER | c.-93+14187_-93+1419 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495691 | |||||||
chr7:135495691 | AAAGAAAG others(8): Show |
A | 1 | a0001c0001t0001g0209 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-93+14183_-93+1419 others(19): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495691 | |||||||
chr7:135495691 | AAAGAAAG others(12): Show |
A | 2 | a0001c0001t0001g0205 a0001c0001t0001g0207 |
2 | HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-93+14179_-93+1419 others(23): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495691 | |||||||
chr7:135495691 | AAAGAAAG others(24): Show |
A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0176 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-93+14167_-93+1419 others(35): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495691 | |||||||
chr7:135495692 | AAGAAAGA others(3): Show |
A | 2 | a0001c0001t0001g0191 a0006c0006t0001g0194 |
2 | HG01255.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-93+14187_-93+1419 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495692 | |||||||
chr7:135495692 | AAGAAAGA others(23): Show |
A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0175 |
2 | HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-93+14167_-93+1419 others(34): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495692 | |||||||
chr7:135495698 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-93+14191C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495698 | |||||||
chr7:135495703 | A | G | 1 | a0001c0001t0001g0191 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-93+14186T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495703 | |||||||
chr7:135495734 | G | C | 2 | a0001c0001t0001g0325 a0001c0001t0001g0326 |
2 | NA18953.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-93+14155C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495734 | |||||||
chr7:135495735 | A | G | 15 | a0002c0002t0001g0002 a0002c0002t0001g0043 a0002c0002t0001g0044 others(12): Show |
16 | HG00438.hp1 HG01071.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.-93+14154T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495735 | |||||||
chr7:135495738 | G | C | 12 | a0001c0001t0001g0141 a0001c0001t0003g0347 a0001c0001t0003g0348 others(9): Show |
12 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(9): Show |
intron_variant | MODIFIER | c.-93+14151C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495738 | |||||||
chr7:135495739 | A | G | 2 | a0002c0002t0001g0033 a0002c0002t0001g0034 |
2 | NA19003.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-93+14150T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495739 | |||||||
chr7:135495742 | GAAAGAAA others(15): Show |
G | 1 | a0002c0002t0001g0042 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-93+14125_-93+1414 others(26): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495742 | |||||||
chr7:135495746 | GAAAGAAA others(7): Show |
G | 1 | a0001c0001t0001g0160 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-93+14129_-93+1414 others(18): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495746 | |||||||
chr7:135495754 | G | T | 1 | a0001c0001t0001g0319 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-93+14135C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495754 | |||||||
chr7:135495758 | G | T | 1 | a0001c0001t0001g0319 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-93+14131C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495758 | |||||||
chr7:135495762 | G | T | 7 | a0001c0001t0001g0145 a0001c0001t0001g0295 a0001c0001t0001g0296 others(4): Show |
7 | HG01243.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-93+14127C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495762 | |||||||
chr7:135495763 | A | T | 4 | a0001c0001t0001g0145 a0001c0001t0001g0296 a0001c0001t0001g0297 others(1): Show |
4 | HG01243.hp2 HG02622.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+14126T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495763 | |||||||
chr7:135495803 | A | G | 2 | a0001c0001t0001g0237 a0001c0001t0001g0238 |
2 | HG00738.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-93+14086T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495803 | |||||||
chr7:135495806 | T | A | 1 | a0001c0001t0001g0229 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-93+14083A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495806 | |||||||
chr7:135496121 | CTCACTCC others(32): Show |
C | 4 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
4 | HG00673.hp2 HG02083.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+13729_-93+1376 others(43): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135496121 | |||||||
chr7:135496281 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0172 |
2 | HG01943.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-93+13608G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135496281 | |||||||
chr7:135496289 | C | T | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+13600G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135496289 | |||||||
chr7:135496631 | C | CCT | 23 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(20): Show |
23 | HG00597.hp2 HG00609.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.-93+13256_-93+1325 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135496631 | |||||||
chr7:135496631 | CCT | C | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+13256_-93+1325 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135496631 | |||||||
chr7:135496631 | CCTCT | C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0172 a0001c0001t0001g0173 others(1): Show |
4 | HG01943.hp2 HG03490.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93+13254_-93+1325 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135496631 | |||||||
chr7:135496633 | T | G | 3 | a0001c0001t0001g0312 a0001c0001t0001g0313 a0001c0001t0001g0314 |
3 | HG01123.hp1 HG03654.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-93+13256A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135496633 | |||||||
chr7:135496707 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-93+13182T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135496707 | |||||||
chr7:135496969 | G | A | 4 | a0001c0001t0001g0152 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
4 | HG00738.hp1 HG01106.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93+12920C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135496969 | |||||||
chr7:135497084 | G | T | 8 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93+12805C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135497084 | |||||||
chr7:135497144 | A | G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0153 |
2 | NA18967.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-93+12745T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135497144 | |||||||
chr7:135497168 | G | A | 6 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(3): Show |
6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+12721C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135497168 | |||||||
chr7:135497586 | C | G | 5 | a0002c0002t0001g0035 a0002c0002t0001g0036 a0002c0002t0001g0037 others(2): Show |
5 | NA18941.hp2 NA18980.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-93+12303G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135497586 | |||||||
chr7:135497696 | T | C | 12 | a0002c0002t0001g0001 a0002c0002t0001g0023 a0002c0002t0001g0024 others(9): Show |
13 | NA18947.hp2 NA18948.hp1 NA18951.hp1 others(10): Show |
intron_variant | MODIFIER | c.-93+12193A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135497696 | |||||||
chr7:135498162 | A | ATACTAC | 17 | a0001c0001t0001g0318 a0001c0001t0002g0285 a0001c0001t0002g0286 others(14): Show |
17 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-93+11721_-93+1172 others(10): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135498162 | |||||||
chr7:135498241 | T | C | 9 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(6): Show |
9 | NA18944.hp1 NA18945.hp2 NA18986.hp1 others(6): Show |
intron_variant | MODIFIER | c.-93+11648A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135498241 | |||||||
chr7:135498599 | AGTGCAAT | A | 3 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0140 |
3 | HG02572.hp2 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-93+11283_-93+1128 others(11): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135498599 | |||||||
chr7:135498851 | A | G | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+11038T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135498851 | |||||||
chr7:135499111 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-93+10778G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135499111 | |||||||
chr7:135499246 | G | T | 2 | a0001c0001t0001g0334 a0001c0001t0001g0335 |
2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-93+10643C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135499246 | |||||||
chr7:135499333 | T | C | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+10556A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135499333 | |||||||
chr7:135499876 | A | C | 2 | a0001c0001t0003g0347 a0001c0001t0003g0348 |
2 | HG00597.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.-93+10013T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135499876 | |||||||
chr7:135499976 | C | T | 1 | a0002c0002t0001g0093 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-93+9913G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135499976 | |||||||
chr7:135500206 | A | T | 2 | a0002c0002t0001g0033 a0002c0002t0001g0034 |
2 | NA19003.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-93+9683T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135500206 | |||||||
chr7:135500471 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+9418A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135500471 | |||||||
chr7:135500472 | T | A | 28 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(25): Show |
28 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.-93+9417A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135500472 | |||||||
chr7:135500574 | A | G | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 |
3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-93+9315T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135500574 | |||||||
chr7:135500765 | T | C | 4 | a0001c0001t0002g0130 a0001c0001t0002g0132 a0001c0001t0002g0133 others(1): Show |
4 | HG02818.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93+9124A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135500765 | |||||||
chr7:135500912 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-93+8977A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135500912 | |||||||
chr7:135500948 | C | T | 1 | a0001c0001t0001g0304 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-93+8941G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135500948 | |||||||
chr7:135500983 | C | CT | 68 | a0001c0001t0001g0141 a0001c0001t0001g0145 a0001c0001t0001g0147 others(65): Show |
68 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.-93+8905dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135500983 | |||||||
chr7:135500983 | C | CTT | 57 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0230 others(54): Show |
59 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-93+8904_-93+8905d others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135500983 | |||||||
chr7:135501009 | A | C | 1 | a0001c0010t0002g0324 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-93+8880T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135501009 | |||||||
chr7:135501028 | G | C | 1 | a0001c0001t0003g0348 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-93+8861C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135501028 | |||||||
chr7:135501069 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0008g0346 |
2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-93+8820G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135501069 | |||||||
chr7:135501114 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-93+8775T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135501114 | |||||||
chr7:135501183 | C | G | 2 | a0001c0001t0001g0189 a0001c0001t0007g0190 |
2 | HG00733.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-93+8706G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135501183 | |||||||
chr7:135501618 | A | C | 2 | a0001c0001t0001g0322 a0002c0002t0006g0006 |
2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-93+8271T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135501618 | |||||||
chr7:135501623 | C | A | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+8266G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135501623 | |||||||
chr7:135501942 | T | C | 1 | a0001c0010t0002g0324 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-93+7947A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135501942 | |||||||
chr7:135502040 | C | G | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0008g0346 |
3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-93+7849G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502040 | |||||||
chr7:135502084 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-93+7805G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502084 | |||||||
chr7:135502092 | C | T | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+7797G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502092 | |||||||
chr7:135502330 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-93+7559G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502330 | |||||||
chr7:135502400 | T | C | 1 | a0002c0002t0001g0302 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-93+7489A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502400 | |||||||
chr7:135502566 | A | G | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+7323T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502566 | |||||||
chr7:135502571 | T | C | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+7318A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502571 | |||||||
chr7:135502581 | G | A | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+7308C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502581 | |||||||
chr7:135502583 | A | G | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+7306T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502583 | |||||||
chr7:135502589 | C | T | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+7300G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502589 | |||||||
chr7:135502590 | A | G | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+7299T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502590 | |||||||
chr7:135502631 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-93+7258T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502631 | |||||||
chr7:135502681 | T | C | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+7208A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502681 | |||||||
chr7:135502689 | G | A | 1 | a0002c0002t0001g0129 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-93+7200C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502689 | |||||||
chr7:135502816 | C | CA | 35 | a0001c0001t0001g0020 a0001c0001t0001g0119 a0001c0001t0001g0177 others(32): Show |
35 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.-93+7072dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502816 | |||||||
chr7:135502816 | CA | C | 24 | a0001c0001t0001g0141 a0001c0001t0001g0150 a0001c0001t0001g0231 others(21): Show |
24 | HG00597.hp2 HG01515.hp2 HG01517.hp1 others(21): Show |
intron_variant | MODIFIER | c.-93+7072delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502816 | |||||||
chr7:135502994 | A | G | 62 | a0001c0001t0001g0003 a0001c0001t0001g0228 a0001c0001t0001g0229 others(59): Show |
64 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.-93+6895T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502994 | |||||||
chr7:135503126 | C | A | 1 | a0002c0002t0001g0106 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-93+6763G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135503126 | |||||||
chr7:135503325 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-93+6564G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135503325 | |||||||
chr7:135503333 | T | C | 233 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(230): Show |
235 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.-93+6556A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135503333 | |||||||
chr7:135503456 | C | CA | 9 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 others(6): Show |
9 | HG02486.hp2 HG02622.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-93+6432dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135503456 | |||||||
chr7:135503456 | C | CAA | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+6431_-93+6432d others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135503456 | |||||||
chr7:135503456 | CA | C | 8 | a0001c0001t0001g0229 a0001c0001t0002g0135 a0001c0001t0002g0136 others(5): Show |
8 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-93+6432delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135503456 | |||||||
chr7:135503479 | C | A | 20 | a0001c0001t0001g0141 a0001c0001t0001g0304 a0001c0001t0001g0305 others(17): Show |
20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+6410G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135503479 | |||||||
chr7:135503722 | T | C | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+6167A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135503722 | |||||||
chr7:135503839 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-93+6050A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135503839 | |||||||
chr7:135504160 | A | G | 2 | a0002c0002t0001g0001 a0002c0002t0001g0023 |
3 | NA18986.hp2 NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-93+5729T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504160 | |||||||
chr7:135504190 | T | C | 5 | a0002c0002t0001g0298 a0002c0002t0001g0299 a0002c0002t0001g0300 others(2): Show |
5 | HG02055.hp1 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+5699A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504190 | |||||||
chr7:135504254 | T | C | 7 | a0001c0001t0002g0120 a0001c0001t0002g0121 a0001c0001t0002g0122 others(4): Show |
7 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(4): Show |
intron_variant | MODIFIER | c.-93+5635A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504254 | |||||||
chr7:135504263 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-93+5626A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504263 | |||||||
chr7:135504295 | A | AT | 8 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0228 others(5): Show |
8 | HG02486.hp1 HG02717.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-93+5593dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504295 | |||||||
chr7:135504451 | ACATCCGG others(327): Show |
A | 136 | a0001c0001t0001g0003 a0001c0001t0001g0141 a0001c0001t0001g0145 others(133): Show |
138 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.-93+5104_-93+5437d others(2): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504451 | |||||||
chr7:135504462 | A | AT | 6 | a0001c0001t0001g0119 a0001c0001t0002g0118 a0001c0003t0002g0183 others(3): Show |
6 | HG01106.hp1 HG01255.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+5426dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504462 | |||||||
chr7:135504462 | A | ATT | 8 | a0001c0001t0001g0009 a0001c0001t0001g0169 a0001c0001t0001g0170 others(5): Show |
8 | HG00673.hp2 HG01069.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-93+5425_-93+5426d others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504462 | |||||||
chr7:135504462 | AT | A | 82 | a0001c0001t0002g0130 a0001c0001t0002g0132 a0001c0001t0002g0133 others(79): Show |
84 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.-93+5426delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504462 | |||||||
chr7:135504462 | ATT | A | 10 | a0002c0002t0001g0033 a0002c0002t0001g0066 a0002c0002t0001g0076 others(7): Show |
10 | HG02257.hp2 NA18747.hp1 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.-93+5425_-93+5426d others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504462 | |||||||
chr7:135504478 | T | A | 1 | a0002c0002t0001g0102 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-93+5411A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504478 | |||||||
chr7:135504484 | T | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0113 a0001c0001t0001g0154 others(4): Show |
7 | HG00099.hp2 HG00621.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.-93+5405A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504484 | |||||||
chr7:135504484 | T | TA | 13 | a0001c0001t0001g0017 a0001c0001t0001g0148 a0001c0001t0001g0150 others(10): Show |
13 | HG00099.hp1 HG01074.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.-93+5404_-93+5405i others(3): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504484 | |||||||
chr7:135504484 | T | TTA | 56 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(53): Show |
56 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.-93+5404_-93+5405i others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504484 | |||||||
chr7:135504484 | T | TTTA | 21 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0163 others(18): Show |
21 | HG00733.hp1 HG01358.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.-93+5404_-93+5405i others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504484 | |||||||
chr7:135504496 | A | T | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-93+5393T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504496 | |||||||
chr7:135504549 | G | C | 96 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(93): Show |
96 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.-93+5340C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504549 | |||||||
chr7:135504569 | C | G | 1 | a0001c0001t0001g0166 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93+5320G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504569 | |||||||
chr7:135504574 | C | A | 11 | a0002c0002t0001g0002 a0002c0002t0001g0043 a0002c0002t0001g0044 others(8): Show |
12 | HG01071.hp1 HG01256.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-93+5315G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504574 | |||||||
chr7:135504612 | A | G | 1 | a0002c0002t0001g0032 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-93+5277T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504612 | |||||||
chr7:135504641 | T | C | 4 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
4 | HG00673.hp2 HG02083.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+5248A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504641 | |||||||
chr7:135504690 | T | A | 1 | a0001c0001t0001g0203 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-93+5199A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504690 | |||||||
chr7:135504775 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-93+5114G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504775 | |||||||
chr7:135504907 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-93+4982G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504907 | |||||||
chr7:135505061 | A | G | 1 | a0001c0001t0001g0007 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-93+4828T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135505061 | |||||||
chr7:135505114 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-93+4775C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135505114 | |||||||
chr7:135505176 | C | T | 50 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(47): Show |
50 | HG00642.hp2 HG00673.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.-93+4713G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135505176 | |||||||
chr7:135505265 | G | A | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+4624C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135505265 | |||||||
chr7:135505357 | A | G | 2 | a0001c0001t0001g0322 a0002c0002t0006g0006 |
2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-93+4532T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135505357 | |||||||
chr7:135505404 | T | C | 8 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(5): Show |
8 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93+4485A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135505404 | |||||||
chr7:135505494 | G | C | 8 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(5): Show |
8 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93+4395C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135505494 | |||||||
chr7:135505516 | C | T | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+4373G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135505516 | |||||||
chr7:135506017 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-93+3872C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135506017 | |||||||
chr7:135506210 | T | C | 1 | a0001c0001t0001g0318 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-93+3679A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135506210 | |||||||
chr7:135506410 | G | C | 97 | a0001c0001t0001g0319 a0002c0002t0001g0001 a0002c0002t0001g0002 others(94): Show |
99 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.-93+3479C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135506410 | |||||||
chr7:135506624 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-93+3265G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135506624 | |||||||
chr7:135506716 | C | T | 1 | a0001c0001t0001g0344 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-93+3173G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135506716 | |||||||
chr7:135506802 | C | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-93+3087G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135506802 | |||||||
chr7:135506830 | A | G | 14 | a0001c0001t0001g0141 a0001c0001t0001g0325 a0001c0001t0001g0326 others(11): Show |
14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+3059T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135506830 | |||||||
chr7:135506877 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-93+3012C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135506877 | |||||||
chr7:135506957 | A | G | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+2932T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135506957 | |||||||
chr7:135506993 | C | T | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+2896G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135506993 | |||||||
chr7:135507022 | T | C | 4 | a0002c0002t0001g0108 a0002c0002t0001g0109 a0002c0002t0001g0110 others(1): Show |
4 | HG00438.hp1 NA18956.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+2867A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135507022 | |||||||
chr7:135507091 | T | C | 1 | a0001c0001t0001g0321 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-93+2798A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135507091 | |||||||
chr7:135507711 | A | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG01123.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.-93+2178T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135507711 | |||||||
chr7:135507849 | A | T | 1 | a0001c0001t0001g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-93+2040T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135507849 | |||||||
chr7:135508281 | G | T | 34 | a0001c0001t0001g0141 a0001c0001t0001g0322 a0001c0001t0001g0325 others(31): Show |
34 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.-93+1608C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135508281 | |||||||
chr7:135508543 | G | T | 2 | a0001c0001t0001g0322 a0002c0002t0006g0006 |
2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-93+1346C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135508543 | |||||||
chr7:135508683 | G | A | 2 | a0001c0001t0001g0322 a0002c0002t0006g0006 |
2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-93+1206C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135508683 | |||||||
chr7:135508721 | A | G | 6 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+1168T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135508721 | |||||||
chr7:135508930 | GA | G | 18 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(15): Show |
18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+958delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135508930 | |||||||
chr7:135509024 | T | C | 1 | a0001c0001t0001g0344 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-93+865A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135509024 | |||||||
chr7:135509266 | A | T | 5 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0132 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+623T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135509266 | |||||||
chr7:135509306 | T | C | 1 | a0001c0008t0001g0323 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-93+583A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135509306 | |||||||
chr7:135509453 | G | T | 121 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(118): Show |
123 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(120): Show |
intron_variant | MODIFIER | c.-93+436C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135509453 | |||||||
chr7:135509518 | G | C | 19 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(16): Show |
20 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+371C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135509518 | |||||||
chr7:135509530 | T | C | 1 | a0001c0010t0002g0324 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-93+359A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135509530 | |||||||
chr7:135509555 | C | G | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | HG00621.hp2 HG01433.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.-93+334G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135509555 | |||||||
chr7:135509692 | T | G | 33 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0327 others(30): Show |
34 | HG00597.hp2 HG00642.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.-93+197A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135509692 | |||||||
chr7:135509865 | A | G | 108 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(105): Show |
110 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.-93+24T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135509865 | |||||||
chr7:135509880 | T | C | 1 | a0001c0003t0002g0345 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-93+9A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135509880 |