Item | Value |
---|---|
geneid | 55160 |
ensemblid | ENSG00000074964.17 |
hgncid | 25540 |
symbol | ARHGEF10L |
name | Rho guanine nucleotide exchange factor 10 like |
refseq_nuc | NM_018125.4 |
refseq_prot | NP_060595.3 |
ensembl_nuc | ENST00000361221.8 |
ensembl_prot | ENSP00000355060.3 |
mane_status | MANE Select |
chr | chr1 |
start | 17539698 |
end | 17697869 |
strand | + |
ver | v1.2 |
region | chr1:17539698-17697869 |
region5000 | chr1:17534698-17702869 |
regionname0 | ARHGEF10L_chr1_17539698_17697869 |
regionname5000 | ARHGEF10L_chr1_17534698_17702869 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1279 | 96 | 30 | 33 | 16 | 3 | 13 | 6 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | MASSN others(1274): Show |
chr1 | 17534698 | 17702869 |
a0002 | 1/0 | 1279 | 31 | 11 | 7 | 8 | 0 | 4 | 5 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | MASSN others(1274): Show |
chr1 | 17534698 | 17702869 |
a0003 | 0/0 | 1279 | 8 | 1 | 2 | 1 | 0 | 4 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | MASSN others(1274): Show |
chr1 | 17534698 | 17702869 |
a0004 | 0/0 | 1279 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | MASSN others(1274): Show |
chr1 | 17534698 | 17702869 |
a0005 | 0/0 | 1279 | 4 | 1 | 2 | 0 | 0 | 1 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | MASSN others(1274): Show |
chr1 | 17534698 | 17702869 |
a0006 | 0/0 | 1279 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | MASSN others(1274): Show |
chr1 | 17534698 | 17702869 |
a0007 | 0/0 | 1279 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | MASSN others(1274): Show |
chr1 | 17534698 | 17702869 |
a0008 | 0/0 | 1279 | 3 | 1 | 0 | 2 | 0 | 0 | 2 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | MASSN others(1274): Show |
chr1 | 17534698 | 17702869 |
a0009 | 0/0 | 1279 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | MASSN others(1274): Show |
chr1 | 17534698 | 17702869 |
a0010 | 0/0 | 1279 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | MASSN others(1274): Show |
chr1 | 17534698 | 17702869 |
a0011 | 0/0 | 1279 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | MASSN others(1274): Show |
chr1 | 17534698 | 17702869 |
a0012 | 0/0 | 1279 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | MASSN others(1274): Show |
chr1 | 17534698 | 17702869 |
a0013 | 0/0 | 1279 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | MASSN others(1274): Show |
chr1 | 17534698 | 17702869 |
a0014 | 0/0 | 1279 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | MASSN others(1274): Show |
chr1 | 17534698 | 17702869 |
a0015 | 0/0 | 1279 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | MASSN others(1274): Show |
chr1 | 17534698 | 17702869 |
a0016 | 0/0 | 1279 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | MASSN others(1274): Show |
chr1 | 17534698 | 17702869 |
a0017 | 0/0 | 1279 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | MASSN others(1274): Show |
chr1 | 17534698 | 17702869 |
a0018 | 0/0 | 1279 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | MASSN others(1274): Show |
chr1 | 17534698 | 17702869 |
a0019 | 0/0 | 1279 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | MASSN others(1274): Show |
chr1 | 17534698 | 17702869 |
a0020 | 0/0 | 1279 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | MASSN others(1274): Show |
chr1 | 17534698 | 17702869 |
a0021 | 0/0 | 1279 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | MASSN others(1274): Show |
chr1 | 17534698 | 17702869 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3837 | 66 | 18 | 22 | 13 | 1 | 11 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0001c0006 | 0/0 | 3837 | 6 | 4 | 2 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0001c0011 | 0/0 | 3837 | 3 | 0 | 2 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0001c0012 | 0/0 | 3837 | 3 | 0 | 2 | 0 | 1 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0001c0013 | 0/0 | 3837 | 3 | 0 | 2 | 0 | 1 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0001c0014 | 0/0 | 3837 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0001c0017 | 0/0 | 3837 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0001c0019 | 0/0 | 3837 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0001c0020 | 0/0 | 3837 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0001c0033 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0001c0038 | 0/0 | 3837 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0001c0042 | 0/0 | 3837 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0001c0043 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0001c0044 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0001c0045 | 0/0 | 3837 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0001c0048 | 0/0 | 3837 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0002c0003 | 0/0 | 3837 | 8 | 0 | 3 | 4 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0002c0004 | 1/0 | 3837 | 7 | 3 | 2 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0002c0007 | 0/0 | 3837 | 5 | 4 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0002c0008 | 0/0 | 3837 | 4 | 0 | 1 | 0 | 0 | 3 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0002c0018 | 0/0 | 3837 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0002c0021 | 0/0 | 3837 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0002c0022 | 0/0 | 3837 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0002c0034 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0002c0036 | 0/0 | 3837 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0002c0041 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0003c0002 | 0/0 | 3837 | 8 | 1 | 2 | 1 | 0 | 4 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0004c0005 | 0/0 | 3837 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0005c0015 | 0/0 | 3837 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0005c0023 | 0/0 | 3837 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0005c0024 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0006c0009 | 0/0 | 3837 | 3 | 1 | 2 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0007c0010 | 0/0 | 3837 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0008c0016 | 0/0 | 3837 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0008c0027 | 0/0 | 3837 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0009c0039 | 0/0 | 3837 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0009c0040 | 0/0 | 3837 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0010c0046 | 0/0 | 3837 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0011c0025 | 0/0 | 3837 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0012c0031 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0013c0035 | 0/0 | 3837 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0014c0029 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0015c0032 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0016c0047 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0017c0037 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0018c0028 | 0/0 | 3837 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0019c0026 | 0/0 | 3837 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0020c0049 | 0/0 | 3837 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 | ||
a0021c0030 | 0/0 | 3837 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | ATGGC others(3832): Show |
chr1 | 17534698 | 17702869 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4626 | 54 | 12 | 19 | 12 | 1 | 10 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0001c0001t0003 | 0/1 | 4626 | 11 | 5 | 3 | 1 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0001c0001t0005 | 0/0 | 4626 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0001c0006t0001 | 0/0 | 4626 | 4 | 2 | 2 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0001c0006t0003 | 0/0 | 4626 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0001c0006t0007 | 0/0 | 4626 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0001c0011t0001 | 0/0 | 4626 | 3 | 0 | 2 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0001c0012t0001 | 0/0 | 4626 | 3 | 0 | 2 | 0 | 1 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0001c0013t0001 | 0/0 | 4626 | 3 | 0 | 2 | 0 | 1 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0001c0014t0001 | 0/0 | 4626 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0001c0017t0002 | 0/0 | 4625 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0001c0019t0001 | 0/0 | 4626 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0001c0020t0001 | 0/0 | 4626 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0001c0033t0002 | 0/0 | 4625 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0001c0038t0003 | 0/0 | 4626 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0001c0042t0001 | 0/0 | 4626 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0001c0043t0002 | 0/0 | 4625 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0001c0044t0004 | 0/0 | 4625 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0001c0045t0001 | 0/0 | 4626 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0001c0048t0001 | 0/0 | 4626 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0002c0003t0002 | 0/0 | 4625 | 8 | 0 | 3 | 4 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0002c0004t0002 | 1/0 | 4625 | 7 | 3 | 2 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0002c0007t0002 | 0/0 | 4625 | 5 | 4 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0002c0008t0002 | 0/0 | 4625 | 4 | 0 | 1 | 0 | 0 | 3 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0002c0018t0002 | 0/0 | 4625 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0002c0021t0002 | 0/0 | 4625 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0002c0022t0002 | 0/0 | 4625 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0002c0034t0002 | 0/0 | 4625 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0002c0036t0002 | 0/0 | 4625 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0002c0041t0008 | 0/0 | 4625 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0003c0002t0001 | 0/0 | 4626 | 8 | 1 | 2 | 1 | 0 | 4 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0004c0005t0002 | 0/0 | 4625 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0005c0015t0002 | 0/0 | 4625 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0005c0023t0002 | 0/0 | 4625 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0005c0024t0002 | 0/0 | 4625 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0006c0009t0001 | 0/0 | 4626 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0006c0009t0003 | 0/0 | 4626 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0007c0010t0001 | 0/0 | 4626 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0008c0016t0002 | 0/0 | 4625 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0008c0027t0002 | 0/0 | 4625 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0009c0039t0001 | 0/0 | 4626 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0009c0040t0001 | 0/0 | 4626 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0010c0046t0001 | 0/0 | 4626 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0011c0025t0002 | 0/0 | 4625 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0012c0031t0006 | 0/0 | 4625 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0013c0035t0001 | 0/0 | 4626 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0014c0029t0001 | 0/0 | 4626 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0015c0032t0001 | 0/0 | 4626 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0016c0047t0002 | 0/0 | 4625 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0017c0037t0001 | 0/0 | 4626 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0018c0028t0003 | 0/0 | 4626 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0019c0026t0001 | 0/0 | 4626 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4621): Show |
chr1 | 17534698 | 17702869 |
a0020c0049t0004 | 0/0 | 4625 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
a0021c0030t0002 | 0/0 | 4625 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | GCGTC others(4620): Show |
chr1 | 17534698 | 17702869 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0003g0123 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0006t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0006t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0006t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0006t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0006t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0006t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0011t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0011t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0011t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0012t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0012t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0012t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0013t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0013t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0013t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0014t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0014t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0017t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0017t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0019t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0019t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0020t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0020t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0033t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0038t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0042t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0043t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0044t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0045t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0001c0048t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0003t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0003t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0003t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0003t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0003t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0003t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0004t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0004t0002g0091 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0004t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0004t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0004t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0004t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0004t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0007t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0007t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0007t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0007t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0007t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0008t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0008t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0008t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0008t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0018t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0018t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0021t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0022t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0034t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0036t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0002c0041t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0003c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0003c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0003c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0003c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0003c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0003c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0003c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0003c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0004c0005t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0004c0005t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0004c0005t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0004c0005t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0004c0005t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0004c0005t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0005c0015t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0005c0015t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0005c0023t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0005c0024t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0006c0009t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0006c0009t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0006c0009t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0007c0010t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0007c0010t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0007c0010t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0008c0016t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0008c0016t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0008c0027t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0009c0039t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0009c0040t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0010c0046t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0011c0025t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0012c0031t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0013c0035t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0014c0029t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0015c0032t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0016c0047t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0017c0037t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0018c0028t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0019c0026t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0020c0049t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
a0021c0030t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00323 | hp1 | a0001 | c0012 | t0001 | g0102 | EUR | FIN | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG00323 | hp2 | a0010 | c0046 | t0001 | g0020 | EUR | FIN | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG00544 | hp1 | a0001 | c0014 | t0001 | g0094 | EAS | CHS | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG00544 | hp2 | a0002 | c0022 | t0002 | g0050 | EAS | CHS | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG00642 | hp1 | a0002 | c0007 | t0002 | g0105 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG00642 | hp2 | a0003 | c0002 | t0001 | g0056 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG00733 | hp1 | a0002 | c0008 | t0002 | g0104 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG00738 | hp1 | a0001 | c0013 | t0001 | g0008 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG00738 | hp2 | a0001 | c0012 | t0001 | g0064 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG00741 | hp1 | a0001 | c0042 | t0001 | g0035 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01069 | hp1 | a0001 | c0006 | t0001 | g0129 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01070 | hp1 | a0002 | c0004 | t0002 | g0120 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01071 | hp1 | a0001 | c0006 | t0001 | g0130 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01071 | hp2 | a0002 | c0004 | t0002 | g0121 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01074 | hp1 | a0003 | c0002 | t0001 | g0081 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01074 | hp2 | a0002 | c0003 | t0002 | g0116 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01081 | hp1 | a0001 | c0012 | t0001 | g0072 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01106 | hp1 | a0011 | c0025 | t0002 | g0049 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01109 | hp1 | a0001 | c0020 | t0001 | g0052 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01169 | hp2 | a0006 | c0009 | t0003 | g0007 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0090 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01175 | hp2 | a0002 | c0003 | t0002 | g0083 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01192 | hp1 | a0005 | c0023 | t0002 | g0101 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01257 | hp1 | a0001 | c0011 | t0001 | g0152 | AMR | CLM | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01258 | hp2 | a0002 | c0003 | t0002 | g0089 | AMR | CLM | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01261 | hp1 | a0001 | c0013 | t0001 | g0023 | AMR | CLM | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01261 | hp2 | a0009 | c0040 | t0001 | g0087 | AMR | CLM | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01433 | hp1 | a0001 | c0045 | t0001 | g0031 | AMR | CLM | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01433 | hp2 | a0005 | c0015 | t0002 | g0068 | AMR | CLM | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | CLM | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01884 | hp1 | a0012 | c0031 | t0006 | g0165 | AFR | ACB | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0162 | AFR | ACB | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02071 | hp1 | a0001 | c0011 | t0001 | g0004 | EAS | KHV | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02080 | hp1 | a0013 | c0035 | t0001 | g0018 | EAS | KHV | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02135 | hp2 | a0002 | c0004 | t0002 | g0036 | EAS | KHV | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02148 | hp2 | a0001 | c0011 | t0001 | g0138 | AMR | PEL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02280 | hp1 | a0001 | c0006 | t0007 | g0150 | AFR | ACB | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02280 | hp2 | a0002 | c0007 | t0002 | g0058 | AFR | ACB | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02451 | hp1 | a0003 | c0002 | t0001 | g0106 | AFR | ACB | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02572 | hp2 | a0015 | c0032 | t0001 | g0086 | AFR | GWD | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02602 | hp1 | a0002 | c0008 | t0002 | g0126 | SAS | PJL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02602 | hp2 | a0003 | c0002 | t0001 | g0074 | SAS | PJL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02622 | hp1 | a0006 | c0009 | t0001 | g0166 | AFR | GWD | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02622 | hp2 | a0001 | c0044 | t0004 | g0161 | AFR | GWD | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02630 | hp1 | a0001 | c0043 | t0002 | g0051 | AFR | GWD | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02630 | hp2 | a0002 | c0018 | t0002 | g0015 | AFR | GWD | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02683 | hp2 | a0003 | c0002 | t0001 | g0073 | SAS | PJL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02717 | hp2 | a0002 | c0034 | t0002 | g0149 | AFR | GWD | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | GWD | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02809 | hp2 | a0002 | c0004 | t0002 | g0167 | AFR | GWD | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | GWD | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02896 | hp2 | a0002 | c0007 | t0002 | g0085 | AFR | GWD | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | GWD | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02897 | hp2 | a0001 | c0017 | t0002 | g0113 | AFR | GWD | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02922 | hp1 | a0004 | c0005 | t0002 | g0112 | AFR | ESN | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02922 | hp2 | a0001 | c0006 | t0001 | g0001 | AFR | ESN | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02976 | hp2 | a0005 | c0024 | t0002 | g0059 | AFR | ESN | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03017 | hp1 | a0003 | c0002 | t0001 | g0069 | SAS | PJL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03098 | hp1 | a0016 | c0047 | t0002 | g0147 | AFR | MSL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03098 | hp2 | a0004 | c0005 | t0002 | g0117 | AFR | MSL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03130 | hp1 | a0004 | c0005 | t0002 | g0060 | AFR | ESN | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03130 | hp2 | a0002 | c0018 | t0002 | g0155 | AFR | ESN | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03195 | hp1 | a0001 | c0006 | t0003 | g0139 | AFR | ESN | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03195 | hp2 | a0001 | c0020 | t0001 | g0016 | AFR | ESN | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03225 | hp1 | a0002 | c0007 | t0002 | g0111 | AFR | MSL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03225 | hp2 | a0017 | c0037 | t0001 | g0142 | AFR | MSL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03486 | hp2 | a0001 | c0017 | t0002 | g0148 | AFR | MSL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03491 | hp2 | a0002 | c0008 | t0002 | g0042 | SAS | PJL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0135 | SAS | PJL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03540 | hp1 | a0001 | c0019 | t0001 | g0095 | AFR | GWD | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03540 | hp2 | a0007 | c0010 | t0001 | g0065 | AFR | GWD | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03579 | hp1 | a0002 | c0041 | t0008 | g0054 | AFR | MSL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03579 | hp2 | a0004 | c0005 | t0002 | g0157 | AFR | MSL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03688 | hp2 | a0003 | c0002 | t0001 | g0144 | SAS | STU | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03710 | hp2 | a0002 | c0003 | t0002 | g0055 | SAS | PJL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03834 | hp1 | a0001 | c0038 | t0003 | g0124 | SAS | BEB | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03834 | hp2 | a0001 | c0048 | t0001 | g0005 | SAS | BEB | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | STU | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG04115 | hp2 | a0005 | c0015 | t0002 | g0067 | SAS | STU | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG04204 | hp1 | a0002 | c0008 | t0002 | g0100 | SAS | STU | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | STU | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | YRI | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | YRI | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18612 | hp1 | a0002 | c0003 | t0002 | g0133 | EAS | CHB | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHB | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | CHB | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | YRI | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18946 | hp1 | a0001 | c0014 | t0001 | g0145 | EAS | JPT | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18946 | hp2 | a0002 | c0003 | t0002 | g0025 | EAS | JPT | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18951 | hp1 | a0002 | c0021 | t0002 | g0137 | EAS | JPT | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18951 | hp2 | a0018 | c0028 | t0003 | g0044 | EAS | JPT | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18954 | hp1 | a0008 | c0027 | t0002 | g0029 | EAS | JPT | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18962 | hp2 | a0002 | c0003 | t0002 | g0141 | EAS | JPT | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18966 | hp1 | a0002 | c0003 | t0002 | g0037 | EAS | JPT | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18966 | hp2 | a0019 | c0026 | t0001 | g0026 | EAS | JPT | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18982 | hp1 | a0020 | c0049 | t0004 | g0075 | EAS | JPT | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18982 | hp2 | a0009 | c0039 | t0001 | g0039 | EAS | JPT | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA19010 | hp2 | a0002 | c0036 | t0002 | g0160 | EAS | JPT | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA19043 | hp1 | a0004 | c0005 | t0002 | g0006 | AFR | LWK | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA19074 | hp1 | a0008 | c0016 | t0002 | g0132 | EAS | JPT | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA19074 | hp2 | a0003 | c0002 | t0001 | g0038 | EAS | JPT | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0131 | AFR | YRI | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA19240 | hp2 | a0007 | c0010 | t0001 | g0115 | AFR | YRI | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA20805 | hp1 | a0001 | c0013 | t0001 | g0017 | EUR | TSI | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01123 | hp1 | a0006 | c0009 | t0001 | g0107 | AMR | CLM | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02109 | hp1 | a0014 | c0029 | t0001 | g0122 | AFR | ACB | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02109 | hp2 | a0002 | c0004 | t0002 | g0146 | AFR | ACB | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02486 | hp1 | a0002 | c0004 | t0002 | g0118 | AFR | ACB | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02559 | hp1 | a0001 | c0033 | t0002 | g0110 | AFR | ACB | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03471 | hp1 | a0002 | c0007 | t0002 | g0013 | AFR | MSL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG03471 | hp2 | a0007 | c0010 | t0001 | g0053 | AFR | MSL | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG06807 | hp1 | a0004 | c0005 | t0002 | g0108 | AFR | USA | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
HG06807 | hp2 | a0001 | c0019 | t0001 | g0066 | AFR | USA | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA20300 | hp1 | a0001 | c0006 | t0001 | g0156 | AFR | USA | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA20300 | hp2 | a0008 | c0016 | t0002 | g0082 | AFR | USA | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | LWK | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
NA21309 | hp2 | a0021 | c0030 | t0002 | g0109 | AFR | LWK | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0123 | REF | REF | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
homoSapiens | grch38p0 | a0002 | c0004 | t0002 | g0091 | REF | REF | ARHGEF10L_chr1_17534698_17702869 | ARHGEF10L | chr1 | 17534698 | 17702869 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:17587562 | G | A | 2 | a0005 a0006 |
7 | HG01123.hp1 HG01169.hp2 HG01192.hp1 others(4): Show |
missense_variant | MODERATE | c.140G>A | p.Ser47Asn | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 3/29 | 436/4625 | 140/3840 | 47/1279 | chr1 | 17587562 | |||
chr1:17587608 | C | A | 1 | a0011 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.186C>A | p.Asp62Glu | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 3/29 | 482/4625 | 186/3840 | 62/1279 | chr1 | 17587608 | |||
chr1:17587627 | G | A | 4 | a0003 a0008 a0018 others(1): Show |
13 | HG00642.hp2 HG01074.hp1 HG02451.hp1 others(10): Show |
missense_variant | MODERATE | c.205G>A | p.Asp69Asn | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 3/29 | 501/4625 | 205/3840 | 69/1279 | chr1 | 17587627 | |||
chr1:17602164 | G | A | 2 | a0004 a0014 |
7 | HG02109.hp1 HG02922.hp1 HG03098.hp2 others(4): Show |
missense_variant | MODERATE | c.295G>A | p.Ala99Thr | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 5/29 | 591/4625 | 295/3840 | 99/1279 | chr1 | 17602164 | |||
chr1:17602183 | G | A | 2 | a0012 a0021 |
2 | HG01884.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.314G>A | p.Arg105Gln | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 5/29 | 610/4625 | 314/3840 | 105/1279 | chr1 | 17602183 | |||
chr1:17603583 | A | G | 1 | a0020 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.425A>G | p.His142Arg | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/29 | 721/4625 | 425/3840 | 142/1279 | chr1 | 17603583 | |||
chr1:17607859 | C | T | 1 | a0016 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.491C>T | p.Ala164Val | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/29 | 787/4625 | 491/3840 | 164/1279 | chr1 | 17607859 | |||
chr1:17607936 | G | A | 1 | a0015 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.568G>A | p.Glu190Lys | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/29 | 864/4625 | 568/3840 | 190/1279 | chr1 | 17607936 | |||
chr1:17616194 | A | T | 1 | a0018 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.827A>T | p.Asp276Val | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/29 | 1123/4625 | 827/3840 | 276/1279 | chr1 | 17616194 | |||
chr1:17623042 | C | T | 1 | a0010 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.1067C>T | p.Ala356Val | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 12/29 | 1363/4625 | 1067/3840 | 356/1279 | chr1 | 17623042 | |||
chr1:17656077 | A | G | 1 | a0009 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.2680A>G | p.Ile894Val | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 24/29 | 2976/4625 | 2680/3840 | 894/1279 | chr1 | 17656077 | |||
chr1:17656079 | C | G | 1 | a0009 | 1 | NA18982.hp2 | missense_variant | MODERATE | c.2682C>G | p.Ile894Met | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 24/29 | 2978/4625 | 2682/3840 | 894/1279 | chr1 | 17656079 | |||
chr1:17696908 | C | T | 1 | a0017 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.3368C>T | p.Thr1123Ile | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 29/29 | 3664/4625 | 3368/3840 | 1123/1279 | chr1 | 17696908 | |||
chr1:17697135 | G | A | 1 | a0019 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.3595G>A | p.Ala1199Thr | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 29/29 | 3891/4625 | 3595/3840 | 1199/1279 | chr1 | 17697135 | |||
chr1:17697195 | A | G | 15 | a0001 a0003 a0006 others(12): Show |
121 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(118): Show |
missense_variant | MODERATE | c.3655A>G | p.Ile1219Val | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 29/29 | 3951/4625 | 3655/3840 | 1219/1279 | chr1 | 17697195 | |||
chr1:17697204 | C | T | 1 | a0007 | 3 | HG03471.hp2 HG03540.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.3664C>T | p.Arg1222Cys | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 29/29 | 3960/4625 | 3664/3840 | 1222/1279 | chr1 | 17697204 | |||
chr1:17697223 | G | A | 1 | a0013 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.3683G>A | p.Arg1228His | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 29/29 | 3979/4625 | 3683/3840 | 1228/1279 | chr1 | 17697223 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:17580613 | T | G | 3 | a0001c0014 a0002c0021 a0002c0022 |
4 | HG00544.hp1 HG00544.hp2 NA18946.hp1 others(1): Show |
synonymous_variant | LOW | c.18T>G | p.Pro6Pro | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/29 | 314/4625 | 18/3840 | 6/1279 | chr1 | 17580613 | |||
chr1:17607824 | C | T | 3 | a0001c0048 a0002c0008 a0005c0015 |
7 | HG00733.hp1 HG01433.hp2 HG02602.hp1 others(4): Show |
synonymous_variant | LOW | c.456C>T | p.Tyr152Tyr | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/29 | 752/4625 | 456/3840 | 152/1279 | chr1 | 17607824 | |||
chr1:17621914 | C | T | 1 | a0008c0027 | 1 | NA18954.hp1 | synonymous_variant | LOW | c.993C>T | p.Tyr331Tyr | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 11/29 | 1289/4625 | 993/3840 | 331/1279 | chr1 | 17621914 | |||
chr1:17623067 | C | T | 1 | a0001c0013 | 3 | HG00738.hp1 HG01261.hp1 NA20805.hp1 |
synonymous_variant | LOW | c.1092C>T | p.Phe364Phe | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 12/29 | 1388/4625 | 1092/3840 | 364/1279 | chr1 | 17623067 | |||
chr1:17625982 | T | C | 4 | a0001c0033 a0002c0034 a0004c0005 others(1): Show |
9 | HG02109.hp1 HG02559.hp1 HG02717.hp2 others(6): Show |
synonymous_variant | LOW | c.1344T>C | p.Arg448Arg | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 14/29 | 1640/4625 | 1344/3840 | 448/1279 | chr1 | 17625982 | |||
chr1:17626036 | A | C | 6 | a0001c0033 a0002c0007 a0002c0034 others(3): Show |
15 | HG00642.hp1 HG02109.hp1 HG02280.hp2 others(12): Show |
synonymous_variant | LOW | c.1398A>C | p.Ile466Ile | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 14/29 | 1694/4625 | 1398/3840 | 466/1279 | chr1 | 17626036 | |||
chr1:17632368 | G | A | 3 | a0002c0021 a0002c0036 a0013c0035 |
3 | HG02080.hp1 NA18951.hp1 NA19010.hp2 |
synonymous_variant | LOW | c.1632G>A | p.Thr544Thr | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 16/29 | 1928/4625 | 1632/3840 | 544/1279 | chr1 | 17632368 | |||
chr1:17632449 | T | C | 4 | a0001c0033 a0002c0034 a0004c0005 others(1): Show |
9 | HG02109.hp1 HG02559.hp1 HG02717.hp2 others(6): Show |
synonymous_variant | LOW | c.1713T>C | p.Cys571Cys | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 16/29 | 2009/4625 | 1713/3840 | 571/1279 | chr1 | 17632449 | |||
chr1:17634850 | C | T | 3 | a0001c0012 a0001c0013 a0001c0045 |
7 | HG00323.hp1 HG00738.hp1 HG00738.hp2 others(4): Show |
synonymous_variant | LOW | c.1761C>T | p.Ile587Ile | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/29 | 2057/4625 | 1761/3840 | 587/1279 | chr1 | 17634850 | |||
chr1:17637979 | C | T | 7 | a0001c0006 a0001c0033 a0001c0044 others(4): Show |
17 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(14): Show |
synonymous_variant | LOW | c.2019C>T | p.Ile673Ile | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 19/29 | 2315/4625 | 2019/3840 | 673/1279 | chr1 | 17637979 | |||
chr1:17637985 | G | A | 1 | a0001c0045 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.2025G>A | p.Thr675Thr | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 19/29 | 2321/4625 | 2025/3840 | 675/1279 | chr1 | 17637985 | |||
chr1:17640214 | C | T | 1 | a0001c0043 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.2184C>T | p.Pro728Pro | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/29 | 2480/4625 | 2184/3840 | 728/1279 | chr1 | 17640214 | |||
chr1:17640295 | C | T | 1 | a0001c0042 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.2265C>T | p.Ile755Ile | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/29 | 2561/4625 | 2265/3840 | 755/1279 | chr1 | 17640295 | |||
chr1:17654689 | A | C | 25 | a0001c0011 a0001c0017 a0001c0019 others(22): Show |
48 | HG00544.hp2 HG00733.hp1 HG00741.hp1 others(45): Show |
synonymous_variant | LOW | c.2448A>C | p.Ala816Ala | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 23/29 | 2744/4625 | 2448/3840 | 816/1279 | chr1 | 17654689 | |||
chr1:17656064 | G | A | 13 | a0001c0011 a0001c0042 a0002c0003 others(10): Show |
27 | HG00544.hp2 HG00733.hp1 HG00741.hp1 others(24): Show |
synonymous_variant | LOW | c.2667G>A | p.Thr889Thr | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 24/29 | 2963/4625 | 2667/3840 | 889/1279 | chr1 | 17656064 | |||
chr1:17687581 | C | T | 1 | a0011c0025 | 1 | HG01106.hp1 | synonymous_variant | LOW | c.3018C>T | p.Phe1006Phe | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/29 | 3314/4625 | 3018/3840 | 1006/1279 | chr1 | 17687581 | |||
chr1:17687659 | C | T | 3 | a0001c0011 a0001c0020 a0001c0042 |
6 | HG00741.hp1 HG01109.hp1 HG01257.hp1 others(3): Show |
synonymous_variant | LOW | c.3096C>T | p.Ser1032Ser | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/29 | 3392/4625 | 3096/3840 | 1032/1279 | chr1 | 17687659 | |||
chr1:17687713 | C | T | 1 | a0001c0038 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.3150C>T | p.Ile1050Ile | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/29 | 3446/4625 | 3150/3840 | 1050/1279 | chr1 | 17687713 | |||
chr1:17696870 | C | T | 24 | a0001c0001 a0001c0006 a0001c0011 others(21): Show |
113 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(110): Show |
synonymous_variant | LOW | c.3330C>T | p.Asn1110Asn | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 29/29 | 3626/4625 | 3330/3840 | 1110/1279 | chr1 | 17696870 | |||
chr1:17697014 | T | C | 33 | a0001c0001 a0001c0006 a0001c0011 others(30): Show |
123 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(120): Show |
synonymous_variant | LOW | c.3474T>C | p.Asp1158Asp | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 29/29 | 3770/4625 | 3474/3840 | 1158/1279 | chr1 | 17697014 | |||
chr1:17697122 | G | A | 1 | a0001c0033 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.3582G>A | p.Ala1194Ala | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 29/29 | 3878/4625 | 3582/3840 | 1194/1279 | chr1 | 17697122 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:17539744 | G | A | 1 | a0001c0001t0005 | 1 | HG01884.hp2 | 5_prime_UTR_variant | MODIFIER | c.-250G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/29 | 40852 | chr1 | 17539744 | ||||||
chr1:17539846 | G | A | 1 | a0012c0031t0006 | 1 | HG01884.hp1 | 5_prime_UTR_variant | MODIFIER | c.-148G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/29 | 40750 | chr1 | 17539846 | ||||||
chr1:17697382 | G | A | 5 | a0001c0001t0003 a0001c0006t0003 a0001c0038t0003 others(2): Show |
14 | HG01069.hp2 HG01169.hp2 HG01175.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 29/29 | 2 | chr1 | 17697382 | ||||||
chr1:17697446 | C | T | 1 | a0002c0041t0008 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*66C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 29/29 | 66 | chr1 | 17697446 | ||||||
chr1:17697502 | G | GC | 29 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(26): Show |
113 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*123dupC | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 29/29 | 124 | INFO_REALIGN_3_PRIME | chr1 | 17697502 | |||||
chr1:17697681 | C | T | 1 | a0001c0006t0007 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*301C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 29/29 | 301 | chr1 | 17697681 | ||||||
chr1:17697702 | C | T | 3 | a0001c0044t0004 a0012c0031t0006 a0020c0049t0004 |
3 | HG01884.hp1 HG02622.hp2 NA18982.hp1 |
3_prime_UTR_variant | MODIFIER | c.*322C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 29/29 | 322 | chr1 | 17697702 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:17539981 | C | T | 8 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0003g0168 others(5): Show |
8 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-44+31C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17539981 | |||||||
chr1:17540213 | T | TTG | 2 | a0001c0001t0001g0159 a0002c0036t0002g0160 |
2 | NA18954.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-44+276_-44+277dup others(2): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17540213 | ||||||
chr1:17540267 | CA | C | 5 | a0001c0001t0001g0154 a0001c0001t0001g0158 a0001c0006t0001g0156 others(2): Show |
5 | HG02976.hp1 HG03130.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+318delA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17540267 | |||||||
chr1:17540326 | G | A | 1 | a0001c0006t0001g0001 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-44+376G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17540326 | |||||||
chr1:17540403 | C | T | 1 | a0001c0001t0003g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-44+453C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17540403 | |||||||
chr1:17540502 | C | T | 1 | a0001c0011t0001g0152 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-44+552C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17540502 | |||||||
chr1:17540510 | C | G | 6 | a0001c0001t0003g0151 a0001c0006t0007g0150 a0001c0017t0002g0148 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+560C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17540510 | |||||||
chr1:17540636 | C | T | 3 | a0001c0001t0003g0143 a0001c0014t0001g0145 a0003c0002t0001g0144 |
3 | HG03688.hp2 NA18747.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.-44+686C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17540636 | |||||||
chr1:17540642 | C | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-44+692C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17540642 | |||||||
chr1:17540862 | G | A | 3 | a0001c0001t0003g0143 a0001c0014t0001g0145 a0003c0002t0001g0144 |
3 | HG03688.hp2 NA18747.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.-44+912G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17540862 | |||||||
chr1:17540984 | T | C | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(57): Show |
60 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.-44+1034T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17540984 | |||||||
chr1:17541161 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-44+1211C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17541161 | |||||||
chr1:17541279 | A | C | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(72): Show |
75 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.-44+1329A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17541279 | |||||||
chr1:17541310 | G | C | 1 | a0001c0001t0003g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-44+1360G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17541310 | |||||||
chr1:17541353 | A | G | 4 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0038t0003g0124 others(1): Show |
4 | HG02602.hp1 HG03834.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+1403A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17541353 | |||||||
chr1:17541549 | G | T | 1 | a0001c0001t0003g0168 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-44+1599G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17541549 | |||||||
chr1:17541806 | A | G | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+1856A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17541806 | |||||||
chr1:17541835 | C | T | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+1885C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17541835 | |||||||
chr1:17541836 | A | G | 20 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(17): Show |
20 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.-44+1886A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17541836 | |||||||
chr1:17541877 | G | T | 1 | a0001c0001t0003g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-44+1927G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17541877 | |||||||
chr1:17541900 | C | G | 1 | a0006c0009t0001g0107 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-44+1950C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17541900 | |||||||
chr1:17541954 | T | C | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+2004T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17541954 | |||||||
chr1:17541979 | G | A | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+2029G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17541979 | |||||||
chr1:17542063 | C | T | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(94): Show |
97 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.-44+2113C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17542063 | |||||||
chr1:17542099 | A | G | 1 | a0001c0001t0003g0151 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-44+2149A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17542099 | |||||||
chr1:17542150 | AG | A | 2 | a0001c0006t0001g0001 a0002c0003t0002g0116 |
2 | HG01074.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-44+2201delG | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17542150 | |||||||
chr1:17542151 | G | A | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(100): Show |
103 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.-44+2201G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17542151 | |||||||
chr1:17542274 | C | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(71): Show |
74 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.-44+2324C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17542274 | |||||||
chr1:17542323 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-44+2373C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17542323 | |||||||
chr1:17542335 | G | C | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+2385G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17542335 | |||||||
chr1:17542375 | G | A | 1 | a0001c0001t0003g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-44+2425G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17542375 | |||||||
chr1:17542451 | T | A | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+2501T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17542451 | |||||||
chr1:17542464 | A | G | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+2514A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17542464 | |||||||
chr1:17542602 | T | C | 1 | a0002c0003t0002g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-44+2652T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17542602 | |||||||
chr1:17542684 | T | C | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+2734T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17542684 | |||||||
chr1:17542826 | C | T | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+2876C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17542826 | |||||||
chr1:17542941 | G | A | 3 | a0001c0001t0003g0143 a0001c0014t0001g0145 a0003c0002t0001g0144 |
3 | HG03688.hp2 NA18747.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.-44+2991G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17542941 | |||||||
chr1:17543029 | T | C | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+3079T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17543029 | |||||||
chr1:17543136 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-44+3186G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17543136 | |||||||
chr1:17543278 | A | G | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+3328A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17543278 | |||||||
chr1:17543281 | A | G | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+3331A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17543281 | |||||||
chr1:17543294 | A | T | 3 | a0001c0001t0003g0143 a0001c0014t0001g0145 a0003c0002t0001g0144 |
3 | HG03688.hp2 NA18747.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.-44+3344A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17543294 | |||||||
chr1:17543500 | T | G | 1 | a0004c0005t0002g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-44+3550T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17543500 | |||||||
chr1:17543501 | G | T | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+3551G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17543501 | |||||||
chr1:17543583 | C | CA | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+3644dupA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17543583 | ||||||
chr1:17543603 | G | C | 1 | a0003c0002t0001g0056 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-44+3653G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17543603 | |||||||
chr1:17543607 | G | A | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+3657G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17543607 | |||||||
chr1:17543733 | C | T | 1 | a0003c0002t0001g0106 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-44+3783C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17543733 | |||||||
chr1:17543845 | A | G | 1 | a0002c0007t0002g0105 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-44+3895A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17543845 | |||||||
chr1:17543902 | C | T | 1 | a0014c0029t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-44+3952C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17543902 | |||||||
chr1:17544101 | T | C | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+4151T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17544101 | |||||||
chr1:17544135 | T | G | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+4185T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17544135 | |||||||
chr1:17544178 | G | C | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+4228G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17544178 | |||||||
chr1:17544278 | G | A | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+4328G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17544278 | |||||||
chr1:17544278 | G | GTA | 2 | a0002c0004t0002g0167 a0006c0009t0001g0166 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-44+4341_-44+4342d others(4): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17544278 | ||||||
chr1:17544291 | T | A | 1 | a0004c0005t0002g0006 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-44+4341T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17544291 | |||||||
chr1:17544291 | T | TATGA | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+4342_-44+4343i others(6): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17544291 | ||||||
chr1:17544296 | AT | A | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+4356delT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17544296 | ||||||
chr1:17544359 | C | T | 12 | a0001c0001t0001g0128 a0001c0001t0001g0134 a0001c0001t0001g0136 others(9): Show |
12 | HG00558.hp2 HG02080.hp2 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+4409C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17544359 | |||||||
chr1:17544447 | A | C | 4 | a0001c0020t0001g0052 a0001c0043t0002g0051 a0002c0041t0008g0054 others(1): Show |
4 | HG01109.hp1 HG02630.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+4497A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17544447 | |||||||
chr1:17544499 | G | T | 12 | a0001c0001t0001g0119 a0001c0001t0001g0125 a0001c0001t0001g0127 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+4549G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17544499 | |||||||
chr1:17544577 | G | T | 10 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0006t0001g0001 others(7): Show |
10 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.-44+4627G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17544577 | |||||||
chr1:17544627 | C | T | 12 | a0001c0001t0001g0128 a0001c0001t0001g0134 a0001c0001t0001g0136 others(9): Show |
12 | HG00558.hp2 HG02080.hp2 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+4677C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17544627 | |||||||
chr1:17544702 | G | A | 10 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0006t0001g0001 others(7): Show |
10 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.-44+4752G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17544702 | |||||||
chr1:17544829 | T | C | 10 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0006t0001g0001 others(7): Show |
10 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.-44+4879T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17544829 | |||||||
chr1:17544872 | T | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(103): Show |
106 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.-44+4922T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17544872 | |||||||
chr1:17544889 | G | A | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(100): Show |
103 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.-44+4939G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17544889 | |||||||
chr1:17544904 | A | G | 10 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0006t0001g0001 others(7): Show |
10 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.-44+4954A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17544904 | |||||||
chr1:17545036 | G | T | 10 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0006t0001g0001 others(7): Show |
10 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.-44+5086G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17545036 | |||||||
chr1:17545110 | G | T | 9 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0006t0001g0001 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.-44+5160G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17545110 | |||||||
chr1:17545146 | A | G | 4 | a0001c0001t0001g0103 a0001c0012t0001g0102 a0002c0008t0002g0104 others(1): Show |
4 | HG00323.hp1 HG00733.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+5196A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17545146 | |||||||
chr1:17545150 | C | T | 1 | a0017c0037t0001g0142 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-44+5200C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17545150 | |||||||
chr1:17545198 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-44+5248G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17545198 | |||||||
chr1:17545200 | G | A | 1 | a0008c0016t0002g0132 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-44+5250G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17545200 | |||||||
chr1:17545533 | G | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(72): Show |
75 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.-44+5583G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17545533 | |||||||
chr1:17545615 | A | G | 10 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0006t0001g0001 others(7): Show |
10 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.-44+5665A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17545615 | |||||||
chr1:17545817 | C | T | 3 | a0002c0004t0002g0120 a0002c0004t0002g0121 a0014c0029t0001g0122 |
3 | HG01070.hp1 HG01071.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-44+5867C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17545817 | |||||||
chr1:17545860 | A | T | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(84): Show |
87 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.-44+5910A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17545860 | |||||||
chr1:17546045 | C | A | 1 | a0006c0009t0003g0007 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-44+6095C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17546045 | |||||||
chr1:17546164 | G | T | 9 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0006t0001g0001 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.-44+6214G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17546164 | |||||||
chr1:17546314 | T | C | 6 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0003g0168 others(3): Show |
6 | HG01106.hp2 HG01884.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+6364T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17546314 | |||||||
chr1:17546425 | T | C | 3 | a0001c0001t0003g0143 a0001c0014t0001g0145 a0003c0002t0001g0144 |
3 | HG03688.hp2 NA18747.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.-44+6475T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17546425 | |||||||
chr1:17546603 | G | A | 1 | a0001c0013t0001g0008 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-44+6653G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17546603 | |||||||
chr1:17546654 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-44+6704G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17546654 | |||||||
chr1:17546685 | G | A | 3 | a0001c0001t0001g0163 a0001c0001t0005g0162 a0001c0044t0004g0161 |
3 | HG01106.hp2 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-44+6735G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17546685 | |||||||
chr1:17546799 | C | T | 12 | a0001c0001t0001g0128 a0001c0001t0001g0134 a0001c0001t0001g0136 others(9): Show |
12 | HG00558.hp2 HG02080.hp2 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+6849C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17546799 | |||||||
chr1:17546928 | G | A | 1 | a0001c0006t0001g0001 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-44+6978G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17546928 | |||||||
chr1:17547031 | CT | C | 9 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0006t0001g0001 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.-44+7083delT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17547031 | ||||||
chr1:17547268 | C | T | 1 | a0001c0001t0003g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-44+7318C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17547268 | |||||||
chr1:17547351 | C | G | 1 | a0001c0001t0001g0163 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-44+7401C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17547351 | |||||||
chr1:17547392 | C | T | 1 | a0012c0031t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-44+7442C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17547392 | |||||||
chr1:17547432 | A | G | 1 | a0017c0037t0001g0142 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-44+7482A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17547432 | |||||||
chr1:17547464 | A | G | 1 | a0001c0001t0003g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-44+7514A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17547464 | |||||||
chr1:17547638 | G | A | 1 | a0006c0009t0001g0166 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-44+7688G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17547638 | |||||||
chr1:17548077 | G | C | 2 | a0001c0001t0001g0159 a0002c0036t0002g0160 |
2 | NA18954.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-44+8127G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17548077 | |||||||
chr1:17548348 | C | T | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0019 others(33): Show |
36 | HG00323.hp2 HG00733.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.-44+8398C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17548348 | |||||||
chr1:17548646 | C | CT | 15 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG01081.hp2 HG01106.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.-44+8721dupT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17548646 | ||||||
chr1:17548646 | C | CTTTT | 7 | a0001c0001t0003g0114 a0001c0017t0002g0113 a0001c0033t0002g0110 others(4): Show |
7 | HG02559.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-44+8718_-44+8721d others(6): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17548646 | ||||||
chr1:17548646 | CT | C | 11 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(8): Show |
11 | HG00323.hp2 HG01070.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-44+8721delT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17548646 | ||||||
chr1:17548795 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-44+8845C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17548795 | |||||||
chr1:17548912 | G | C | 5 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0001c0038t0003g0124 others(2): Show |
5 | HG01074.hp2 HG02602.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+8962G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17548912 | |||||||
chr1:17549121 | C | T | 1 | a0001c0001t0005g0162 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-44+9171C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17549121 | |||||||
chr1:17549229 | G | A | 2 | a0001c0001t0001g0063 a0001c0012t0001g0064 |
2 | HG00738.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-44+9279G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17549229 | |||||||
chr1:17549508 | G | A | 13 | a0001c0001t0001g0163 a0001c0001t0003g0114 a0001c0001t0005g0162 others(10): Show |
13 | HG01106.hp2 HG01884.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-44+9558G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17549508 | |||||||
chr1:17549524 | A | C | 3 | a0001c0001t0001g0163 a0001c0001t0005g0162 a0001c0044t0004g0161 |
3 | HG01106.hp2 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-44+9574A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17549524 | |||||||
chr1:17549595 | G | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0048 others(1): Show |
4 | HG01346.hp2 HG01496.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+9645G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17549595 | |||||||
chr1:17549751 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | NA18612.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-44+9801A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17549751 | |||||||
chr1:17549891 | G | A | 1 | a0001c0019t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-44+9941G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17549891 | |||||||
chr1:17549894 | C | T | 64 | a0001c0001t0001g0014 a0001c0001t0001g0045 a0001c0001t0001g0046 others(61): Show |
64 | HG00544.hp1 HG00544.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.-44+9944C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17549894 | |||||||
chr1:17549915 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-44+9965C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17549915 | |||||||
chr1:17549983 | T | G | 1 | a0001c0001t0003g0092 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-44+10033T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17549983 | |||||||
chr1:17550353 | A | T | 2 | a0001c0001t0001g0063 a0001c0012t0001g0064 |
2 | HG00738.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-44+10403A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17550353 | |||||||
chr1:17550355 | G | A | 5 | a0005c0015t0002g0067 a0005c0015t0002g0068 a0005c0023t0002g0101 others(2): Show |
5 | HG01123.hp1 HG01169.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44+10405G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17550355 | |||||||
chr1:17550364 | C | T | 5 | a0001c0013t0001g0008 a0001c0013t0001g0017 a0001c0044t0004g0161 others(2): Show |
5 | HG00738.hp1 HG02109.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+10414C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17550364 | |||||||
chr1:17550555 | T | C | 4 | a0001c0001t0001g0163 a0001c0001t0005g0162 a0001c0020t0001g0052 others(1): Show |
4 | HG01106.hp2 HG01109.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+10605T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17550555 | |||||||
chr1:17550625 | G | A | 1 | a0003c0002t0001g0069 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-44+10675G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17550625 | |||||||
chr1:17550650 | G | GA | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(147): Show |
150 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.-44+10711dupA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17550650 | ||||||
chr1:17550876 | G | A | 1 | a0011c0025t0002g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-44+10926G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17550876 | |||||||
chr1:17550988 | C | T | 7 | a0001c0001t0001g0061 a0001c0001t0003g0168 a0001c0019t0001g0095 others(4): Show |
7 | HG00642.hp1 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44+11038C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17550988 | |||||||
chr1:17550995 | C | T | 13 | a0001c0001t0003g0131 a0001c0006t0001g0001 a0001c0006t0001g0129 others(10): Show |
13 | HG01069.hp1 HG01071.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-44+11045C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17550995 | |||||||
chr1:17551326 | C | A | 2 | a0001c0001t0001g0163 a0001c0001t0005g0162 |
2 | HG01106.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-44+11376C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17551326 | |||||||
chr1:17551351 | T | TC | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(138): Show |
141 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.-44+11403dupC | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17551351 | ||||||
chr1:17551440 | A | G | 10 | a0001c0001t0001g0119 a0001c0006t0007g0150 a0001c0019t0001g0066 others(7): Show |
10 | HG02109.hp1 HG02280.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-44+11490A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17551440 | |||||||
chr1:17551451 | G | T | 1 | a0009c0039t0001g0039 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-44+11501G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17551451 | |||||||
chr1:17551512 | A | T | 1 | a0002c0034t0002g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-44+11562A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17551512 | |||||||
chr1:17551516 | T | C | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(150): Show |
153 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.-44+11566T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17551516 | |||||||
chr1:17551614 | T | C | 4 | a0001c0001t0001g0024 a0001c0001t0001g0070 a0001c0001t0001g0097 others(1): Show |
4 | HG00733.hp2 HG01123.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+11664T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17551614 | |||||||
chr1:17551747 | A | G | 1 | a0003c0002t0001g0144 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-44+11797A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17551747 | |||||||
chr1:17551778 | C | A | 5 | a0001c0033t0002g0110 a0002c0007t0002g0111 a0004c0005t0002g0112 others(2): Show |
5 | HG02559.hp1 HG02922.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+11828C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17551778 | |||||||
chr1:17551875 | A | G | 12 | a0001c0001t0001g0021 a0001c0001t0001g0057 a0001c0001t0001g0103 others(9): Show |
12 | HG00323.hp1 HG00733.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.-44+11925A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17551875 | |||||||
chr1:17551932 | G | A | 1 | a0001c0038t0003g0124 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-44+11982G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17551932 | |||||||
chr1:17552124 | T | C | 75 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(72): Show |
75 | HG00544.hp1 HG00544.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.-44+12174T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17552124 | |||||||
chr1:17552226 | A | G | 1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-44+12276A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17552226 | |||||||
chr1:17552287 | T | G | 6 | a0001c0001t0001g0062 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
6 | HG02602.hp1 HG03579.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44+12337T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17552287 | |||||||
chr1:17552291 | C | T | 1 | a0001c0044t0004g0161 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-44+12341C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17552291 | |||||||
chr1:17552300 | A | G | 2 | a0001c0020t0001g0052 a0001c0043t0002g0051 |
2 | HG01109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-44+12350A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17552300 | |||||||
chr1:17552315 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-44+12365T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17552315 | |||||||
chr1:17552336 | A | G | 1 | a0001c0020t0001g0052 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-44+12386A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17552336 | |||||||
chr1:17552571 | G | GT | 11 | a0001c0001t0001g0043 a0001c0006t0003g0139 a0001c0011t0001g0004 others(8): Show |
11 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.-44+12653dupT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17552571 | ||||||
chr1:17552571 | GT | G | 60 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(57): Show |
60 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.-44+12653delT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17552571 | ||||||
chr1:17552571 | GTT | G | 28 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(25): Show |
28 | HG00558.hp2 HG01081.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.-44+12652_-44+1265 others(6): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17552571 | ||||||
chr1:17552571 | GTTTT | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0062 a0001c0001t0001g0125 others(5): Show |
8 | HG02572.hp1 HG02602.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-44+12650_-44+1265 others(8): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17552571 | ||||||
chr1:17552571 | GTTTTTTT others(10): Show |
G | 1 | a0001c0020t0001g0016 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-44+12637_-44+1265 others(21): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17552571 | ||||||
chr1:17552571 | GTTTTTTT others(11): Show |
G | 7 | a0001c0012t0001g0072 a0003c0002t0001g0144 a0005c0015t0002g0067 others(4): Show |
7 | HG01081.hp1 HG01123.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.-44+12636_-44+1265 others(22): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17552571 | ||||||
chr1:17552582 | T | G | 12 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0088 others(9): Show |
12 | HG00741.hp2 HG01109.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.-44+12632T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17552582 | |||||||
chr1:17553049 | G | A | 4 | a0001c0014t0001g0094 a0001c0014t0001g0145 a0002c0021t0002g0137 others(1): Show |
4 | HG00544.hp1 HG00544.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+13099G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17553049 | |||||||
chr1:17553103 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0154 a0001c0001t0003g0153 |
3 | HG02572.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-44+13153C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17553103 | |||||||
chr1:17553165 | C | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0154 a0001c0001t0003g0153 |
3 | HG02572.hp1 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-44+13215C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17553165 | |||||||
chr1:17553189 | C | G | 6 | a0001c0001t0001g0062 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
6 | HG02602.hp1 HG03579.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44+13239C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17553189 | |||||||
chr1:17553469 | C | T | 4 | a0001c0014t0001g0094 a0001c0014t0001g0145 a0002c0021t0002g0137 others(1): Show |
4 | HG00544.hp1 HG00544.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+13519C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17553469 | |||||||
chr1:17553521 | C | T | 1 | a0003c0002t0001g0038 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-44+13571C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17553521 | |||||||
chr1:17553570 | C | T | 1 | a0014c0029t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-44+13620C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17553570 | |||||||
chr1:17553803 | T | C | 1 | a0018c0028t0003g0044 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-44+13853T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17553803 | |||||||
chr1:17553865 | C | A | 5 | a0001c0001t0003g0131 a0001c0006t0001g0001 a0001c0006t0001g0129 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+13915C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17553865 | |||||||
chr1:17553964 | T | C | 14 | a0001c0001t0001g0043 a0001c0001t0003g0131 a0001c0006t0001g0001 others(11): Show |
14 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-44+14014T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17553964 | |||||||
chr1:17554129 | G | A | 4 | a0001c0014t0001g0094 a0001c0014t0001g0145 a0002c0021t0002g0137 others(1): Show |
4 | HG00544.hp1 HG00544.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+14179G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17554129 | |||||||
chr1:17554273 | C | A | 2 | a0001c0006t0007g0150 a0014c0029t0001g0122 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-44+14323C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17554273 | |||||||
chr1:17554344 | G | C | 3 | a0003c0002t0001g0069 a0003c0002t0001g0073 a0003c0002t0001g0074 |
3 | HG02602.hp2 HG02683.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-44+14394G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17554344 | |||||||
chr1:17554391 | G | A | 1 | a0001c0048t0001g0005 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-44+14441G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17554391 | |||||||
chr1:17554474 | G | T | 1 | a0002c0022t0002g0050 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-44+14524G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17554474 | |||||||
chr1:17554519 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0005g0162 |
2 | HG01106.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-44+14569C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17554519 | |||||||
chr1:17554520 | A | G | 1 | a0019c0026t0001g0026 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-44+14570A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17554520 | |||||||
chr1:17554583 | C | CT | 8 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0163 others(5): Show |
8 | HG01074.hp2 HG01106.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-44+14655dupT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17554583 | ||||||
chr1:17554583 | C | CTT | 5 | a0001c0033t0002g0110 a0002c0007t0002g0111 a0004c0005t0002g0112 others(2): Show |
5 | HG02559.hp1 HG02922.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+14654_-44+1465 others(6): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17554583 | ||||||
chr1:17554583 | CT | C | 16 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0062 others(13): Show |
16 | HG01070.hp2 HG01496.hp1 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.-44+14655delT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17554583 | ||||||
chr1:17554583 | CTT | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0154 a0001c0001t0003g0153 others(2): Show |
5 | HG02572.hp1 HG02976.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+14654_-44+1465 others(6): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17554583 | ||||||
chr1:17554666 | G | A | 2 | a0001c0006t0007g0150 a0014c0029t0001g0122 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-44+14716G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17554666 | |||||||
chr1:17554985 | A | G | 1 | a0005c0024t0002g0059 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-44+15035A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17554985 | |||||||
chr1:17555273 | G | A | 2 | a0001c0020t0001g0052 a0001c0043t0002g0051 |
2 | HG01109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-44+15323G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17555273 | |||||||
chr1:17555298 | C | T | 1 | a0002c0007t0002g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-44+15348C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17555298 | |||||||
chr1:17555368 | C | CT | 6 | a0002c0004t0002g0118 a0002c0007t0002g0013 a0002c0007t0002g0085 others(3): Show |
6 | HG01884.hp1 HG02486.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+15432dupT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17555368 | ||||||
chr1:17555762 | C | T | 1 | a0008c0027t0002g0029 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-44+15812C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17555762 | |||||||
chr1:17555837 | C | T | 4 | a0002c0004t0002g0118 a0002c0007t0002g0013 a0002c0007t0002g0085 others(1): Show |
4 | HG01884.hp1 HG02486.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+15887C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17555837 | |||||||
chr1:17555981 | A | G | 1 | a0006c0009t0003g0007 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-44+16031A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17555981 | |||||||
chr1:17556033 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-44+16083T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17556033 | |||||||
chr1:17556072 | C | T | 1 | a0002c0004t0002g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-44+16122C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17556072 | |||||||
chr1:17556104 | T | G | 2 | a0001c0020t0001g0052 a0001c0043t0002g0051 |
2 | HG01109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-44+16154T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17556104 | |||||||
chr1:17556119 | G | C | 2 | a0001c0020t0001g0052 a0001c0043t0002g0051 |
2 | HG01109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-44+16169G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17556119 | |||||||
chr1:17556134 | G | T | 1 | a0001c0001t0001g0099 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-44+16184G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17556134 | |||||||
chr1:17556234 | A | C | 1 | a0002c0007t0002g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-44+16284A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17556234 | |||||||
chr1:17556234 | AGCCTGGG others(79): Show |
A | 4 | a0001c0001t0003g0114 a0001c0017t0002g0113 a0004c0005t0002g0108 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+16297_-44+1638 others(90): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17556234 | ||||||
chr1:17556249 | A | G | 1 | a0001c0001t0003g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-44+16299A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17556249 | |||||||
chr1:17556269 | C | CGG | 7 | a0001c0001t0001g0154 a0001c0001t0003g0131 a0001c0006t0001g0001 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-44+16320_-44+1632 others(6): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17556269 | ||||||
chr1:17556270 | GGC | G | 19 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0084 others(16): Show |
19 | HG00544.hp2 HG00741.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-44+16322_-44+1632 others(6): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17556270 | ||||||
chr1:17556271 | GC | G | 25 | a0001c0001t0001g0014 a0001c0001t0001g0045 a0001c0001t0001g0062 others(22): Show |
25 | HG00544.hp1 HG01069.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-44+16322delC | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17556271 | |||||||
chr1:17556272 | C | CG | 15 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0022 others(12): Show |
15 | HG00642.hp2 HG01106.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.-44+16332dupG | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17556272 | ||||||
chr1:17556272 | C | G | 25 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0046 others(22): Show |
25 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.-44+16322C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17556272 | |||||||
chr1:17556273 | G | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0062 a0001c0001t0001g0125 others(4): Show |
7 | HG02602.hp1 HG03579.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44+16323G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17556273 | |||||||
chr1:17556275 | G | C | 5 | a0001c0033t0002g0110 a0002c0007t0002g0111 a0004c0005t0002g0112 others(2): Show |
5 | HG02559.hp1 HG02922.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+16325G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17556275 | |||||||
chr1:17556276 | G | C | 1 | a0016c0047t0002g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-44+16326G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17556276 | |||||||
chr1:17556279 | G | C | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0084 others(12): Show |
15 | HG00741.hp2 HG01109.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-44+16329G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17556279 | |||||||
chr1:17556279 | GGGGCCTG others(12): Show |
G | 1 | a0001c0001t0001g0034 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-44+16344_-44+1636 others(23): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17556279 | ||||||
chr1:17556281 | G | C | 1 | a0005c0015t0002g0067 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-44+16331G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17556281 | |||||||
chr1:17556293 | C | CG | 30 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(27): Show |
30 | HG00323.hp2 HG00558.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.-44+16343_-44+1634 others(5): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17556293 | |||||||
chr1:17556294 | A | G | 30 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(27): Show |
30 | HG00323.hp2 HG00558.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.-44+16344A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17556294 | |||||||
chr1:17556298 | C | G | 1 | a0001c0001t0003g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-44+16348C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17556298 | |||||||
chr1:17556465 | C | T | 4 | a0002c0004t0002g0118 a0002c0007t0002g0013 a0002c0007t0002g0085 others(1): Show |
4 | HG01884.hp1 HG02486.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+16515C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17556465 | |||||||
chr1:17556564 | T | C | 1 | a0002c0034t0002g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-44+16614T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17556564 | |||||||
chr1:17557033 | T | TA | 15 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0084 others(12): Show |
15 | HG00741.hp2 HG01109.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-44+17102dupA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17557033 | ||||||
chr1:17557033 | TA | T | 14 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0024 others(11): Show |
14 | HG00323.hp1 HG00558.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+17102delA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17557033 | ||||||
chr1:17557062 | G | A | 1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-44+17112G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17557062 | |||||||
chr1:17557346 | A | C | 24 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(21): Show |
24 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.-44+17396A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17557346 | |||||||
chr1:17557352 | A | C | 2 | a0001c0001t0001g0163 a0001c0001t0005g0162 |
2 | HG01106.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-44+17402A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17557352 | |||||||
chr1:17557356 | C | CA | 18 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0019 others(15): Show |
18 | HG00558.hp2 HG01081.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-44+17414dupA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17557356 | ||||||
chr1:17557364 | A | C | 2 | a0001c0001t0001g0010 a0002c0004t0002g0167 |
2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-44+17414A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17557364 | |||||||
chr1:17557365 | C | A | 28 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(25): Show |
28 | HG00544.hp1 HG00544.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.-44+17415C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17557365 | |||||||
chr1:17557388 | C | T | 1 | a0001c0001t0003g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-44+17438C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17557388 | |||||||
chr1:17557448 | G | T | 4 | a0001c0033t0002g0110 a0002c0007t0002g0111 a0004c0005t0002g0112 others(1): Show |
4 | HG02559.hp1 HG02922.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+17498G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17557448 | |||||||
chr1:17557548 | T | G | 24 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(21): Show |
24 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.-44+17598T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17557548 | |||||||
chr1:17557584 | G | A | 4 | a0001c0033t0002g0110 a0002c0007t0002g0111 a0004c0005t0002g0112 others(1): Show |
4 | HG02559.hp1 HG02922.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44+17634G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17557584 | |||||||
chr1:17557659 | G | A | 2 | a0001c0006t0007g0150 a0014c0029t0001g0122 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-44+17709G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17557659 | |||||||
chr1:17557662 | C | T | 1 | a0004c0005t0002g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-44+17712C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17557662 | |||||||
chr1:17557724 | C | T | 5 | a0001c0033t0002g0110 a0002c0007t0002g0111 a0004c0005t0002g0112 others(2): Show |
5 | HG02559.hp1 HG02922.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+17774C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17557724 | |||||||
chr1:17557853 | G | A | 1 | a0001c0001t0003g0080 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-44+17903G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17557853 | |||||||
chr1:17557862 | T | C | 14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0084 others(11): Show |
14 | HG00741.hp2 HG01109.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.-44+17912T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17557862 | |||||||
chr1:17558023 | C | T | 10 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0071 others(7): Show |
10 | HG01069.hp2 HG02080.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.-44+18073C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17558023 | |||||||
chr1:17558224 | T | A | 2 | a0001c0006t0007g0150 a0014c0029t0001g0122 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-44+18274T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17558224 | |||||||
chr1:17558253 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-44+18303C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17558253 | |||||||
chr1:17558633 | C | T | 8 | a0001c0001t0001g0043 a0001c0011t0001g0004 a0001c0013t0001g0008 others(5): Show |
8 | HG00738.hp1 HG01952.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44+18683C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17558633 | |||||||
chr1:17558828 | T | A | 2 | a0002c0004t0002g0120 a0002c0004t0002g0121 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-44+18878T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17558828 | |||||||
chr1:17558886 | G | C | 14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0084 others(11): Show |
14 | HG00741.hp2 HG01109.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.-44+18936G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17558886 | |||||||
chr1:17559022 | A | G | 1 | a0008c0027t0002g0029 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-44+19072A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17559022 | |||||||
chr1:17559188 | G | C | 1 | a0001c0001t0001g0062 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-44+19238G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17559188 | |||||||
chr1:17559347 | C | T | 13 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0088 others(10): Show |
13 | HG00741.hp2 HG01109.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.-44+19397C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17559347 | |||||||
chr1:17559361 | G | A | 23 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0061 others(20): Show |
23 | HG00642.hp1 HG01069.hp2 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.-44+19411G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17559361 | |||||||
chr1:17559500 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-44+19550C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17559500 | |||||||
chr1:17559666 | T | C | 57 | a0001c0001t0001g0021 a0001c0001t0001g0043 a0001c0001t0001g0045 others(54): Show |
57 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.-44+19716T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17559666 | |||||||
chr1:17559929 | C | T | 1 | a0001c0020t0001g0016 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-44+19979C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17559929 | |||||||
chr1:17560189 | G | A | 1 | a0001c0045t0001g0031 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-44+20239G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17560189 | |||||||
chr1:17560329 | TC | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0127 a0002c0008t0002g0126 |
3 | HG02602.hp1 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-43-20220delC | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17560329 | ||||||
chr1:17560424 | T | G | 1 | a0001c0001t0001g0093 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-43-20129T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17560424 | |||||||
chr1:17560494 | A | G | 2 | a0001c0006t0007g0150 a0014c0029t0001g0122 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-43-20059A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17560494 | |||||||
chr1:17560507 | A | C | 1 | a0001c0001t0001g0159 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-43-20046A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17560507 | |||||||
chr1:17560521 | A | T | 1 | a0001c0001t0001g0159 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-43-20032A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17560521 | |||||||
chr1:17560522 | T | G | 1 | a0001c0001t0001g0159 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-43-20031T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17560522 | |||||||
chr1:17560523 | G | T | 1 | a0001c0001t0001g0159 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-43-20030G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17560523 | |||||||
chr1:17560526 | G | T | 1 | a0001c0001t0001g0159 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-43-20027G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17560526 | |||||||
chr1:17560528 | C | A | 1 | a0001c0001t0001g0159 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-43-20025C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17560528 | |||||||
chr1:17560570 | C | T | 1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-43-19983C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17560570 | |||||||
chr1:17560606 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(52): Show |
55 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.-43-19947C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17560606 | |||||||
chr1:17560621 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0003 |
2 | HG02486.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-43-19932A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17560621 | |||||||
chr1:17560792 | T | C | 18 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0084 others(15): Show |
18 | HG00544.hp1 HG00544.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.-43-19761T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17560792 | |||||||
chr1:17560936 | T | A | 8 | a0001c0001t0001g0043 a0001c0011t0001g0004 a0001c0013t0001g0008 others(5): Show |
8 | HG00738.hp1 HG01952.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-19617T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17560936 | |||||||
chr1:17560950 | C | T | 18 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0084 others(15): Show |
18 | HG00544.hp1 HG00544.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.-43-19603C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17560950 | |||||||
chr1:17561165 | A | G | 1 | a0001c0006t0003g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-43-19388A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17561165 | |||||||
chr1:17561272 | C | A | 2 | a0001c0001t0001g0163 a0001c0001t0005g0162 |
2 | HG01106.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-43-19281C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17561272 | |||||||
chr1:17561276 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-43-19277C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17561276 | |||||||
chr1:17561468 | T | C | 100 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0021 others(97): Show |
100 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.-43-19085T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17561468 | |||||||
chr1:17561507 | C | T | 1 | a0001c0006t0007g0150 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-43-19046C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17561507 | |||||||
chr1:17561523 | C | G | 2 | a0001c0001t0001g0163 a0001c0001t0005g0162 |
2 | HG01106.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-43-19030C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17561523 | |||||||
chr1:17561556 | C | T | 1 | a0001c0014t0001g0094 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-43-18997C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17561556 | |||||||
chr1:17561813 | G | C | 5 | a0001c0001t0001g0084 a0001c0014t0001g0094 a0001c0014t0001g0145 others(2): Show |
5 | HG00544.hp1 HG00544.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-18740G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17561813 | |||||||
chr1:17561912 | G | C | 2 | a0009c0039t0001g0039 a0020c0049t0004g0075 |
2 | NA18982.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.-43-18641G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17561912 | |||||||
chr1:17561931 | A | G | 1 | a0001c0001t0003g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-43-18622A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17561931 | |||||||
chr1:17562251 | C | T | 2 | a0001c0006t0007g0150 a0014c0029t0001g0122 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-43-18302C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17562251 | |||||||
chr1:17562306 | A | G | 13 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0088 others(10): Show |
13 | HG00741.hp2 HG01109.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.-43-18247A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17562306 | |||||||
chr1:17562415 | TCAAA | T | 2 | a0001c0006t0007g0150 a0014c0029t0001g0122 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-43-18125_-43-1812 others(8): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17562415 | ||||||
chr1:17562432 | A | AAG | 7 | a0001c0001t0001g0014 a0001c0001t0001g0062 a0001c0001t0001g0125 others(4): Show |
7 | HG02602.hp1 HG03579.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-18118_-43-1811 others(6): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17562432 | ||||||
chr1:17562475 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0062 a0001c0001t0001g0125 others(4): Show |
7 | HG02602.hp1 HG03579.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-18078C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17562475 | |||||||
chr1:17562728 | G | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0154 a0001c0006t0001g0156 others(1): Show |
4 | HG02572.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-17825G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17562728 | |||||||
chr1:17562905 | G | A | 6 | a0001c0001t0001g0062 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
6 | HG02602.hp1 HG03579.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-17648G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17562905 | |||||||
chr1:17562928 | C | T | 1 | a0004c0005t0002g0112 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-43-17625C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17562928 | |||||||
chr1:17563052 | C | T | 6 | a0001c0001t0001g0062 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
6 | HG02602.hp1 HG03579.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-17501C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17563052 | |||||||
chr1:17563195 | G | A | 6 | a0001c0001t0001g0062 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
6 | HG02602.hp1 HG03579.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-17358G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17563195 | |||||||
chr1:17563236 | T | C | 1 | a0004c0005t0002g0060 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-43-17317T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17563236 | |||||||
chr1:17563237 | C | CT | 16 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0076 others(13): Show |
16 | HG00558.hp2 HG01081.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.-43-17301dupT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17563237 | ||||||
chr1:17563237 | CT | C | 27 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(24): Show |
27 | HG00323.hp1 HG00741.hp2 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-43-17301delT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17563237 | ||||||
chr1:17563249 | T | G | 1 | a0001c0001t0001g0159 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-43-17304T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17563249 | |||||||
chr1:17563380 | G | A | 26 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(23): Show |
26 | HG00741.hp2 HG01106.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.-43-17173G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17563380 | |||||||
chr1:17563517 | G | A | 1 | a0008c0016t0002g0132 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-43-17036G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17563517 | |||||||
chr1:17563634 | G | A | 6 | a0001c0001t0001g0062 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
6 | HG02602.hp1 HG03579.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-16919G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17563634 | |||||||
chr1:17563687 | C | A | 1 | a0002c0003t0002g0133 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-43-16866C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17563687 | |||||||
chr1:17563793 | C | T | 6 | a0001c0001t0001g0062 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
6 | HG02602.hp1 HG03579.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-16760C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17563793 | |||||||
chr1:17563937 | T | C | 3 | a0001c0001t0003g0080 a0001c0012t0001g0102 a0008c0016t0002g0082 |
3 | HG00323.hp1 HG01496.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-43-16616T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17563937 | |||||||
chr1:17564079 | G | A | 6 | a0001c0001t0001g0062 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
6 | HG02602.hp1 HG03579.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-16474G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17564079 | |||||||
chr1:17564187 | G | GGTGAGGG others(136): Show |
1 | a0001c0001t0001g0159 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-43-16366_-43-1636 others(147): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17564187 | |||||||
chr1:17564238 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0154 a0001c0006t0001g0156 others(1): Show |
4 | HG02572.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-16315C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17564238 | |||||||
chr1:17564306 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0002c0008t0002g0042 |
3 | HG01109.hp2 HG03017.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-43-16247G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17564306 | |||||||
chr1:17564478 | C | T | 2 | a0001c0020t0001g0052 a0001c0043t0002g0051 |
2 | HG01109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-43-16075C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17564478 | |||||||
chr1:17564488 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-43-16065C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17564488 | |||||||
chr1:17564803 | C | T | 1 | a0017c0037t0001g0142 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-43-15750C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17564803 | |||||||
chr1:17564981 | C | T | 1 | a0003c0002t0001g0056 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-43-15572C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17564981 | |||||||
chr1:17564982 | C | G | 1 | a0001c0001t0003g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-43-15571C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17564982 | |||||||
chr1:17565099 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0062 a0001c0001t0001g0125 others(4): Show |
7 | HG02602.hp1 HG03579.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-15454C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17565099 | |||||||
chr1:17565155 | G | A | 1 | a0002c0007t0002g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-43-15398G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17565155 | |||||||
chr1:17565285 | C | T | 4 | a0002c0004t0002g0118 a0002c0007t0002g0013 a0002c0007t0002g0085 others(1): Show |
4 | HG01884.hp1 HG02486.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-15268C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17565285 | |||||||
chr1:17565466 | C | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0070 a0001c0001t0001g0097 others(1): Show |
4 | HG00733.hp2 HG01123.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-15087C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17565466 | |||||||
chr1:17565616 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-43-14937C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17565616 | |||||||
chr1:17565695 | G | T | 5 | a0001c0001t0001g0084 a0001c0014t0001g0094 a0001c0014t0001g0145 others(2): Show |
5 | HG00544.hp1 HG00544.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-14858G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17565695 | |||||||
chr1:17565730 | G | A | 11 | a0001c0001t0001g0021 a0001c0001t0001g0103 a0001c0001t0001g0136 others(8): Show |
11 | HG00323.hp1 HG00733.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.-43-14823G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17565730 | |||||||
chr1:17565901 | T | C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(29): Show |
32 | HG00323.hp2 HG00558.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.-43-14652T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17565901 | |||||||
chr1:17566011 | T | C | 1 | a0005c0024t0002g0059 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-43-14542T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17566011 | |||||||
chr1:17566024 | GTGTT | G | 6 | a0001c0001t0001g0062 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
6 | HG02602.hp1 HG03579.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-14525_-43-1452 others(8): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17566024 | ||||||
chr1:17566162 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0154 a0001c0006t0001g0156 others(1): Show |
4 | HG02572.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-14391C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17566162 | |||||||
chr1:17566184 | T | C | 1 | a0001c0001t0001g0012 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-43-14369T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17566184 | |||||||
chr1:17566247 | G | A | 6 | a0001c0001t0001g0062 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
6 | HG02602.hp1 HG03579.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-14306G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17566247 | |||||||
chr1:17566321 | A | C | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(152): Show |
155 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.-43-14232A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17566321 | |||||||
chr1:17566441 | T | C | 2 | a0001c0020t0001g0052 a0001c0043t0002g0051 |
2 | HG01109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-43-14112T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17566441 | |||||||
chr1:17566621 | C | T | 1 | a0007c0010t0001g0065 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-43-13932C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17566621 | |||||||
chr1:17566691 | A | T | 7 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0078 others(4): Show |
7 | HG00741.hp1 HG01169.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.-43-13862A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17566691 | |||||||
chr1:17566817 | C | T | 1 | a0001c0001t0003g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-43-13736C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17566817 | |||||||
chr1:17566913 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0154 a0001c0006t0001g0156 others(1): Show |
4 | HG02572.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-13640G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17566913 | |||||||
chr1:17567021 | C | G | 5 | a0001c0001t0001g0084 a0001c0014t0001g0094 a0001c0014t0001g0145 others(2): Show |
5 | HG00544.hp1 HG00544.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-13532C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17567021 | |||||||
chr1:17567321 | G | T | 4 | a0002c0004t0002g0118 a0002c0007t0002g0013 a0002c0007t0002g0085 others(1): Show |
4 | HG01884.hp1 HG02486.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-13232G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17567321 | |||||||
chr1:17567359 | C | G | 2 | a0001c0020t0001g0052 a0001c0043t0002g0051 |
2 | HG01109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.-43-13194C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17567359 | |||||||
chr1:17567406 | G | A | 2 | a0001c0011t0001g0152 a0001c0042t0001g0035 |
2 | HG00741.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.-43-13147G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17567406 | |||||||
chr1:17567435 | C | T | 6 | a0001c0033t0002g0110 a0002c0007t0002g0111 a0004c0005t0002g0112 others(3): Show |
6 | HG02559.hp1 HG02922.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-13118C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17567435 | |||||||
chr1:17567606 | G | C | 25 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(22): Show |
25 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-43-12947G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17567606 | |||||||
chr1:17567612 | C | A | 2 | a0001c0006t0007g0150 a0014c0029t0001g0122 |
2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-43-12941C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17567612 | |||||||
chr1:17568172 | C | T | 1 | a0001c0011t0001g0138 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-43-12381C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17568172 | |||||||
chr1:17568231 | CA | C | 2 | a0001c0001t0001g0163 a0001c0001t0005g0162 |
2 | HG01106.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-43-12319delA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17568231 | ||||||
chr1:17568418 | C | T | 15 | a0001c0001t0001g0014 a0001c0001t0001g0062 a0001c0001t0001g0125 others(12): Show |
15 | HG00544.hp1 HG00544.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-43-12135C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17568418 | |||||||
chr1:17568432 | A | G | 2 | a0001c0001t0001g0163 a0001c0001t0005g0162 |
2 | HG01106.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-43-12121A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17568432 | |||||||
chr1:17568447 | C | T | 1 | a0002c0003t0002g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-43-12106C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17568447 | |||||||
chr1:17568448 | C | G | 1 | a0002c0003t0002g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-43-12105C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17568448 | |||||||
chr1:17568598 | G | A | 1 | a0001c0001t0003g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-43-11955G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17568598 | |||||||
chr1:17568686 | C | A | 14 | a0001c0001t0001g0043 a0001c0001t0003g0131 a0001c0006t0001g0001 others(11): Show |
14 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-43-11867C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17568686 | |||||||
chr1:17568710 | C | T | 6 | a0001c0001t0003g0131 a0001c0006t0001g0001 a0001c0006t0001g0129 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-11843C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17568710 | |||||||
chr1:17568717 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0062 a0001c0001t0001g0125 others(4): Show |
7 | HG02602.hp1 HG03579.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-11836C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17568717 | |||||||
chr1:17568729 | T | C | 6 | a0001c0033t0002g0110 a0002c0007t0002g0111 a0004c0005t0002g0112 others(3): Show |
6 | HG02559.hp1 HG02922.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-11824T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17568729 | |||||||
chr1:17568867 | G | T | 1 | a0001c0001t0003g0090 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-43-11686G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17568867 | |||||||
chr1:17569148 | T | C | 2 | a0001c0001t0001g0063 a0001c0012t0001g0064 |
2 | HG00738.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-43-11405T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17569148 | |||||||
chr1:17569228 | CA | C | 2 | a0001c0001t0001g0163 a0001c0001t0005g0162 |
2 | HG01106.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-43-11324delA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17569228 | |||||||
chr1:17569249 | G | T | 37 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0040 others(34): Show |
37 | HG00544.hp1 HG00544.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.-43-11304G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17569249 | |||||||
chr1:17569250 | C | T | 2 | a0001c0001t0001g0041 a0002c0008t0002g0042 |
2 | HG03017.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-43-11303C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17569250 | |||||||
chr1:17569320 | G | T | 1 | a0017c0037t0001g0142 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-43-11233G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17569320 | |||||||
chr1:17569775 | C | T | 6 | a0001c0033t0002g0110 a0002c0007t0002g0111 a0004c0005t0002g0112 others(3): Show |
6 | HG02559.hp1 HG02922.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-10778C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17569775 | |||||||
chr1:17569798 | G | A | 6 | a0001c0033t0002g0110 a0002c0007t0002g0111 a0004c0005t0002g0112 others(3): Show |
6 | HG02559.hp1 HG02922.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-10755G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17569798 | |||||||
chr1:17570039 | T | A | 14 | a0001c0001t0001g0043 a0001c0001t0003g0131 a0001c0006t0001g0001 others(11): Show |
14 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-43-10514T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17570039 | |||||||
chr1:17570107 | G | A | 6 | a0001c0033t0002g0110 a0002c0007t0002g0111 a0004c0005t0002g0112 others(3): Show |
6 | HG02559.hp1 HG02922.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-10446G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17570107 | |||||||
chr1:17570344 | T | C | 4 | a0002c0004t0002g0118 a0002c0007t0002g0013 a0002c0007t0002g0085 others(1): Show |
4 | HG01884.hp1 HG02486.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-10209T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17570344 | |||||||
chr1:17570450 | A | G | 7 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0078 others(4): Show |
7 | HG00741.hp1 HG01169.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.-43-10103A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17570450 | |||||||
chr1:17570460 | A | C | 2 | a0001c0001t0001g0103 a0002c0008t0002g0104 |
2 | HG00733.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-43-10093A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17570460 | |||||||
chr1:17570523 | T | G | 1 | a0002c0003t0002g0116 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-43-10030T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17570523 | |||||||
chr1:17570551 | G | T | 1 | a0001c0001t0003g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-43-10002G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17570551 | |||||||
chr1:17570807 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0154 a0001c0006t0001g0156 others(1): Show |
4 | HG02572.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-9746G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17570807 | |||||||
chr1:17570814 | G | T | 1 | a0015c0032t0001g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-43-9739G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17570814 | |||||||
chr1:17570849 | GGT | G | 26 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(23): Show |
26 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.-43-9700_-43-9699d others(4): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17570849 | ||||||
chr1:17570939 | A | G | 2 | a0001c0011t0001g0152 a0001c0042t0001g0035 |
2 | HG00741.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.-43-9614A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17570939 | |||||||
chr1:17571107 | A | G | 1 | a0007c0010t0001g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-43-9446A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17571107 | |||||||
chr1:17571154 | C | T | 1 | a0001c0013t0001g0008 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-43-9399C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17571154 | |||||||
chr1:17571163 | G | A | 1 | a0014c0029t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-43-9390G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17571163 | |||||||
chr1:17571206 | C | A | 5 | a0001c0001t0001g0061 a0002c0007t0002g0105 a0004c0005t0002g0060 others(2): Show |
5 | HG00642.hp1 HG02572.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-9347C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17571206 | |||||||
chr1:17571435 | C | T | 1 | a0002c0004t0002g0146 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-43-9118C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17571435 | |||||||
chr1:17571594 | T | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0062 a0001c0001t0001g0125 others(3): Show |
6 | HG02602.hp1 HG04115.hp1 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-8959T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17571594 | |||||||
chr1:17572052 | G | A | 1 | a0019c0026t0001g0026 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-43-8501G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17572052 | |||||||
chr1:17572171 | G | A | 66 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0040 others(63): Show |
66 | HG00544.hp1 HG00544.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.-43-8382G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17572171 | |||||||
chr1:17572656 | C | T | 25 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(22): Show |
25 | HG00738.hp1 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-43-7897C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17572656 | |||||||
chr1:17572814 | G | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0062 a0001c0001t0001g0125 others(4): Show |
7 | HG02602.hp1 HG03579.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-7739G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17572814 | |||||||
chr1:17572878 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-43-7675A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17572878 | |||||||
chr1:17573042 | A | C | 1 | a0001c0001t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-43-7511A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17573042 | |||||||
chr1:17573064 | G | A | 14 | a0001c0001t0001g0043 a0001c0001t0003g0131 a0001c0006t0001g0001 others(11): Show |
14 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-43-7489G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17573064 | |||||||
chr1:17573113 | T | G | 12 | a0001c0001t0001g0014 a0001c0001t0001g0062 a0001c0001t0001g0084 others(9): Show |
12 | HG00544.hp1 HG00544.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.-43-7440T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17573113 | |||||||
chr1:17573224 | C | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0062 a0001c0001t0001g0125 others(8): Show |
11 | HG00544.hp1 HG00544.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.-43-7329C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17573224 | |||||||
chr1:17573250 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0062 a0001c0001t0001g0125 others(4): Show |
7 | HG02602.hp1 HG03579.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-7303C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17573250 | |||||||
chr1:17573314 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-43-7239G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17573314 | |||||||
chr1:17573834 | G | A | 6 | a0001c0001t0001g0062 a0001c0001t0001g0125 a0001c0001t0001g0127 others(3): Show |
6 | HG02602.hp1 HG03579.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.-43-6719G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17573834 | |||||||
chr1:17573856 | CTG | C | 11 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0088 others(8): Show |
11 | HG00741.hp2 HG01109.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.-43-6696_-43-6695d others(4): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17573856 | |||||||
chr1:17573881 | G | C | 5 | a0001c0001t0001g0084 a0001c0014t0001g0094 a0001c0014t0001g0145 others(2): Show |
5 | HG00544.hp1 HG00544.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-6672G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17573881 | |||||||
chr1:17573893 | A | G | 1 | a0001c0006t0007g0150 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-43-6660A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17573893 | |||||||
chr1:17573989 | C | T | 12 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0088 others(9): Show |
12 | HG00741.hp2 HG01109.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.-43-6564C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17573989 | |||||||
chr1:17574000 | C | T | 1 | a0008c0016t0002g0082 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-43-6553C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17574000 | |||||||
chr1:17574028 | C | G | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(152): Show |
155 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.-43-6525C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17574028 | |||||||
chr1:17574079 | G | T | 1 | a0001c0045t0001g0031 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-43-6474G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17574079 | |||||||
chr1:17574203 | G | A | 4 | a0002c0004t0002g0118 a0002c0007t0002g0013 a0002c0007t0002g0085 others(1): Show |
4 | HG01884.hp1 HG02486.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-6350G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17574203 | |||||||
chr1:17574259 | C | T | 7 | a0001c0001t0001g0062 a0001c0001t0001g0125 a0001c0001t0001g0127 others(4): Show |
7 | HG02602.hp1 HG02630.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.-43-6294C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17574259 | |||||||
chr1:17574310 | G | A | 12 | a0001c0001t0001g0043 a0001c0001t0003g0131 a0001c0006t0001g0001 others(9): Show |
12 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.-43-6243G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17574310 | |||||||
chr1:17574479 | A | G | 12 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0088 others(9): Show |
12 | HG00741.hp2 HG01109.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.-43-6074A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17574479 | |||||||
chr1:17574502 | T | C | 4 | a0002c0004t0002g0118 a0002c0007t0002g0013 a0002c0007t0002g0085 others(1): Show |
4 | HG01884.hp1 HG02486.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-6051T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17574502 | |||||||
chr1:17574573 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-43-5980G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17574573 | |||||||
chr1:17574714 | A | G | 2 | a0001c0019t0001g0066 a0002c0018t0002g0015 |
2 | HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-43-5839A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17574714 | |||||||
chr1:17574733 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0103 a0002c0003t0002g0083 others(1): Show |
4 | HG00733.hp1 HG01070.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-5820C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17574733 | |||||||
chr1:17574734 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0005g0162 |
2 | HG01106.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-43-5819G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17574734 | |||||||
chr1:17575094 | G | A | 1 | a0013c0035t0001g0018 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-43-5459G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17575094 | |||||||
chr1:17575349 | C | G | 1 | a0001c0001t0001g0071 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-43-5204C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17575349 | |||||||
chr1:17575433 | C | T | 1 | a0001c0043t0002g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-43-5120C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17575433 | |||||||
chr1:17575575 | G | A | 4 | a0002c0004t0002g0118 a0002c0007t0002g0013 a0002c0007t0002g0085 others(1): Show |
4 | HG01884.hp1 HG02486.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-4978G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17575575 | |||||||
chr1:17575596 | G | A | 4 | a0002c0004t0002g0118 a0002c0007t0002g0013 a0002c0007t0002g0085 others(1): Show |
4 | HG01884.hp1 HG02486.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-4957G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17575596 | |||||||
chr1:17575805 | G | A | 8 | a0001c0033t0002g0110 a0001c0043t0002g0051 a0002c0007t0002g0111 others(5): Show |
8 | HG02559.hp1 HG02630.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-4748G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17575805 | |||||||
chr1:17575851 | C | A | 4 | a0001c0014t0001g0094 a0001c0014t0001g0145 a0002c0021t0002g0137 others(1): Show |
4 | HG00544.hp1 HG00544.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-4702C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17575851 | |||||||
chr1:17575938 | C | T | 1 | a0001c0011t0001g0004 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-43-4615C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17575938 | |||||||
chr1:17576012 | C | T | 12 | a0001c0001t0001g0043 a0001c0001t0003g0131 a0001c0006t0001g0001 others(9): Show |
12 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.-43-4541C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17576012 | |||||||
chr1:17576055 | T | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(159): Show |
162 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.-43-4498T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17576055 | |||||||
chr1:17576071 | C | T | 1 | a0001c0001t0003g0168 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-43-4482C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17576071 | |||||||
chr1:17576535 | G | A | 1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-43-4018G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17576535 | |||||||
chr1:17576559 | T | G | 1 | a0004c0005t0002g0060 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-43-3994T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17576559 | |||||||
chr1:17576628 | T | G | 2 | a0001c0001t0003g0153 a0001c0020t0001g0052 |
2 | HG01109.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-43-3925T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17576628 | |||||||
chr1:17576634 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-43-3919T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17576634 | |||||||
chr1:17576803 | G | A | 55 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(52): Show |
55 | HG00738.hp1 HG00741.hp2 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.-43-3750G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17576803 | |||||||
chr1:17576865 | G | A | 1 | a0001c0006t0007g0150 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-43-3688G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17576865 | |||||||
chr1:17576874 | G | A | 6 | a0001c0033t0002g0110 a0002c0007t0002g0111 a0004c0005t0002g0112 others(3): Show |
6 | HG02559.hp1 HG02922.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-3679G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17576874 | |||||||
chr1:17576897 | C | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0154 a0001c0006t0001g0156 others(5): Show |
8 | HG01884.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-3656C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17576897 | |||||||
chr1:17577170 | G | A | 1 | a0001c0043t0002g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-43-3383G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17577170 | |||||||
chr1:17577234 | TG | T | 4 | a0001c0014t0001g0094 a0001c0014t0001g0145 a0002c0021t0002g0137 others(1): Show |
4 | HG00544.hp1 HG00544.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-3315delG | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17577234 | ||||||
chr1:17578281 | G | A | 6 | a0001c0001t0003g0131 a0001c0006t0001g0001 a0001c0006t0001g0129 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-2272G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17578281 | |||||||
chr1:17578438 | A | G | 21 | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0001g0041 others(18): Show |
21 | HG00738.hp1 HG00741.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-43-2115A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17578438 | |||||||
chr1:17578549 | TG | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(111): Show |
114 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.-43-2002delG | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | 17578549 | ||||||
chr1:17578668 | C | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(83): Show |
86 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.-43-1885C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17578668 | |||||||
chr1:17578682 | C | T | 1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-43-1871C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17578682 | |||||||
chr1:17578695 | C | T | 28 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0061 others(25): Show |
28 | HG00642.hp1 HG01069.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.-43-1858C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17578695 | |||||||
chr1:17578902 | A | T | 1 | a0002c0003t0002g0089 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-43-1651A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17578902 | |||||||
chr1:17579030 | T | A | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(159): Show |
162 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.-43-1523T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17579030 | |||||||
chr1:17579083 | C | T | 2 | a0001c0043t0002g0051 a0002c0041t0008g0054 |
2 | HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-43-1470C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17579083 | |||||||
chr1:17579704 | G | A | 3 | a0003c0002t0001g0069 a0003c0002t0001g0073 a0003c0002t0001g0074 |
3 | HG02602.hp2 HG02683.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-43-849G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17579704 | |||||||
chr1:17579810 | C | T | 4 | a0002c0004t0002g0118 a0002c0007t0002g0013 a0002c0007t0002g0085 others(1): Show |
4 | HG01884.hp1 HG02486.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-743C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17579810 | |||||||
chr1:17579878 | C | T | 1 | a0001c0019t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-43-675C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17579878 | |||||||
chr1:17580171 | C | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0154 a0001c0006t0001g0156 others(5): Show |
8 | HG01884.hp1 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-382C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | chr1 | 17580171 | |||||||
chr1:17580684 | G | T | 1 | a0008c0016t0002g0132 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.37+52G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17580684 | |||||||
chr1:17580787 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.37+155G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17580787 | |||||||
chr1:17580973 | G | A | 4 | a0001c0014t0001g0094 a0001c0043t0002g0051 a0002c0021t0002g0137 others(1): Show |
4 | HG00544.hp1 HG00544.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.37+341G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17580973 | |||||||
chr1:17581010 | A | G | 100 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(97): Show |
100 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.37+378A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17581010 | |||||||
chr1:17581080 | C | T | 87 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(84): Show |
87 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.37+448C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17581080 | |||||||
chr1:17581112 | C | T | 161 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(158): Show |
161 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.37+480C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17581112 | |||||||
chr1:17581202 | C | T | 4 | a0002c0004t0002g0118 a0002c0007t0002g0013 a0002c0007t0002g0085 others(1): Show |
4 | HG01884.hp1 HG02486.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+570C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17581202 | |||||||
chr1:17581288 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.37+656G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17581288 | |||||||
chr1:17581309 | C | CA | 99 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(96): Show |
99 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.37+700dupA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr1 | 17581309 | ||||||
chr1:17581309 | C | CAA | 6 | a0001c0042t0001g0035 a0002c0003t0002g0083 a0002c0004t0002g0036 others(3): Show |
6 | HG00741.hp1 HG01175.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.37+699_37+700dupAA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr1 | 17581309 | ||||||
chr1:17581309 | CA | C | 17 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0040 others(14): Show |
17 | HG00738.hp2 HG01106.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.37+700delA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr1 | 17581309 | ||||||
chr1:17581510 | A | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(159): Show |
162 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.37+878A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17581510 | |||||||
chr1:17581682 | A | T | 24 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0061 others(21): Show |
24 | HG00642.hp1 HG01069.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.37+1050A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17581682 | |||||||
chr1:17581953 | G | A | 1 | a0004c0005t0002g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.37+1321G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17581953 | |||||||
chr1:17581966 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.37+1334G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17581966 | |||||||
chr1:17582155 | C | T | 20 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0062 others(17): Show |
20 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.37+1523C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17582155 | |||||||
chr1:17582236 | G | A | 6 | a0001c0001t0003g0131 a0001c0006t0001g0001 a0001c0006t0001g0129 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.37+1604G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17582236 | |||||||
chr1:17582240 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.37+1608C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17582240 | |||||||
chr1:17582446 | T | C | 4 | a0001c0001t0001g0163 a0001c0001t0003g0153 a0001c0020t0001g0052 others(1): Show |
4 | HG01106.hp2 HG01109.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.37+1814T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17582446 | |||||||
chr1:17582468 | C | T | 3 | a0001c0001t0003g0168 a0001c0014t0001g0094 a0002c0021t0002g0137 |
3 | HG00544.hp1 HG02809.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.37+1836C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17582468 | |||||||
chr1:17582661 | G | A | 4 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 others(1): Show |
4 | HG02630.hp1 HG02897.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+2029G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17582661 | |||||||
chr1:17582665 | G | A | 162 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(159): Show |
162 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.37+2033G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17582665 | |||||||
chr1:17582733 | G | A | 2 | a0001c0014t0001g0094 a0002c0021t0002g0137 |
2 | HG00544.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.37+2101G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17582733 | |||||||
chr1:17582753 | T | A | 10 | a0001c0001t0003g0131 a0001c0001t0003g0168 a0001c0006t0001g0129 others(7): Show |
10 | HG00544.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.37+2121T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17582753 | |||||||
chr1:17582764 | T | C | 5 | a0001c0014t0001g0094 a0001c0017t0002g0113 a0001c0017t0002g0148 others(2): Show |
5 | HG00544.hp1 HG02630.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.37+2132T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17582764 | |||||||
chr1:17582789 | C | G | 18 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0027 others(15): Show |
18 | HG00642.hp2 HG00733.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.37+2157C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17582789 | |||||||
chr1:17582917 | A | C | 32 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0019 others(29): Show |
32 | HG00544.hp2 HG00558.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.37+2285A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17582917 | |||||||
chr1:17583006 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(155): Show |
158 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.37+2374A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17583006 | |||||||
chr1:17583059 | G | GA | 106 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(103): Show |
106 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.37+2441dupA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr1 | 17583059 | ||||||
chr1:17583113 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.37+2481G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17583113 | |||||||
chr1:17583201 | T | TAA | 4 | a0001c0006t0007g0150 a0001c0017t0002g0113 a0001c0017t0002g0148 others(1): Show |
4 | HG02280.hp1 HG02630.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+2569_37+2570ins others(2): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17583201 | |||||||
chr1:17583202 | T | A | 7 | a0001c0001t0001g0077 a0001c0006t0007g0150 a0001c0017t0002g0113 others(4): Show |
7 | HG02280.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.37+2570T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17583202 | |||||||
chr1:17583202 | T | TA | 100 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(97): Show |
100 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.37+2591dupA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr1 | 17583202 | ||||||
chr1:17583202 | T | TAA | 29 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0040 others(26): Show |
29 | HG00733.hp2 HG00738.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.37+2590_37+2591dup others(2): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr1 | 17583202 | ||||||
chr1:17583301 | G | A | 1 | a0001c0019t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.37+2669G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17583301 | |||||||
chr1:17583428 | C | A | 22 | a0001c0001t0001g0024 a0001c0001t0001g0040 a0001c0001t0001g0041 others(19): Show |
22 | HG00733.hp2 HG00738.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.37+2796C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17583428 | |||||||
chr1:17583489 | T | A | 4 | a0002c0003t0002g0116 a0002c0007t0002g0058 a0002c0018t0002g0015 others(1): Show |
4 | HG01074.hp2 HG02280.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.37+2857T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17583489 | |||||||
chr1:17583579 | G | A | 8 | a0001c0001t0001g0077 a0001c0017t0002g0113 a0001c0017t0002g0148 others(5): Show |
8 | HG01074.hp2 HG02280.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.37+2947G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17583579 | |||||||
chr1:17583827 | A | G | 7 | a0001c0001t0001g0077 a0002c0003t0002g0116 a0002c0004t0002g0036 others(4): Show |
7 | HG01074.hp2 HG02135.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.37+3195A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17583827 | |||||||
chr1:17583860 | AT | A | 7 | a0001c0001t0001g0077 a0002c0003t0002g0116 a0002c0004t0002g0036 others(4): Show |
7 | HG01074.hp2 HG02135.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.37+3237delT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr1 | 17583860 | ||||||
chr1:17583886 | C | G | 2 | a0001c0001t0001g0136 a0001c0001t0003g0135 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.37+3254C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17583886 | |||||||
chr1:17583900 | G | A | 1 | a0001c0019t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.37+3268G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17583900 | |||||||
chr1:17583956 | A | G | 3 | a0002c0004t0002g0120 a0002c0004t0002g0121 a0007c0010t0001g0065 |
3 | HG01070.hp1 HG01071.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.37+3324A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17583956 | |||||||
chr1:17583967 | A | T | 7 | a0001c0001t0001g0077 a0002c0003t0002g0116 a0002c0004t0002g0036 others(4): Show |
7 | HG01074.hp2 HG02135.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.37+3335A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17583967 | |||||||
chr1:17584011 | C | A | 1 | a0002c0003t0002g0037 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.37+3379C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17584011 | |||||||
chr1:17584053 | A | AT | 7 | a0001c0001t0001g0077 a0002c0003t0002g0116 a0002c0004t0002g0036 others(4): Show |
7 | HG01074.hp2 HG02135.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.38-3398dupT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr1 | 17584053 | ||||||
chr1:17584087 | C | T | 1 | a0012c0031t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.38-3373C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17584087 | |||||||
chr1:17584205 | T | C | 5 | a0001c0001t0001g0077 a0002c0003t0002g0116 a0002c0004t0002g0036 others(2): Show |
5 | HG01074.hp2 HG02135.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.38-3255T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17584205 | |||||||
chr1:17584418 | G | A | 2 | a0002c0003t0002g0116 a0002c0007t0002g0058 |
2 | HG01074.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.38-3042G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17584418 | |||||||
chr1:17584428 | C | T | 1 | a0003c0002t0001g0069 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.38-3032C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17584428 | |||||||
chr1:17584429 | G | A | 2 | a0002c0003t0002g0116 a0002c0007t0002g0058 |
2 | HG01074.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.38-3031G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17584429 | |||||||
chr1:17584501 | C | T | 2 | a0002c0003t0002g0116 a0002c0007t0002g0058 |
2 | HG01074.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.38-2959C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17584501 | |||||||
chr1:17584591 | C | T | 2 | a0002c0003t0002g0116 a0002c0007t0002g0058 |
2 | HG01074.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.38-2869C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17584591 | |||||||
chr1:17584678 | G | A | 2 | a0002c0018t0002g0015 a0004c0005t0002g0117 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.38-2782G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17584678 | |||||||
chr1:17584749 | G | A | 7 | a0005c0015t0002g0067 a0005c0015t0002g0068 a0005c0023t0002g0101 others(4): Show |
7 | HG01123.hp1 HG01169.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.38-2711G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17584749 | |||||||
chr1:17584792 | G | C | 2 | a0002c0003t0002g0116 a0002c0007t0002g0058 |
2 | HG01074.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.38-2668G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17584792 | |||||||
chr1:17584857 | G | GCA | 2 | a0001c0001t0001g0079 a0001c0001t0001g0088 |
2 | HG00741.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.38-2581_38-2580dup others(2): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr1 | 17584857 | ||||||
chr1:17584857 | GCA | G | 24 | a0001c0001t0001g0062 a0001c0001t0001g0077 a0001c0001t0001g0119 others(21): Show |
24 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.38-2581_38-2580del others(2): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr1 | 17584857 | ||||||
chr1:17584857 | GCACA | G | 5 | a0001c0001t0003g0168 a0001c0011t0001g0004 a0001c0013t0001g0008 others(2): Show |
5 | HG00738.hp1 HG02071.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.38-2583_38-2580del others(4): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr1 | 17584857 | ||||||
chr1:17584861 | A | G | 2 | a0002c0018t0002g0015 a0004c0005t0002g0117 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.38-2599A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17584861 | |||||||
chr1:17584879 | A | C | 9 | a0001c0001t0003g0131 a0001c0006t0001g0129 a0001c0006t0001g0130 others(6): Show |
9 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.38-2581A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17584879 | |||||||
chr1:17585181 | C | T | 4 | a0001c0001t0003g0131 a0001c0006t0001g0129 a0001c0006t0001g0130 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-2279C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17585181 | |||||||
chr1:17585283 | G | A | 1 | a0019c0026t0001g0026 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.38-2177G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17585283 | |||||||
chr1:17585295 | A | G | 4 | a0002c0003t0002g0116 a0002c0007t0002g0058 a0002c0018t0002g0015 others(1): Show |
4 | HG01074.hp2 HG02280.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-2165A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17585295 | |||||||
chr1:17585388 | G | C | 2 | a0001c0001t0005g0162 a0002c0007t0002g0105 |
2 | HG00642.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.38-2072G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17585388 | |||||||
chr1:17585551 | G | A | 2 | a0002c0003t0002g0116 a0002c0007t0002g0058 |
2 | HG01074.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.38-1909G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17585551 | |||||||
chr1:17585622 | G | A | 2 | a0002c0003t0002g0116 a0002c0007t0002g0058 |
2 | HG01074.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.38-1838G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17585622 | |||||||
chr1:17585644 | T | C | 2 | a0002c0003t0002g0116 a0002c0007t0002g0058 |
2 | HG01074.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.38-1816T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17585644 | |||||||
chr1:17585648 | A | C | 1 | a0001c0001t0001g0057 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.38-1812A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17585648 | |||||||
chr1:17585782 | C | T | 2 | a0002c0003t0002g0116 a0002c0007t0002g0058 |
2 | HG01074.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.38-1678C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17585782 | |||||||
chr1:17585850 | C | T | 1 | a0003c0002t0001g0144 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.38-1610C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17585850 | |||||||
chr1:17585851 | C | T | 2 | a0002c0003t0002g0116 a0002c0007t0002g0058 |
2 | HG01074.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.38-1609C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17585851 | |||||||
chr1:17585966 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.38-1494C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17585966 | |||||||
chr1:17586124 | T | G | 1 | a0003c0002t0001g0056 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.38-1336T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17586124 | |||||||
chr1:17586152 | CCCAAGTA others(9): Show |
C | 2 | a0002c0003t0002g0116 a0002c0007t0002g0058 |
2 | HG01074.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.38-1302_38-1287del others(16): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr1 | 17586152 | ||||||
chr1:17586267 | A | G | 2 | a0002c0003t0002g0116 a0002c0007t0002g0058 |
2 | HG01074.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.38-1193A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17586267 | |||||||
chr1:17586366 | T | C | 4 | a0002c0003t0002g0116 a0002c0007t0002g0058 a0002c0018t0002g0015 others(1): Show |
4 | HG01074.hp2 HG02280.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.38-1094T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17586366 | |||||||
chr1:17586502 | CAG | C | 103 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(100): Show |
103 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.38-955_38-954delAG | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr1 | 17586502 | ||||||
chr1:17586629 | C | A | 2 | a0002c0003t0002g0116 a0002c0007t0002g0058 |
2 | HG01074.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.38-831C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17586629 | |||||||
chr1:17586663 | G | T | 2 | a0002c0003t0002g0116 a0002c0007t0002g0058 |
2 | HG01074.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.38-797G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17586663 | |||||||
chr1:17586779 | C | T | 2 | a0002c0003t0002g0116 a0002c0007t0002g0058 |
2 | HG01074.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.38-681C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17586779 | |||||||
chr1:17586821 | G | A | 1 | a0008c0016t0002g0082 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.38-639G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17586821 | |||||||
chr1:17586839 | T | G | 2 | a0002c0018t0002g0015 a0004c0005t0002g0117 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.38-621T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17586839 | |||||||
chr1:17586850 | G | T | 1 | a0001c0001t0001g0027 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.38-610G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17586850 | |||||||
chr1:17587014 | A | G | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(139): Show |
142 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.38-446A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17587014 | |||||||
chr1:17587168 | C | T | 13 | a0001c0001t0001g0010 a0001c0001t0001g0045 a0001c0001t0001g0071 others(10): Show |
13 | HG00544.hp1 HG01069.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.38-292C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17587168 | |||||||
chr1:17587200 | T | A | 2 | a0002c0003t0002g0116 a0002c0007t0002g0058 |
2 | HG01074.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.38-260T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17587200 | |||||||
chr1:17587213 | A | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0119 |
2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.38-247A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17587213 | |||||||
chr1:17587219 | G | A | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(137): Show |
140 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.38-241G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17587219 | |||||||
chr1:17587378 | C | G | 1 | a0001c0001t0001g0019 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.38-82C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 2/28 | chr1 | 17587378 | |||||||
chr1:17587823 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.223+178T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 3/28 | chr1 | 17587823 | |||||||
chr1:17587972 | A | G | 3 | a0002c0004t0002g0120 a0002c0004t0002g0121 a0007c0010t0001g0065 |
3 | HG01070.hp1 HG01071.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.223+327A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 3/28 | chr1 | 17587972 | |||||||
chr1:17587989 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(162): Show |
165 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.223+344T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 3/28 | chr1 | 17587989 | |||||||
chr1:17588017 | G | A | 1 | a0001c0019t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.223+372G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 3/28 | chr1 | 17588017 | |||||||
chr1:17588105 | C | G | 7 | a0001c0048t0001g0005 a0005c0015t0002g0067 a0005c0015t0002g0068 others(4): Show |
7 | HG01123.hp1 HG01192.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.224-341C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 3/28 | chr1 | 17588105 | |||||||
chr1:17588124 | G | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0119 |
2 | HG03486.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.224-322G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 3/28 | chr1 | 17588124 | |||||||
chr1:17588169 | G | T | 43 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(40): Show |
43 | HG00558.hp2 HG00642.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.224-277G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 3/28 | chr1 | 17588169 | |||||||
chr1:17588351 | C | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(115): Show |
118 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.224-95C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 3/28 | chr1 | 17588351 | |||||||
chr1:17588530 | G | A | 3 | a0003c0002t0001g0069 a0003c0002t0001g0073 a0003c0002t0001g0074 |
3 | HG02602.hp2 HG02683.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.257+51G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17588530 | |||||||
chr1:17588849 | A | AGT | 12 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0040 others(9): Show |
12 | HG00642.hp1 HG00733.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.257+419_257+420dup others(2): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17588849 | ||||||
chr1:17588849 | A | AGTGT | 10 | a0001c0001t0001g0002 a0001c0001t0001g0097 a0001c0001t0003g0168 others(7): Show |
10 | HG00323.hp2 HG00738.hp1 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.257+417_257+420dup others(4): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17588849 | ||||||
chr1:17588849 | A | AGTGTGT | 15 | a0001c0001t0001g0043 a0001c0001t0001g0057 a0001c0001t0001g0088 others(12): Show |
15 | HG00741.hp2 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.257+415_257+420dup others(6): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17588849 | ||||||
chr1:17588849 | A | AGTGTGTG others(1): Show |
12 | a0001c0001t0001g0071 a0001c0001t0001g0098 a0001c0001t0001g0164 others(9): Show |
12 | HG00323.hp1 HG00741.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.257+413_257+420dup others(8): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17588849 | ||||||
chr1:17588849 | A | AGTGTGTG others(3): Show |
12 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(9): Show |
12 | HG00558.hp1 HG01169.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.257+411_257+420dup others(10): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17588849 | ||||||
chr1:17588849 | A | AGTGTGTG others(5): Show |
7 | a0001c0001t0001g0032 a0001c0001t0001g0045 a0001c0001t0001g0099 others(4): Show |
7 | HG01433.hp1 HG02071.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.257+409_257+420dup others(12): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17588849 | ||||||
chr1:17588849 | A | AGTGTGTG others(7): Show |
4 | a0001c0001t0001g0022 a0001c0001t0001g0034 a0001c0001t0001g0158 others(1): Show |
4 | HG01496.hp2 HG02148.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+407_257+420dup others(14): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17588849 | ||||||
chr1:17588849 | A | AGTGTGTG others(9): Show |
2 | a0001c0001t0001g0079 a0001c0001t0003g0143 |
2 | HG02451.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.257+405_257+420dup others(16): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17588849 | ||||||
chr1:17588849 | A | AGTGTGTG others(11): Show |
10 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0093 others(7): Show |
10 | HG00544.hp2 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.257+403_257+420dup others(18): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17588849 | ||||||
chr1:17588849 | A | AGTGTGTG others(13): Show |
4 | a0001c0001t0003g0131 a0001c0006t0007g0150 a0007c0010t0001g0053 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+401_257+420dup others(20): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17588849 | ||||||
chr1:17588849 | A | AGTGTGTG others(15): Show |
1 | a0001c0006t0001g0001 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.257+399_257+420dup others(22): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17588849 | ||||||
chr1:17588849 | AGTGTGTG others(11): Show |
A | 1 | a0014c0029t0001g0122 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.257+403_257+420del others(18): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17588849 | ||||||
chr1:17588878 | G | GTGTGTGT others(1): Show |
3 | a0003c0002t0001g0069 a0003c0002t0001g0073 a0003c0002t0001g0074 |
3 | HG02602.hp2 HG02683.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.257+406_257+407ins others(8): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17588878 | ||||||
chr1:17588878 | G | GTGTGTGT others(5): Show |
1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.257+410_257+411ins others(12): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17588878 | ||||||
chr1:17588880 | G | GTGTGTC | 36 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(33): Show |
36 | HG00558.hp2 HG00642.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.257+406_257+407ins others(6): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17588880 | ||||||
chr1:17588880 | G | GTGTGTGT others(3): Show |
14 | a0001c0001t0001g0077 a0001c0019t0001g0066 a0001c0048t0001g0005 others(11): Show |
14 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.257+410_257+411ins others(10): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17588880 | ||||||
chr1:17588880 | G | GTGTGTGT others(5): Show |
7 | a0001c0001t0001g0062 a0001c0001t0001g0119 a0001c0001t0003g0114 others(4): Show |
7 | HG01433.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.257+412_257+413ins others(12): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17588880 | ||||||
chr1:17588880 | G | GTGTGTGT others(7): Show |
2 | a0002c0018t0002g0015 a0004c0005t0002g0117 |
2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.257+414_257+415ins others(14): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17588880 | ||||||
chr1:17588975 | C | T | 3 | a0001c0001t0001g0077 a0002c0004t0002g0036 a0002c0021t0002g0137 |
3 | HG02135.hp2 NA18951.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.257+496C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17588975 | |||||||
chr1:17589227 | A | C | 1 | a0001c0011t0001g0004 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.257+748A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17589227 | |||||||
chr1:17589250 | C | A | 1 | a0001c0001t0001g0030 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.257+771C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17589250 | |||||||
chr1:17589338 | T | C | 53 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(50): Show |
53 | HG00323.hp2 HG00558.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.257+859T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17589338 | |||||||
chr1:17589831 | G | A | 2 | a0002c0004t0002g0120 a0002c0004t0002g0121 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.257+1352G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17589831 | |||||||
chr1:17589887 | C | T | 62 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(59): Show |
62 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.257+1408C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17589887 | |||||||
chr1:17590156 | C | T | 2 | a0002c0004t0002g0120 a0002c0004t0002g0121 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.257+1677C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17590156 | |||||||
chr1:17590193 | C | T | 2 | a0002c0004t0002g0120 a0002c0004t0002g0121 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.257+1714C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17590193 | |||||||
chr1:17590338 | G | A | 4 | a0001c0001t0003g0131 a0001c0006t0001g0129 a0001c0006t0001g0130 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+1859G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17590338 | |||||||
chr1:17590424 | T | A | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(107): Show |
110 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.257+1945T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17590424 | |||||||
chr1:17590446 | G | A | 61 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(58): Show |
61 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.257+1967G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17590446 | |||||||
chr1:17590465 | A | T | 3 | a0001c0001t0001g0077 a0002c0004t0002g0036 a0002c0021t0002g0137 |
3 | HG02135.hp2 NA18951.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.257+1986A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17590465 | |||||||
chr1:17590467 | A | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(111): Show |
114 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.257+1988A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17590467 | |||||||
chr1:17590585 | A | G | 1 | a0007c0010t0001g0065 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.257+2106A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17590585 | |||||||
chr1:17590623 | G | A | 2 | a0001c0001t0001g0093 a0001c0006t0007g0150 |
2 | HG02280.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.257+2144G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17590623 | |||||||
chr1:17590767 | A | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0096 |
2 | HG02735.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.257+2288A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17590767 | |||||||
chr1:17590976 | T | G | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(110): Show |
113 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.257+2497T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17590976 | |||||||
chr1:17591042 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.257+2563A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17591042 | |||||||
chr1:17591387 | C | A | 45 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(42): Show |
45 | HG00558.hp2 HG00642.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.257+2908C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17591387 | |||||||
chr1:17591396 | T | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(107): Show |
110 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.257+2917T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17591396 | |||||||
chr1:17591408 | A | AT | 6 | a0001c0001t0001g0010 a0001c0001t0001g0061 a0001c0019t0001g0095 others(3): Show |
6 | HG01192.hp1 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.257+2949dupT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17591408 | ||||||
chr1:17591408 | AT | A | 10 | a0001c0001t0001g0063 a0001c0001t0003g0131 a0001c0001t0003g0151 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.257+2949delT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17591408 | ||||||
chr1:17591408 | ATT | A | 26 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0040 others(23): Show |
26 | HG00323.hp2 HG00733.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.257+2948_257+2949d others(4): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17591408 | ||||||
chr1:17591408 | ATTT | A | 67 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(64): Show |
67 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.257+2947_257+2949d others(5): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17591408 | ||||||
chr1:17591568 | G | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(68): Show |
71 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.257+3089G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17591568 | |||||||
chr1:17591571 | G | A | 1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.257+3092G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17591571 | |||||||
chr1:17591586 | A | G | 1 | a0007c0010t0001g0065 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.257+3107A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17591586 | |||||||
chr1:17591852 | T | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(54): Show |
57 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.257+3373T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17591852 | |||||||
chr1:17591898 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.257+3419T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17591898 | |||||||
chr1:17592105 | G | A | 56 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0014 others(53): Show |
56 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.257+3626G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17592105 | |||||||
chr1:17592332 | T | A | 1 | a0004c0005t0002g0112 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.257+3853T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17592332 | |||||||
chr1:17592385 | C | T | 1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.257+3906C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17592385 | |||||||
chr1:17592476 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.257+3997C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17592476 | |||||||
chr1:17592541 | G | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(162): Show |
165 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.257+4062G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17592541 | |||||||
chr1:17592594 | C | T | 1 | a0001c0033t0002g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.257+4115C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17592594 | |||||||
chr1:17592672 | G | A | 3 | a0002c0004t0002g0036 a0002c0021t0002g0137 a0002c0041t0008g0054 |
3 | HG02135.hp2 HG03579.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.257+4193G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17592672 | |||||||
chr1:17592712 | C | T | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(154): Show |
157 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(154): Show |
intron_variant | MODIFIER | c.257+4233C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17592712 | |||||||
chr1:17592741 | T | C | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(149): Show |
152 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.257+4262T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17592741 | |||||||
chr1:17593031 | A | G | 3 | a0001c0001t0003g0143 a0001c0014t0001g0145 a0003c0002t0001g0073 |
3 | HG02683.hp2 NA18747.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.257+4552A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17593031 | |||||||
chr1:17593092 | G | A | 6 | a0001c0001t0001g0046 a0002c0003t0002g0133 a0002c0004t0002g0167 others(3): Show |
6 | HG02809.hp2 HG06807.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.257+4613G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17593092 | |||||||
chr1:17593176 | A | T | 1 | a0017c0037t0001g0142 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.257+4697A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17593176 | |||||||
chr1:17593207 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.257+4728G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17593207 | |||||||
chr1:17593260 | C | T | 2 | a0001c0001t0001g0159 a0019c0026t0001g0026 |
2 | NA18954.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.257+4781C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17593260 | |||||||
chr1:17593266 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.257+4787C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17593266 | |||||||
chr1:17593267 | G | A | 1 | a0004c0005t0002g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.257+4788G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17593267 | |||||||
chr1:17593283 | A | G | 1 | a0001c0011t0001g0152 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.257+4804A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17593283 | |||||||
chr1:17593322 | T | C | 23 | a0001c0001t0001g0071 a0001c0001t0001g0119 a0001c0001t0001g0163 others(20): Show |
23 | HG00544.hp1 HG00544.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.257+4843T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17593322 | |||||||
chr1:17593652 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0062 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+5173C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17593652 | |||||||
chr1:17593660 | G | A | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(107): Show |
110 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.257+5181G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17593660 | |||||||
chr1:17593759 | CACT | C | 20 | a0001c0001t0001g0012 a0001c0001t0001g0119 a0001c0001t0001g0140 others(17): Show |
20 | HG00558.hp1 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.257+5282_257+5284d others(5): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17593759 | ||||||
chr1:17593773 | T | C | 2 | a0001c0001t0001g0159 a0020c0049t0004g0075 |
2 | NA18954.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.257+5294T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17593773 | |||||||
chr1:17593952 | A | G | 3 | a0001c0006t0003g0139 a0001c0044t0004g0161 a0002c0004t0002g0167 |
3 | HG02622.hp2 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.257+5473A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17593952 | |||||||
chr1:17594019 | C | T | 1 | a0001c0020t0001g0016 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.257+5540C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17594019 | |||||||
chr1:17594132 | G | A | 2 | a0001c0006t0001g0129 a0001c0006t0001g0130 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.257+5653G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17594132 | |||||||
chr1:17594179 | G | A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0103 a0002c0008t0002g0104 |
3 | HG00733.hp1 HG01346.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.257+5700G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17594179 | |||||||
chr1:17594384 | G | A | 1 | a0001c0006t0001g0156 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.257+5905G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17594384 | |||||||
chr1:17594412 | C | T | 3 | a0001c0001t0001g0119 a0002c0004t0002g0120 a0002c0004t0002g0121 |
3 | HG01070.hp1 HG01071.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.257+5933C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17594412 | |||||||
chr1:17594631 | C | T | 2 | a0012c0031t0006g0165 a0021c0030t0002g0109 |
2 | HG01884.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.257+6152C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17594631 | |||||||
chr1:17594728 | GCCTGCCT others(8): Show |
G | 1 | a0001c0012t0001g0102 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.257+6251_257+6265d others(17): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17594728 | ||||||
chr1:17594883 | G | A | 9 | a0001c0001t0001g0119 a0002c0004t0002g0120 a0002c0004t0002g0121 others(6): Show |
9 | HG00642.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.257+6404G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17594883 | |||||||
chr1:17595042 | A | T | 6 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.257+6563A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17595042 | |||||||
chr1:17595220 | C | CA | 3 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0011t0001g0004 |
3 | HG02071.hp1 HG02135.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.257+6741_257+6742i others(3): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17595220 | |||||||
chr1:17595220 | C | CT | 10 | a0001c0001t0001g0030 a0001c0001t0001g0057 a0001c0012t0001g0072 others(7): Show |
10 | HG00642.hp1 HG01081.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.257+6766dupT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17595220 | ||||||
chr1:17595220 | CT | C | 14 | a0001c0001t0001g0027 a0001c0001t0001g0078 a0001c0001t0001g0098 others(11): Show |
14 | HG00323.hp2 HG01081.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.257+6766delT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17595220 | ||||||
chr1:17595220 | CTT | C | 9 | a0001c0001t0001g0119 a0001c0043t0002g0051 a0002c0004t0002g0120 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.257+6765_257+6766d others(4): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17595220 | ||||||
chr1:17595220 | CTTT | C | 10 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0062 others(7): Show |
10 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.257+6764_257+6766d others(5): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17595220 | ||||||
chr1:17595220 | CTTTTTTT others(5): Show |
C | 8 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(5): Show |
8 | HG01069.hp1 HG01071.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.257+6755_257+6766d others(14): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17595220 | ||||||
chr1:17595317 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.258-6810C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17595317 | |||||||
chr1:17595499 | C | T | 2 | a0001c0001t0001g0163 a0007c0010t0001g0053 |
2 | HG01106.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.258-6628C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17595499 | |||||||
chr1:17595592 | G | T | 2 | a0001c0001t0001g0159 a0020c0049t0004g0075 |
2 | NA18954.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.258-6535G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17595592 | |||||||
chr1:17595666 | G | A | 3 | a0001c0001t0001g0119 a0002c0004t0002g0120 a0002c0004t0002g0121 |
3 | HG01070.hp1 HG01071.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.258-6461G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17595666 | |||||||
chr1:17595707 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.258-6420G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17595707 | |||||||
chr1:17595764 | A | G | 71 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(68): Show |
71 | HG00544.hp2 HG00558.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.258-6363A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17595764 | |||||||
chr1:17595977 | T | C | 2 | a0002c0008t0002g0104 a0005c0015t0002g0068 |
2 | HG00733.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.258-6150T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17595977 | |||||||
chr1:17596054 | C | A | 7 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.258-6073C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17596054 | |||||||
chr1:17596058 | C | T | 3 | a0001c0001t0001g0119 a0002c0004t0002g0120 a0002c0004t0002g0121 |
3 | HG01070.hp1 HG01071.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.258-6069C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17596058 | |||||||
chr1:17596105 | A | G | 29 | a0001c0001t0001g0012 a0001c0001t0001g0140 a0001c0001t0001g0164 others(26): Show |
29 | HG00544.hp2 HG00558.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.258-6022A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17596105 | |||||||
chr1:17596177 | C | A | 56 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(53): Show |
56 | HG00544.hp2 HG00558.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.258-5950C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17596177 | |||||||
chr1:17596248 | A | C | 2 | a0001c0001t0001g0159 a0020c0049t0004g0075 |
2 | NA18954.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.258-5879A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17596248 | |||||||
chr1:17596267 | A | G | 1 | a0001c0011t0001g0152 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.258-5860A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17596267 | |||||||
chr1:17596370 | G | T | 7 | a0004c0005t0002g0006 a0004c0005t0002g0060 a0004c0005t0002g0108 others(4): Show |
7 | HG02109.hp1 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-5757G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17596370 | |||||||
chr1:17596556 | T | C | 1 | a0002c0007t0002g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.258-5571T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17596556 | |||||||
chr1:17596565 | G | A | 4 | a0001c0001t0001g0062 a0001c0001t0003g0114 a0001c0001t0003g0151 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-5562G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17596565 | |||||||
chr1:17596588 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.258-5539T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17596588 | |||||||
chr1:17596609 | G | A | 4 | a0001c0011t0001g0138 a0001c0011t0001g0152 a0001c0042t0001g0035 others(1): Show |
4 | HG00741.hp1 HG01257.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-5518G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17596609 | |||||||
chr1:17596617 | C | G | 1 | a0005c0023t0002g0101 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.258-5510C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17596617 | |||||||
chr1:17596768 | C | A | 33 | a0001c0001t0001g0140 a0001c0006t0001g0001 a0001c0006t0001g0129 others(30): Show |
33 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.258-5359C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17596768 | |||||||
chr1:17597023 | G | A | 13 | a0001c0001t0001g0046 a0001c0001t0001g0071 a0001c0001t0001g0077 others(10): Show |
13 | HG00323.hp2 HG02602.hp2 HG03017.hp1 others(10): Show |
intron_variant | MODIFIER | c.258-5104G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17597023 | |||||||
chr1:17597308 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.258-4819A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17597308 | |||||||
chr1:17597352 | G | A | 3 | a0001c0012t0001g0064 a0001c0012t0001g0072 a0001c0045t0001g0031 |
3 | HG00738.hp2 HG01081.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.258-4775G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17597352 | |||||||
chr1:17597519 | T | A | 3 | a0001c0001t0001g0096 a0001c0001t0001g0099 a0001c0011t0001g0004 |
3 | HG02071.hp1 HG02135.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.258-4608T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17597519 | |||||||
chr1:17597593 | C | A | 1 | a0012c0031t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.258-4534C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17597593 | |||||||
chr1:17597780 | C | T | 1 | a0001c0001t0001g0030 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.258-4347C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17597780 | |||||||
chr1:17597807 | A | C | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.258-4320A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17597807 | |||||||
chr1:17597811 | G | A | 5 | a0001c0001t0001g0119 a0002c0004t0002g0120 a0002c0004t0002g0121 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.258-4316G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17597811 | |||||||
chr1:17598102 | CT | C | 24 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0043 others(21): Show |
24 | HG00642.hp1 HG01069.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.258-4008delT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17598102 | ||||||
chr1:17598175 | C | T | 7 | a0004c0005t0002g0006 a0004c0005t0002g0060 a0004c0005t0002g0108 others(4): Show |
7 | HG02109.hp1 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-3952C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17598175 | |||||||
chr1:17598308 | G | A | 1 | a0002c0003t0002g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.258-3819G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17598308 | |||||||
chr1:17598362 | G | A | 3 | a0001c0001t0003g0080 a0001c0001t0003g0090 a0001c0001t0003g0092 |
3 | HG01069.hp2 HG01175.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.258-3765G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17598362 | |||||||
chr1:17598473 | G | C | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.258-3654G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17598473 | |||||||
chr1:17598515 | G | A | 7 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.258-3612G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17598515 | |||||||
chr1:17598685 | T | A | 1 | a0002c0004t0002g0036 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.258-3442T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17598685 | |||||||
chr1:17598773 | CT | C | 5 | a0001c0001t0003g0114 a0001c0001t0005g0162 a0001c0019t0001g0066 others(2): Show |
5 | HG01884.hp2 HG02896.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.258-3341delT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17598773 | ||||||
chr1:17598795 | G | T | 7 | a0004c0005t0002g0006 a0004c0005t0002g0060 a0004c0005t0002g0108 others(4): Show |
7 | HG02109.hp1 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-3332G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17598795 | |||||||
chr1:17598814 | C | T | 1 | a0001c0014t0001g0094 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.258-3313C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17598814 | |||||||
chr1:17598875 | C | T | 2 | a0001c0001t0001g0096 a0001c0011t0001g0004 |
2 | HG02071.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.258-3252C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17598875 | |||||||
chr1:17598878 | C | A | 2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.258-3249C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17598878 | |||||||
chr1:17598897 | A | T | 1 | a0001c0014t0001g0094 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.258-3230A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17598897 | |||||||
chr1:17599033 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.258-3094C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17599033 | |||||||
chr1:17599064 | T | C | 69 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(66): Show |
69 | HG00544.hp2 HG00558.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.258-3063T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17599064 | |||||||
chr1:17599119 | T | C | 2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.258-3008T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17599119 | |||||||
chr1:17599331 | C | CA | 46 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0071 others(43): Show |
46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.258-2783dupA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17599331 | ||||||
chr1:17599331 | CA | C | 8 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(5): Show |
8 | HG01069.hp1 HG01071.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.258-2783delA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17599331 | ||||||
chr1:17599362 | C | T | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.258-2765C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17599362 | |||||||
chr1:17599401 | G | A | 4 | a0001c0001t0001g0096 a0001c0011t0001g0004 a0001c0020t0001g0016 others(1): Show |
4 | HG01109.hp1 HG02071.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-2726G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17599401 | |||||||
chr1:17599788 | C | T | 3 | a0001c0001t0001g0119 a0002c0004t0002g0120 a0002c0004t0002g0121 |
3 | HG01070.hp1 HG01071.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.258-2339C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17599788 | |||||||
chr1:17599862 | A | G | 2 | a0004c0005t0002g0117 a0014c0029t0001g0122 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.258-2265A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17599862 | |||||||
chr1:17599928 | A | T | 1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.258-2199A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17599928 | |||||||
chr1:17600178 | G | A | 6 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.258-1949G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17600178 | |||||||
chr1:17600309 | G | A | 6 | a0001c0001t0001g0119 a0001c0019t0001g0095 a0002c0004t0002g0120 others(3): Show |
6 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.258-1818G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17600309 | |||||||
chr1:17600671 | T | C | 56 | a0001c0001t0001g0012 a0001c0001t0001g0062 a0001c0001t0001g0096 others(53): Show |
56 | HG00544.hp2 HG00558.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.258-1456T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17600671 | |||||||
chr1:17600889 | A | G | 2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.258-1238A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17600889 | |||||||
chr1:17601049 | C | CA | 9 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0057 others(6): Show |
9 | HG00741.hp1 HG01192.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.258-1059dupA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17601049 | ||||||
chr1:17601056 | A | C | 8 | a0001c0020t0001g0016 a0001c0020t0001g0052 a0002c0007t0002g0013 others(5): Show |
8 | HG00642.hp1 HG01109.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.258-1071A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17601056 | |||||||
chr1:17601062 | A | C | 1 | a0001c0001t0001g0032 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.258-1065A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17601062 | |||||||
chr1:17601064 | A | C | 6 | a0001c0001t0001g0093 a0001c0001t0001g0119 a0001c0011t0001g0004 others(3): Show |
6 | HG01070.hp1 HG01071.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.258-1063A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17601064 | |||||||
chr1:17601065 | A | AAC | 23 | a0001c0001t0001g0012 a0001c0001t0001g0140 a0001c0001t0001g0164 others(20): Show |
23 | HG00558.hp1 HG00733.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.258-1061_258-1060i others(4): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | 17601065 | ||||||
chr1:17601065 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.258-1062A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17601065 | |||||||
chr1:17601066 | A | AC | 14 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0019t0001g0066 others(11): Show |
14 | HG02109.hp1 HG02572.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.258-1061_258-1060i others(3): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17601066 | |||||||
chr1:17601066 | A | C | 14 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(11): Show |
14 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.258-1061A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17601066 | |||||||
chr1:17601069 | C | A | 66 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(63): Show |
66 | HG00558.hp1 HG00642.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.258-1058C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17601069 | |||||||
chr1:17601072 | A | C | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.258-1055A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17601072 | |||||||
chr1:17601074 | A | C | 1 | a0002c0003t0002g0037 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.258-1053A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17601074 | |||||||
chr1:17601075 | A | C | 9 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(6): Show |
9 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.258-1052A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17601075 | |||||||
chr1:17601076 | C | A | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.258-1051C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17601076 | |||||||
chr1:17601210 | T | C | 39 | a0001c0001t0001g0012 a0001c0001t0001g0096 a0001c0001t0001g0140 others(36): Show |
39 | HG00558.hp1 HG00733.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.258-917T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17601210 | |||||||
chr1:17601303 | G | C | 28 | a0001c0001t0001g0012 a0001c0001t0001g0140 a0001c0001t0001g0164 others(25): Show |
28 | HG00558.hp1 HG00733.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.258-824G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17601303 | |||||||
chr1:17601527 | C | G | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.258-600C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17601527 | |||||||
chr1:17601652 | G | T | 7 | a0004c0005t0002g0006 a0004c0005t0002g0060 a0004c0005t0002g0108 others(4): Show |
7 | HG02109.hp1 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-475G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17601652 | |||||||
chr1:17601687 | C | T | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.258-440C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17601687 | |||||||
chr1:17601764 | A | G | 17 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0021 others(14): Show |
17 | HG00642.hp2 HG00733.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.258-363A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17601764 | |||||||
chr1:17601855 | A | G | 1 | a0002c0007t0002g0058 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.258-272A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17601855 | |||||||
chr1:17601928 | G | A | 2 | a0001c0014t0001g0145 a0002c0003t0002g0025 |
2 | NA18946.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.258-199G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17601928 | |||||||
chr1:17602033 | T | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(1): Show |
4 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-94T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17602033 | |||||||
chr1:17602049 | G | A | 2 | a0001c0001t0001g0096 a0001c0011t0001g0004 |
2 | HG02071.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.258-78G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | chr1 | 17602049 | |||||||
chr1:17602233 | C | T | 1 | a0002c0022t0002g0050 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.349+15C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 5/28 | chr1 | 17602233 | |||||||
chr1:17602510 | C | T | 1 | a0003c0002t0001g0073 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.349+292C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 5/28 | chr1 | 17602510 | |||||||
chr1:17602713 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.349+495T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 5/28 | chr1 | 17602713 | |||||||
chr1:17602719 | C | T | 37 | a0001c0001t0001g0096 a0001c0001t0001g0140 a0001c0006t0001g0001 others(34): Show |
37 | HG00733.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.349+501C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 5/28 | chr1 | 17602719 | |||||||
chr1:17602732 | T | A | 3 | a0001c0033t0002g0110 a0012c0031t0006g0165 a0021c0030t0002g0109 |
3 | HG01884.hp1 HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.349+514T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 5/28 | chr1 | 17602732 | |||||||
chr1:17602733 | C | A | 3 | a0001c0033t0002g0110 a0012c0031t0006g0165 a0021c0030t0002g0109 |
3 | HG01884.hp1 HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.349+515C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 5/28 | chr1 | 17602733 | |||||||
chr1:17602867 | G | GA | 27 | a0001c0001t0001g0012 a0001c0001t0001g0140 a0001c0017t0002g0113 others(24): Show |
27 | HG00558.hp1 HG00733.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.350-639dupA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr1 | 17602867 | ||||||
chr1:17603082 | G | A | 7 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-426G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 5/28 | chr1 | 17603082 | |||||||
chr1:17603122 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.350-386C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 5/28 | chr1 | 17603122 | |||||||
chr1:17603309 | T | C | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.350-199T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 5/28 | chr1 | 17603309 | |||||||
chr1:17603338 | G | C | 2 | a0012c0031t0006g0165 a0021c0030t0002g0109 |
2 | HG01884.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.350-170G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 5/28 | chr1 | 17603338 | |||||||
chr1:17603417 | C | T | 2 | a0004c0005t0002g0117 a0014c0029t0001g0122 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.350-91C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 5/28 | chr1 | 17603417 | |||||||
chr1:17603477 | G | T | 57 | a0001c0001t0001g0012 a0001c0001t0001g0062 a0001c0001t0001g0096 others(54): Show |
57 | HG00558.hp1 HG00733.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.350-31G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 5/28 | chr1 | 17603477 | |||||||
chr1:17603485 | C | G | 54 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0027 others(51): Show |
54 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.350-23C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 5/28 | chr1 | 17603485 | |||||||
chr1:17603495 | A | C | 57 | a0001c0001t0001g0012 a0001c0001t0001g0062 a0001c0001t0001g0096 others(54): Show |
57 | HG00558.hp1 HG00733.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.350-13A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 5/28 | chr1 | 17603495 | |||||||
chr1:17603688 | C | T | 4 | a0001c0001t0001g0062 a0001c0001t0003g0114 a0001c0001t0003g0151 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.433+97C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17603688 | |||||||
chr1:17603736 | C | G | 1 | a0001c0001t0001g0098 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.433+145C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17603736 | |||||||
chr1:17603917 | G | A | 1 | a0001c0019t0001g0095 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.433+326G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17603917 | |||||||
chr1:17604211 | C | CG | 5 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.433+622dupG | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr1 | 17604211 | ||||||
chr1:17604304 | G | A | 17 | a0001c0001t0001g0062 a0001c0001t0001g0096 a0001c0001t0003g0114 others(14): Show |
17 | HG01109.hp1 HG02071.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.433+713G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17604304 | |||||||
chr1:17604543 | C | T | 4 | a0001c0001t0001g0062 a0001c0001t0003g0114 a0001c0001t0003g0151 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.433+952C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17604543 | |||||||
chr1:17604605 | C | T | 8 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(5): Show |
8 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.433+1014C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17604605 | |||||||
chr1:17604811 | C | T | 3 | a0001c0001t0001g0119 a0002c0004t0002g0120 a0002c0004t0002g0121 |
3 | HG01070.hp1 HG01071.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.433+1220C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17604811 | |||||||
chr1:17604814 | C | T | 7 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.433+1223C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17604814 | |||||||
chr1:17605091 | A | T | 1 | a0011c0025t0002g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.433+1500A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17605091 | |||||||
chr1:17605143 | G | A | 2 | a0001c0001t0001g0096 a0001c0011t0001g0004 |
2 | HG02071.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.433+1552G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17605143 | |||||||
chr1:17605207 | G | A | 24 | a0001c0001t0001g0062 a0001c0001t0001g0096 a0001c0001t0003g0114 others(21): Show |
24 | HG01069.hp1 HG01071.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.433+1616G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17605207 | |||||||
chr1:17605372 | A | C | 8 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(5): Show |
8 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.433+1781A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17605372 | |||||||
chr1:17605397 | C | T | 2 | a0004c0005t0002g0117 a0014c0029t0001g0122 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.433+1806C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17605397 | |||||||
chr1:17605400 | A | G | 12 | a0001c0001t0001g0062 a0001c0001t0003g0114 a0001c0001t0003g0151 others(9): Show |
12 | HG02109.hp1 HG02717.hp2 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.433+1809A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17605400 | |||||||
chr1:17605423 | G | A | 3 | a0002c0007t0002g0058 a0002c0007t0002g0085 a0005c0024t0002g0059 |
3 | HG02280.hp2 HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.433+1832G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17605423 | |||||||
chr1:17605450 | C | G | 1 | a0001c0012t0001g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.433+1859C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17605450 | |||||||
chr1:17605572 | C | T | 3 | a0001c0001t0001g0127 a0003c0002t0001g0056 a0009c0040t0001g0087 |
3 | HG00642.hp2 HG01261.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.433+1981C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17605572 | |||||||
chr1:17605856 | C | T | 1 | a0003c0002t0001g0106 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.434-1946C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17605856 | |||||||
chr1:17605958 | C | T | 7 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.434-1844C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17605958 | |||||||
chr1:17606106 | G | A | 1 | a0005c0015t0002g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.434-1696G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17606106 | |||||||
chr1:17606356 | C | T | 3 | a0001c0001t0001g0119 a0002c0004t0002g0120 a0002c0004t0002g0121 |
3 | HG01070.hp1 HG01071.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.434-1446C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17606356 | |||||||
chr1:17606363 | G | T | 1 | a0003c0002t0001g0069 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.434-1439G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17606363 | |||||||
chr1:17606600 | CT | C | 43 | a0001c0001t0001g0041 a0001c0001t0001g0079 a0001c0001t0001g0096 others(40): Show |
43 | HG00733.hp1 HG01071.hp1 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.434-1187delT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr1 | 17606600 | ||||||
chr1:17606600 | CTT | C | 12 | a0001c0006t0001g0129 a0002c0003t0002g0116 a0002c0007t0002g0085 others(9): Show |
12 | HG01069.hp1 HG01074.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.434-1188_434-1187d others(4): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr1 | 17606600 | ||||||
chr1:17606615 | T | A | 8 | a0001c0001t0001g0163 a0001c0001t0005g0162 a0001c0006t0003g0139 others(5): Show |
8 | HG01106.hp2 HG01884.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.434-1187T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17606615 | |||||||
chr1:17606635 | A | C | 6 | a0001c0001t0001g0062 a0001c0001t0003g0114 a0001c0001t0003g0151 others(3): Show |
6 | HG01109.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.434-1167A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17606635 | |||||||
chr1:17606790 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.434-1012A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17606790 | |||||||
chr1:17607026 | G | T | 1 | a0001c0044t0004g0161 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.434-776G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17607026 | |||||||
chr1:17607192 | C | T | 8 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(5): Show |
8 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.434-610C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17607192 | |||||||
chr1:17607303 | C | T | 1 | a0019c0026t0001g0026 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.434-499C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17607303 | |||||||
chr1:17607399 | C | T | 5 | a0001c0001t0001g0119 a0002c0004t0002g0120 a0002c0004t0002g0121 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.434-403C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17607399 | |||||||
chr1:17607466 | C | A | 2 | a0002c0003t0002g0037 a0008c0016t0002g0132 |
2 | NA18966.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.434-336C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17607466 | |||||||
chr1:17607565 | C | T | 1 | a0002c0007t0002g0013 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.434-237C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17607565 | |||||||
chr1:17607618 | C | T | 1 | a0007c0010t0001g0065 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.434-184C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17607618 | |||||||
chr1:17607644 | C | T | 2 | a0001c0001t0003g0114 a0001c0001t0003g0151 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.434-158C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17607644 | |||||||
chr1:17607661 | G | A | 2 | a0001c0001t0001g0096 a0001c0011t0001g0004 |
2 | HG02071.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.434-141G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 6/28 | chr1 | 17607661 | |||||||
chr1:17607994 | T | C | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.609+17T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17607994 | |||||||
chr1:17608017 | C | T | 1 | a0001c0006t0007g0150 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.609+40C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17608017 | |||||||
chr1:17608018 | G | A | 8 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(5): Show |
8 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.609+41G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17608018 | |||||||
chr1:17608183 | G | A | 2 | a0001c0001t0003g0114 a0001c0001t0003g0151 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.609+206G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17608183 | |||||||
chr1:17608426 | C | G | 4 | a0001c0001t0001g0062 a0001c0001t0003g0114 a0001c0001t0003g0151 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.609+449C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17608426 | |||||||
chr1:17608603 | G | A | 8 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(5): Show |
8 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.609+626G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17608603 | |||||||
chr1:17608659 | C | T | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.609+682C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17608659 | |||||||
chr1:17608682 | T | C | 17 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0021 others(14): Show |
17 | HG00642.hp2 HG00733.hp2 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.609+705T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17608682 | |||||||
chr1:17608756 | G | A | 7 | a0001c0048t0001g0005 a0002c0008t0002g0042 a0002c0008t0002g0100 others(4): Show |
7 | HG00733.hp1 HG01433.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.609+779G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17608756 | |||||||
chr1:17608810 | A | G | 3 | a0002c0007t0002g0058 a0002c0007t0002g0085 a0005c0024t0002g0059 |
3 | HG02280.hp2 HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.609+833A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17608810 | |||||||
chr1:17609112 | C | T | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.609+1135C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17609112 | |||||||
chr1:17609218 | G | T | 2 | a0012c0031t0006g0165 a0021c0030t0002g0109 |
2 | HG01884.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.609+1241G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17609218 | |||||||
chr1:17609276 | G | T | 2 | a0001c0001t0001g0136 a0001c0001t0003g0135 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.609+1299G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17609276 | |||||||
chr1:17609460 | C | G | 1 | a0001c0038t0003g0124 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.609+1483C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17609460 | |||||||
chr1:17609534 | A | G | 8 | a0001c0001t0001g0062 a0001c0001t0001g0096 a0001c0001t0003g0114 others(5): Show |
8 | HG01109.hp1 HG02071.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.609+1557A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17609534 | |||||||
chr1:17609660 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.609+1683C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17609660 | |||||||
chr1:17609936 | C | T | 3 | a0002c0007t0002g0058 a0002c0007t0002g0085 a0005c0024t0002g0059 |
3 | HG02280.hp2 HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.609+1959C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17609936 | |||||||
chr1:17610042 | C | T | 4 | a0002c0007t0002g0058 a0002c0007t0002g0085 a0005c0024t0002g0059 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.609+2065C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17610042 | |||||||
chr1:17610233 | C | T | 8 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(5): Show |
8 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.609+2256C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17610233 | |||||||
chr1:17610319 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.609+2342C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17610319 | |||||||
chr1:17610496 | G | C | 1 | a0001c0019t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.609+2519G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17610496 | |||||||
chr1:17610523 | C | T | 2 | a0001c0006t0001g0129 a0001c0006t0001g0130 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.610-2535C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17610523 | |||||||
chr1:17610737 | T | C | 3 | a0001c0033t0002g0110 a0012c0031t0006g0165 a0021c0030t0002g0109 |
3 | HG01884.hp1 HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.610-2321T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17610737 | |||||||
chr1:17610815 | C | T | 5 | a0001c0001t0001g0096 a0001c0011t0001g0004 a0001c0033t0002g0110 others(2): Show |
5 | HG01884.hp1 HG02071.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.610-2243C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17610815 | |||||||
chr1:17610951 | G | GT | 17 | a0001c0001t0001g0119 a0001c0001t0003g0114 a0001c0001t0003g0151 others(14): Show |
17 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.610-2095dupT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr1 | 17610951 | ||||||
chr1:17610952 | T | G | 27 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0140 others(24): Show |
27 | HG00558.hp1 HG00733.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.610-2106T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17610952 | |||||||
chr1:17610953 | T | G | 1 | a0013c0035t0001g0018 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.610-2105T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17610953 | |||||||
chr1:17611058 | A | G | 4 | a0001c0001t0001g0010 a0002c0007t0002g0013 a0002c0007t0002g0105 others(1): Show |
4 | HG00642.hp1 HG02572.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.610-2000A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17611058 | |||||||
chr1:17611083 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.610-1975C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17611083 | |||||||
chr1:17611301 | A | G | 1 | a0002c0004t0002g0036 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.610-1757A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17611301 | |||||||
chr1:17611502 | T | C | 31 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(28): Show |
31 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.610-1556T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17611502 | |||||||
chr1:17611533 | T | TATCC | 24 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0033 others(21): Show |
24 | HG00323.hp1 HG01106.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.610-1483_610-1480d others(6): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr1 | 17611533 | ||||||
chr1:17611533 | T | TATCCATC others(1): Show |
4 | a0001c0001t0001g0003 a0001c0001t0001g0158 a0001c0019t0001g0095 others(1): Show |
4 | HG02451.hp1 HG02559.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.610-1487_610-1480d others(10): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr1 | 17611533 | ||||||
chr1:17611533 | T | TATCCATC others(5): Show |
1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.610-1491_610-1480d others(14): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr1 | 17611533 | ||||||
chr1:17611533 | TATCC | T | 27 | a0001c0001t0001g0140 a0001c0017t0002g0113 a0001c0017t0002g0148 others(24): Show |
27 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.610-1483_610-1480d others(6): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr1 | 17611533 | ||||||
chr1:17611533 | TATCCATC others(5): Show |
T | 4 | a0001c0001t0001g0096 a0001c0011t0001g0004 a0001c0033t0002g0110 others(1): Show |
4 | HG01884.hp1 HG02071.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.610-1491_610-1480d others(14): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr1 | 17611533 | ||||||
chr1:17611533 | TATCCATC others(9): Show |
T | 5 | a0001c0001t0001g0021 a0001c0001t0001g0119 a0002c0004t0002g0120 others(2): Show |
5 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.610-1495_610-1480d others(18): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr1 | 17611533 | ||||||
chr1:17611534 | A | G | 1 | a0010c0046t0001g0020 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.610-1524A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17611534 | |||||||
chr1:17611920 | C | T | 1 | a0002c0004t0002g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.610-1138C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17611920 | |||||||
chr1:17611977 | G | GTCCA | 42 | a0001c0001t0001g0096 a0001c0001t0001g0140 a0001c0001t0003g0114 others(39): Show |
42 | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.610-1053_610-1050d others(6): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr1 | 17611977 | ||||||
chr1:17611977 | G | GTCCATCC others(1): Show |
4 | a0002c0007t0002g0058 a0002c0007t0002g0085 a0002c0041t0008g0054 others(1): Show |
4 | HG02280.hp2 HG02896.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.610-1057_610-1050d others(10): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr1 | 17611977 | ||||||
chr1:17611987 | C | CCAT | 3 | a0002c0007t0002g0013 a0002c0007t0002g0105 a0002c0007t0002g0111 |
3 | HG00642.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.610-1069_610-1067d others(5): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr1 | 17611987 | ||||||
chr1:17612346 | C | G | 2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.610-712C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17612346 | |||||||
chr1:17612878 | C | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0001t0001g0034 others(2): Show |
5 | HG01346.hp2 HG01496.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.610-180C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17612878 | |||||||
chr1:17612879 | G | T | 4 | a0001c0001t0001g0096 a0001c0011t0001g0004 a0012c0031t0006g0165 others(1): Show |
4 | HG01884.hp1 HG02071.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.610-179G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17612879 | |||||||
chr1:17612910 | C | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.610-148C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17612910 | |||||||
chr1:17612936 | G | A | 2 | a0001c0001t0005g0162 a0007c0010t0001g0053 |
2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.610-122G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | chr1 | 17612936 | |||||||
chr1:17613866 | A | C | 28 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0140 others(25): Show |
28 | HG00558.hp1 HG00733.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.726+692A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17613866 | |||||||
chr1:17613872 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(1): Show |
4 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.726+698G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17613872 | |||||||
chr1:17613937 | C | T | 1 | a0003c0002t0001g0144 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.726+763C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17613937 | |||||||
chr1:17614028 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.726+854C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17614028 | |||||||
chr1:17614109 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.726+935G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17614109 | |||||||
chr1:17614194 | T | C | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.726+1020T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17614194 | |||||||
chr1:17614233 | G | GT | 62 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
62 | HG00558.hp1 HG00642.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.726+1061dupT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr1 | 17614233 | ||||||
chr1:17614233 | G | T | 1 | a0002c0034t0002g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.726+1059G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17614233 | |||||||
chr1:17614257 | C | A | 3 | a0001c0001t0003g0114 a0001c0001t0003g0151 a0002c0041t0008g0054 |
3 | HG02896.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.726+1083C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17614257 | |||||||
chr1:17614258 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.726+1084G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17614258 | |||||||
chr1:17614323 | T | G | 63 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(60): Show |
63 | HG00558.hp1 HG00642.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.726+1149T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17614323 | |||||||
chr1:17614356 | T | C | 2 | a0002c0018t0002g0155 a0007c0010t0001g0115 |
2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.726+1182T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17614356 | |||||||
chr1:17614397 | T | G | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.726+1223T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17614397 | |||||||
chr1:17614409 | G | T | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.726+1235G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17614409 | |||||||
chr1:17614515 | G | A | 8 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(5): Show |
8 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.726+1341G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17614515 | |||||||
chr1:17614609 | C | G | 1 | a0001c0001t0001g0010 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.726+1435C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17614609 | |||||||
chr1:17614628 | T | C | 14 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(11): Show |
14 | HG00642.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.726+1454T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17614628 | |||||||
chr1:17614732 | C | T | 14 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(11): Show |
14 | HG00642.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.727-1362C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17614732 | |||||||
chr1:17614964 | C | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.727-1130C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17614964 | |||||||
chr1:17615079 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.727-1015G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17615079 | |||||||
chr1:17615090 | T | G | 8 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(5): Show |
8 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.727-1004T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17615090 | |||||||
chr1:17615327 | C | T | 14 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(11): Show |
14 | HG00642.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.727-767C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17615327 | |||||||
chr1:17615408 | A | G | 8 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(5): Show |
8 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.727-686A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17615408 | |||||||
chr1:17615421 | T | A | 1 | a0001c0006t0003g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.727-673T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17615421 | |||||||
chr1:17615672 | T | G | 2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.727-422T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17615672 | |||||||
chr1:17615784 | T | G | 14 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(11): Show |
14 | HG00642.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.727-310T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17615784 | |||||||
chr1:17615851 | T | C | 14 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(11): Show |
14 | HG00642.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.727-243T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17615851 | |||||||
chr1:17615914 | C | A | 1 | a0001c0038t0003g0124 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.727-180C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 8/28 | chr1 | 17615914 | |||||||
chr1:17616215 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.835+13C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17616215 | |||||||
chr1:17616400 | G | A | 62 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
62 | HG00558.hp1 HG00642.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.835+198G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17616400 | |||||||
chr1:17616441 | C | T | 2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.835+239C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17616441 | |||||||
chr1:17616531 | C | A | 3 | a0001c0001t0001g0119 a0002c0004t0002g0120 a0002c0004t0002g0121 |
3 | HG01070.hp1 HG01071.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.835+329C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17616531 | |||||||
chr1:17616575 | A | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.835+373A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17616575 | |||||||
chr1:17616595 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.835+393C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17616595 | |||||||
chr1:17616780 | G | A | 1 | a0001c0019t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.835+578G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17616780 | |||||||
chr1:17617042 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.835+840A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17617042 | |||||||
chr1:17617101 | C | T | 8 | a0001c0001t0001g0096 a0001c0001t0001g0119 a0001c0011t0001g0004 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.835+899C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17617101 | |||||||
chr1:17617102 | G | A | 2 | a0001c0001t0003g0114 a0001c0001t0003g0151 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.835+900G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17617102 | |||||||
chr1:17617108 | G | A | 27 | a0001c0001t0001g0012 a0001c0001t0001g0140 a0001c0017t0002g0113 others(24): Show |
27 | HG00558.hp1 HG00733.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.835+906G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17617108 | |||||||
chr1:17617113 | C | T | 8 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(5): Show |
8 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.835+911C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17617113 | |||||||
chr1:17617223 | A | C | 1 | a0003c0002t0001g0038 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.835+1021A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17617223 | |||||||
chr1:17617573 | G | T | 1 | a0004c0005t0002g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.835+1371G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17617573 | |||||||
chr1:17617639 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.835+1437G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17617639 | |||||||
chr1:17618179 | C | T | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.836-1160C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17618179 | |||||||
chr1:17618325 | C | T | 1 | a0001c0001t0003g0143 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.836-1014C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17618325 | |||||||
chr1:17618396 | A | C | 16 | a0001c0033t0002g0110 a0002c0007t0002g0013 a0002c0007t0002g0058 others(13): Show |
16 | HG00642.hp1 HG02109.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.836-943A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17618396 | |||||||
chr1:17618459 | C | A | 1 | a0001c0042t0001g0035 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.836-880C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17618459 | |||||||
chr1:17618476 | C | T | 1 | a0001c0019t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.836-863C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17618476 | |||||||
chr1:17618494 | C | G | 1 | a0001c0001t0005g0162 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.836-845C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17618494 | |||||||
chr1:17618615 | C | G | 1 | a0001c0019t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.836-724C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17618615 | |||||||
chr1:17618817 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.836-522G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17618817 | |||||||
chr1:17618876 | A | G | 1 | a0001c0019t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.836-463A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17618876 | |||||||
chr1:17618900 | C | T | 6 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.836-439C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17618900 | |||||||
chr1:17619260 | G | A | 4 | a0001c0001t0001g0096 a0001c0011t0001g0004 a0012c0031t0006g0165 others(1): Show |
4 | HG01884.hp1 HG02071.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.836-79G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17619260 | |||||||
chr1:17619279 | G | A | 2 | a0012c0031t0006g0165 a0021c0030t0002g0109 |
2 | HG01884.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.836-60G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 9/28 | chr1 | 17619279 | |||||||
chr1:17619603 | T | C | 4 | a0001c0001t0001g0096 a0001c0011t0001g0004 a0012c0031t0006g0165 others(1): Show |
4 | HG01884.hp1 HG02071.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.942+158T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | chr1 | 17619603 | |||||||
chr1:17619604 | C | T | 4 | a0001c0001t0001g0096 a0001c0011t0001g0004 a0012c0031t0006g0165 others(1): Show |
4 | HG01884.hp1 HG02071.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.942+159C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | chr1 | 17619604 | |||||||
chr1:17619679 | C | T | 2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.942+234C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | chr1 | 17619679 | |||||||
chr1:17619698 | G | C | 61 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(58): Show |
61 | HG00558.hp1 HG00642.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.942+253G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | chr1 | 17619698 | |||||||
chr1:17619927 | G | A | 3 | a0001c0001t0003g0114 a0001c0001t0003g0151 a0002c0041t0008g0054 |
3 | HG02896.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.942+482G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | chr1 | 17619927 | |||||||
chr1:17619928 | C | T | 3 | a0001c0001t0003g0114 a0001c0001t0003g0151 a0002c0041t0008g0054 |
3 | HG02896.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.942+483C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | chr1 | 17619928 | |||||||
chr1:17619960 | C | A | 15 | a0001c0033t0002g0110 a0002c0007t0002g0013 a0002c0007t0002g0058 others(12): Show |
15 | HG00642.hp1 HG02109.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.942+515C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | chr1 | 17619960 | |||||||
chr1:17620205 | C | CA | 67 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0030 others(64): Show |
67 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.942+778dupA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr1 | 17620205 | ||||||
chr1:17620224 | T | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.942+779T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | chr1 | 17620224 | |||||||
chr1:17620296 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.942+851T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | chr1 | 17620296 | |||||||
chr1:17620312 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.942+867G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | chr1 | 17620312 | |||||||
chr1:17620382 | GT | G | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.942+939delT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr1 | 17620382 | ||||||
chr1:17620420 | A | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.942+975A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | chr1 | 17620420 | |||||||
chr1:17620755 | C | A | 6 | a0002c0003t0002g0083 a0002c0003t0002g0089 a0002c0003t0002g0116 others(3): Show |
6 | HG01074.hp2 HG01106.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.943-1109C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | chr1 | 17620755 | |||||||
chr1:17620992 | C | T | 5 | a0001c0001t0001g0061 a0001c0001t0001g0154 a0001c0001t0003g0131 others(2): Show |
5 | HG02976.hp1 HG03098.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.943-872C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | chr1 | 17620992 | |||||||
chr1:17621115 | C | A | 1 | a0002c0004t0002g0146 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.943-749C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | chr1 | 17621115 | |||||||
chr1:17621206 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.943-658C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | chr1 | 17621206 | |||||||
chr1:17621223 | A | G | 3 | a0001c0001t0003g0114 a0001c0001t0003g0151 a0002c0041t0008g0054 |
3 | HG02896.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.943-641A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | chr1 | 17621223 | |||||||
chr1:17621370 | C | T | 3 | a0001c0001t0003g0114 a0001c0001t0003g0151 a0002c0041t0008g0054 |
3 | HG02896.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.943-494C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | chr1 | 17621370 | |||||||
chr1:17621389 | C | A | 1 | a0002c0003t0002g0133 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.943-475C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | chr1 | 17621389 | |||||||
chr1:17621629 | A | G | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.943-235A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | chr1 | 17621629 | |||||||
chr1:17621704 | G | A | 7 | a0001c0048t0001g0005 a0002c0008t0002g0042 a0002c0008t0002g0100 others(4): Show |
7 | HG00733.hp1 HG01433.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.943-160G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | chr1 | 17621704 | |||||||
chr1:17621810 | G | GGGCCACA others(9): Show |
59 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(56): Show |
59 | HG00558.hp1 HG00733.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.943-50_943-49insAC others(14): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr1 | 17621810 | ||||||
chr1:17621842 | C | G | 2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.943-22C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | chr1 | 17621842 | |||||||
chr1:17621981 | G | A | 1 | a0001c0033t0002g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1020+40G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 11/28 | chr1 | 17621981 | |||||||
chr1:17622148 | T | C | 3 | a0001c0001t0003g0114 a0001c0001t0003g0151 a0002c0041t0008g0054 |
3 | HG02896.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1020+207T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 11/28 | chr1 | 17622148 | |||||||
chr1:17622443 | G | C | 3 | a0001c0001t0001g0119 a0002c0004t0002g0120 a0002c0004t0002g0121 |
3 | HG01070.hp1 HG01071.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1020+502G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 11/28 | chr1 | 17622443 | |||||||
chr1:17622549 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0011 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1021-447G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 11/28 | chr1 | 17622549 | |||||||
chr1:17622687 | T | A | 1 | a0002c0018t0002g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1021-309T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 11/28 | chr1 | 17622687 | |||||||
chr1:17622818 | G | A | 2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1021-178G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 11/28 | chr1 | 17622818 | |||||||
chr1:17622850 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1021-146C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 11/28 | chr1 | 17622850 | |||||||
chr1:17622959 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1021-37G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 11/28 | chr1 | 17622959 | |||||||
chr1:17622985 | C | G | 1 | a0002c0007t0002g0013 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1021-11C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 11/28 | chr1 | 17622985 | |||||||
chr1:17622992 | G | T | 7 | a0001c0019t0001g0066 a0002c0007t0002g0013 a0002c0007t0002g0058 others(4): Show |
7 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1021-4G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 11/28 | chr1 | 17622992 | |||||||
chr1:17623185 | C | T | 3 | a0001c0001t0001g0096 a0001c0011t0001g0004 a0021c0030t0002g0109 |
3 | HG02071.hp1 HG03710.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1200+10C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 12/28 | chr1 | 17623185 | |||||||
chr1:17623198 | C | T | 1 | a0003c0002t0001g0038 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1200+23C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 12/28 | chr1 | 17623198 | |||||||
chr1:17623419 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1200+244T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 12/28 | chr1 | 17623419 | |||||||
chr1:17623474 | C | T | 2 | a0004c0005t0002g0060 a0004c0005t0002g0108 |
2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1200+299C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 12/28 | chr1 | 17623474 | |||||||
chr1:17623494 | C | T | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1200+319C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 12/28 | chr1 | 17623494 | |||||||
chr1:17623554 | G | A | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1200+379G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 12/28 | chr1 | 17623554 | |||||||
chr1:17623599 | T | A | 9 | a0001c0033t0002g0110 a0002c0034t0002g0149 a0004c0005t0002g0006 others(6): Show |
9 | HG02109.hp1 HG02559.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1200+424T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 12/28 | chr1 | 17623599 | |||||||
chr1:17623637 | A | C | 2 | a0001c0001t0001g0096 a0001c0011t0001g0004 |
2 | HG02071.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1200+462A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 12/28 | chr1 | 17623637 | |||||||
chr1:17623826 | C | CT | 5 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1201-553dupT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr1 | 17623826 | ||||||
chr1:17623895 | G | A | 1 | a0001c0012t0001g0064 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1201-492G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 12/28 | chr1 | 17623895 | |||||||
chr1:17623959 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0003g0135 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1201-428G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 12/28 | chr1 | 17623959 | |||||||
chr1:17623967 | G | T | 18 | a0001c0001t0001g0096 a0001c0001t0001g0119 a0001c0001t0003g0114 others(15): Show |
18 | HG00642.hp1 HG01070.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1201-420G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 12/28 | chr1 | 17623967 | |||||||
chr1:17624133 | C | T | 1 | a0002c0004t0002g0036 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1201-254C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 12/28 | chr1 | 17624133 | |||||||
chr1:17624138 | G | A | 2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1201-249G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 12/28 | chr1 | 17624138 | |||||||
chr1:17624219 | G | T | 1 | a0003c0002t0001g0081 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1201-168G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 12/28 | chr1 | 17624219 | |||||||
chr1:17624641 | G | T | 1 | a0001c0019t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1317+138G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 13/28 | chr1 | 17624641 | |||||||
chr1:17624729 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1317+226T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 13/28 | chr1 | 17624729 | |||||||
chr1:17625051 | T | G | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1317+548T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 13/28 | chr1 | 17625051 | |||||||
chr1:17625070 | C | T | 8 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(5): Show |
8 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1317+567C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 13/28 | chr1 | 17625070 | |||||||
chr1:17625083 | C | T | 8 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(5): Show |
8 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1317+580C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 13/28 | chr1 | 17625083 | |||||||
chr1:17625186 | G | A | 3 | a0001c0001t0001g0119 a0002c0004t0002g0120 a0002c0004t0002g0121 |
3 | HG01070.hp1 HG01071.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1317+683G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 13/28 | chr1 | 17625186 | |||||||
chr1:17625462 | T | G | 1 | a0001c0001t0001g0046 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1318-494T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 13/28 | chr1 | 17625462 | |||||||
chr1:17625608 | A | C | 1 | a0001c0001t0001g0028 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1318-348A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 13/28 | chr1 | 17625608 | |||||||
chr1:17625661 | A | G | 3 | a0001c0001t0003g0114 a0001c0001t0003g0151 a0002c0041t0008g0054 |
3 | HG02896.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1318-295A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 13/28 | chr1 | 17625661 | |||||||
chr1:17625754 | G | A | 1 | a0010c0046t0001g0020 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1318-202G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 13/28 | chr1 | 17625754 | |||||||
chr1:17626223 | AC | A | 2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1410+176delC | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 14/28 | chr1 | 17626223 | |||||||
chr1:17626281 | T | G | 1 | a0001c0001t0001g0010 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1410+233T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 14/28 | chr1 | 17626281 | |||||||
chr1:17626763 | G | A | 1 | a0002c0003t0002g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1411-567G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 14/28 | chr1 | 17626763 | |||||||
chr1:17626907 | C | G | 2 | a0001c0001t0001g0078 a0007c0010t0001g0065 |
2 | HG01169.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1411-423C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 14/28 | chr1 | 17626907 | |||||||
chr1:17627000 | G | C | 8 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(5): Show |
8 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1411-330G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 14/28 | chr1 | 17627000 | |||||||
chr1:17627016 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1411-314G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 14/28 | chr1 | 17627016 | |||||||
chr1:17627131 | T | C | 8 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(5): Show |
8 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1411-199T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 14/28 | chr1 | 17627131 | |||||||
chr1:17627253 | G | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1411-77G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 14/28 | chr1 | 17627253 | |||||||
chr1:17627685 | T | G | 1 | a0003c0002t0001g0081 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1584+182T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17627685 | |||||||
chr1:17627916 | T | C | 62 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(59): Show |
62 | HG00558.hp1 HG00642.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.1584+413T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17627916 | |||||||
chr1:17627991 | A | C | 37 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0096 others(34): Show |
37 | HG00558.hp1 HG00733.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.1584+488A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17627991 | |||||||
chr1:17628016 | C | T | 1 | a0007c0010t0001g0065 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1584+513C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17628016 | |||||||
chr1:17628034 | T | TA | 26 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0098 others(23): Show |
26 | HG00558.hp1 HG00733.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1584+544dupA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | INFO_REALIGN_3_PRIME | chr1 | 17628034 | ||||||
chr1:17628034 | TA | T | 11 | a0001c0001t0003g0151 a0001c0006t0001g0129 a0001c0011t0001g0152 others(8): Show |
11 | HG01069.hp1 HG01257.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1584+544delA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | INFO_REALIGN_3_PRIME | chr1 | 17628034 | ||||||
chr1:17628073 | C | T | 8 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(5): Show |
8 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1584+570C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17628073 | |||||||
chr1:17628127 | C | A | 1 | a0002c0003t0002g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1584+624C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17628127 | |||||||
chr1:17628317 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1584+814G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17628317 | |||||||
chr1:17628343 | C | A | 3 | a0001c0001t0003g0114 a0001c0001t0003g0151 a0002c0041t0008g0054 |
3 | HG02896.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1584+840C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17628343 | |||||||
chr1:17628344 | C | G | 8 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(5): Show |
8 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1584+841C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17628344 | |||||||
chr1:17628802 | C | T | 13 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0076 others(10): Show |
13 | HG00558.hp2 HG00741.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.1584+1299C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17628802 | |||||||
chr1:17628836 | G | A | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1584+1333G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17628836 | |||||||
chr1:17628896 | A | C | 1 | a0002c0022t0002g0050 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1584+1393A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17628896 | |||||||
chr1:17629100 | A | C | 2 | a0001c0001t0001g0096 a0001c0011t0001g0004 |
2 | HG02071.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1584+1597A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17629100 | |||||||
chr1:17629191 | A | AT | 8 | a0001c0001t0001g0021 a0001c0006t0001g0001 a0001c0006t0001g0129 others(5): Show |
8 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1584+1704dupT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | INFO_REALIGN_3_PRIME | chr1 | 17629191 | ||||||
chr1:17629191 | AT | A | 33 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(30): Show |
33 | HG00642.hp1 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1584+1704delT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | INFO_REALIGN_3_PRIME | chr1 | 17629191 | ||||||
chr1:17629439 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1584+1936C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17629439 | |||||||
chr1:17629589 | C | T | 8 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(5): Show |
8 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1584+2086C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17629589 | |||||||
chr1:17629603 | G | A | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1584+2100G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17629603 | |||||||
chr1:17629927 | T | G | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1585-2394T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17629927 | |||||||
chr1:17629938 | C | T | 7 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1585-2383C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17629938 | |||||||
chr1:17629939 | G | A | 1 | a0010c0046t0001g0020 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1585-2382G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17629939 | |||||||
chr1:17629951 | C | T | 12 | a0001c0001t0001g0119 a0001c0006t0001g0001 a0001c0006t0001g0129 others(9): Show |
12 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1585-2370C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17629951 | |||||||
chr1:17629968 | G | T | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1585-2353G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17629968 | |||||||
chr1:17630054 | G | A | 12 | a0001c0001t0001g0119 a0001c0006t0001g0001 a0001c0006t0001g0129 others(9): Show |
12 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1585-2267G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17630054 | |||||||
chr1:17630183 | A | G | 9 | a0001c0033t0002g0110 a0002c0034t0002g0149 a0004c0005t0002g0006 others(6): Show |
9 | HG02109.hp1 HG02559.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1585-2138A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17630183 | |||||||
chr1:17630280 | G | A | 3 | a0001c0001t0001g0154 a0001c0001t0003g0131 a0016c0047t0002g0147 |
3 | HG02976.hp1 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1585-2041G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17630280 | |||||||
chr1:17630612 | G | A | 7 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1585-1709G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17630612 | |||||||
chr1:17630713 | G | C | 1 | a0001c0001t0001g0159 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1585-1608G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17630713 | |||||||
chr1:17630714 | C | G | 1 | a0001c0001t0001g0159 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1585-1607C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17630714 | |||||||
chr1:17630759 | A | C | 9 | a0001c0033t0002g0110 a0002c0034t0002g0149 a0004c0005t0002g0006 others(6): Show |
9 | HG02109.hp1 HG02559.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1585-1562A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17630759 | |||||||
chr1:17630765 | C | T | 1 | a0001c0006t0007g0150 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1585-1556C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17630765 | |||||||
chr1:17630766 | C | T | 9 | a0001c0033t0002g0110 a0002c0034t0002g0149 a0004c0005t0002g0006 others(6): Show |
9 | HG02109.hp1 HG02559.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1585-1555C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17630766 | |||||||
chr1:17630778 | C | T | 15 | a0001c0001t0001g0096 a0001c0001t0001g0119 a0001c0006t0001g0001 others(12): Show |
15 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1585-1543C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17630778 | |||||||
chr1:17630912 | T | C | 9 | a0001c0033t0002g0110 a0002c0034t0002g0149 a0004c0005t0002g0006 others(6): Show |
9 | HG02109.hp1 HG02559.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1585-1409T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17630912 | |||||||
chr1:17630944 | G | C | 26 | a0001c0001t0001g0012 a0001c0001t0001g0140 a0001c0017t0002g0113 others(23): Show |
26 | HG00558.hp1 HG00733.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.1585-1377G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17630944 | |||||||
chr1:17630954 | T | A | 44 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(41): Show |
44 | HG00558.hp1 HG00733.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.1585-1367T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17630954 | |||||||
chr1:17630960 | C | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1585-1361C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17630960 | |||||||
chr1:17631063 | G | T | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1585-1258G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17631063 | |||||||
chr1:17631141 | A | G | 9 | a0001c0033t0002g0110 a0002c0034t0002g0149 a0004c0005t0002g0006 others(6): Show |
9 | HG02109.hp1 HG02559.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1585-1180A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17631141 | |||||||
chr1:17631192 | A | G | 9 | a0001c0033t0002g0110 a0002c0034t0002g0149 a0004c0005t0002g0006 others(6): Show |
9 | HG02109.hp1 HG02559.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1585-1129A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17631192 | |||||||
chr1:17631543 | C | T | 2 | a0001c0001t0003g0090 a0001c0001t0003g0092 |
2 | HG01069.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1585-778C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17631543 | |||||||
chr1:17631637 | C | T | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1585-684C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17631637 | |||||||
chr1:17631673 | C | A | 1 | a0009c0039t0001g0039 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1585-648C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17631673 | |||||||
chr1:17631673 | C | T | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1585-648C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17631673 | |||||||
chr1:17631745 | T | C | 69 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(66): Show |
69 | HG00558.hp1 HG00642.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.1585-576T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17631745 | |||||||
chr1:17631828 | G | A | 1 | a0002c0003t0002g0089 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1585-493G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17631828 | |||||||
chr1:17632003 | C | A | 1 | a0001c0001t0001g0096 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1585-318C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17632003 | |||||||
chr1:17632061 | G | A | 2 | a0001c0001t0003g0114 a0001c0001t0003g0151 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1585-260G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17632061 | |||||||
chr1:17632283 | C | T | 1 | a0001c0001t0003g0168 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1585-38C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 15/28 | chr1 | 17632283 | |||||||
chr1:17632549 | A | T | 14 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(11): Show |
14 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.1730+83A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 16/28 | chr1 | 17632549 | |||||||
chr1:17632607 | T | A | 1 | a0003c0002t0001g0074 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1730+141T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 16/28 | chr1 | 17632607 | |||||||
chr1:17632681 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1730+215C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 16/28 | chr1 | 17632681 | |||||||
chr1:17632698 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1730+232A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 16/28 | chr1 | 17632698 | |||||||
chr1:17632885 | G | A | 9 | a0001c0033t0002g0110 a0002c0034t0002g0149 a0004c0005t0002g0006 others(6): Show |
9 | HG02109.hp1 HG02559.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1730+419G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 16/28 | chr1 | 17632885 | |||||||
chr1:17632898 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1730+432C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 16/28 | chr1 | 17632898 | |||||||
chr1:17632958 | C | T | 8 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(5): Show |
8 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1730+492C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 16/28 | chr1 | 17632958 | |||||||
chr1:17633039 | C | T | 2 | a0001c0001t0001g0096 a0001c0011t0001g0004 |
2 | HG02071.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1730+573C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 16/28 | chr1 | 17633039 | |||||||
chr1:17633132 | G | T | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1730+666G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 16/28 | chr1 | 17633132 | |||||||
chr1:17633178 | C | T | 2 | a0001c0001t0003g0114 a0001c0001t0003g0151 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1730+712C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 16/28 | chr1 | 17633178 | |||||||
chr1:17633541 | G | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1731-1007G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 16/28 | chr1 | 17633541 | |||||||
chr1:17633632 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1731-916G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 16/28 | chr1 | 17633632 | |||||||
chr1:17633641 | C | T | 7 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1731-907C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 16/28 | chr1 | 17633641 | |||||||
chr1:17633939 | G | A | 14 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(11): Show |
14 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.1731-609G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 16/28 | chr1 | 17633939 | |||||||
chr1:17634317 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(162): Show |
165 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.1731-231T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 16/28 | chr1 | 17634317 | |||||||
chr1:17634543 | C | G | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | splice_region_variant&intron_variant | LOW | c.1731-5C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 16/28 | chr1 | 17634543 | |||||||
chr1:17634620 | C | T | 17 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1745+58C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 17/28 | chr1 | 17634620 | |||||||
chr1:17634642 | C | T | 2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1745+80C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 17/28 | chr1 | 17634642 | |||||||
chr1:17635222 | A | G | 17 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1927+206A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | chr1 | 17635222 | |||||||
chr1:17635343 | C | T | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1927+327C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | chr1 | 17635343 | |||||||
chr1:17635439 | A | C | 17 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1927+423A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | chr1 | 17635439 | |||||||
chr1:17635519 | T | C | 72 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(69): Show |
72 | HG00558.hp1 HG00642.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.1927+503T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | chr1 | 17635519 | |||||||
chr1:17635534 | C | T | 16 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(13): Show |
16 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1927+518C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | chr1 | 17635534 | |||||||
chr1:17635615 | C | G | 1 | a0012c0031t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1927+599C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | chr1 | 17635615 | |||||||
chr1:17636087 | G | A | 2 | a0001c0001t0001g0003 a0003c0002t0001g0106 |
2 | HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1927+1071G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | chr1 | 17636087 | |||||||
chr1:17636335 | C | T | 1 | a0001c0001t0003g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1927+1319C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | chr1 | 17636335 | |||||||
chr1:17636454 | C | G | 1 | a0017c0037t0001g0142 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1928-1434C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | chr1 | 17636454 | |||||||
chr1:17636501 | T | C | 72 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(69): Show |
72 | HG00558.hp1 HG00642.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.1928-1387T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | chr1 | 17636501 | |||||||
chr1:17636520 | T | G | 17 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1928-1368T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | chr1 | 17636520 | |||||||
chr1:17636521 | C | T | 25 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0140 others(22): Show |
25 | HG00558.hp1 HG00733.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.1928-1367C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | chr1 | 17636521 | |||||||
chr1:17636752 | A | C | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1928-1136A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | chr1 | 17636752 | |||||||
chr1:17636824 | T | G | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1928-1064T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | chr1 | 17636824 | |||||||
chr1:17637019 | C | A | 1 | a0001c0001t0001g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1928-869C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | chr1 | 17637019 | |||||||
chr1:17637396 | A | G | 17 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1928-492A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | chr1 | 17637396 | |||||||
chr1:17637425 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0034 a0001c0001t0001g0048 |
3 | HG01496.hp2 HG01934.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.1928-463C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | chr1 | 17637425 | |||||||
chr1:17637506 | C | CT | 68 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(65): Show |
68 | HG00558.hp1 HG00642.hp1 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.1928-372dupT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr1 | 17637506 | ||||||
chr1:17637516 | T | TG | 3 | a0001c0001t0003g0114 a0001c0001t0003g0151 a0002c0041t0008g0054 |
3 | HG02896.hp1 HG02897.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1928-369dupG | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr1 | 17637516 | ||||||
chr1:17637559 | C | T | 2 | a0001c0001t0003g0114 a0001c0001t0003g0151 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1928-329C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | chr1 | 17637559 | |||||||
chr1:17637567 | C | T | 4 | a0001c0001t0001g0070 a0001c0013t0001g0008 a0001c0013t0001g0017 others(1): Show |
4 | HG00738.hp1 HG01123.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1928-321C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | chr1 | 17637567 | |||||||
chr1:17637667 | T | A | 17 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1928-221T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | chr1 | 17637667 | |||||||
chr1:17637793 | C | T | 28 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0140 others(25): Show |
28 | HG00558.hp1 HG00733.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.1928-95C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 18/28 | chr1 | 17637793 | |||||||
chr1:17638025 | T | C | 17 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2043+22T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 19/28 | chr1 | 17638025 | |||||||
chr1:17638103 | G | A | 17 | a0001c0006t0001g0001 a0001c0006t0001g0129 a0001c0006t0001g0130 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2043+100G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 19/28 | chr1 | 17638103 | |||||||
chr1:17638122 | C | T | 33 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(30): Show |
33 | HG00558.hp1 HG00733.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.2043+119C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 19/28 | chr1 | 17638122 | |||||||
chr1:17638192 | C | T | 1 | a0003c0002t0001g0074 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2043+189C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 19/28 | chr1 | 17638192 | |||||||
chr1:17638222 | T | G | 1 | a0001c0001t0001g0062 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2043+219T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 19/28 | chr1 | 17638222 | |||||||
chr1:17638307 | G | A | 21 | a0001c0001t0001g0125 a0001c0001t0003g0080 a0001c0001t0003g0090 others(18): Show |
21 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.2044-255G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 19/28 | chr1 | 17638307 | |||||||
chr1:17638341 | C | G | 9 | a0001c0033t0002g0110 a0002c0034t0002g0149 a0004c0005t0002g0006 others(6): Show |
9 | HG02109.hp1 HG02559.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2044-221C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 19/28 | chr1 | 17638341 | |||||||
chr1:17638699 | G | A | 23 | a0001c0001t0001g0096 a0001c0001t0001g0125 a0001c0001t0003g0080 others(20): Show |
23 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.2171+10G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 20/28 | chr1 | 17638699 | |||||||
chr1:17638796 | A | G | 5 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0105 others(2): Show |
5 | HG00642.hp1 HG02280.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2171+107A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 20/28 | chr1 | 17638796 | |||||||
chr1:17638939 | T | G | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2171+250T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 20/28 | chr1 | 17638939 | |||||||
chr1:17638961 | A | G | 7 | a0001c0001t0001g0012 a0002c0003t0002g0037 a0002c0003t0002g0133 others(4): Show |
7 | HG00558.hp1 HG02080.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.2171+272A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 20/28 | chr1 | 17638961 | |||||||
chr1:17639135 | C | A | 13 | a0001c0001t0001g0125 a0001c0001t0003g0080 a0001c0001t0003g0090 others(10): Show |
13 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.2171+446C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 20/28 | chr1 | 17639135 | |||||||
chr1:17639246 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2171+557G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 20/28 | chr1 | 17639246 | |||||||
chr1:17639263 | C | T | 9 | a0001c0033t0002g0110 a0002c0034t0002g0149 a0004c0005t0002g0006 others(6): Show |
9 | HG02109.hp1 HG02559.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2171+574C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 20/28 | chr1 | 17639263 | |||||||
chr1:17639366 | T | C | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2171+677T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 20/28 | chr1 | 17639366 | |||||||
chr1:17639532 | T | C | 1 | a0004c0005t0002g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2172-670T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 20/28 | chr1 | 17639532 | |||||||
chr1:17639565 | C | T | 7 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(4): Show |
7 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.2172-637C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 20/28 | chr1 | 17639565 | |||||||
chr1:17639586 | C | T | 1 | a0001c0019t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2172-616C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 20/28 | chr1 | 17639586 | |||||||
chr1:17639587 | G | A | 5 | a0001c0001t0001g0119 a0001c0001t0001g0164 a0002c0004t0002g0120 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2172-615G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 20/28 | chr1 | 17639587 | |||||||
chr1:17640009 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2172-193C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 20/28 | chr1 | 17640009 | |||||||
chr1:17640010 | G | A | 1 | a0001c0012t0001g0102 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2172-192G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 20/28 | chr1 | 17640010 | |||||||
chr1:17640351 | G | A | 2 | a0001c0012t0001g0064 a0001c0012t0001g0072 |
2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.2272+49G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17640351 | |||||||
chr1:17640549 | C | T | 1 | a0001c0019t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2272+247C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17640549 | |||||||
chr1:17640564 | T | C | 2 | a0012c0031t0006g0165 a0021c0030t0002g0109 |
2 | HG01884.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2272+262T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17640564 | |||||||
chr1:17640591 | A | G | 22 | a0001c0001t0001g0125 a0001c0001t0003g0080 a0001c0001t0003g0090 others(19): Show |
22 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2272+289A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17640591 | |||||||
chr1:17640631 | GAGGTGAT others(10): Show |
G | 1 | a0001c0001t0001g0099 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2272+330_2272+346d others(19): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17640631 | |||||||
chr1:17640818 | G | C | 1 | a0001c0001t0001g0012 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2272+516G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17640818 | |||||||
chr1:17641099 | T | G | 1 | a0012c0031t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2272+797T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17641099 | |||||||
chr1:17641269 | A | G | 1 | a0002c0003t0002g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2272+967A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17641269 | |||||||
chr1:17641736 | T | C | 1 | a0001c0001t0001g0028 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2272+1434T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17641736 | |||||||
chr1:17641800 | G | A | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2272+1498G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17641800 | |||||||
chr1:17641874 | G | C | 1 | a0001c0001t0001g0040 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2272+1572G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17641874 | |||||||
chr1:17641912 | C | T | 1 | a0008c0016t0002g0132 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2272+1610C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17641912 | |||||||
chr1:17641976 | G | A | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2272+1674G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17641976 | |||||||
chr1:17642046 | G | T | 66 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0096 others(63): Show |
66 | HG00558.hp1 HG00642.hp1 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.2272+1744G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17642046 | |||||||
chr1:17642146 | G | T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0163 |
2 | HG01106.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2272+1844G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17642146 | |||||||
chr1:17642165 | A | G | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2272+1863A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17642165 | |||||||
chr1:17642190 | G | A | 1 | a0005c0023t0002g0101 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2272+1888G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17642190 | |||||||
chr1:17642426 | C | T | 1 | a0002c0003t0002g0037 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2272+2124C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17642426 | |||||||
chr1:17642427 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2272+2125G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17642427 | |||||||
chr1:17642479 | G | A | 2 | a0001c0006t0001g0129 a0001c0006t0001g0130 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2272+2177G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17642479 | |||||||
chr1:17642493 | C | T | 38 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0096 others(35): Show |
38 | HG00558.hp1 HG00733.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.2272+2191C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17642493 | |||||||
chr1:17642799 | C | T | 1 | a0001c0019t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2272+2497C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17642799 | |||||||
chr1:17642813 | G | A | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2272+2511G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17642813 | |||||||
chr1:17642858 | C | T | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2272+2556C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17642858 | |||||||
chr1:17643039 | T | G | 2 | a0001c0001t0003g0090 a0001c0001t0003g0092 |
2 | HG01069.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.2272+2737T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17643039 | |||||||
chr1:17643083 | G | T | 26 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0140 others(23): Show |
26 | HG00558.hp1 HG00733.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.2272+2781G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17643083 | |||||||
chr1:17643170 | T | C | 8 | a0001c0033t0002g0110 a0002c0034t0002g0149 a0004c0005t0002g0006 others(5): Show |
8 | HG02559.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2272+2868T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17643170 | |||||||
chr1:17643224 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.2272+2922G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17643224 | |||||||
chr1:17643294 | T | G | 8 | a0001c0033t0002g0110 a0002c0034t0002g0149 a0004c0005t0002g0006 others(5): Show |
8 | HG02559.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2272+2992T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17643294 | |||||||
chr1:17643338 | C | G | 14 | a0001c0001t0001g0125 a0001c0001t0003g0080 a0001c0001t0003g0090 others(11): Show |
14 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.2272+3036C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17643338 | |||||||
chr1:17643390 | T | C | 7 | a0001c0048t0001g0005 a0002c0008t0002g0042 a0002c0008t0002g0100 others(4): Show |
7 | HG00733.hp1 HG01433.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.2272+3088T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17643390 | |||||||
chr1:17643426 | C | T | 5 | a0001c0001t0001g0125 a0001c0001t0003g0080 a0001c0001t0003g0090 others(2): Show |
5 | HG01069.hp2 HG01169.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.2272+3124C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17643426 | |||||||
chr1:17643429 | C | T | 2 | a0001c0001t0001g0071 a0002c0003t0002g0025 |
2 | NA18747.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.2272+3127C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17643429 | |||||||
chr1:17643573 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2272+3271T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17643573 | |||||||
chr1:17643859 | T | A | 1 | a0001c0038t0003g0124 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2272+3557T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17643859 | |||||||
chr1:17643898 | A | C | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2272+3596A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17643898 | |||||||
chr1:17644004 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2272+3702G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17644004 | |||||||
chr1:17644186 | C | T | 8 | a0001c0033t0002g0110 a0002c0034t0002g0149 a0004c0005t0002g0006 others(5): Show |
8 | HG02559.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2272+3884C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17644186 | |||||||
chr1:17644255 | C | T | 1 | a0001c0044t0004g0161 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2272+3953C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17644255 | |||||||
chr1:17644261 | T | C | 27 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0098 others(24): Show |
27 | HG00558.hp1 HG00733.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.2272+3959T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17644261 | |||||||
chr1:17644328 | C | G | 1 | a0001c0001t0003g0090 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2272+4026C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17644328 | |||||||
chr1:17644527 | C | T | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2273-4027C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17644527 | |||||||
chr1:17644634 | G | A | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2273-3920G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17644634 | |||||||
chr1:17644824 | G | A | 8 | a0001c0033t0002g0110 a0002c0034t0002g0149 a0004c0005t0002g0006 others(5): Show |
8 | HG02559.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2273-3730G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17644824 | |||||||
chr1:17644836 | C | T | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2273-3718C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17644836 | |||||||
chr1:17644837 | G | C | 3 | a0001c0011t0001g0138 a0001c0011t0001g0152 a0001c0042t0001g0035 |
3 | HG00741.hp1 HG01257.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.2273-3717G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17644837 | |||||||
chr1:17644964 | G | A | 1 | a0001c0033t0002g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2273-3590G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17644964 | |||||||
chr1:17645254 | C | T | 8 | a0001c0033t0002g0110 a0002c0034t0002g0149 a0004c0005t0002g0006 others(5): Show |
8 | HG02559.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2273-3300C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17645254 | |||||||
chr1:17645307 | A | G | 1 | a0001c0001t0001g0028 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2273-3247A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17645307 | |||||||
chr1:17645324 | C | T | 4 | a0001c0001t0001g0096 a0001c0011t0001g0004 a0001c0020t0001g0016 others(1): Show |
4 | HG01109.hp1 HG02071.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2273-3230C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17645324 | |||||||
chr1:17645715 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2273-2839G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17645715 | |||||||
chr1:17645730 | G | A | 1 | a0001c0001t0003g0080 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2273-2824G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17645730 | |||||||
chr1:17645826 | A | G | 11 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0028 others(8): Show |
11 | HG00544.hp1 HG00544.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.2273-2728A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17645826 | |||||||
chr1:17645900 | G | A | 1 | a0019c0026t0001g0026 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2273-2654G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17645900 | |||||||
chr1:17646073 | C | T | 1 | a0002c0003t0002g0141 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2273-2481C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17646073 | |||||||
chr1:17646120 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2273-2434C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17646120 | |||||||
chr1:17646229 | A | C | 1 | a0001c0013t0001g0008 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2273-2325A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17646229 | |||||||
chr1:17646368 | C | T | 2 | a0002c0003t0002g0141 a0008c0027t0002g0029 |
2 | NA18954.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.2273-2186C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17646368 | |||||||
chr1:17646549 | C | T | 22 | a0001c0001t0001g0125 a0001c0001t0003g0080 a0001c0001t0003g0090 others(19): Show |
22 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2273-2005C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17646549 | |||||||
chr1:17646577 | C | T | 15 | a0001c0001t0001g0125 a0001c0001t0003g0080 a0001c0001t0003g0090 others(12): Show |
15 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.2273-1977C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17646577 | |||||||
chr1:17646588 | G | A | 2 | a0002c0007t0002g0058 a0002c0007t0002g0085 |
2 | HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2273-1966G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17646588 | |||||||
chr1:17646684 | G | A | 26 | a0001c0001t0001g0012 a0001c0001t0001g0093 a0001c0001t0001g0140 others(23): Show |
26 | HG00558.hp1 HG00733.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.2273-1870G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17646684 | |||||||
chr1:17646770 | G | C | 15 | a0001c0001t0001g0125 a0001c0001t0003g0080 a0001c0001t0003g0090 others(12): Show |
15 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.2273-1784G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17646770 | |||||||
chr1:17646782 | G | A | 1 | a0006c0009t0001g0107 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2273-1772G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17646782 | |||||||
chr1:17646798 | G | A | 14 | a0001c0001t0001g0096 a0001c0001t0001g0164 a0001c0011t0001g0004 others(11): Show |
14 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2273-1756G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17646798 | |||||||
chr1:17646846 | C | T | 1 | a0001c0019t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2273-1708C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17646846 | |||||||
chr1:17646988 | T | C | 1 | a0001c0012t0001g0102 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2273-1566T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17646988 | |||||||
chr1:17646995 | C | T | 1 | a0005c0023t0002g0101 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2273-1559C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17646995 | |||||||
chr1:17647084 | C | A | 1 | a0001c0001t0001g0159 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2273-1470C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17647084 | |||||||
chr1:17647087 | C | T | 1 | a0001c0042t0001g0035 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2273-1467C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17647087 | |||||||
chr1:17647120 | C | T | 10 | a0001c0001t0001g0164 a0001c0017t0002g0113 a0001c0017t0002g0148 others(7): Show |
10 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.2273-1434C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17647120 | |||||||
chr1:17647158 | C | T | 13 | a0001c0001t0001g0125 a0001c0001t0003g0080 a0001c0001t0003g0090 others(10): Show |
13 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.2273-1396C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17647158 | |||||||
chr1:17647266 | T | C | 5 | a0001c0001t0001g0164 a0002c0004t0002g0120 a0002c0004t0002g0121 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.2273-1288T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17647266 | |||||||
chr1:17647383 | T | A | 1 | a0007c0010t0001g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2273-1171T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17647383 | |||||||
chr1:17647419 | C | T | 9 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0028 others(6): Show |
9 | HG00544.hp2 HG02683.hp1 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.2273-1135C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17647419 | |||||||
chr1:17647461 | G | C | 8 | a0001c0033t0002g0110 a0002c0034t0002g0149 a0004c0005t0002g0006 others(5): Show |
8 | HG02559.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2273-1093G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17647461 | |||||||
chr1:17647772 | G | T | 1 | a0019c0026t0001g0026 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2273-782G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17647772 | |||||||
chr1:17647850 | C | T | 2 | a0002c0003t0002g0141 a0008c0027t0002g0029 |
2 | NA18954.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.2273-704C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17647850 | |||||||
chr1:17647967 | G | T | 1 | a0006c0009t0001g0166 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2273-587G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17647967 | |||||||
chr1:17648249 | G | A | 5 | a0001c0019t0001g0066 a0001c0020t0001g0016 a0001c0020t0001g0052 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2273-305G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17648249 | |||||||
chr1:17648250 | C | A | 5 | a0001c0019t0001g0066 a0001c0020t0001g0016 a0001c0020t0001g0052 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2273-304C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17648250 | |||||||
chr1:17648294 | G | A | 8 | a0001c0033t0002g0110 a0002c0034t0002g0149 a0004c0005t0002g0006 others(5): Show |
8 | HG02559.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2273-260G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17648294 | |||||||
chr1:17648376 | C | T | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2273-178C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17648376 | |||||||
chr1:17648411 | C | T | 2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2273-143C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17648411 | |||||||
chr1:17648412 | G | A | 1 | a0018c0028t0003g0044 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2273-142G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17648412 | |||||||
chr1:17648412 | G | T | 1 | a0003c0002t0001g0106 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2273-142G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 21/28 | chr1 | 17648412 | |||||||
chr1:17648720 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2394+45G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17648720 | |||||||
chr1:17648864 | A | G | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2394+189A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17648864 | |||||||
chr1:17649041 | G | A | 1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2394+366G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17649041 | |||||||
chr1:17649089 | G | A | 1 | a0002c0004t0002g0036 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2394+414G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17649089 | |||||||
chr1:17649319 | G | A | 1 | a0001c0012t0001g0064 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2394+644G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17649319 | |||||||
chr1:17649350 | C | T | 8 | a0001c0033t0002g0110 a0002c0034t0002g0149 a0004c0005t0002g0006 others(5): Show |
8 | HG02559.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2394+675C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17649350 | |||||||
chr1:17649971 | C | T | 3 | a0001c0013t0001g0008 a0001c0013t0001g0023 a0003c0002t0001g0081 |
3 | HG00738.hp1 HG01074.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.2394+1296C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17649971 | |||||||
chr1:17649995 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2394+1320T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17649995 | |||||||
chr1:17650065 | C | T | 62 | a0001c0001t0001g0125 a0001c0001t0001g0154 a0001c0001t0003g0080 others(59): Show |
62 | HG00544.hp2 HG00733.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.2394+1390C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17650065 | |||||||
chr1:17650187 | G | T | 14 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0033 others(11): Show |
14 | HG01070.hp2 HG01123.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.2394+1512G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17650187 | |||||||
chr1:17650324 | G | T | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2394+1649G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17650324 | |||||||
chr1:17650329 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2394+1654G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17650329 | |||||||
chr1:17650405 | C | A | 1 | a0001c0001t0001g0014 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2394+1730C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17650405 | |||||||
chr1:17650481 | C | T | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2394+1806C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17650481 | |||||||
chr1:17650712 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2394+2037G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17650712 | |||||||
chr1:17650713 | A | G | 8 | a0001c0033t0002g0110 a0002c0034t0002g0149 a0004c0005t0002g0006 others(5): Show |
8 | HG02559.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2394+2038A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17650713 | |||||||
chr1:17650732 | C | CA | 24 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0040 others(21): Show |
24 | HG01081.hp2 HG01109.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.2394+2080dupA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr1 | 17650732 | ||||||
chr1:17650732 | CA | C | 15 | a0001c0006t0001g0129 a0001c0013t0001g0008 a0001c0013t0001g0023 others(12): Show |
15 | HG00738.hp1 HG01069.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.2394+2080delA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | INFO_REALIGN_3_PRIME | chr1 | 17650732 | ||||||
chr1:17650883 | C | T | 45 | a0001c0001t0001g0125 a0001c0001t0001g0154 a0001c0001t0003g0114 others(42): Show |
45 | HG00544.hp2 HG00733.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.2394+2208C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17650883 | |||||||
chr1:17651002 | G | A | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2394+2327G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17651002 | |||||||
chr1:17651145 | C | A | 4 | a0002c0004t0002g0120 a0002c0004t0002g0121 a0002c0018t0002g0155 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.2394+2470C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17651145 | |||||||
chr1:17651147 | A | C | 25 | a0002c0003t0002g0025 a0002c0003t0002g0037 a0002c0003t0002g0055 others(22): Show |
25 | HG00544.hp2 HG00733.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.2394+2472A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17651147 | |||||||
chr1:17651182 | C | G | 1 | a0001c0001t0001g0024 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2394+2507C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17651182 | |||||||
chr1:17651329 | G | T | 1 | a0003c0002t0001g0038 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2394+2654G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17651329 | |||||||
chr1:17651405 | G | A | 4 | a0002c0004t0002g0120 a0002c0004t0002g0121 a0002c0018t0002g0155 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.2394+2730G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17651405 | |||||||
chr1:17651439 | A | G | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2394+2764A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17651439 | |||||||
chr1:17651674 | C | A | 1 | a0001c0001t0001g0014 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2395-2962C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17651674 | |||||||
chr1:17651691 | G | C | 25 | a0002c0003t0002g0025 a0002c0003t0002g0037 a0002c0003t0002g0055 others(22): Show |
25 | HG00544.hp2 HG00733.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.2395-2945G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17651691 | |||||||
chr1:17651714 | C | T | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2395-2922C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17651714 | |||||||
chr1:17651994 | A | G | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2395-2642A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17651994 | |||||||
chr1:17652097 | G | A | 8 | a0001c0033t0002g0110 a0002c0034t0002g0149 a0004c0005t0002g0006 others(5): Show |
8 | HG02559.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.2395-2539G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17652097 | |||||||
chr1:17652149 | G | C | 25 | a0002c0003t0002g0025 a0002c0003t0002g0037 a0002c0003t0002g0055 others(22): Show |
25 | HG00544.hp2 HG00733.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.2395-2487G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17652149 | |||||||
chr1:17652623 | A | G | 74 | a0001c0001t0001g0022 a0001c0001t0001g0034 a0001c0001t0001g0043 others(71): Show |
74 | HG00544.hp2 HG00733.hp1 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.2395-2013A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17652623 | |||||||
chr1:17652716 | C | T | 4 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(1): Show |
4 | HG00741.hp1 HG01257.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.2395-1920C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17652716 | |||||||
chr1:17653176 | T | C | 1 | a0002c0004t0002g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2395-1460T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17653176 | |||||||
chr1:17653180 | T | C | 24 | a0002c0003t0002g0025 a0002c0003t0002g0037 a0002c0003t0002g0055 others(21): Show |
24 | HG00544.hp2 HG00733.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.2395-1456T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17653180 | |||||||
chr1:17653229 | G | A | 1 | a0002c0004t0002g0118 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2395-1407G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17653229 | |||||||
chr1:17653394 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2395-1242C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17653394 | |||||||
chr1:17653522 | G | A | 1 | a0017c0037t0001g0142 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2395-1114G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17653522 | |||||||
chr1:17653650 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2395-986T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17653650 | |||||||
chr1:17653683 | A | C | 5 | a0001c0019t0001g0066 a0001c0020t0001g0016 a0001c0020t0001g0052 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2395-953A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17653683 | |||||||
chr1:17653859 | C | T | 5 | a0001c0019t0001g0066 a0001c0020t0001g0016 a0001c0020t0001g0052 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2395-777C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17653859 | |||||||
chr1:17653873 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2395-763G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17653873 | |||||||
chr1:17653938 | T | C | 69 | a0001c0001t0001g0125 a0001c0001t0001g0154 a0001c0001t0003g0080 others(66): Show |
69 | HG00544.hp2 HG00733.hp1 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.2395-698T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17653938 | |||||||
chr1:17654035 | C | T | 24 | a0002c0003t0002g0025 a0002c0003t0002g0037 a0002c0003t0002g0055 others(21): Show |
24 | HG00544.hp2 HG00733.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.2395-601C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17654035 | |||||||
chr1:17654235 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2395-401C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17654235 | |||||||
chr1:17654251 | C | T | 1 | a0001c0012t0001g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2395-385C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17654251 | |||||||
chr1:17654461 | G | A | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2395-175G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 22/28 | chr1 | 17654461 | |||||||
chr1:17654793 | G | A | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2481+71G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 23/28 | chr1 | 17654793 | |||||||
chr1:17654936 | A | T | 18 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0019t0001g0066 others(15): Show |
18 | HG01109.hp1 HG01884.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.2481+214A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 23/28 | chr1 | 17654936 | |||||||
chr1:17655214 | C | G | 1 | a0002c0003t0002g0141 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2481+492C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 23/28 | chr1 | 17655214 | |||||||
chr1:17655259 | C | T | 1 | a0002c0003t0002g0141 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2481+537C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 23/28 | chr1 | 17655259 | |||||||
chr1:17655418 | A | G | 27 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(24): Show |
27 | HG00544.hp2 HG00733.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.2482-461A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 23/28 | chr1 | 17655418 | |||||||
chr1:17655437 | G | GTCCA | 4 | a0001c0001t0001g0012 a0001c0001t0001g0071 a0001c0001t0001g0159 others(1): Show |
4 | HG00558.hp1 HG06807.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.2482-403_2482-400d others(6): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr1 | 17655437 | ||||||
chr1:17655437 | GTCCA | G | 78 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(75): Show |
78 | HG00558.hp2 HG01069.hp1 HG01069.hp2 others(75): Show |
intron_variant | MODIFIER | c.2482-403_2482-400d others(6): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr1 | 17655437 | ||||||
chr1:17655437 | GTCCATCC others(1): Show |
G | 4 | a0002c0004t0002g0120 a0002c0004t0002g0121 a0002c0018t0002g0155 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.2482-407_2482-400d others(10): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr1 | 17655437 | ||||||
chr1:17655464 | CATCCATC others(9): Show |
C | 23 | a0002c0003t0002g0025 a0002c0003t0002g0037 a0002c0003t0002g0055 others(20): Show |
23 | HG00544.hp2 HG00733.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.2482-399_2482-384d others(18): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr1 | 17655464 | ||||||
chr1:17655468 | CATCCATC others(5): Show |
C | 4 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(1): Show |
4 | HG00741.hp1 HG01257.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.2482-399_2482-388d others(14): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr1 | 17655468 | ||||||
chr1:17655484 | C | T | 27 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(24): Show |
27 | HG00544.hp2 HG00733.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.2482-395C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 23/28 | chr1 | 17655484 | |||||||
chr1:17655616 | T | C | 4 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(1): Show |
4 | HG00741.hp1 HG01257.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.2482-263T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 23/28 | chr1 | 17655616 | |||||||
chr1:17655760 | G | T | 1 | a0002c0004t0002g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2482-119G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 23/28 | chr1 | 17655760 | |||||||
chr1:17655821 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2482-58C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 23/28 | chr1 | 17655821 | |||||||
chr1:17655829 | C | T | 2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2482-50C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 23/28 | chr1 | 17655829 | |||||||
chr1:17656312 | A | G | 9 | a0001c0020t0001g0016 a0001c0020t0001g0052 a0002c0034t0002g0149 others(6): Show |
9 | HG01109.hp1 HG02717.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.2705+210A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 24/28 | chr1 | 17656312 | |||||||
chr1:17656457 | C | A | 1 | a0001c0001t0003g0080 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2706-97C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 24/28 | chr1 | 17656457 | |||||||
chr1:17656781 | G | C | 1 | a0008c0016t0002g0082 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2860+73G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17656781 | |||||||
chr1:17656962 | G | T | 5 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 others(2): Show |
5 | HG02622.hp2 HG02630.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2860+254G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17656962 | |||||||
chr1:17657112 | T | C | 2 | a0002c0004t0002g0118 a0002c0004t0002g0146 |
2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2860+404T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17657112 | |||||||
chr1:17657185 | G | C | 25 | a0001c0019t0001g0095 a0002c0003t0002g0025 a0002c0003t0002g0037 others(22): Show |
25 | HG00544.hp2 HG00733.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.2860+477G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17657185 | |||||||
chr1:17657269 | A | C | 2 | a0001c0001t0001g0088 a0001c0045t0001g0031 |
2 | HG00741.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.2860+561A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17657269 | |||||||
chr1:17657294 | G | A | 51 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(48): Show |
51 | HG00544.hp2 HG00733.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.2860+586G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17657294 | |||||||
chr1:17657462 | T | A | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2860+754T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17657462 | |||||||
chr1:17657490 | G | A | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2860+782G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17657490 | |||||||
chr1:17657612 | A | T | 2 | a0002c0004t0002g0118 a0002c0004t0002g0146 |
2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2860+904A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17657612 | |||||||
chr1:17657818 | C | T | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2860+1110C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17657818 | |||||||
chr1:17657973 | A | T | 22 | a0002c0003t0002g0025 a0002c0003t0002g0037 a0002c0003t0002g0055 others(19): Show |
22 | HG00544.hp2 HG00733.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.2860+1265A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17657973 | |||||||
chr1:17658018 | T | G | 1 | a0001c0001t0001g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2860+1310T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17658018 | |||||||
chr1:17658030 | T | C | 1 | a0010c0046t0001g0020 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2860+1322T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17658030 | |||||||
chr1:17658034 | C | T | 1 | a0001c0020t0001g0016 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2860+1326C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17658034 | |||||||
chr1:17658261 | G | C | 2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2860+1553G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17658261 | |||||||
chr1:17658313 | C | T | 1 | a0002c0036t0002g0160 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2860+1605C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17658313 | |||||||
chr1:17658364 | C | G | 23 | a0002c0003t0002g0025 a0002c0003t0002g0037 a0002c0003t0002g0055 others(20): Show |
23 | HG00544.hp2 HG00733.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.2860+1656C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17658364 | |||||||
chr1:17658556 | A | C | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2860+1848A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17658556 | |||||||
chr1:17658614 | T | C | 22 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0019t0001g0095 others(19): Show |
22 | HG01109.hp1 HG01884.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.2860+1906T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17658614 | |||||||
chr1:17658778 | A | G | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2860+2070A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17658778 | |||||||
chr1:17658782 | GA | G | 7 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(4): Show |
7 | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2860+2077delA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr1 | 17658782 | ||||||
chr1:17658813 | A | G | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2860+2105A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17658813 | |||||||
chr1:17659094 | G | A | 7 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(4): Show |
7 | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2860+2386G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17659094 | |||||||
chr1:17659129 | T | C | 22 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0019t0001g0095 others(19): Show |
22 | HG01109.hp1 HG01884.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.2860+2421T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17659129 | |||||||
chr1:17659382 | T | C | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2860+2674T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17659382 | |||||||
chr1:17659404 | C | G | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2860+2696C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17659404 | |||||||
chr1:17659452 | C | A | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2860+2744C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17659452 | |||||||
chr1:17659453 | C | T | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2860+2745C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17659453 | |||||||
chr1:17659551 | C | T | 23 | a0002c0003t0002g0025 a0002c0003t0002g0037 a0002c0003t0002g0055 others(20): Show |
23 | HG00544.hp2 HG00733.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.2860+2843C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17659551 | |||||||
chr1:17659738 | G | A | 6 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0033t0002g0110 others(3): Show |
6 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2860+3030G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17659738 | |||||||
chr1:17659989 | G | A | 7 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(4): Show |
7 | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.2860+3281G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17659989 | |||||||
chr1:17660116 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2860+3408C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17660116 | |||||||
chr1:17660162 | G | T | 4 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(1): Show |
4 | HG00741.hp1 HG01257.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.2860+3454G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17660162 | |||||||
chr1:17660193 | C | T | 1 | a0002c0004t0002g0036 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2860+3485C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17660193 | |||||||
chr1:17660386 | C | T | 1 | a0010c0046t0001g0020 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2860+3678C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17660386 | |||||||
chr1:17660395 | G | A | 5 | a0001c0019t0001g0095 a0002c0004t0002g0118 a0002c0004t0002g0146 others(2): Show |
5 | HG02109.hp2 HG02486.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.2860+3687G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17660395 | |||||||
chr1:17660461 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2860+3753C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17660461 | |||||||
chr1:17660538 | G | C | 1 | a0001c0001t0001g0040 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2860+3830G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17660538 | |||||||
chr1:17660730 | C | T | 1 | a0002c0004t0002g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2861-3717C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17660730 | |||||||
chr1:17660779 | A | G | 23 | a0002c0003t0002g0025 a0002c0003t0002g0037 a0002c0003t0002g0055 others(20): Show |
23 | HG00544.hp2 HG00733.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.2861-3668A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17660779 | |||||||
chr1:17660941 | C | T | 1 | a0002c0004t0002g0036 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2861-3506C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17660941 | |||||||
chr1:17661031 | C | A | 1 | a0001c0001t0001g0021 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2861-3416C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17661031 | |||||||
chr1:17661171 | G | A | 1 | a0001c0001t0003g0143 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2861-3276G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17661171 | |||||||
chr1:17661223 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2861-3224G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17661223 | |||||||
chr1:17661322 | G | T | 1 | a0001c0001t0003g0080 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2861-3125G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17661322 | |||||||
chr1:17661711 | T | C | 1 | a0001c0011t0001g0004 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2861-2736T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17661711 | |||||||
chr1:17661885 | C | CAGAAACC others(317): Show |
1 | a0017c0037t0001g0142 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2861-2547_2861-254 others(328): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr1 | 17661885 | ||||||
chr1:17661893 | TGA | T | 2 | a0002c0004t0002g0120 a0002c0004t0002g0121 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2861-2550_2861-254 others(6): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr1 | 17661893 | ||||||
chr1:17661939 | C | T | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2861-2508C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17661939 | |||||||
chr1:17661945 | C | T | 1 | a0001c0001t0003g0080 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2861-2502C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17661945 | |||||||
chr1:17662045 | C | T | 1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2861-2402C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17662045 | |||||||
chr1:17662099 | C | T | 1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2861-2348C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17662099 | |||||||
chr1:17662150 | G | A | 8 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0020t0001g0016 others(5): Show |
8 | HG01109.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2861-2297G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17662150 | |||||||
chr1:17662207 | G | T | 8 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0020t0001g0016 others(5): Show |
8 | HG01109.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2861-2240G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17662207 | |||||||
chr1:17662216 | G | C | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2861-2231G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17662216 | |||||||
chr1:17662271 | C | T | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2861-2176C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17662271 | |||||||
chr1:17662311 | A | T | 1 | a0002c0004t0002g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2861-2136A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17662311 | |||||||
chr1:17662316 | T | C | 2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2861-2131T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17662316 | |||||||
chr1:17662327 | T | C | 8 | a0001c0001t0001g0164 a0001c0006t0007g0150 a0002c0004t0002g0118 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2861-2120T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17662327 | |||||||
chr1:17662362 | G | A | 2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2861-2085G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17662362 | |||||||
chr1:17662364 | G | A | 4 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(1): Show |
4 | HG00741.hp1 HG01257.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.2861-2083G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17662364 | |||||||
chr1:17662400 | G | A | 1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2861-2047G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17662400 | |||||||
chr1:17662466 | C | G | 1 | a0001c0011t0001g0138 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2861-1981C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17662466 | |||||||
chr1:17662502 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2861-1945C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17662502 | |||||||
chr1:17662536 | G | C | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2861-1911G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17662536 | |||||||
chr1:17662710 | G | A | 1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2861-1737G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17662710 | |||||||
chr1:17662764 | G | A | 7 | a0001c0001t0001g0002 a0002c0007t0002g0013 a0002c0007t0002g0058 others(4): Show |
7 | HG00642.hp1 HG02280.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2861-1683G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17662764 | |||||||
chr1:17662846 | C | T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2861-1601C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17662846 | |||||||
chr1:17662849 | T | C | 1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2861-1598T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17662849 | |||||||
chr1:17663005 | T | G | 17 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(14): Show |
17 | HG00642.hp1 HG00741.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2861-1442T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17663005 | |||||||
chr1:17663125 | G | A | 2 | a0001c0001t0001g0164 a0002c0041t0008g0054 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2861-1322G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17663125 | |||||||
chr1:17663200 | A | G | 5 | a0001c0013t0001g0008 a0001c0013t0001g0017 a0001c0013t0001g0023 others(2): Show |
5 | HG00323.hp2 HG00738.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.2861-1247A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17663200 | |||||||
chr1:17663270 | G | T | 41 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(38): Show |
41 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.2861-1177G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17663270 | |||||||
chr1:17663350 | A | G | 51 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(48): Show |
51 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.2861-1097A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17663350 | |||||||
chr1:17663425 | C | T | 2 | a0007c0010t0001g0053 a0007c0010t0001g0115 |
2 | HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2861-1022C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17663425 | |||||||
chr1:17663467 | C | T | 2 | a0002c0003t0002g0037 a0008c0016t0002g0132 |
2 | NA18966.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.2861-980C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17663467 | |||||||
chr1:17663468 | G | A | 1 | a0002c0018t0002g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2861-979G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17663468 | |||||||
chr1:17663557 | G | GA | 37 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0033t0002g0110 others(34): Show |
37 | HG00544.hp2 HG00733.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.2861-877dupA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr1 | 17663557 | ||||||
chr1:17663565 | A | C | 1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2861-882A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17663565 | |||||||
chr1:17663847 | C | T | 2 | a0002c0041t0008g0054 a0021c0030t0002g0109 |
2 | HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2861-600C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17663847 | |||||||
chr1:17663907 | G | T | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2861-540G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17663907 | |||||||
chr1:17663980 | A | G | 51 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(48): Show |
51 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.2861-467A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17663980 | |||||||
chr1:17664000 | C | T | 1 | a0009c0039t0001g0039 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2861-447C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17664000 | |||||||
chr1:17664064 | C | T | 12 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0033t0002g0110 others(9): Show |
12 | HG00642.hp1 HG01884.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.2861-383C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17664064 | |||||||
chr1:17664295 | C | T | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2861-152C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 25/28 | chr1 | 17664295 | |||||||
chr1:17664701 | A | G | 51 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(48): Show |
51 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.3009+106A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17664701 | |||||||
chr1:17664766 | C | T | 2 | a0001c0001t0003g0135 a0018c0028t0003g0044 |
2 | HG03492.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.3009+171C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17664766 | |||||||
chr1:17665078 | A | G | 38 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0033t0002g0110 others(35): Show |
38 | HG00544.hp2 HG00733.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.3009+483A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17665078 | |||||||
chr1:17665128 | C | T | 1 | a0006c0009t0001g0107 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3009+533C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17665128 | |||||||
chr1:17665160 | C | T | 1 | a0005c0015t0002g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3009+565C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17665160 | |||||||
chr1:17665318 | GCAGCTGT others(4): Show |
G | 5 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 others(2): Show |
5 | HG01884.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.3009+730_3009+740d others(13): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17665318 | ||||||
chr1:17665561 | G | A | 4 | a0001c0013t0001g0008 a0001c0013t0001g0017 a0001c0013t0001g0023 others(1): Show |
4 | HG00738.hp1 HG01074.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.3009+966G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17665561 | |||||||
chr1:17665566 | C | T | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3009+971C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17665566 | |||||||
chr1:17665672 | C | T | 1 | a0001c0001t0003g0168 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3009+1077C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17665672 | |||||||
chr1:17665717 | G | A | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3009+1122G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17665717 | |||||||
chr1:17665783 | T | C | 7 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(4): Show |
7 | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.3009+1188T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17665783 | |||||||
chr1:17665819 | G | A | 6 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.3009+1224G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17665819 | |||||||
chr1:17665925 | C | T | 1 | a0010c0046t0001g0020 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3009+1330C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17665925 | |||||||
chr1:17666127 | A | G | 27 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(24): Show |
27 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.3009+1532A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17666127 | |||||||
chr1:17666511 | C | T | 1 | a0003c0002t0001g0073 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3009+1916C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17666511 | |||||||
chr1:17666625 | C | T | 29 | a0001c0033t0002g0110 a0002c0003t0002g0025 a0002c0003t0002g0037 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.3009+2030C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17666625 | |||||||
chr1:17666637 | C | T | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3009+2042C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17666637 | |||||||
chr1:17666886 | C | T | 2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3009+2291C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17666886 | |||||||
chr1:17666930 | G | A | 1 | a0001c0013t0001g0023 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3009+2335G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17666930 | |||||||
chr1:17666990 | G | GGAA | 27 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(24): Show |
27 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.3009+2397_3009+239 others(7): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17666990 | ||||||
chr1:17667149 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3009+2554C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17667149 | |||||||
chr1:17667261 | G | C | 5 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 others(2): Show |
5 | HG01884.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.3009+2666G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17667261 | |||||||
chr1:17667366 | G | A | 1 | a0001c0006t0007g0150 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3009+2771G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17667366 | |||||||
chr1:17667551 | A | G | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3009+2956A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17667551 | |||||||
chr1:17667553 | G | T | 1 | a0001c0033t0002g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3009+2958G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17667553 | |||||||
chr1:17667738 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3009+3143C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17667738 | |||||||
chr1:17667739 | G | A | 56 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(53): Show |
56 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.3009+3144G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17667739 | |||||||
chr1:17667740 | C | T | 5 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 others(2): Show |
5 | HG01884.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.3009+3145C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17667740 | |||||||
chr1:17667901 | C | T | 1 | a0001c0013t0001g0017 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3009+3306C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17667901 | |||||||
chr1:17667909 | T | G | 1 | a0001c0001t0001g0077 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3009+3314T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17667909 | |||||||
chr1:17668213 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0158 |
2 | NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3009+3618G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17668213 | |||||||
chr1:17668355 | C | T | 23 | a0002c0003t0002g0025 a0002c0003t0002g0037 a0002c0003t0002g0055 others(20): Show |
23 | HG00544.hp2 HG00733.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.3009+3760C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17668355 | |||||||
chr1:17668383 | G | A | 5 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 others(2): Show |
5 | HG01884.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.3009+3788G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17668383 | |||||||
chr1:17668409 | T | C | 6 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.3009+3814T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17668409 | |||||||
chr1:17668472 | TG | T | 5 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 others(2): Show |
5 | HG01884.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.3009+3878delG | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17668472 | |||||||
chr1:17668561 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3009+3966G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17668561 | |||||||
chr1:17668786 | A | G | 22 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(19): Show |
22 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3009+4191A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17668786 | |||||||
chr1:17668810 | T | TA | 22 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(19): Show |
22 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.3009+4217dupA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17668810 | ||||||
chr1:17668975 | G | C | 1 | a0006c0009t0001g0107 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3009+4380G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17668975 | |||||||
chr1:17669029 | G | A | 1 | a0001c0006t0007g0150 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3009+4434G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17669029 | |||||||
chr1:17669164 | C | A | 1 | a0001c0042t0001g0035 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3009+4569C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17669164 | |||||||
chr1:17669192 | G | A | 1 | a0006c0009t0001g0166 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3009+4597G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17669192 | |||||||
chr1:17669197 | A | G | 24 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(21): Show |
24 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.3009+4602A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17669197 | |||||||
chr1:17669337 | G | A | 27 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(24): Show |
27 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.3009+4742G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17669337 | |||||||
chr1:17669351 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3009+4756T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17669351 | |||||||
chr1:17669818 | G | T | 2 | a0002c0003t0002g0089 a0011c0025t0002g0049 |
2 | HG01106.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.3009+5223G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17669818 | |||||||
chr1:17669970 | C | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0034 a0001c0001t0001g0043 others(2): Show |
5 | HG01346.hp2 HG01496.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.3009+5375C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17669970 | |||||||
chr1:17670020 | C | T | 1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3009+5425C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17670020 | |||||||
chr1:17670028 | C | T | 16 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(13): Show |
16 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.3009+5433C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17670028 | |||||||
chr1:17670067 | T | A | 1 | a0001c0012t0001g0102 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3009+5472T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17670067 | |||||||
chr1:17670185 | A | G | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3009+5590A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17670185 | |||||||
chr1:17670397 | C | T | 1 | a0003c0002t0001g0038 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3009+5802C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17670397 | |||||||
chr1:17670420 | A | G | 1 | a0002c0003t0002g0083 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3009+5825A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17670420 | |||||||
chr1:17670526 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3009+5931A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17670526 | |||||||
chr1:17670735 | G | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0134 a0009c0039t0001g0039 |
3 | HG00558.hp2 HG02080.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.3009+6140G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17670735 | |||||||
chr1:17670745 | G | A | 7 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(4): Show |
7 | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.3009+6150G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17670745 | |||||||
chr1:17670754 | C | T | 2 | a0001c0001t0001g0076 a0001c0001t0001g0099 |
2 | HG02135.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.3009+6159C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17670754 | |||||||
chr1:17671005 | C | G | 1 | a0003c0002t0001g0069 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3009+6410C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17671005 | |||||||
chr1:17671053 | T | C | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3009+6458T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17671053 | |||||||
chr1:17671121 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0034 a0001c0001t0001g0048 |
3 | HG01496.hp2 HG01934.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.3009+6526C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17671121 | |||||||
chr1:17671356 | G | T | 2 | a0002c0004t0002g0120 a0002c0004t0002g0121 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.3009+6761G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17671356 | |||||||
chr1:17671489 | T | C | 20 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(17): Show |
20 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.3009+6894T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17671489 | |||||||
chr1:17671508 | C | T | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3009+6913C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17671508 | |||||||
chr1:17671542 | G | A | 8 | a0002c0034t0002g0149 a0002c0041t0008g0054 a0004c0005t0002g0006 others(5): Show |
8 | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.3009+6947G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17671542 | |||||||
chr1:17671664 | G | A | 5 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(2): Show |
5 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3009+7069G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17671664 | |||||||
chr1:17671738 | T | C | 29 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(26): Show |
29 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.3009+7143T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17671738 | |||||||
chr1:17671745 | C | A | 1 | a0001c0001t0001g0046 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3009+7150C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17671745 | |||||||
chr1:17671931 | C | G | 20 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(17): Show |
20 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.3009+7336C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17671931 | |||||||
chr1:17671940 | A | C | 1 | a0006c0009t0001g0166 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3009+7345A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17671940 | |||||||
chr1:17671954 | G | C | 6 | a0001c0001t0001g0154 a0001c0001t0003g0114 a0001c0001t0003g0131 others(3): Show |
6 | HG02896.hp1 HG02897.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.3009+7359G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17671954 | |||||||
chr1:17672002 | G | A | 9 | a0002c0018t0002g0155 a0002c0034t0002g0149 a0002c0041t0008g0054 others(6): Show |
9 | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.3009+7407G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17672002 | |||||||
chr1:17672138 | A | G | 2 | a0002c0004t0002g0120 a0002c0004t0002g0121 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.3009+7543A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17672138 | |||||||
chr1:17672282 | C | T | 16 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(13): Show |
16 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.3009+7687C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17672282 | |||||||
chr1:17672294 | G | A | 2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3009+7699G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17672294 | |||||||
chr1:17672394 | G | A | 9 | a0002c0018t0002g0155 a0002c0034t0002g0149 a0002c0041t0008g0054 others(6): Show |
9 | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.3009+7799G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17672394 | |||||||
chr1:17672425 | G | C | 12 | a0001c0001t0001g0154 a0001c0001t0003g0080 a0001c0001t0003g0090 others(9): Show |
12 | HG01069.hp2 HG01169.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.3009+7830G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17672425 | |||||||
chr1:17672537 | A | G | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3009+7942A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17672537 | |||||||
chr1:17672723 | T | C | 20 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(17): Show |
20 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.3009+8128T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17672723 | |||||||
chr1:17672790 | G | A | 9 | a0002c0018t0002g0155 a0002c0034t0002g0149 a0002c0041t0008g0054 others(6): Show |
9 | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.3009+8195G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17672790 | |||||||
chr1:17672847 | A | G | 3 | a0001c0001t0001g0154 a0001c0001t0003g0131 a0001c0001t0003g0153 |
3 | HG02976.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3009+8252A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17672847 | |||||||
chr1:17672947 | G | A | 8 | a0001c0001t0001g0024 a0001c0001t0001g0127 a0001c0012t0001g0064 others(5): Show |
8 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.3009+8352G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17672947 | |||||||
chr1:17673006 | C | G | 1 | a0002c0008t0002g0100 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3009+8411C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17673006 | |||||||
chr1:17673142 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3009+8547C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17673142 | |||||||
chr1:17673163 | C | T | 4 | a0001c0033t0002g0110 a0001c0044t0004g0161 a0012c0031t0006g0165 others(1): Show |
4 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.3009+8568C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17673163 | |||||||
chr1:17673187 | G | A | 8 | a0002c0034t0002g0149 a0002c0041t0008g0054 a0004c0005t0002g0006 others(5): Show |
8 | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.3009+8592G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17673187 | |||||||
chr1:17673296 | CTG | C | 6 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.3009+8707_3009+870 others(6): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17673296 | ||||||
chr1:17673549 | G | A | 28 | a0002c0003t0002g0025 a0002c0003t0002g0037 a0002c0003t0002g0055 others(25): Show |
28 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.3009+8954G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17673549 | |||||||
chr1:17673625 | T | C | 56 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(53): Show |
56 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.3009+9030T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17673625 | |||||||
chr1:17673661 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3009+9066A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17673661 | |||||||
chr1:17673788 | T | C | 6 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.3009+9193T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17673788 | |||||||
chr1:17673958 | C | T | 8 | a0002c0034t0002g0149 a0002c0041t0008g0054 a0004c0005t0002g0006 others(5): Show |
8 | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.3009+9363C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17673958 | |||||||
chr1:17674019 | T | C | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3009+9424T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17674019 | |||||||
chr1:17674118 | G | A | 3 | a0001c0001t0003g0080 a0001c0001t0003g0090 a0001c0001t0003g0092 |
3 | HG01069.hp2 HG01175.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.3009+9523G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17674118 | |||||||
chr1:17674132 | A | G | 28 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(25): Show |
28 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.3009+9537A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17674132 | |||||||
chr1:17674219 | C | T | 28 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(25): Show |
28 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.3009+9624C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17674219 | |||||||
chr1:17674359 | A | C | 1 | a0001c0001t0001g0032 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3009+9764A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17674359 | |||||||
chr1:17674482 | T | C | 28 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(25): Show |
28 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.3009+9887T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17674482 | |||||||
chr1:17674501 | C | T | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3009+9906C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17674501 | |||||||
chr1:17674562 | G | T | 8 | a0002c0034t0002g0149 a0002c0041t0008g0054 a0004c0005t0002g0006 others(5): Show |
8 | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.3009+9967G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17674562 | |||||||
chr1:17674749 | A | C | 28 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(25): Show |
28 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.3009+10154A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17674749 | |||||||
chr1:17675005 | C | T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3009+10410C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17675005 | |||||||
chr1:17675019 | A | G | 28 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(25): Show |
28 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.3009+10424A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17675019 | |||||||
chr1:17675174 | C | T | 28 | a0002c0003t0002g0025 a0002c0003t0002g0037 a0002c0003t0002g0055 others(25): Show |
28 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.3009+10579C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17675174 | |||||||
chr1:17675206 | G | A | 28 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(25): Show |
28 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.3009+10611G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17675206 | |||||||
chr1:17675219 | A | G | 1 | a0001c0033t0002g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3009+10624A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17675219 | |||||||
chr1:17675255 | C | T | 4 | a0001c0001t0003g0080 a0001c0001t0003g0090 a0001c0001t0003g0092 others(1): Show |
4 | HG01069.hp2 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.3009+10660C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17675255 | |||||||
chr1:17675356 | C | A | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3009+10761C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17675356 | |||||||
chr1:17675393 | G | A | 2 | a0002c0004t0002g0118 a0002c0004t0002g0146 |
2 | HG02109.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3009+10798G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17675393 | |||||||
chr1:17675554 | C | T | 1 | a0003c0002t0001g0144 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3009+10959C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17675554 | |||||||
chr1:17675621 | G | A | 20 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(17): Show |
20 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.3009+11026G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17675621 | |||||||
chr1:17675622 | TGTG | T | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3009+11029_3009+11 others(9): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17675622 | ||||||
chr1:17675649 | T | G | 8 | a0002c0034t0002g0149 a0002c0041t0008g0054 a0004c0005t0002g0006 others(5): Show |
8 | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.3009+11054T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17675649 | |||||||
chr1:17675660 | T | TGGGTGCA others(16): Show |
1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3009+11066_3009+11 others(29): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17675660 | ||||||
chr1:17675691 | G | GGT | 28 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(25): Show |
28 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.3009+11101_3009+11 others(8): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17675691 | ||||||
chr1:17675696 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3009+11101G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17675696 | |||||||
chr1:17675830 | G | T | 1 | a0001c0001t0005g0162 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3009+11235G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17675830 | |||||||
chr1:17675863 | C | T | 1 | a0002c0008t0002g0042 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3009+11268C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17675863 | |||||||
chr1:17676022 | A | G | 1 | a0003c0002t0001g0106 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3009+11427A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17676022 | |||||||
chr1:17676024 | G | A | 1 | a0003c0002t0001g0106 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3009+11429G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17676024 | |||||||
chr1:17676025 | T | G | 1 | a0003c0002t0001g0106 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3009+11430T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17676025 | |||||||
chr1:17676041 | C | A | 6 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.3009+11446C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17676041 | |||||||
chr1:17676046 | G | A | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3009+11451G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17676046 | |||||||
chr1:17676109 | C | G | 28 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(25): Show |
28 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.3010-11464C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17676109 | |||||||
chr1:17676127 | G | A | 4 | a0001c0001t0001g0128 a0001c0001t0001g0134 a0003c0002t0001g0038 others(1): Show |
4 | HG00558.hp2 HG02080.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.3010-11446G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17676127 | |||||||
chr1:17676208 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3010-11365G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17676208 | |||||||
chr1:17676282 | A | C | 29 | a0001c0019t0001g0095 a0002c0003t0002g0025 a0002c0003t0002g0037 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.3010-11291A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17676282 | |||||||
chr1:17676283 | G | A | 2 | a0002c0004t0002g0120 a0002c0004t0002g0121 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.3010-11290G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17676283 | |||||||
chr1:17676344 | CGTGGGTG others(5): Show |
C | 6 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.3010-11209_3010-11 others(18): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17676344 | ||||||
chr1:17676428 | ATGGGTGC others(17): Show |
A | 1 | a0003c0002t0001g0106 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3010-11140_3010-11 others(30): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17676428 | ||||||
chr1:17676554 | G | A | 1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3010-11019G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17676554 | |||||||
chr1:17676809 | C | G | 1 | a0001c0013t0001g0023 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3010-10764C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17676809 | |||||||
chr1:17677303 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0034 a0001c0001t0001g0048 |
3 | HG01496.hp2 HG01934.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.3010-10270C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17677303 | |||||||
chr1:17677405 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3010-10168C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17677405 | |||||||
chr1:17677415 | T | C | 19 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(16): Show |
19 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.3010-10158T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17677415 | |||||||
chr1:17677451 | C | T | 8 | a0002c0034t0002g0149 a0002c0041t0008g0054 a0004c0005t0002g0006 others(5): Show |
8 | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.3010-10122C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17677451 | |||||||
chr1:17677679 | A | G | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3010-9894A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17677679 | |||||||
chr1:17677754 | A | G | 1 | a0001c0038t0003g0124 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3010-9819A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17677754 | |||||||
chr1:17677965 | G | A | 4 | a0001c0033t0002g0110 a0001c0044t0004g0161 a0012c0031t0006g0165 others(1): Show |
4 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.3010-9608G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17677965 | |||||||
chr1:17678203 | T | C | 1 | a0001c0044t0004g0161 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3010-9370T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17678203 | |||||||
chr1:17678259 | C | T | 6 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.3010-9314C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17678259 | |||||||
chr1:17678378 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3010-9195C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17678378 | |||||||
chr1:17678399 | G | A | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3010-9174G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17678399 | |||||||
chr1:17678417 | G | GT | 19 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0084 others(16): Show |
19 | HG00544.hp1 HG00558.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.3010-9137dupT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17678417 | ||||||
chr1:17678417 | GT | G | 11 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0096 others(8): Show |
11 | HG01070.hp2 HG01257.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.3010-9137delT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17678417 | ||||||
chr1:17678502 | A | C | 9 | a0001c0033t0002g0110 a0001c0044t0004g0161 a0002c0007t0002g0013 others(6): Show |
9 | HG00642.hp1 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.3010-9071A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17678502 | |||||||
chr1:17678505 | T | C | 24 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(21): Show |
24 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.3010-9068T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17678505 | |||||||
chr1:17678525 | C | T | 18 | a0001c0033t0002g0110 a0001c0044t0004g0161 a0002c0007t0002g0013 others(15): Show |
18 | HG00642.hp1 HG01884.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.3010-9048C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17678525 | |||||||
chr1:17678531 | G | T | 12 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 others(9): Show |
12 | HG02630.hp1 HG02717.hp2 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.3010-9042G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17678531 | |||||||
chr1:17678565 | A | G | 5 | a0001c0033t0002g0110 a0001c0044t0004g0161 a0012c0031t0006g0165 others(2): Show |
5 | HG01884.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3010-9008A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17678565 | |||||||
chr1:17678575 | A | G | 1 | a0001c0006t0001g0001 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3010-8998A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17678575 | |||||||
chr1:17678638 | T | C | 28 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(25): Show |
28 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.3010-8935T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17678638 | |||||||
chr1:17678728 | A | T | 16 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(13): Show |
16 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.3010-8845A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17678728 | |||||||
chr1:17678820 | T | G | 28 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(25): Show |
28 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.3010-8753T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17678820 | |||||||
chr1:17678884 | T | G | 28 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(25): Show |
28 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.3010-8689T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17678884 | |||||||
chr1:17679294 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3010-8279A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17679294 | |||||||
chr1:17679318 | C | T | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3010-8255C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17679318 | |||||||
chr1:17679321 | A | T | 1 | a0002c0034t0002g0149 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3010-8252A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17679321 | |||||||
chr1:17679413 | G | A | 1 | a0006c0009t0001g0166 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3010-8160G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17679413 | |||||||
chr1:17679445 | G | A | 1 | a0001c0001t0001g0014 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3010-8128G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17679445 | |||||||
chr1:17679517 | T | C | 6 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.3010-8056T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17679517 | |||||||
chr1:17679577 | A | G | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3010-7996A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17679577 | |||||||
chr1:17679607 | C | G | 6 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.3010-7966C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17679607 | |||||||
chr1:17679612 | A | C | 29 | a0001c0019t0001g0095 a0002c0003t0002g0025 a0002c0003t0002g0037 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.3010-7961A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17679612 | |||||||
chr1:17679661 | G | A | 1 | a0002c0003t0002g0055 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3010-7912G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17679661 | |||||||
chr1:17679712 | C | T | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3010-7861C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17679712 | |||||||
chr1:17679801 | G | C | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3010-7772G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17679801 | |||||||
chr1:17680055 | T | C | 57 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(54): Show |
57 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.3010-7518T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17680055 | |||||||
chr1:17680124 | G | A | 29 | a0001c0019t0001g0095 a0002c0003t0002g0025 a0002c0003t0002g0037 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.3010-7449G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17680124 | |||||||
chr1:17680183 | G | C | 1 | a0001c0001t0001g0024 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3010-7390G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17680183 | |||||||
chr1:17680271 | G | C | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3010-7302G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17680271 | |||||||
chr1:17680417 | G | T | 1 | a0002c0018t0002g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3010-7156G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17680417 | |||||||
chr1:17680488 | C | T | 3 | a0001c0033t0002g0110 a0001c0044t0004g0161 a0012c0031t0006g0165 |
3 | HG01884.hp1 HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3010-7085C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17680488 | |||||||
chr1:17680550 | A | G | 29 | a0001c0019t0001g0095 a0002c0003t0002g0025 a0002c0003t0002g0037 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.3010-7023A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17680550 | |||||||
chr1:17680649 | C | A | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3010-6924C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17680649 | |||||||
chr1:17680743 | CT | C | 5 | a0001c0001t0001g0128 a0001c0001t0003g0092 a0001c0006t0001g0001 others(2): Show |
5 | HG01069.hp2 HG01070.hp1 HG02080.hp2 others(2): Show |
intron_variant | MODIFIER | c.3010-6813delT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17680743 | ||||||
chr1:17680787 | C | CT | 59 | a0001c0001t0003g0135 a0001c0011t0001g0004 a0001c0011t0001g0138 others(56): Show |
59 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.3010-6773dupT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17680787 | ||||||
chr1:17680844 | C | T | 1 | a0001c0012t0001g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3010-6729C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17680844 | |||||||
chr1:17680853 | G | A | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3010-6720G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17680853 | |||||||
chr1:17680886 | C | A | 1 | a0001c0012t0001g0102 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3010-6687C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17680886 | |||||||
chr1:17681065 | G | A | 1 | a0002c0022t0002g0050 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3010-6508G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17681065 | |||||||
chr1:17681103 | A | G | 29 | a0001c0019t0001g0095 a0002c0003t0002g0025 a0002c0003t0002g0037 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.3010-6470A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17681103 | |||||||
chr1:17681221 | T | A | 3 | a0001c0033t0002g0110 a0001c0044t0004g0161 a0012c0031t0006g0165 |
3 | HG01884.hp1 HG02559.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3010-6352T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17681221 | |||||||
chr1:17681221 | T | C | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3010-6352T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17681221 | |||||||
chr1:17681256 | C | T | 6 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.3010-6317C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17681256 | |||||||
chr1:17681314 | A | G | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3010-6259A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17681314 | |||||||
chr1:17681434 | C | T | 6 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.3010-6139C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17681434 | |||||||
chr1:17681592 | A | G | 1 | a0015c0032t0001g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3010-5981A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17681592 | |||||||
chr1:17681621 | T | C | 29 | a0001c0019t0001g0095 a0002c0003t0002g0025 a0002c0003t0002g0037 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.3010-5952T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17681621 | |||||||
chr1:17681626 | C | T | 29 | a0001c0019t0001g0095 a0002c0003t0002g0025 a0002c0003t0002g0037 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.3010-5947C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17681626 | |||||||
chr1:17681717 | C | T | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3010-5856C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17681717 | |||||||
chr1:17681746 | C | T | 29 | a0001c0019t0001g0095 a0002c0003t0002g0025 a0002c0003t0002g0037 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.3010-5827C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17681746 | |||||||
chr1:17681989 | T | A | 2 | a0001c0044t0004g0161 a0012c0031t0006g0165 |
2 | HG01884.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3010-5584T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17681989 | |||||||
chr1:17681989 | T | TA | 48 | a0001c0001t0001g0154 a0001c0001t0003g0114 a0001c0001t0003g0131 others(45): Show |
48 | HG00544.hp2 HG00733.hp1 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.3010-5572dupA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17681989 | ||||||
chr1:17682035 | T | C | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3010-5538T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17682035 | |||||||
chr1:17682181 | T | G | 1 | a0002c0018t0002g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3010-5392T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17682181 | |||||||
chr1:17682331 | G | A | 5 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 others(2): Show |
5 | HG01884.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.3010-5242G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17682331 | |||||||
chr1:17682345 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3010-5228T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17682345 | |||||||
chr1:17682359 | G | A | 1 | a0001c0001t0003g0135 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.3010-5214G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17682359 | |||||||
chr1:17682647 | G | T | 1 | a0001c0001t0001g0010 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3010-4926G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17682647 | |||||||
chr1:17682802 | C | T | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3010-4771C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17682802 | |||||||
chr1:17682858 | G | A | 1 | a0002c0022t0002g0050 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3010-4715G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17682858 | |||||||
chr1:17682920 | T | C | 29 | a0001c0033t0002g0110 a0002c0003t0002g0025 a0002c0003t0002g0037 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.3010-4653T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17682920 | |||||||
chr1:17682931 | G | A | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3010-4642G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17682931 | |||||||
chr1:17682989 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3010-4584A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17682989 | |||||||
chr1:17683088 | AGGGTGCT others(21): Show |
A | 2 | a0001c0044t0004g0161 a0012c0031t0006g0165 |
2 | HG01884.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3010-4456_3010-442 others(32): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17683088 | ||||||
chr1:17683110 | C | T | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3010-4463C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17683110 | |||||||
chr1:17683116 | G | T | 29 | a0001c0033t0002g0110 a0002c0003t0002g0025 a0002c0003t0002g0037 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.3010-4457G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17683116 | |||||||
chr1:17683173 | T | C | 32 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0033t0002g0110 others(29): Show |
32 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.3010-4400T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17683173 | |||||||
chr1:17683173 | T | G | 1 | a0001c0011t0001g0004 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3010-4400T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17683173 | |||||||
chr1:17683173 | T | TGGTGCTC others(49): Show |
1 | a0001c0001t0001g0084 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3010-4374_3010-437 others(60): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17683173 | ||||||
chr1:17683173 | TGGTGCTC others(21): Show |
T | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3010-4373_3010-434 others(32): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17683173 | ||||||
chr1:17683173 | TGGTGCTC others(77): Show |
T | 1 | a0001c0001t0001g0047 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3010-4317_3010-423 others(88): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17683173 | ||||||
chr1:17683200 | G | GGGGTGCT others(21): Show |
4 | a0001c0001t0001g0071 a0001c0001t0001g0154 a0001c0001t0003g0131 others(1): Show |
4 | HG02976.hp1 NA18747.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.3010-4317_3010-429 others(32): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17683200 | ||||||
chr1:17683200 | GGGGTGCT others(217): Show |
G | 1 | a0002c0022t0002g0050 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3010-4346_3010-412 others(4): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17683200 | ||||||
chr1:17683201 | G | C | 28 | a0001c0033t0002g0110 a0002c0003t0002g0025 a0002c0003t0002g0037 others(25): Show |
28 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.3010-4372G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17683201 | |||||||
chr1:17683214 | CCCCTGCT others(190): Show |
C | 1 | a0002c0021t0002g0137 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3010-4356_3010-416 others(4): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17683214 | ||||||
chr1:17683215 | CCCTGCTC others(189): Show |
C | 27 | a0001c0033t0002g0110 a0002c0003t0002g0025 a0002c0003t0002g0037 others(24): Show |
27 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.3010-4318_3010-412 others(4): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17683215 | ||||||
chr1:17683243 | C | G | 1 | a0010c0046t0001g0020 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3010-4330C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17683243 | |||||||
chr1:17683256 | C | G | 1 | a0001c0001t0001g0084 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3010-4317C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17683256 | |||||||
chr1:17683256 | CGGGTGCT others(77): Show |
C | 7 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(4): Show |
7 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.3010-4261_3010-417 others(88): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17683256 | ||||||
chr1:17683312 | C | CGGGTGCT others(21): Show |
1 | a0001c0001t0001g0084 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3010-4190_3010-416 others(32): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17683312 | ||||||
chr1:17683312 | CGGGTGCT others(21): Show |
C | 12 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(9): Show |
12 | HG00738.hp1 HG00741.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.3010-4190_3010-416 others(32): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17683312 | ||||||
chr1:17683424 | C | G | 28 | a0001c0033t0002g0110 a0002c0003t0002g0025 a0002c0003t0002g0037 others(25): Show |
28 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.3010-4149C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17683424 | |||||||
chr1:17683425 | G | C | 29 | a0001c0033t0002g0110 a0002c0003t0002g0025 a0002c0003t0002g0037 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.3010-4148G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17683425 | |||||||
chr1:17683562 | C | G | 1 | a0002c0008t0002g0126 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3010-4011C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17683562 | |||||||
chr1:17683572 | G | A | 29 | a0001c0033t0002g0110 a0002c0003t0002g0025 a0002c0003t0002g0037 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.3010-4001G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17683572 | |||||||
chr1:17683595 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3010-3978C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17683595 | |||||||
chr1:17683603 | A | G | 1 | a0002c0003t0002g0025 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3010-3970A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17683603 | |||||||
chr1:17683616 | CAGGCTG | C | 29 | a0001c0033t0002g0110 a0002c0003t0002g0025 a0002c0003t0002g0037 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.3010-3956_3010-395 others(10): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17683616 | |||||||
chr1:17683617 | A | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(134): Show |
137 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.3010-3956A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17683617 | |||||||
chr1:17683634 | A | G | 53 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(50): Show |
53 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.3010-3939A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17683634 | |||||||
chr1:17683659 | T | C | 29 | a0001c0033t0002g0110 a0002c0003t0002g0025 a0002c0003t0002g0037 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.3010-3914T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17683659 | |||||||
chr1:17683694 | G | C | 53 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(50): Show |
53 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.3010-3879G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17683694 | |||||||
chr1:17683703 | G | A | 29 | a0001c0033t0002g0110 a0002c0003t0002g0025 a0002c0003t0002g0037 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.3010-3870G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17683703 | |||||||
chr1:17683738 | T | A | 56 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(53): Show |
56 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.3010-3835T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17683738 | |||||||
chr1:17683917 | C | T | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3010-3656C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17683917 | |||||||
chr1:17684008 | T | A | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3010-3565T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17684008 | |||||||
chr1:17684040 | C | T | 29 | a0001c0033t0002g0110 a0002c0003t0002g0025 a0002c0003t0002g0037 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.3010-3533C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17684040 | |||||||
chr1:17684093 | G | A | 1 | a0001c0014t0001g0145 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3010-3480G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17684093 | |||||||
chr1:17684114 | G | A | 1 | a0006c0009t0001g0166 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3010-3459G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17684114 | |||||||
chr1:17684370 | G | A | 1 | a0002c0007t0002g0013 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3010-3203G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17684370 | |||||||
chr1:17684394 | G | T | 1 | a0001c0001t0001g0014 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3010-3179G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17684394 | |||||||
chr1:17684454 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3010-3119G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17684454 | |||||||
chr1:17684515 | C | T | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3010-3058C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17684515 | |||||||
chr1:17684584 | A | G | 2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3010-2989A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17684584 | |||||||
chr1:17684604 | C | T | 1 | a0010c0046t0001g0020 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3010-2969C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17684604 | |||||||
chr1:17684608 | T | A | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3010-2965T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17684608 | |||||||
chr1:17684673 | GAGACACC others(52): Show |
G | 1 | a0002c0003t0002g0141 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3010-2899_3010-284 others(63): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17684673 | |||||||
chr1:17684855 | A | C | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3010-2718A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17684855 | |||||||
chr1:17684866 | T | G | 34 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0033t0002g0110 others(31): Show |
34 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.3010-2707T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17684866 | |||||||
chr1:17685419 | C | A | 8 | a0002c0034t0002g0149 a0002c0041t0008g0054 a0004c0005t0002g0006 others(5): Show |
8 | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.3010-2154C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17685419 | |||||||
chr1:17685539 | T | A | 30 | a0001c0033t0002g0110 a0002c0003t0002g0025 a0002c0003t0002g0037 others(27): Show |
30 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.3010-2034T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17685539 | |||||||
chr1:17685541 | G | A | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3010-2032G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17685541 | |||||||
chr1:17685953 | G | C | 3 | a0001c0013t0001g0008 a0001c0013t0001g0023 a0003c0002t0001g0081 |
3 | HG00738.hp1 HG01074.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.3010-1620G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17685953 | |||||||
chr1:17686074 | TTTTTTTT others(9): Show |
T | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3010-1495_3010-148 others(20): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17686074 | ||||||
chr1:17686078 | T | C | 50 | a0001c0001t0001g0032 a0001c0017t0002g0113 a0001c0017t0002g0148 others(47): Show |
50 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.3010-1495T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17686078 | |||||||
chr1:17686078 | T | TTTTC | 15 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0011 others(12): Show |
15 | HG00558.hp2 HG01257.hp2 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.3010-1467_3010-146 others(8): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17686078 | ||||||
chr1:17686078 | TTTTC | T | 5 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(2): Show |
5 | HG00741.hp1 HG01109.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.3010-1467_3010-146 others(8): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17686078 | ||||||
chr1:17686101 | TCTTTC | T | 8 | a0002c0034t0002g0149 a0002c0041t0008g0054 a0004c0005t0002g0006 others(5): Show |
8 | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.3010-1471_3010-146 others(9): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17686101 | |||||||
chr1:17686105 | TC | T | 31 | a0001c0033t0002g0110 a0002c0003t0002g0025 a0002c0003t0002g0037 others(28): Show |
31 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.3010-1467delC | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17686105 | |||||||
chr1:17686106 | C | T | 5 | a0001c0044t0004g0161 a0002c0008t0002g0126 a0012c0031t0006g0165 others(2): Show |
5 | HG01884.hp1 HG02602.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3010-1467C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17686106 | |||||||
chr1:17686108 | T | TTCTTTCT others(31): Show |
1 | a0001c0017t0002g0113 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.3010-1464_3010-146 others(42): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17686108 | ||||||
chr1:17686108 | T | TTCTTTCT others(35): Show |
1 | a0001c0017t0002g0148 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3010-1464_3010-146 others(46): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | 17686108 | ||||||
chr1:17686109 | T | TCTTTCTT others(26): Show |
1 | a0001c0043t0002g0051 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3010-1464_3010-146 others(37): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17686109 | |||||||
chr1:17686521 | G | A | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3010-1052G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17686521 | |||||||
chr1:17686579 | T | C | 1 | a0003c0002t0001g0144 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3010-994T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17686579 | |||||||
chr1:17686593 | T | TG | 3 | a0002c0003t0002g0025 a0002c0008t0002g0126 a0004c0005t0002g0117 |
3 | HG02602.hp1 HG03098.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.3010-980_3010-979i others(3): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17686593 | |||||||
chr1:17686594 | C | G | 50 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0033t0002g0110 others(47): Show |
50 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.3010-979C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17686594 | |||||||
chr1:17686608 | G | A | 1 | a0017c0037t0001g0142 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3010-965G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17686608 | |||||||
chr1:17686935 | T | A | 41 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0033t0002g0110 others(38): Show |
41 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.3010-638T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17686935 | |||||||
chr1:17687107 | G | A | 41 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0033t0002g0110 others(38): Show |
41 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.3010-466G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17687107 | |||||||
chr1:17687183 | G | A | 1 | a0002c0004t0002g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3010-390G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17687183 | |||||||
chr1:17687204 | C | T | 3 | a0001c0001t0001g0061 a0001c0001t0001g0158 a0016c0047t0002g0147 |
3 | HG03098.hp1 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3010-369C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17687204 | |||||||
chr1:17687239 | G | C | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3010-334G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17687239 | |||||||
chr1:17687244 | C | T | 1 | a0002c0004t0002g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3010-329C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17687244 | |||||||
chr1:17687325 | T | C | 50 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0033t0002g0110 others(47): Show |
50 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.3010-248T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17687325 | |||||||
chr1:17687340 | G | C | 41 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0033t0002g0110 others(38): Show |
41 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.3010-233G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | chr1 | 17687340 | |||||||
chr1:17687775 | G | A | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3184+28G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17687775 | |||||||
chr1:17687798 | C | T | 1 | a0002c0004t0002g0036 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3184+51C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17687798 | |||||||
chr1:17687925 | C | T | 2 | a0001c0044t0004g0161 a0012c0031t0006g0165 |
2 | HG01884.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3184+178C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17687925 | |||||||
chr1:17688083 | C | G | 5 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 others(2): Show |
5 | HG01884.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.3184+336C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17688083 | |||||||
chr1:17688157 | C | T | 1 | a0002c0007t0002g0085 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3184+410C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17688157 | |||||||
chr1:17688265 | G | A | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3184+518G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17688265 | |||||||
chr1:17688456 | G | A | 1 | a0002c0018t0002g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3184+709G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17688456 | |||||||
chr1:17688605 | G | A | 29 | a0001c0033t0002g0110 a0002c0003t0002g0025 a0002c0003t0002g0037 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.3184+858G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17688605 | |||||||
chr1:17688645 | G | A | 2 | a0002c0003t0002g0141 a0008c0027t0002g0029 |
2 | NA18954.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.3184+898G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17688645 | |||||||
chr1:17688648 | G | C | 2 | a0002c0003t0002g0141 a0008c0027t0002g0029 |
2 | NA18954.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.3184+901G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17688648 | |||||||
chr1:17688815 | G | T | 1 | a0001c0001t0003g0143 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3184+1068G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17688815 | |||||||
chr1:17689010 | G | A | 8 | a0002c0034t0002g0149 a0002c0041t0008g0054 a0004c0005t0002g0006 others(5): Show |
8 | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.3184+1263G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689010 | |||||||
chr1:17689050 | A | G | 54 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(51): Show |
54 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.3184+1303A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689050 | |||||||
chr1:17689350 | G | T | 1 | a0001c0001t0001g0010 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3184+1603G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689350 | |||||||
chr1:17689423 | A | G | 40 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0033t0002g0110 others(37): Show |
40 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.3184+1676A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689423 | |||||||
chr1:17689450 | T | C | 1 | a0002c0003t0002g0025 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3184+1703T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689450 | |||||||
chr1:17689458 | T | C | 56 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(53): Show |
56 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.3184+1711T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689458 | |||||||
chr1:17689462 | C | CCTCCCTC others(1023): Show |
1 | a0011c0025t0002g0049 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3184+1731_3184+173 others(1034): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689462 | ||||||
chr1:17689479 | T | C | 45 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(42): Show |
45 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.3184+1732T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689479 | |||||||
chr1:17689481 | C | CCCCCCTC others(1258): Show |
1 | a0001c0012t0001g0064 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1269): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(659): Show |
1 | a0001c0045t0001g0031 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(670): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1298): Show |
5 | a0001c0001t0001g0063 a0001c0001t0001g0077 a0001c0001t0001g0084 others(2): Show |
5 | HG00741.hp2 HG02735.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.3184+1737_3184+173 others(1309): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1290): Show |
1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1301): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1282): Show |
1 | a0001c0001t0003g0168 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1293): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1298): Show |
2 | a0001c0001t0001g0061 a0001c0001t0001g0158 |
2 | NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3184+1737_3184+173 others(1309): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1302): Show |
1 | a0003c0002t0001g0081 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1313): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1328): Show |
1 | a0001c0001t0001g0136 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1339): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(659): Show |
6 | a0001c0001t0001g0024 a0001c0001t0001g0127 a0001c0019t0001g0066 others(3): Show |
6 | HG00642.hp2 HG00733.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.3184+1737_3184+173 others(670): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1328): Show |
1 | a0001c0001t0001g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1339): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1092): Show |
1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1103): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1295): Show |
1 | a0001c0006t0001g0156 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1306): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1299): Show |
1 | a0015c0032t0001g0086 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1310): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1299): Show |
1 | a0001c0001t0001g0128 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1310): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1236): Show |
1 | a0004c0005t0002g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1247): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1299): Show |
1 | a0001c0001t0001g0062 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1310): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1298): Show |
4 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0079 others(1): Show |
4 | HG01257.hp2 HG01258.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.3184+1737_3184+173 others(1309): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1328): Show |
1 | a0001c0001t0001g0027 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1339): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1294): Show |
1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1305): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1294): Show |
5 | a0002c0034t0002g0149 a0004c0005t0002g0006 a0004c0005t0002g0060 others(2): Show |
5 | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.3184+1737_3184+173 others(1305): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1298): Show |
62 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0014 others(59): Show |
62 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.3184+1737_3184+173 others(1309): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1294): Show |
1 | a0007c0010t0001g0065 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1305): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1472): Show |
1 | a0004c0005t0002g0108 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1483): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1298): Show |
1 | a0013c0035t0001g0018 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1309): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1298): Show |
1 | a0001c0001t0001g0032 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1309): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1293): Show |
1 | a0003c0002t0001g0106 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1304): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1298): Show |
1 | a0001c0038t0003g0124 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1309): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1272): Show |
2 | a0001c0001t0001g0093 a0001c0012t0001g0102 |
2 | HG00323.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.3184+1737_3184+173 others(1283): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1294): Show |
2 | a0001c0001t0003g0135 a0003c0002t0001g0073 |
2 | HG02683.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3184+1737_3184+173 others(1305): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1260): Show |
1 | a0001c0012t0001g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1271): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1386): Show |
1 | a0001c0014t0001g0145 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1397): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1323): Show |
1 | a0003c0002t0001g0069 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1334): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1293): Show |
1 | a0001c0001t0003g0151 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1304): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1298): Show |
2 | a0007c0010t0001g0053 a0007c0010t0001g0115 |
2 | HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3184+1737_3184+173 others(1309): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1297): Show |
1 | a0001c0006t0007g0150 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1308): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1334): Show |
1 | a0001c0001t0001g0002 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1345): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1294): Show |
1 | a0001c0001t0003g0143 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1305): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1284): Show |
1 | a0001c0001t0001g0003 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1295): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1268): Show |
1 | a0001c0011t0001g0004 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1279): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1298): Show |
3 | a0001c0011t0001g0138 a0001c0011t0001g0152 a0001c0042t0001g0035 |
3 | HG00741.hp1 HG01257.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.3184+1737_3184+173 others(1309): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CCCCCTCC others(1258): Show |
2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3184+1737_3184+173 others(1269): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689481 | ||||||
chr1:17689481 | C | CTCCCTCC others(1057): Show |
6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3184+1734_3184+173 others(1068): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689481 | |||||||
chr1:17689483 | C | CCCTCCCT others(1022): Show |
1 | a0002c0003t0002g0083 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1033): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689483 | ||||||
chr1:17689483 | C | CCCTCCCT others(743): Show |
1 | a0001c0033t0002g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(754): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689483 | ||||||
chr1:17689483 | C | CCCTCCCT others(1826): Show |
1 | a0002c0003t0002g0116 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1837): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689483 | ||||||
chr1:17689483 | C | CCCTCCCT others(1021): Show |
1 | a0002c0008t0002g0126 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1032): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689483 | ||||||
chr1:17689483 | C | CCCTCCCT others(713): Show |
1 | a0002c0003t0002g0089 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(724): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689483 | ||||||
chr1:17689483 | C | CCCTCCCT others(1020): Show |
18 | a0002c0003t0002g0037 a0002c0003t0002g0055 a0002c0003t0002g0133 others(15): Show |
18 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.3184+1737_3184+173 others(1031): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689483 | ||||||
chr1:17689483 | C | CCCTCCCT others(1025): Show |
2 | a0001c0044t0004g0161 a0012c0031t0006g0165 |
2 | HG01884.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3184+1737_3184+173 others(1036): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689483 | ||||||
chr1:17689483 | C | CCCTCCCT others(1132): Show |
1 | a0001c0001t0001g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1143): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689483 | ||||||
chr1:17689483 | C | CCCTCCCT others(1016): Show |
1 | a0002c0003t0002g0025 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1027): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689483 | ||||||
chr1:17689483 | C | CCCTCCCT others(1019): Show |
1 | a0002c0021t0002g0137 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1030): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689483 | ||||||
chr1:17689483 | C | CCCTCCCT others(992): Show |
3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3184+1737_3184+173 others(1003): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689483 | ||||||
chr1:17689484 | C | CCCTCCCT others(1020): Show |
1 | a0008c0016t0002g0082 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3184+1737_3184+173 others(1031): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689484 | |||||||
chr1:17689485 | T | C | 32 | a0001c0001t0001g0164 a0001c0017t0002g0113 a0001c0017t0002g0148 others(29): Show |
32 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.3184+1738T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689485 | |||||||
chr1:17689485 | T | TCCCTCCC others(1079): Show |
1 | a0002c0003t0002g0141 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3184+1738_3184+173 others(1090): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689485 | |||||||
chr1:17689486 | A | C | 33 | a0001c0001t0001g0164 a0001c0017t0002g0113 a0001c0017t0002g0148 others(30): Show |
33 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.3184+1739A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689486 | |||||||
chr1:17689495 | T | C | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3184+1748T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689495 | |||||||
chr1:17689512 | C | T | 2 | a0001c0044t0004g0161 a0012c0031t0006g0165 |
2 | HG01884.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3184+1765C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689512 | |||||||
chr1:17689515 | C | CCCCTCCC others(999): Show |
1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3184+1769_3184+177 others(1010): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689515 | ||||||
chr1:17689523 | T | C | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3184+1776T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689523 | |||||||
chr1:17689526 | T | G | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3184+1779T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689526 | |||||||
chr1:17689528 | T | C | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3184+1781T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689528 | |||||||
chr1:17689529 | T | G | 2 | a0001c0044t0004g0161 a0012c0031t0006g0165 |
2 | HG01884.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3184+1782T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689529 | |||||||
chr1:17689544 | T | TTCCTCCC others(28): Show |
2 | a0001c0044t0004g0161 a0012c0031t0006g0165 |
2 | HG01884.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3184+1800_3184+180 others(39): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689544 | ||||||
chr1:17689555 | T | C | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3184+1808T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689555 | |||||||
chr1:17689558 | T | C | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3184+1811T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689558 | |||||||
chr1:17689558 | TCTTCCCT others(9): Show |
T | 37 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0033t0002g0110 others(34): Show |
37 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.3184+1828_3184+184 others(20): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689558 | ||||||
chr1:17689563 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3184+1816C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689563 | |||||||
chr1:17689571 | C | T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3184+1824C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689571 | |||||||
chr1:17689574 | C | CCTTCCCT others(9): Show |
2 | a0001c0044t0004g0161 a0012c0031t0006g0165 |
2 | HG01884.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3184+1839_3184+184 others(20): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17689574 | ||||||
chr1:17689574 | C | T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3184+1827C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689574 | |||||||
chr1:17689667 | G | A | 50 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0033t0002g0110 others(47): Show |
50 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.3184+1920G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689667 | |||||||
chr1:17689696 | T | A | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3184+1949T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689696 | |||||||
chr1:17689738 | C | G | 2 | a0001c0044t0004g0161 a0012c0031t0006g0165 |
2 | HG01884.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3184+1991C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689738 | |||||||
chr1:17689773 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3184+2026T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689773 | |||||||
chr1:17689857 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3184+2110G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689857 | |||||||
chr1:17689907 | A | G | 32 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0033t0002g0110 others(29): Show |
32 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.3184+2160A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689907 | |||||||
chr1:17689946 | T | C | 41 | a0001c0001t0001g0125 a0001c0017t0002g0113 a0001c0017t0002g0148 others(38): Show |
41 | HG00544.hp2 HG00642.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.3184+2199T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689946 | |||||||
chr1:17689996 | G | A | 29 | a0001c0033t0002g0110 a0002c0003t0002g0025 a0002c0003t0002g0037 others(26): Show |
29 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.3184+2249G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17689996 | |||||||
chr1:17690095 | A | G | 33 | a0001c0001t0003g0114 a0001c0001t0003g0151 a0001c0017t0002g0148 others(30): Show |
33 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.3184+2348A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17690095 | |||||||
chr1:17690162 | G | A | 32 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0033t0002g0110 others(29): Show |
32 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.3184+2415G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17690162 | |||||||
chr1:17690192 | C | T | 32 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0033t0002g0110 others(29): Show |
32 | HG00544.hp2 HG00733.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.3184+2445C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17690192 | |||||||
chr1:17690240 | G | A | 1 | a0012c0031t0006g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3184+2493G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17690240 | |||||||
chr1:17690289 | C | T | 1 | a0001c0044t0004g0161 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3184+2542C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17690289 | |||||||
chr1:17690328 | A | C | 9 | a0001c0033t0002g0110 a0001c0044t0004g0161 a0002c0007t0002g0013 others(6): Show |
9 | HG00642.hp1 HG01884.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.3184+2581A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17690328 | |||||||
chr1:17690410 | G | A | 1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3184+2663G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17690410 | |||||||
chr1:17690410 | G | GTCTCAAG others(23): Show |
1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3184+2664_3184+269 others(34): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17690410 | ||||||
chr1:17690423 | A | G | 4 | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(1): Show |
4 | HG00741.hp1 HG01257.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.3184+2676A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17690423 | |||||||
chr1:17690574 | G | A | 8 | a0001c0044t0004g0161 a0002c0007t0002g0013 a0002c0007t0002g0058 others(5): Show |
8 | HG00642.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3184+2827G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17690574 | |||||||
chr1:17690579 | T | C | 8 | a0001c0044t0004g0161 a0002c0007t0002g0013 a0002c0007t0002g0058 others(5): Show |
8 | HG00642.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3184+2832T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17690579 | |||||||
chr1:17690658 | G | T | 2 | a0001c0044t0004g0161 a0012c0031t0006g0165 |
2 | HG01884.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3184+2911G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17690658 | |||||||
chr1:17691027 | T | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(135): Show |
138 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.3184+3280T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17691027 | |||||||
chr1:17691039 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3184+3292C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17691039 | |||||||
chr1:17691063 | A | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(134): Show |
137 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.3184+3316A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17691063 | |||||||
chr1:17691209 | C | T | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(134): Show |
137 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.3184+3462C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17691209 | |||||||
chr1:17691308 | G | C | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3184+3561G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17691308 | |||||||
chr1:17691364 | G | A | 8 | a0002c0034t0002g0149 a0002c0041t0008g0054 a0004c0005t0002g0006 others(5): Show |
8 | HG02717.hp2 HG02922.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.3184+3617G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17691364 | |||||||
chr1:17691411 | G | A | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3184+3664G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17691411 | |||||||
chr1:17691665 | T | C | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3185-3493T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17691665 | |||||||
chr1:17691705 | G | GTA | 5 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 others(2): Show |
5 | HG02109.hp2 HG02486.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.3185-3443_3185-344 others(6): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17691705 | ||||||
chr1:17691725 | A | G | 2 | a0002c0003t0002g0037 a0008c0016t0002g0132 |
2 | NA18966.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.3185-3433A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17691725 | |||||||
chr1:17691760 | A | C | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(113): Show |
116 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.3185-3398A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17691760 | |||||||
chr1:17692229 | G | A | 2 | a0001c0020t0001g0016 a0001c0020t0001g0052 |
2 | HG01109.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3185-2929G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692229 | |||||||
chr1:17692285 | G | A | 6 | a0001c0001t0003g0114 a0001c0001t0003g0131 a0001c0001t0003g0151 others(3): Show |
6 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3185-2873G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692285 | |||||||
chr1:17692334 | G | A | 1 | a0005c0024t0002g0059 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3185-2824G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692334 | |||||||
chr1:17692362 | T | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(123): Show |
126 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.3185-2796T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692362 | |||||||
chr1:17692365 | G | A | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3185-2793G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692365 | |||||||
chr1:17692393 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3185-2765C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692393 | |||||||
chr1:17692432 | G | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(123): Show |
126 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.3185-2726G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692432 | |||||||
chr1:17692521 | T | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(124): Show |
127 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.3185-2637T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692521 | |||||||
chr1:17692522 | G | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0062 a0001c0001t0001g0163 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.3185-2636G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692522 | |||||||
chr1:17692558 | G | A | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3185-2600G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692558 | |||||||
chr1:17692685 | T | G | 3 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 |
3 | HG02630.hp1 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3185-2473T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692685 | |||||||
chr1:17692712 | C | G | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(160): Show |
163 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.3185-2446C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692712 | |||||||
chr1:17692748 | T | A | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2410T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692748 | |||||||
chr1:17692754 | C | T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2404C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692754 | |||||||
chr1:17692765 | A | T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2393A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692765 | |||||||
chr1:17692767 | T | C | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2391T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692767 | |||||||
chr1:17692783 | G | C | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2375G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692783 | |||||||
chr1:17692784 | G | T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2374G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692784 | |||||||
chr1:17692786 | C | T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2372C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692786 | |||||||
chr1:17692824 | TTCTGTGC others(20): Show |
T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2329_3185-230 others(31): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17692824 | ||||||
chr1:17692860 | G | C | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2298G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692860 | |||||||
chr1:17692861 | C | T | 1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3185-2297C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692861 | |||||||
chr1:17692862 | G | A | 8 | a0001c0044t0004g0161 a0002c0007t0002g0013 a0002c0007t0002g0058 others(5): Show |
8 | HG00642.hp1 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.3185-2296G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692862 | |||||||
chr1:17692868 | G | C | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2290G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692868 | |||||||
chr1:17692918 | T | C | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2240T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692918 | |||||||
chr1:17692936 | T | A | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2222T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692936 | |||||||
chr1:17692937 | G | T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2221G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692937 | |||||||
chr1:17692959 | A | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(124): Show |
127 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.3185-2199A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692959 | |||||||
chr1:17692978 | C | T | 1 | a0001c0044t0004g0161 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3185-2180C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17692978 | |||||||
chr1:17693023 | C | T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2135C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693023 | |||||||
chr1:17693029 | C | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(117): Show |
120 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.3185-2129C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693029 | |||||||
chr1:17693036 | T | A | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2122T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693036 | |||||||
chr1:17693037 | G | T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2121G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693037 | |||||||
chr1:17693038 | C | G | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2120C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693038 | |||||||
chr1:17693067 | G | T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2091G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693067 | |||||||
chr1:17693079 | CCTTGTTT others(6): Show |
C | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2078_3185-206 others(17): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693079 | |||||||
chr1:17693104 | A | T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2054A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693104 | |||||||
chr1:17693105 | T | C | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2053T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693105 | |||||||
chr1:17693108 | C | T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2050C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693108 | |||||||
chr1:17693136 | T | TAGCCATC others(12): Show |
1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2016_3185-201 others(23): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17693136 | ||||||
chr1:17693150 | A | T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2008A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693150 | |||||||
chr1:17693154 | A | C | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-2004A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693154 | |||||||
chr1:17693162 | A | T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-1996A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693162 | |||||||
chr1:17693179 | A | G | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-1979A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693179 | |||||||
chr1:17693180 | G | A | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-1978G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693180 | |||||||
chr1:17693194 | AT | A | 2 | a0002c0018t0002g0155 a0003c0002t0001g0038 |
2 | HG03130.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.3185-1961delT | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | 17693194 | ||||||
chr1:17693230 | T | A | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-1928T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693230 | |||||||
chr1:17693235 | A | T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-1923A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693235 | |||||||
chr1:17693237 | T | G | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-1921T>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693237 | |||||||
chr1:17693247 | C | A | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-1911C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693247 | |||||||
chr1:17693247 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(117): Show |
120 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.3185-1911C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693247 | |||||||
chr1:17693248 | G | T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-1910G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693248 | |||||||
chr1:17693250 | T | A | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-1908T>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693250 | |||||||
chr1:17693253 | G | T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-1905G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693253 | |||||||
chr1:17693254 | G | C | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-1904G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693254 | |||||||
chr1:17693255 | A | T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-1903A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693255 | |||||||
chr1:17693257 | C | G | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-1901C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693257 | |||||||
chr1:17693263 | C | T | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-1895C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693263 | |||||||
chr1:17693265 | T | C | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-1893T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693265 | |||||||
chr1:17693266 | C | G | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-1892C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693266 | |||||||
chr1:17693275 | A | C | 1 | a0002c0018t0002g0155 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3185-1883A>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693275 | |||||||
chr1:17693366 | A | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(113): Show |
116 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.3185-1792A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693366 | |||||||
chr1:17693462 | G | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0032 others(17): Show |
20 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.3185-1696G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693462 | |||||||
chr1:17693607 | C | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0070 |
2 | HG01123.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.3185-1551C>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693607 | |||||||
chr1:17693689 | G | A | 23 | a0002c0003t0002g0025 a0002c0003t0002g0037 a0002c0003t0002g0055 others(20): Show |
23 | HG00544.hp2 HG00733.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.3185-1469G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693689 | |||||||
chr1:17693706 | C | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(120): Show |
123 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.3185-1452C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693706 | |||||||
chr1:17693803 | A | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(120): Show |
123 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.3185-1355A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17693803 | |||||||
chr1:17694121 | C | T | 2 | a0001c0044t0004g0161 a0012c0031t0006g0165 |
2 | HG01884.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.3185-1037C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17694121 | |||||||
chr1:17694143 | A | G | 1 | a0021c0030t0002g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3185-1015A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17694143 | |||||||
chr1:17694158 | G | C | 1 | a0001c0001t0001g0014 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3185-1000G>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17694158 | |||||||
chr1:17694190 | A | G | 1 | a0001c0033t0002g0110 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3185-968A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17694190 | |||||||
chr1:17694693 | C | T | 1 | a0020c0049t0004g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3185-465C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17694693 | |||||||
chr1:17694899 | C | G | 1 | a0002c0004t0002g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3185-259C>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17694899 | |||||||
chr1:17694911 | T | C | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(119): Show |
122 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.3185-247T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17694911 | |||||||
chr1:17694914 | G | A | 6 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 others(3): Show |
6 | HG01884.hp1 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.3185-244G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17694914 | |||||||
chr1:17694949 | G | T | 3 | a0001c0013t0001g0008 a0001c0013t0001g0023 a0003c0002t0001g0081 |
3 | HG00738.hp1 HG01074.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.3185-209G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17694949 | |||||||
chr1:17695035 | G | A | 1 | a0002c0004t0002g0036 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3185-123G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17695035 | |||||||
chr1:17695090 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3185-68G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | 17695090 | |||||||
chr1:17695363 | T | C | 23 | a0001c0001t0001g0079 a0002c0003t0002g0025 a0002c0003t0002g0037 others(20): Show |
23 | HG00544.hp2 HG00733.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.3307+83T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | chr1 | 17695363 | |||||||
chr1:17695372 | T | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(118): Show |
121 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.3307+92T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | chr1 | 17695372 | |||||||
chr1:17695432 | G | A | 6 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0043t0002g0051 others(3): Show |
6 | HG01884.hp1 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.3307+152G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | chr1 | 17695432 | |||||||
chr1:17695571 | G | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(121): Show |
124 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.3307+291G>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | chr1 | 17695571 | |||||||
chr1:17695790 | T | TCTG | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(121): Show |
124 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.3307+511_3307+512i others(5): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr1 | 17695790 | ||||||
chr1:17695795 | C | T | 1 | a0004c0005t0002g0060 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3307+515C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | chr1 | 17695795 | |||||||
chr1:17695961 | C | T | 4 | a0002c0003t0002g0133 a0002c0021t0002g0137 a0002c0022t0002g0050 others(1): Show |
4 | HG00544.hp2 NA18612.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.3307+681C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | chr1 | 17695961 | |||||||
chr1:17695994 | T | C | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(113): Show |
116 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.3307+714T>C | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | chr1 | 17695994 | |||||||
chr1:17696045 | A | AAAAAAT | 6 | a0002c0007t0002g0013 a0002c0007t0002g0058 a0002c0007t0002g0085 others(3): Show |
6 | HG00642.hp1 HG02280.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3307+777_3307+782d others(8): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr1 | 17696045 | ||||||
chr1:17696047 | A | T | 1 | a0001c0001t0001g0028 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3307+767A>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | chr1 | 17696047 | |||||||
chr1:17696160 | C | T | 1 | a0017c0037t0001g0142 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3308-688C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | chr1 | 17696160 | |||||||
chr1:17696170 | G | A | 1 | a0002c0003t0002g0133 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3308-678G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | chr1 | 17696170 | |||||||
chr1:17696212 | C | CA | 40 | a0001c0001t0001g0119 a0001c0001t0001g0128 a0001c0001t0001g0159 others(37): Show |
40 | HG00544.hp2 HG00733.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.3308-620dupA | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr1 | 17696212 | ||||||
chr1:17696212 | C | CAA | 104 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(101): Show |
104 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.3308-621_3308-620d others(4): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr1 | 17696212 | ||||||
chr1:17696212 | C | CAAA | 5 | a0001c0001t0001g0125 a0001c0013t0001g0008 a0001c0044t0004g0161 others(2): Show |
5 | HG00738.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3308-622_3308-620d others(5): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr1 | 17696212 | ||||||
chr1:17696386 | C | T | 1 | a0017c0037t0001g0142 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3308-462C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | chr1 | 17696386 | |||||||
chr1:17696438 | G | A | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(111): Show |
114 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.3308-410G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | chr1 | 17696438 | |||||||
chr1:17696616 | C | T | 6 | a0001c0017t0002g0113 a0001c0017t0002g0148 a0001c0033t0002g0110 others(3): Show |
6 | HG02559.hp1 HG02630.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3308-232C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | chr1 | 17696616 | |||||||
chr1:17696617 | A | G | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(119): Show |
122 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.3308-231A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | chr1 | 17696617 | |||||||
chr1:17696659 | A | G | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(120): Show |
123 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.3308-189A>G | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | chr1 | 17696659 | |||||||
chr1:17696766 | G | A | 2 | a0001c0012t0001g0064 a0001c0012t0001g0072 |
2 | HG00738.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.3308-82G>A | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | chr1 | 17696766 | |||||||
chr1:17696795 | C | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(111): Show |
114 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.3308-53C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | chr1 | 17696795 | |||||||
chr1:17696803 | C | T | 1 | a0002c0041t0008g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3308-45C>T | ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | chr1 | 17696803 |