Item | Value |
---|---|
geneid | 57189 |
ensemblid | ENSG00000257093.7 |
hgncid | 29472 |
symbol | DENND11 |
name | DENN domain containing 11 |
refseq_nuc | NM_001080392.2 |
refseq_prot | NP_001073861.1 |
ensembl_nuc | ENST00000536163.6 |
ensembl_prot | ENSP00000445768.1 |
mane_status | MANE Select |
chr | chr7 |
start | 141656728 |
end | 141702166 |
strand | - |
ver | v1.2 |
region | chr7:141656728-141702166 |
region5000 | chr7:141651728-141707166 |
regionname0 | DENND11_chr7_141656728_141702166 |
regionname5000 | DENND11_chr7_141651728_141707166 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 455 | 342 | 75 | 62 | 150 | 16 | 38 | 112 | DENND11_chr7_141651728_141707166 | DENND11 | MVEQG others(450): Show |
chr7 | 141651728 | 141707166 |
a0002 | 0/0 | 455 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | MVEQG others(450): Show |
chr7 | 141651728 | 141707166 |
a0003 | 0/0 | 455 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | MVEQG others(450): Show |
chr7 | 141651728 | 141707166 |
a0004 | 0/0 | 455 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | MVEQG others(450): Show |
chr7 | 141651728 | 141707166 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1365 | 234 | 65 | 48 | 82 | 14 | 25 | DENND11_chr7_141651728_141707166 | DENND11 | ATGGT others(1360): Show |
chr7 | 141651728 | 141707166 | ||
a0001c0002 | 0/1 | 1365 | 103 | 8 | 12 | 67 | 2 | 13 | DENND11_chr7_141651728_141707166 | DENND11 | ATGGT others(1360): Show |
chr7 | 141651728 | 141707166 | ||
a0001c0003 | 0/0 | 1365 | 2 | 0 | 2 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | ATGGT others(1360): Show |
chr7 | 141651728 | 141707166 | ||
a0001c0005 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | ATGGT others(1360): Show |
chr7 | 141651728 | 141707166 | ||
a0001c0007 | 0/0 | 1365 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | ATGGT others(1360): Show |
chr7 | 141651728 | 141707166 | ||
a0001c0008 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | ATGGT others(1360): Show |
chr7 | 141651728 | 141707166 | ||
a0002c0004 | 0/0 | 1365 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | ATGGT others(1360): Show |
chr7 | 141651728 | 141707166 | ||
a0003c0009 | 0/0 | 1365 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | ATGGT others(1360): Show |
chr7 | 141651728 | 141707166 | ||
a0004c0006 | 0/0 | 1365 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | ATGGT others(1360): Show |
chr7 | 141651728 | 141707166 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7309 | 73 | 23 | 10 | 21 | 10 | 9 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0002 | 0/0 | 7309 | 113 | 15 | 25 | 57 | 4 | 12 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0005 | 0/0 | 7309 | 5 | 5 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0006 | 0/0 | 7309 | 5 | 0 | 4 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0007 | 0/0 | 7309 | 4 | 0 | 4 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0008 | 0/0 | 7309 | 4 | 4 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0010 | 0/0 | 7309 | 3 | 0 | 1 | 0 | 0 | 2 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0011 | 0/0 | 7309 | 3 | 2 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0012 | 0/0 | 7309 | 3 | 3 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0013 | 0/0 | 7309 | 3 | 1 | 1 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0014 | 0/0 | 7309 | 2 | 2 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0016 | 0/0 | 7309 | 2 | 2 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0019 | 0/0 | 7309 | 2 | 2 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0020 | 0/0 | 7309 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0021 | 0/0 | 7309 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0022 | 0/0 | 7309 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0023 | 0/0 | 7309 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0024 | 0/0 | 7309 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0025 | 0/0 | 7309 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0026 | 0/0 | 7309 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0028 | 0/0 | 7309 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0029 | 0/0 | 7309 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0030 | 0/0 | 7309 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0032 | 0/0 | 7309 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0001t0035 | 0/0 | 7309 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0002t0001 | 0/1 | 7309 | 63 | 0 | 1 | 53 | 2 | 6 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0002t0003 | 0/0 | 7309 | 22 | 5 | 2 | 8 | 0 | 7 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0002t0004 | 0/0 | 7309 | 7 | 0 | 7 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0002t0009 | 0/0 | 7309 | 3 | 0 | 0 | 3 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0002t0015 | 0/0 | 7309 | 2 | 2 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0002t0017 | 0/0 | 7309 | 2 | 0 | 0 | 2 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0002t0018 | 0/0 | 7309 | 2 | 0 | 2 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0002t0031 | 0/0 | 7309 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0002t0034 | 0/0 | 7309 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0003t0002 | 0/0 | 7309 | 2 | 0 | 2 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0005t0001 | 0/0 | 7309 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0007t0001 | 0/0 | 7309 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0001c0008t0033 | 0/0 | 7309 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0002c0004t0001 | 0/0 | 7309 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0003c0009t0002 | 0/0 | 7309 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
a0004c0006t0027 | 0/0 | 7309 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | GCCTC others(7304): Show |
chr7 | 141651728 | 141707166 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0001 | 0/0 | 9 | 0 | 5 | 4 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0010 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0013 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0005g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0005g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0006g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0006g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0006g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0006g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0006g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0007g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0007g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0007g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0008g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0010g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0010g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0011g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0012g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0012g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0012g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0013g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0013g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0013g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0014g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0014g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0016g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0019g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0019g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0020g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0021g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0022g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0023g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0024g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0025g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0026g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0028g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0029g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0030g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0032g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0001t0035g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0003 | 0/0 | 7 | 0 | 0 | 6 | 1 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0230 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0003g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0003g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0003g0020 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0003g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0004g0002 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0009g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0009g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0009g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0015g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0015g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0017g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0017g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0018g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0031g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0002t0034g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0003t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0003t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0005t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0007t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0001c0008t0033g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0002c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0003c0009t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
a0004c0006t0027g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | GBR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | GBR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | FIN | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0205 | EUR | FIN | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | FIN | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00408 | hp1 | a0001 | c0002 | t0003 | g0019 | EAS | CHS | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | CHS | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00423 | hp1 | a0002 | c0004 | t0001 | g0047 | EAS | CHS | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | CHS | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | CHS | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | CHS | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | CHS | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00733 | hp2 | a0001 | c0001 | t0006 | g0188 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01070 | hp1 | a0001 | c0001 | t0007 | g0045 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01070 | hp2 | a0001 | c0003 | t0002 | g0067 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01071 | hp2 | a0001 | c0003 | t0002 | g0068 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01099 | hp1 | a0001 | c0001 | t0007 | g0045 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01168 | hp2 | a0001 | c0002 | t0003 | g0186 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01175 | hp1 | a0001 | c0001 | t0006 | g0191 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01192 | hp1 | a0001 | c0001 | t0006 | g0185 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01256 | hp2 | a0001 | c0002 | t0018 | g0023 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01257 | hp2 | a0001 | c0001 | t0007 | g0257 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01258 | hp1 | a0001 | c0002 | t0018 | g0023 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01261 | hp1 | a0001 | c0001 | t0013 | g0176 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01261 | hp2 | a0001 | c0001 | t0011 | g0018 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01346 | hp2 | a0001 | c0001 | t0006 | g0102 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0218 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01358 | hp2 | a0001 | c0002 | t0004 | g0002 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01361 | hp2 | a0001 | c0001 | t0026 | g0144 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01433 | hp2 | a0001 | c0001 | t0007 | g0256 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01496 | hp2 | a0001 | c0001 | t0010 | g0036 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | IBS | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | IBS | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0108 | EUR | IBS | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | ACB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01943 | hp1 | a0001 | c0001 | t0020 | g0137 | AMR | PEL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01952 | hp1 | a0001 | c0002 | t0003 | g0014 | AMR | PEL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01952 | hp2 | a0001 | c0002 | t0004 | g0002 | AMR | PEL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01993 | hp2 | a0001 | c0002 | t0004 | g0002 | AMR | PEL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02015 | hp1 | a0001 | c0002 | t0003 | g0020 | EAS | KHV | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | KHV | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02027 | hp1 | a0001 | c0001 | t0025 | g0146 | EAS | KHV | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | KHV | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | KHV | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02055 | hp1 | a0001 | c0002 | t0015 | g0240 | AFR | ACB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | KHV | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | KHV | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02080 | hp1 | a0003 | c0009 | t0002 | g0114 | EAS | KHV | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | KHV | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | KHV | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | KHV | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | KHV | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02145 | hp2 | a0001 | c0001 | t0016 | g0037 | AFR | ACB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PEL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02148 | hp2 | a0001 | c0002 | t0004 | g0002 | AMR | PEL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02155 | hp2 | a0001 | c0002 | t0003 | g0019 | EAS | CDX | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CDX | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02258 | hp2 | a0001 | c0001 | t0035 | g0242 | AFR | ACB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02273 | hp2 | a0001 | c0002 | t0004 | g0002 | AMR | PEL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02280 | hp1 | a0001 | c0001 | t0021 | g0170 | AFR | ACB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02280 | hp2 | a0001 | c0005 | t0001 | g0048 | AFR | ACB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02293 | hp2 | a0001 | c0002 | t0004 | g0002 | AMR | PEL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02602 | hp2 | a0001 | c0002 | t0003 | g0246 | SAS | PJL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02615 | hp1 | a0004 | c0006 | t0027 | g0167 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02615 | hp2 | a0001 | c0001 | t0019 | g0180 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02622 | hp1 | a0001 | c0001 | t0012 | g0052 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02647 | hp2 | a0001 | c0002 | t0003 | g0243 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0202 | SAS | PJL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02698 | hp1 | a0001 | c0001 | t0030 | g0190 | SAS | PJL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02717 | hp1 | a0001 | c0001 | t0012 | g0051 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02723 | hp1 | a0001 | c0001 | t0008 | g0055 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02723 | hp2 | a0001 | c0001 | t0012 | g0255 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02738 | hp2 | a0001 | c0002 | t0003 | g0247 | SAS | PJL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02809 | hp1 | a0001 | c0001 | t0016 | g0037 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02809 | hp2 | a0001 | c0001 | t0008 | g0179 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02896 | hp2 | a0001 | c0001 | t0011 | g0018 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02922 | hp2 | a0001 | c0008 | t0033 | g0050 | AFR | ESN | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0042 | AFR | ESN | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02970 | hp2 | a0001 | c0001 | t0008 | g0054 | AFR | ESN | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0042 | AFR | ESN | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03098 | hp2 | a0001 | c0001 | t0023 | g0103 | AFR | MSL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03130 | hp1 | a0001 | c0002 | t0003 | g0014 | AFR | ESN | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ESN | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | MSL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03225 | hp2 | a0001 | c0001 | t0011 | g0018 | AFR | MSL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03453 | hp1 | a0001 | c0002 | t0034 | g0221 | AFR | MSL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03453 | hp2 | a0001 | c0002 | t0003 | g0159 | AFR | MSL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0027 | SAS | PJL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0027 | SAS | PJL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | ESN | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03540 | hp1 | a0001 | c0001 | t0014 | g0171 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03540 | hp2 | a0001 | c0001 | t0028 | g0184 | AFR | GWD | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03579 | hp1 | a0001 | c0002 | t0003 | g0014 | AFR | MSL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | MSL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03688 | hp2 | a0001 | c0002 | t0003 | g0250 | SAS | STU | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03704 | hp1 | a0001 | c0002 | t0003 | g0020 | SAS | PJL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03704 | hp2 | a0001 | c0001 | t0010 | g0229 | SAS | PJL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03710 | hp2 | a0001 | c0001 | t0010 | g0036 | SAS | PJL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | BEB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03831 | hp2 | a0001 | c0002 | t0003 | g0249 | SAS | BEB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0206 | SAS | BEB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03927 | hp1 | a0001 | c0002 | t0003 | g0225 | SAS | BEB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | BEB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03942 | hp2 | a0001 | c0002 | t0003 | g0020 | SAS | BEB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0070 | SAS | STU | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG04115 | hp2 | a0001 | c0001 | t0006 | g0096 | SAS | STU | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | STU | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | STU | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0139 | SAS | STU | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | YRI | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | CHB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18747 | hp2 | a0001 | c0001 | t0013 | g0183 | EAS | CHB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18906 | hp1 | a0001 | c0001 | t0019 | g0182 | AFR | YRI | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18906 | hp2 | a0001 | c0001 | t0024 | g0238 | AFR | YRI | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18947 | hp1 | a0001 | c0002 | t0031 | g0237 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18949 | hp1 | a0001 | c0002 | t0017 | g0049 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18949 | hp2 | a0001 | c0002 | t0003 | g0019 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18959 | hp2 | a0001 | c0002 | t0003 | g0153 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18960 | hp2 | a0001 | c0001 | t0029 | g0122 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18974 | hp2 | a0001 | c0002 | t0009 | g0213 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18980 | hp2 | a0001 | c0001 | t0022 | g0062 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18987 | hp1 | a0001 | c0002 | t0009 | g0201 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18987 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18992 | hp1 | a0001 | c0002 | t0003 | g0251 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18997 | hp1 | a0001 | c0002 | t0003 | g0252 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19006 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19010 | hp2 | a0001 | c0007 | t0001 | g0200 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19064 | hp2 | a0001 | c0002 | t0003 | g0222 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19066 | hp1 | a0001 | c0002 | t0009 | g0214 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19079 | hp2 | a0001 | c0002 | t0017 | g0056 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | YRI | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA20129 | hp1 | a0001 | c0001 | t0014 | g0239 | AFR | ASW | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ASW | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0003 | EUR | TSI | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0121 | EUR | TSI | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | TSI | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | TSI | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | GIH | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | GIH | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG01123 | hp2 | a0001 | c0002 | t0004 | g0002 | AMR | CLM | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02109 | hp2 | a0001 | c0002 | t0015 | g0241 | AFR | ACB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02486 | hp1 | a0001 | c0002 | t0003 | g0248 | AFR | ACB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02486 | hp2 | a0001 | c0001 | t0032 | g0198 | AFR | ACB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02559 | hp1 | a0001 | c0001 | t0013 | g0166 | AFR | ACB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | MSL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
HG03471 | hp2 | a0001 | c0001 | t0008 | g0053 | AFR | MSL | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | USA | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | USA | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0230 | REF | REF | DENND11_chr7_141651728_141707166 | DENND11 | chr7 | 141651728 | 141707166 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:141674092 | T | C | 1 | a0003 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.656A>G | p.His219Arg | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/9 | 669/7309 | 656/1368 | 219/455 | chr7 | 141674092 | |||
chr7:141685575 | C | G | 1 | a0004 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.430G>C | p.Glu144Gln | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/9 | 443/7309 | 430/1368 | 144/455 | chr7 | 141685575 | |||
chr7:141701958 | G | T | 1 | a0002 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.196C>A | p.Arg66Ser | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/9 | 209/7309 | 196/1368 | 66/455 | chr7 | 141701958 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:141664912 | G | A | 4 | a0001c0002 a0001c0007 a0001c0008 others(1): Show |
105 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
synonymous_variant | LOW | c.1095C>T | p.Asn365Asn | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 7/9 | 1108/7309 | 1095/1368 | 365/455 | chr7 | 141664912 | |||
chr7:141665221 | G | A | 1 | a0001c0008 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.918C>T | p.Ile306Ile | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 6/9 | 931/7309 | 918/1368 | 306/455 | chr7 | 141665221 | |||
chr7:141665233 | G | A | 1 | a0001c0003 | 2 | HG01070.hp2 HG01071.hp2 |
synonymous_variant | LOW | c.906C>T | p.Asn302Asn | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 6/9 | 919/7309 | 906/1368 | 302/455 | chr7 | 141665233 | |||
chr7:141674121 | C | T | 1 | a0001c0007 | 1 | NA19010.hp2 | synonymous_variant | LOW | c.627G>A | p.Leu209Leu | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/9 | 640/7309 | 627/1368 | 209/455 | chr7 | 141674121 | |||
chr7:141701944 | G | T | 1 | a0001c0005 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.210C>A | p.Gly70Gly | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/9 | 223/7309 | 210/1368 | 70/455 | chr7 | 141701944 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:141656840 | T | C | 1 | a0001c0008t0033 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5816A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 5816 | chr7 | 141656840 | ||||||
chr7:141657078 | G | A | 1 | a0001c0001t0019 | 2 | HG02615.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5578C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 5578 | chr7 | 141657078 | ||||||
chr7:141657098 | T | C | 1 | a0004c0006t0027 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5558A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 5558 | chr7 | 141657098 | ||||||
chr7:141657207 | C | T | 2 | a0001c0002t0031 a0001c0002t0034 |
2 | HG03453.hp1 NA18947.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5449G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 5449 | chr7 | 141657207 | ||||||
chr7:141658322 | A | G | 1 | a0001c0002t0034 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4334T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 4334 | chr7 | 141658322 | ||||||
chr7:141658353 | A | G | 1 | a0001c0002t0003 | 22 | HG00408.hp1 HG01168.hp2 HG01952.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4303T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 4303 | chr7 | 141658353 | ||||||
chr7:141658492 | G | A | 1 | a0001c0001t0011 | 3 | HG01261.hp2 HG02896.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4164C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 4164 | chr7 | 141658492 | ||||||
chr7:141658559 | T | C | 1 | a0001c0008t0033 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4097A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 4097 | chr7 | 141658559 | ||||||
chr7:141658595 | A | T | 1 | a0001c0002t0017 | 2 | NA18949.hp1 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4061T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 4061 | chr7 | 141658595 | ||||||
chr7:141658644 | A | T | 1 | a0001c0001t0026 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4012T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 4012 | chr7 | 141658644 | ||||||
chr7:141658720 | A | G | 1 | a0001c0001t0025 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3936T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 3936 | chr7 | 141658720 | ||||||
chr7:141658805 | A | C | 1 | a0001c0001t0012 | 3 | HG02622.hp1 HG02717.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3851T>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 3851 | chr7 | 141658805 | ||||||
chr7:141658806 | C | T | 1 | a0001c0001t0030 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3850G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 3850 | chr7 | 141658806 | ||||||
chr7:141658945 | C | G | 1 | a0001c0001t0016 | 2 | HG02145.hp2 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3711G>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 3711 | chr7 | 141658945 | ||||||
chr7:141658948 | A | G | 1 | a0001c0001t0029 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3708T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 3708 | chr7 | 141658948 | ||||||
chr7:141659298 | C | T | 1 | a0001c0001t0006 | 5 | HG00733.hp2 HG01175.hp1 HG01192.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3358G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 3358 | chr7 | 141659298 | ||||||
chr7:141659595 | A | T | 1 | a0001c0002t0018 | 2 | HG01256.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3061T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 3061 | chr7 | 141659595 | ||||||
chr7:141659827 | C | T | 2 | a0001c0002t0004 a0001c0002t0018 |
9 | HG01123.hp2 HG01256.hp2 HG01258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2829G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 2829 | chr7 | 141659827 | ||||||
chr7:141659868 | G | C | 2 | a0001c0001t0013 a0001c0001t0021 |
4 | HG01261.hp1 HG02280.hp1 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2788C>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 2788 | chr7 | 141659868 | ||||||
chr7:141660119 | A | T | 1 | a0001c0001t0005 | 5 | HG01891.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2537T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 2537 | chr7 | 141660119 | ||||||
chr7:141660634 | T | C | 3 | a0001c0001t0008 a0001c0001t0011 a0001c0002t0034 |
8 | HG01261.hp2 HG02723.hp1 HG02809.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2022A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 2022 | chr7 | 141660634 | ||||||
chr7:141660710 | A | G | 1 | a0001c0001t0028 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1946T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 1946 | chr7 | 141660710 | ||||||
chr7:141660726 | T | C | 1 | a0001c0001t0032 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1930A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 1930 | chr7 | 141660726 | ||||||
chr7:141660744 | T | A | 1 | a0001c0001t0024 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1912A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 1912 | chr7 | 141660744 | ||||||
chr7:141660785 | A | G | 20 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(17): Show |
167 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*1871T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 1871 | chr7 | 141660785 | ||||||
chr7:141660822 | C | T | 5 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0024 others(2): Show |
11 | HG01261.hp2 HG02055.hp1 HG02109.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1834G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 1834 | chr7 | 141660822 | ||||||
chr7:141660897 | A | C | 1 | a0001c0001t0023 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1759T>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 1759 | chr7 | 141660897 | ||||||
chr7:141660981 | T | G | 1 | a0001c0008t0033 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1675A>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 1675 | chr7 | 141660981 | ||||||
chr7:141661192 | C | T | 2 | a0001c0002t0003 a0001c0008t0033 |
23 | HG00408.hp1 HG01168.hp2 HG01952.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1464G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 1464 | chr7 | 141661192 | ||||||
chr7:141661217 | C | T | 1 | a0001c0001t0022 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1439G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 1439 | chr7 | 141661217 | ||||||
chr7:141661261 | G | A | 1 | a0001c0001t0014 | 2 | HG03540.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1395C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 1395 | chr7 | 141661261 | ||||||
chr7:141661315 | A | G | 1 | a0001c0001t0021 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1341T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 1341 | chr7 | 141661315 | ||||||
chr7:141661475 | C | T | 1 | a0001c0001t0014 | 2 | HG03540.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1181G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 1181 | chr7 | 141661475 | ||||||
chr7:141661622 | T | G | 2 | a0001c0002t0003 a0001c0008t0033 |
23 | HG00408.hp1 HG01168.hp2 HG01952.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1034A>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 1034 | chr7 | 141661622 | ||||||
chr7:141661626 | C | T | 1 | a0001c0001t0035 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1030G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 1030 | chr7 | 141661626 | ||||||
chr7:141662055 | T | C | 1 | a0001c0002t0034 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*601A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 601 | chr7 | 141662055 | ||||||
chr7:141662138 | A | G | 1 | a0001c0001t0010 | 3 | HG01496.hp2 HG03704.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*518T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 518 | chr7 | 141662138 | ||||||
chr7:141662265 | A | T | 1 | a0001c0001t0035 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*391T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 391 | chr7 | 141662265 | ||||||
chr7:141662307 | C | A | 1 | a0001c0001t0035 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*349G>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 349 | chr7 | 141662307 | ||||||
chr7:141662319 | A | T | 1 | a0001c0002t0009 | 3 | NA18974.hp2 NA18987.hp1 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*337T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 337 | chr7 | 141662319 | ||||||
chr7:141662415 | G | T | 1 | a0001c0001t0020 | 1 | HG01943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*241C>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 241 | chr7 | 141662415 | ||||||
chr7:141662631 | T | C | 40 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(37): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
3_prime_UTR_variant | MODIFIER | c.*25A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 9/9 | 25 | chr7 | 141662631 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:141662885 | C | G | 17 | a0001c0002t0003g0014 a0001c0002t0003g0019 a0001c0002t0003g0020 others(14): Show |
23 | HG00408.hp1 HG01168.hp2 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.1173-34G>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 8/8 | chr7 | 141662885 | |||||||
chr7:141662889 | G | C | 1 | a0001c0001t0002g0058 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1173-38C>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 8/8 | chr7 | 141662889 | |||||||
chr7:141662889 | G | GGC | 17 | a0001c0002t0003g0014 a0001c0002t0003g0019 a0001c0002t0003g0020 others(14): Show |
23 | HG00408.hp1 HG01168.hp2 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.1173-39_1173-38ins others(2): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 8/8 | chr7 | 141662889 | |||||||
chr7:141662893 | A | T | 85 | a0001c0001t0001g0071 a0001c0001t0001g0104 a0001c0001t0001g0133 others(82): Show |
110 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1173-42T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 8/8 | chr7 | 141662893 | |||||||
chr7:141662972 | G | A | 3 | a0001c0001t0002g0140 a0001c0001t0002g0141 a0001c0001t0002g0253 |
3 | HG02083.hp2 NA19012.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1173-121C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 8/8 | chr7 | 141662972 | |||||||
chr7:141662994 | AAAGAGT | A | 17 | a0001c0002t0003g0014 a0001c0002t0003g0019 a0001c0002t0003g0020 others(14): Show |
23 | HG00408.hp1 HG01168.hp2 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.1173-149_1173-144d others(8): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 8/8 | chr7 | 141662994 | |||||||
chr7:141663233 | G | A | 1 | a0001c0001t0002g0155 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1173-382C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 8/8 | chr7 | 141663233 | |||||||
chr7:141663466 | A | G | 1 | a0001c0008t0033g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1173-615T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 8/8 | chr7 | 141663466 | |||||||
chr7:141663514 | A | G | 1 | a0001c0002t0001g0211 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1172+658T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 8/8 | chr7 | 141663514 | |||||||
chr7:141663553 | A | AG | 252 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(249): Show |
337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.1172+618dupC | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 8/8 | chr7 | 141663553 | |||||||
chr7:141663781 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1172+391G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 8/8 | chr7 | 141663781 | |||||||
chr7:141663950 | T | C | 1 | a0001c0001t0011g0018 | 3 | HG01261.hp2 HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1172+222A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 8/8 | chr7 | 141663950 | |||||||
chr7:141664042 | C | T | 58 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 others(55): Show |
84 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1172+130G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 8/8 | chr7 | 141664042 | |||||||
chr7:141664051 | G | A | 2 | a0001c0002t0004g0002 a0001c0002t0018g0023 |
9 | HG01123.hp2 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1172+121C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 8/8 | chr7 | 141664051 | |||||||
chr7:141664072 | G | A | 2 | a0001c0002t0001g0203 a0001c0002t0001g0216 |
2 | NA18948.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1172+100C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 8/8 | chr7 | 141664072 | |||||||
chr7:141664157 | G | A | 2 | a0001c0002t0017g0049 a0001c0002t0017g0056 |
2 | NA18949.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1172+15C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 8/8 | chr7 | 141664157 | |||||||
chr7:141664416 | T | C | 68 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0009 others(65): Show |
100 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1104-176A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 7/8 | chr7 | 141664416 | |||||||
chr7:141664478 | G | A | 69 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0009 others(66): Show |
101 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1104-238C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 7/8 | chr7 | 141664478 | |||||||
chr7:141664547 | C | T | 2 | a0001c0002t0001g0069 a0001c0002t0001g0086 |
2 | NA18950.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1104-307G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 7/8 | chr7 | 141664547 | |||||||
chr7:141664592 | C | T | 3 | a0001c0002t0003g0019 a0001c0002t0003g0250 a0001c0002t0003g0251 |
5 | HG00408.hp1 HG02155.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.1103+312G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 7/8 | chr7 | 141664592 | |||||||
chr7:141664679 | T | G | 69 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0009 others(66): Show |
101 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1103+225A>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 7/8 | chr7 | 141664679 | |||||||
chr7:141664781 | G | C | 6 | a0001c0001t0001g0028 a0001c0001t0001g0059 a0001c0001t0001g0060 others(3): Show |
7 | HG02165.hp2 NA18956.hp1 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.1103+123C>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 7/8 | chr7 | 141664781 | |||||||
chr7:141665328 | T | C | 73 | a0001c0001t0001g0038 a0001c0001t0001g0193 a0001c0001t0001g0194 others(70): Show |
106 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.821-10A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 5/8 | chr7 | 141665328 | |||||||
chr7:141665335 | G | A | 1 | a0001c0008t0033g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.821-17C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 5/8 | chr7 | 141665335 | |||||||
chr7:141665345 | G | C | 3 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 |
3 | HG02723.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.821-27C>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 5/8 | chr7 | 141665345 | |||||||
chr7:141665377 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.821-59G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 5/8 | chr7 | 141665377 | |||||||
chr7:141665461 | G | A | 1 | a0001c0002t0003g0186 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.821-143C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 5/8 | chr7 | 141665461 | |||||||
chr7:141665597 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.821-279G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 5/8 | chr7 | 141665597 | |||||||
chr7:141665625 | TTCCCCCT others(8): Show |
T | 2 | a0001c0001t0005g0017 a0001c0001t0005g0042 |
5 | HG01891.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.821-322_821-308del others(15): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 5/8 | chr7 | 141665625 | |||||||
chr7:141665691 | C | G | 68 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0009 others(65): Show |
100 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.821-373G>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 5/8 | chr7 | 141665691 | |||||||
chr7:141665811 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.820+476C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 5/8 | chr7 | 141665811 | |||||||
chr7:141665905 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0196 a0001c0001t0001g0197 others(2): Show |
8 | HG00735.hp2 HG02055.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.820+382G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 5/8 | chr7 | 141665905 | |||||||
chr7:141666058 | C | T | 1 | a0001c0002t0001g0219 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.820+229G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 5/8 | chr7 | 141666058 | |||||||
chr7:141666454 | G | C | 2 | a0001c0002t0017g0049 a0001c0002t0017g0056 |
2 | NA18949.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.682-29C>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141666454 | |||||||
chr7:141666522 | A | G | 1 | a0001c0001t0002g0127 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.682-97T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141666522 | |||||||
chr7:141666711 | A | T | 68 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0009 others(65): Show |
100 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.682-286T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141666711 | |||||||
chr7:141666757 | C | T | 1 | a0001c0001t0019g0180 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.682-332G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141666757 | |||||||
chr7:141666839 | A | G | 91 | a0001c0001t0001g0028 a0001c0001t0001g0059 a0001c0001t0001g0060 others(88): Show |
117 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.682-414T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141666839 | |||||||
chr7:141666883 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0089 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.682-458C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141666883 | |||||||
chr7:141666927 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.682-502G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141666927 | |||||||
chr7:141666966 | C | T | 1 | a0001c0001t0035g0242 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.682-541G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141666966 | |||||||
chr7:141666987 | T | C | 68 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0009 others(65): Show |
100 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.682-562A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141666987 | |||||||
chr7:141667149 | G | T | 1 | a0001c0001t0002g0140 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.682-724C>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141667149 | |||||||
chr7:141667218 | G | A | 2 | a0001c0002t0003g0159 a0001c0002t0003g0248 |
2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.682-793C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141667218 | |||||||
chr7:141667328 | G | A | 66 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0009 others(63): Show |
96 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.682-903C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141667328 | |||||||
chr7:141667555 | CCTTGTGA others(1): Show |
C | 67 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0009 others(64): Show |
97 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.682-1138_682-1131d others(10): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141667555 | |||||||
chr7:141667619 | T | G | 67 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0009 others(64): Show |
97 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.682-1194A>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141667619 | |||||||
chr7:141667671 | G | A | 1 | a0001c0002t0003g0014 | 3 | HG01952.hp1 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.682-1246C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141667671 | |||||||
chr7:141667711 | T | C | 68 | a0001c0001t0002g0106 a0001c0002t0001g0003 a0001c0002t0001g0004 others(65): Show |
98 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.682-1286A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141667711 | |||||||
chr7:141667782 | T | C | 67 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0009 others(64): Show |
97 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.682-1357A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141667782 | |||||||
chr7:141667785 | C | G | 5 | a0001c0002t0001g0094 a0001c0002t0001g0142 a0001c0002t0001g0143 others(2): Show |
5 | HG00438.hp1 HG00621.hp2 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.682-1360G>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141667785 | |||||||
chr7:141667876 | A | C | 67 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0009 others(64): Show |
97 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.682-1451T>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141667876 | |||||||
chr7:141667885 | T | C | 1 | a0001c0001t0035g0242 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.682-1460A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141667885 | |||||||
chr7:141667903 | C | T | 67 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0009 others(64): Show |
97 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.682-1478G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141667903 | |||||||
chr7:141667963 | G | A | 4 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 others(1): Show |
4 | HG02723.hp1 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-1538C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141667963 | |||||||
chr7:141667969 | T | G | 2 | a0001c0002t0017g0049 a0001c0002t0017g0056 |
2 | NA18949.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.682-1544A>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141667969 | |||||||
chr7:141668009 | C | A | 1 | a0001c0001t0006g0096 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.682-1584G>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141668009 | |||||||
chr7:141668038 | G | A | 66 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0009 others(63): Show |
96 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.682-1613C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141668038 | |||||||
chr7:141668039 | T | C | 66 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0009 others(63): Show |
96 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.682-1614A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141668039 | |||||||
chr7:141668113 | T | C | 66 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0009 others(63): Show |
96 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.682-1688A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141668113 | |||||||
chr7:141668114 | G | A | 66 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0009 others(63): Show |
96 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.682-1689C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141668114 | |||||||
chr7:141668197 | T | C | 66 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0009 others(63): Show |
96 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.682-1772A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141668197 | |||||||
chr7:141668203 | A | T | 66 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0009 others(63): Show |
96 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.682-1778T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141668203 | |||||||
chr7:141668344 | TG | T | 65 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0009 others(62): Show |
95 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.682-1920delC | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141668344 | |||||||
chr7:141668423 | A | G | 1 | a0001c0002t0034g0221 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.682-1998T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141668423 | |||||||
chr7:141668428 | T | C | 3 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 |
3 | HG02723.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.682-2003A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141668428 | |||||||
chr7:141668500 | T | C | 179 | a0001c0001t0001g0028 a0001c0001t0001g0038 a0001c0001t0001g0059 others(176): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.682-2075A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141668500 | |||||||
chr7:141668509 | C | G | 63 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0009 others(60): Show |
93 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.682-2084G>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141668509 | |||||||
chr7:141668541 | A | G | 65 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0009 others(62): Show |
95 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.682-2116T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141668541 | |||||||
chr7:141668600 | C | A | 3 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 |
3 | HG02723.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.682-2175G>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141668600 | |||||||
chr7:141668600 | C | CA | 67 | a0001c0001t0024g0238 a0001c0002t0001g0003 a0001c0002t0001g0004 others(64): Show |
97 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.682-2176dupT | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141668600 | |||||||
chr7:141668786 | C | G | 68 | a0001c0001t0002g0058 a0001c0001t0024g0238 a0001c0002t0001g0003 others(65): Show |
98 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.682-2361G>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141668786 | |||||||
chr7:141668830 | T | C | 3 | a0001c0001t0011g0018 a0001c0001t0014g0171 a0001c0001t0014g0239 |
5 | HG01261.hp2 HG02896.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.682-2405A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141668830 | |||||||
chr7:141668865 | C | CTG | 69 | a0001c0001t0002g0026 a0001c0001t0002g0058 a0001c0001t0024g0238 others(66): Show |
100 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.682-2442_682-2441d others(4): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141668865 | |||||||
chr7:141668908 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0160 |
3 | HG02109.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.682-2483C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141668908 | |||||||
chr7:141669038 | T | A | 66 | a0001c0001t0002g0026 a0001c0001t0002g0080 a0001c0001t0002g0082 others(63): Show |
97 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.682-2613A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141669038 | |||||||
chr7:141669072 | C | A | 1 | a0001c0008t0033g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.682-2647G>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141669072 | |||||||
chr7:141669207 | A | G | 66 | a0001c0001t0002g0026 a0001c0001t0024g0238 a0001c0002t0001g0003 others(63): Show |
97 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.682-2782T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141669207 | |||||||
chr7:141669244 | G | GT | 65 | a0001c0001t0001g0168 a0001c0001t0002g0026 a0001c0001t0002g0132 others(62): Show |
95 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.682-2820dupA | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141669244 | |||||||
chr7:141669244 | G | GTT | 6 | a0001c0002t0001g0041 a0001c0002t0001g0094 a0001c0002t0001g0105 others(3): Show |
7 | HG02056.hp2 HG02738.hp2 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.682-2821_682-2820d others(4): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141669244 | |||||||
chr7:141669244 | GT | G | 5 | a0001c0001t0002g0138 a0001c0001t0006g0188 a0001c0001t0016g0037 others(2): Show |
6 | HG00733.hp2 HG02145.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.682-2820delA | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141669244 | |||||||
chr7:141669251 | T | G | 2 | a0001c0002t0015g0240 a0001c0002t0015g0241 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.682-2826A>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141669251 | |||||||
chr7:141669254 | T | G | 1 | a0001c0001t0001g0057 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.682-2829A>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141669254 | |||||||
chr7:141669418 | T | C | 1 | a0001c0001t0002g0199 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.682-2993A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141669418 | |||||||
chr7:141669482 | AT | A | 91 | a0001c0001t0001g0028 a0001c0001t0001g0059 a0001c0001t0001g0060 others(88): Show |
116 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.682-3058delA | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141669482 | |||||||
chr7:141669670 | A | T | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.682-3245T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141669670 | |||||||
chr7:141669797 | ATCATACA others(305): Show |
A | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.682-3684_682-3373d others(2): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141669797 | |||||||
chr7:141669809 | A | AT | 39 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(36): Show |
44 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.682-3385dupA | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141669809 | |||||||
chr7:141669809 | A | ATT | 48 | a0001c0001t0001g0008 a0001c0001t0001g0148 a0001c0001t0002g0001 others(45): Show |
57 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.682-3386_682-3385d others(4): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141669809 | |||||||
chr7:141669809 | A | ATTT | 44 | a0001c0001t0001g0028 a0001c0001t0001g0059 a0001c0001t0001g0060 others(41): Show |
54 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.682-3387_682-3385d others(5): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141669809 | |||||||
chr7:141669883 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0197 a0001c0005t0001g0048 |
5 | HG00735.hp2 HG02280.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.682-3458G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141669883 | |||||||
chr7:141669890 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0197 a0001c0005t0001g0048 |
5 | HG00735.hp2 HG02280.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.682-3465C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141669890 | |||||||
chr7:141670029 | C | T | 2 | a0001c0001t0005g0017 a0001c0001t0005g0042 |
5 | HG01891.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.682-3604G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141670029 | |||||||
chr7:141670045 | C | G | 2 | a0001c0001t0002g0005 a0001c0001t0002g0128 |
2 | HG01167.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.682-3620G>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141670045 | |||||||
chr7:141670061 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.682-3636G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141670061 | |||||||
chr7:141670070 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.682-3645T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141670070 | |||||||
chr7:141670092 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.682-3667C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141670092 | |||||||
chr7:141670105 | C | T | 1 | a0001c0001t0002g0011 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.682-3680G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141670105 | |||||||
chr7:141670131 | A | G | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.682-3706T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141670131 | |||||||
chr7:141670618 | C | T | 1 | a0001c0002t0001g0105 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.681+3449G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141670618 | |||||||
chr7:141670673 | T | C | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.681+3394A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141670673 | |||||||
chr7:141670697 | G | A | 2 | a0001c0002t0017g0049 a0001c0002t0017g0056 |
2 | NA18949.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.681+3370C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141670697 | |||||||
chr7:141670737 | A | G | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.681+3330T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141670737 | |||||||
chr7:141670801 | T | C | 2 | a0001c0002t0017g0049 a0001c0002t0017g0056 |
2 | NA18949.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.681+3266A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141670801 | |||||||
chr7:141670805 | C | T | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.681+3262G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141670805 | |||||||
chr7:141670837 | G | A | 1 | a0001c0002t0001g0217 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.681+3230C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141670837 | |||||||
chr7:141670900 | A | G | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.681+3167T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141670900 | |||||||
chr7:141670903 | G | T | 68 | a0001c0001t0002g0026 a0001c0001t0024g0238 a0001c0002t0001g0003 others(65): Show |
99 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.681+3164C>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141670903 | |||||||
chr7:141671014 | C | G | 1 | a0001c0001t0023g0103 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.681+3053G>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141671014 | |||||||
chr7:141671020 | A | G | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.681+3047T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141671020 | |||||||
chr7:141671122 | G | A | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.681+2945C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141671122 | |||||||
chr7:141671205 | C | G | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.681+2862G>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141671205 | |||||||
chr7:141671405 | G | A | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.681+2662C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141671405 | |||||||
chr7:141671476 | C | T | 2 | a0001c0002t0004g0002 a0001c0002t0018g0023 |
9 | HG01123.hp2 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.681+2591G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141671476 | |||||||
chr7:141671479 | T | A | 1 | a0001c0002t0001g0218 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.681+2588A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141671479 | |||||||
chr7:141671542 | C | G | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.681+2525G>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141671542 | |||||||
chr7:141671554 | C | T | 1 | a0001c0002t0003g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.681+2513G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141671554 | |||||||
chr7:141671555 | G | A | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.681+2512C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141671555 | |||||||
chr7:141671765 | G | A | 2 | a0001c0002t0015g0240 a0001c0002t0015g0241 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.681+2302C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141671765 | |||||||
chr7:141671898 | G | T | 1 | a0001c0008t0033g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.681+2169C>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141671898 | |||||||
chr7:141671993 | T | C | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.681+2074A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141671993 | |||||||
chr7:141672007 | G | C | 66 | a0001c0001t0002g0026 a0001c0002t0001g0003 a0001c0002t0001g0004 others(63): Show |
96 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.681+2060C>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141672007 | |||||||
chr7:141672014 | T | C | 1 | a0001c0002t0001g0209 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.681+2053A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141672014 | |||||||
chr7:141672051 | C | T | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.681+2016G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141672051 | |||||||
chr7:141672067 | T | C | 2 | a0001c0001t0002g0026 a0001c0002t0001g0095 |
3 | NA18979.hp1 NA18984.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.681+2000A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141672067 | |||||||
chr7:141672078 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.681+1989G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141672078 | |||||||
chr7:141672277 | T | C | 2 | a0001c0001t0005g0017 a0001c0001t0005g0042 |
5 | HG01891.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+1790A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141672277 | |||||||
chr7:141672404 | T | C | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.681+1663A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141672404 | |||||||
chr7:141672527 | T | A | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.681+1540A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141672527 | |||||||
chr7:141672573 | T | C | 2 | a0001c0002t0017g0049 a0001c0002t0017g0056 |
2 | NA18949.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.681+1494A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141672573 | |||||||
chr7:141672618 | A | T | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.681+1449T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141672618 | |||||||
chr7:141672949 | C | G | 6 | a0001c0001t0001g0028 a0001c0001t0001g0059 a0001c0001t0001g0060 others(3): Show |
7 | HG02165.hp2 NA18956.hp1 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.681+1118G>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141672949 | |||||||
chr7:141673098 | G | A | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.681+969C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141673098 | |||||||
chr7:141673106 | G | A | 50 | a0001c0001t0002g0026 a0001c0002t0001g0003 a0001c0002t0001g0004 others(47): Show |
77 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.681+961C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141673106 | |||||||
chr7:141673228 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.681+839G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141673228 | |||||||
chr7:141673242 | A | T | 68 | a0001c0001t0001g0057 a0001c0001t0002g0026 a0001c0002t0001g0003 others(65): Show |
99 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.681+825T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141673242 | |||||||
chr7:141673244 | A | T | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.681+823T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141673244 | |||||||
chr7:141673245 | A | T | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.681+822T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141673245 | |||||||
chr7:141673250 | A | C | 1 | a0001c0008t0033g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.681+817T>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141673250 | |||||||
chr7:141673256 | A | C | 68 | a0001c0001t0001g0057 a0001c0001t0002g0026 a0001c0002t0001g0003 others(65): Show |
99 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.681+811T>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141673256 | |||||||
chr7:141673257 | C | A | 1 | a0001c0001t0002g0058 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.681+810G>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141673257 | |||||||
chr7:141673299 | A | G | 4 | a0001c0001t0013g0166 a0001c0001t0013g0176 a0001c0001t0013g0183 others(1): Show |
4 | HG01261.hp1 HG02280.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+768T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141673299 | |||||||
chr7:141673423 | C | T | 86 | a0001c0001t0001g0028 a0001c0001t0001g0059 a0001c0001t0001g0060 others(83): Show |
110 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.681+644G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141673423 | |||||||
chr7:141673478 | G | A | 12 | a0001c0001t0001g0104 a0001c0001t0001g0107 a0001c0001t0001g0164 others(9): Show |
14 | HG01261.hp1 HG01891.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.681+589C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141673478 | |||||||
chr7:141673654 | A | C | 1 | a0001c0008t0033g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.681+413T>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141673654 | |||||||
chr7:141673697 | C | T | 2 | a0001c0002t0017g0049 a0001c0002t0017g0056 |
2 | NA18949.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.681+370G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141673697 | |||||||
chr7:141673822 | A | G | 1 | a0001c0001t0035g0242 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.681+245T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141673822 | |||||||
chr7:141673840 | A | G | 3 | a0001c0002t0009g0201 a0001c0002t0009g0213 a0001c0002t0009g0214 |
3 | NA18974.hp2 NA18987.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.681+227T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141673840 | |||||||
chr7:141674000 | G | T | 9 | a0001c0001t0002g0058 a0001c0001t0008g0053 a0001c0001t0008g0054 others(6): Show |
9 | HG02258.hp2 HG02723.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.681+67C>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141674000 | |||||||
chr7:141674025 | T | A | 1 | a0001c0001t0013g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.681+42A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141674025 | |||||||
chr7:141674039 | A | C | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.681+28T>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 4/8 | chr7 | 141674039 | |||||||
chr7:141674227 | A | G | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | splice_region_variant&intron_variant | LOW | c.528-7T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674227 | |||||||
chr7:141674230 | A | AAC | 15 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0175 others(12): Show |
18 | HG00140.hp2 HG00733.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.528-12_528-11dupGT | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674230 | |||||||
chr7:141674230 | A | AACAC | 3 | a0001c0001t0001g0088 a0001c0001t0002g0033 a0001c0001t0006g0096 |
4 | HG02895.hp1 HG02897.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.528-14_528-11dupGT others(2): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674230 | |||||||
chr7:141674230 | A | AACACAC | 3 | a0001c0001t0001g0087 a0001c0001t0011g0018 a0001c0002t0003g0243 |
5 | HG01261.hp2 HG01943.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.528-16_528-11dupGT others(4): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674230 | |||||||
chr7:141674230 | A | AACACACA others(11): Show |
1 | a0001c0001t0002g0058 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.528-28_528-11dupGT others(16): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674230 | |||||||
chr7:141674230 | A | AACACACA others(17): Show |
2 | a0001c0001t0035g0242 a0001c0008t0033g0050 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.528-34_528-11dupGT others(22): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674230 | |||||||
chr7:141674230 | A | AACACACA others(21): Show |
1 | a0001c0002t0017g0049 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.528-38_528-11dupGT others(26): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674230 | |||||||
chr7:141674230 | A | AACACACA others(23): Show |
2 | a0001c0001t0008g0053 a0001c0002t0017g0056 |
2 | HG03471.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.528-11_528-10insGT others(28): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674230 | |||||||
chr7:141674230 | A | AACACACA others(27): Show |
1 | a0001c0001t0008g0055 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.528-11_528-10insGT others(32): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674230 | |||||||
chr7:141674230 | A | AACACACA others(31): Show |
1 | a0001c0001t0008g0054 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.528-11_528-10insGT others(36): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674230 | |||||||
chr7:141674236 | C | CACACACA others(35): Show |
1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.528-17_528-16insAT others(40): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674236 | |||||||
chr7:141674305 | G | A | 1 | a0003c0009t0002g0114 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.528-85C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674305 | |||||||
chr7:141674315 | AG | A | 171 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0059 others(168): Show |
232 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.528-96delC | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674315 | |||||||
chr7:141674350 | T | C | 1 | a0001c0001t0013g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.528-130A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674350 | |||||||
chr7:141674528 | G | C | 1 | a0001c0001t0002g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.528-308C>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674528 | |||||||
chr7:141674532 | G | C | 1 | a0001c0001t0028g0184 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.528-312C>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674532 | |||||||
chr7:141674562 | G | A | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.528-342C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674562 | |||||||
chr7:141674724 | T | C | 3 | a0001c0001t0002g0058 a0001c0001t0035g0242 a0001c0002t0003g0243 |
3 | HG02258.hp2 HG02647.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.528-504A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674724 | |||||||
chr7:141674807 | T | C | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.528-587A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674807 | |||||||
chr7:141674813 | A | G | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.528-593T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674813 | |||||||
chr7:141674928 | C | G | 1 | a0001c0002t0015g0240 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.528-708G>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674928 | |||||||
chr7:141674980 | A | G | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.528-760T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141674980 | |||||||
chr7:141675028 | C | T | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.528-808G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141675028 | |||||||
chr7:141675123 | C | G | 1 | a0001c0001t0002g0234 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.528-903G>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141675123 | |||||||
chr7:141675278 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0024g0238 |
2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.528-1058G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141675278 | |||||||
chr7:141675661 | G | A | 2 | a0001c0001t0002g0132 a0001c0001t0002g0235 |
2 | NA18947.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.528-1441C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141675661 | |||||||
chr7:141675811 | C | T | 2 | a0001c0002t0015g0240 a0001c0002t0015g0241 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.528-1591G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141675811 | |||||||
chr7:141676013 | C | A | 1 | a0001c0002t0001g0224 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.528-1793G>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141676013 | |||||||
chr7:141676025 | A | G | 1 | a0001c0001t0035g0242 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.528-1805T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141676025 | |||||||
chr7:141676315 | T | C | 4 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 others(1): Show |
4 | HG02723.hp1 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.528-2095A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141676315 | |||||||
chr7:141676335 | A | C | 2 | a0001c0002t0017g0049 a0001c0002t0017g0056 |
2 | NA18949.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.528-2115T>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141676335 | |||||||
chr7:141676409 | T | A | 1 | a0001c0002t0003g0246 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.528-2189A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141676409 | |||||||
chr7:141676617 | T | A | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.528-2397A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141676617 | |||||||
chr7:141676657 | C | T | 1 | a0001c0002t0001g0016 | 3 | NA18957.hp1 NA18975.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.528-2437G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141676657 | |||||||
chr7:141676830 | C | T | 1 | a0001c0001t0035g0242 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.528-2610G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141676830 | |||||||
chr7:141676871 | C | T | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.528-2651G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141676871 | |||||||
chr7:141676996 | G | A | 1 | a0001c0002t0001g0206 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.528-2776C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141676996 | |||||||
chr7:141677294 | C | T | 1 | a0001c0002t0001g0212 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.528-3074G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677294 | |||||||
chr7:141677335 | C | T | 2 | a0001c0003t0002g0067 a0001c0003t0002g0068 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.528-3115G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677335 | |||||||
chr7:141677336 | G | A | 2 | a0001c0002t0017g0049 a0001c0002t0017g0056 |
2 | NA18949.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.528-3116C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677336 | |||||||
chr7:141677390 | CA | C | 3 | a0001c0001t0005g0017 a0001c0001t0005g0042 a0001c0002t0001g0211 |
6 | HG01891.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.528-3171delT | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677390 | |||||||
chr7:141677400 | AAAAT | A | 47 | a0001c0001t0001g0028 a0001c0001t0001g0059 a0001c0001t0001g0060 others(44): Show |
55 | HG00140.hp1 HG00438.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.528-3184_528-3181d others(6): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677400 | |||||||
chr7:141677401 | AAAT | A | 14 | a0001c0001t0001g0057 a0001c0001t0002g0080 a0001c0001t0002g0082 others(11): Show |
18 | HG00408.hp1 HG01168.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.528-3184_528-3182d others(5): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677401 | |||||||
chr7:141677402 | A | AT | 3 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0168 |
3 | HG00280.hp2 HG01891.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.528-3183_528-3182i others(3): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677402 | |||||||
chr7:141677402 | A | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0164 a0001c0001t0001g0172 others(5): Show |
8 | HG01346.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.528-3182T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677402 | |||||||
chr7:141677403 | AT | A | 48 | a0001c0001t0002g0026 a0001c0002t0001g0003 a0001c0002t0001g0004 others(45): Show |
73 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.528-3184delA | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677403 | |||||||
chr7:141677403 | ATATAT | A | 1 | a0001c0001t0011g0018 | 3 | HG01261.hp2 HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.528-3188_528-3184d others(7): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677403 | |||||||
chr7:141677404 | T | A | 24 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0043 others(21): Show |
29 | HG00140.hp2 HG00642.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.528-3184A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677404 | |||||||
chr7:141677406 | T | A | 6 | a0001c0001t0006g0185 a0001c0002t0001g0209 a0001c0002t0001g0219 others(3): Show |
6 | HG01192.hp1 HG02647.hp2 NA19006.hp1 others(3): Show |
intron_variant | MODIFIER | c.528-3186A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677406 | |||||||
chr7:141677420 | TATAC | T | 38 | a0001c0001t0001g0061 a0001c0001t0002g0001 a0001c0001t0002g0005 others(35): Show |
53 | HG00558.hp1 HG00673.hp1 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.528-3204_528-3201d others(6): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677420 | |||||||
chr7:141677424 | C | T | 67 | a0001c0001t0001g0028 a0001c0001t0001g0059 a0001c0001t0001g0060 others(64): Show |
84 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.528-3204G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677424 | |||||||
chr7:141677424 | CACAT | C | 60 | a0001c0001t0001g0057 a0001c0001t0002g0026 a0001c0001t0005g0017 others(57): Show |
87 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.528-3208_528-3205d others(6): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677424 | |||||||
chr7:141677426 | C | T | 2 | a0001c0001t0002g0126 a0001c0001t0002g0235 |
2 | HG01346.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.528-3206G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677426 | |||||||
chr7:141677433 | A | G | 5 | a0001c0001t0001g0110 a0001c0001t0002g0126 a0001c0001t0002g0235 others(2): Show |
5 | HG01346.hp1 HG01515.hp1 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.528-3213T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677433 | |||||||
chr7:141677433 | ATG | A | 7 | a0001c0002t0001g0004 a0001c0002t0001g0040 a0001c0002t0001g0076 others(4): Show |
13 | HG00558.hp2 HG00621.hp1 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.528-3215_528-3214d others(4): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677433 | |||||||
chr7:141677435 | G | A | 60 | a0001c0001t0001g0057 a0001c0001t0002g0026 a0001c0001t0005g0017 others(57): Show |
87 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.528-3215C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677435 | |||||||
chr7:141677501 | G | GTA | 6 | a0001c0001t0001g0061 a0001c0001t0002g0022 a0001c0001t0002g0083 others(3): Show |
7 | HG01167.hp1 HG02647.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.528-3282_528-3281i others(4): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677501 | |||||||
chr7:141677503 | G | A | 90 | a0001c0001t0001g0028 a0001c0001t0001g0059 a0001c0001t0001g0060 others(87): Show |
115 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.528-3283C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677503 | |||||||
chr7:141677503 | G | GTA | 6 | a0001c0001t0001g0172 a0001c0001t0010g0036 a0001c0001t0014g0171 others(3): Show |
7 | HG01496.hp2 HG02486.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.528-3285_528-3284d others(4): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677503 | |||||||
chr7:141677503 | GTA | G | 3 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 |
3 | HG02723.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.528-3285_528-3284d others(4): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677503 | |||||||
chr7:141677505 | A | G | 7 | a0001c0001t0002g0058 a0001c0001t0002g0177 a0001c0001t0002g0178 others(4): Show |
10 | HG01891.hp1 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.528-3285T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677505 | |||||||
chr7:141677507 | A | G | 3 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 |
3 | HG02723.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.528-3287T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677507 | |||||||
chr7:141677517 | ATATG | A | 71 | a0001c0001t0001g0057 a0001c0001t0002g0026 a0001c0001t0002g0058 others(68): Show |
105 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.528-3301_528-3298d others(6): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677517 | |||||||
chr7:141677519 | A | ATATG | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
4 | HG00735.hp2 HG03139.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.528-3300_528-3299i others(6): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677519 | |||||||
chr7:141677521 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0197 |
4 | HG00735.hp2 HG03139.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.528-3301C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677521 | |||||||
chr7:141677521 | G | GTA | 19 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(16): Show |
26 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.528-3303_528-3302d others(4): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677521 | |||||||
chr7:141677523 | A | G | 73 | a0001c0001t0001g0044 a0001c0001t0001g0057 a0001c0001t0001g0160 others(70): Show |
108 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.528-3303T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677523 | |||||||
chr7:141677525 | A | G | 1 | a0001c0002t0015g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.528-3305T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677525 | |||||||
chr7:141677709 | G | A | 3 | a0001c0002t0001g0209 a0001c0002t0001g0220 a0001c0002t0001g0223 |
3 | NA19068.hp2 NA19079.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.528-3489C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141677709 | |||||||
chr7:141678029 | C | T | 1 | a0001c0001t0035g0242 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.528-3809G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141678029 | |||||||
chr7:141678111 | A | G | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.528-3891T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141678111 | |||||||
chr7:141678142 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.528-3922T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141678142 | |||||||
chr7:141678182 | C | T | 3 | a0001c0001t0001g0174 a0001c0001t0012g0051 a0001c0001t0012g0052 |
3 | HG02622.hp1 HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.528-3962G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141678182 | |||||||
chr7:141678215 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG00323.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.528-3995C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141678215 | |||||||
chr7:141678280 | G | A | 76 | a0001c0001t0001g0057 a0001c0001t0002g0026 a0001c0001t0002g0058 others(73): Show |
110 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.528-4060C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141678280 | |||||||
chr7:141678336 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG00438.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.528-4116G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141678336 | |||||||
chr7:141678495 | C | T | 1 | a0001c0001t0002g0149 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.528-4275G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141678495 | |||||||
chr7:141678583 | T | A | 3 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 |
3 | HG02723.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.528-4363A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141678583 | |||||||
chr7:141679294 | T | C | 2 | a0001c0001t0002g0064 a0001c0001t0002g0084 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.528-5074A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141679294 | |||||||
chr7:141679502 | C | T | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.528-5282G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141679502 | |||||||
chr7:141679544 | C | T | 1 | a0001c0002t0001g0078 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.528-5324G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141679544 | |||||||
chr7:141679680 | C | T | 3 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 |
3 | HG02723.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.528-5460G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141679680 | |||||||
chr7:141679707 | T | TA | 10 | a0001c0001t0002g0064 a0001c0001t0002g0075 a0001c0001t0002g0077 others(7): Show |
13 | HG01257.hp1 HG01258.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.528-5488dupT | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141679707 | |||||||
chr7:141679707 | TA | T | 14 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0157 others(11): Show |
17 | HG00323.hp2 HG00738.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.528-5488delT | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141679707 | |||||||
chr7:141679732 | A | G | 1 | a0001c0008t0033g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.528-5512T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141679732 | |||||||
chr7:141679850 | T | C | 2 | a0001c0002t0001g0009 a0001c0002t0001g0093 |
4 | NA18972.hp2 NA18991.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.527+5628A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141679850 | |||||||
chr7:141680026 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.527+5452A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141680026 | |||||||
chr7:141680206 | GAC | G | 1 | a0001c0001t0011g0018 | 3 | HG01261.hp2 HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.527+5270_527+5271d others(4): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141680206 | |||||||
chr7:141680208 | C | T | 1 | a0001c0002t0003g0246 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.527+5270G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141680208 | |||||||
chr7:141680292 | AAC | A | 68 | a0001c0001t0001g0057 a0001c0001t0002g0026 a0001c0001t0005g0017 others(65): Show |
102 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.527+5184_527+5185d others(4): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141680292 | |||||||
chr7:141680307 | C | G | 1 | a0001c0002t0001g0070 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.527+5171G>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141680307 | |||||||
chr7:141680362 | T | TAC | 4 | a0001c0001t0001g0038 a0001c0001t0001g0193 a0001c0001t0001g0194 others(1): Show |
5 | HG00280.hp1 HG01081.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.527+5114_527+5115d others(4): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141680362 | |||||||
chr7:141680368 | C | T | 68 | a0001c0001t0001g0057 a0001c0001t0002g0026 a0001c0001t0005g0017 others(65): Show |
102 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.527+5110G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141680368 | |||||||
chr7:141680675 | G | C | 74 | a0001c0001t0001g0057 a0001c0001t0002g0026 a0001c0001t0002g0058 others(71): Show |
108 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.527+4803C>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141680675 | |||||||
chr7:141680720 | T | C | 2 | a0001c0002t0003g0222 a0001c0002t0003g0252 |
2 | NA18997.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.527+4758A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141680720 | |||||||
chr7:141680917 | G | C | 2 | a0001c0002t0017g0049 a0001c0002t0017g0056 |
2 | NA18949.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.527+4561C>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141680917 | |||||||
chr7:141681064 | A | G | 1 | a0001c0001t0007g0045 | 2 | HG01070.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.527+4414T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141681064 | |||||||
chr7:141681364 | G | T | 1 | a0001c0002t0001g0205 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.527+4114C>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141681364 | |||||||
chr7:141681528 | T | C | 3 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 |
3 | HG02723.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.527+3950A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141681528 | |||||||
chr7:141681667 | G | C | 169 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0059 others(166): Show |
230 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.527+3811C>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141681667 | |||||||
chr7:141682057 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.527+3421C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141682057 | |||||||
chr7:141682149 | T | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0187 |
2 | HG02895.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.527+3329A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141682149 | |||||||
chr7:141682620 | C | T | 1 | a0001c0001t0035g0242 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.527+2858G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141682620 | |||||||
chr7:141682707 | A | G | 1 | a0001c0008t0033g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.527+2771T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141682707 | |||||||
chr7:141682932 | CATA | C | 3 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 |
3 | HG02723.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.527+2543_527+2545d others(5): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141682932 | |||||||
chr7:141682945 | C | A | 1 | a0001c0002t0001g0105 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.527+2533G>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141682945 | |||||||
chr7:141682951 | CAA | C | 67 | a0001c0001t0001g0057 a0001c0001t0002g0026 a0001c0001t0005g0017 others(64): Show |
101 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.527+2525_527+2526d others(4): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141682951 | |||||||
chr7:141683304 | G | C | 1 | a0001c0002t0003g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.527+2174C>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141683304 | |||||||
chr7:141683324 | T | C | 1 | a0001c0002t0001g0209 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.527+2154A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141683324 | |||||||
chr7:141683499 | C | T | 1 | a0001c0001t0001g0043 | 2 | HG00642.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.527+1979G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141683499 | |||||||
chr7:141683644 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.527+1834T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141683644 | |||||||
chr7:141683649 | C | A | 1 | a0001c0001t0002g0131 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.527+1829G>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141683649 | |||||||
chr7:141683688 | A | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0160 |
3 | HG02109.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.527+1790T>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141683688 | |||||||
chr7:141683790 | C | T | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.527+1688G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141683790 | |||||||
chr7:141683939 | T | A | 1 | a0001c0001t0002g0129 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.527+1539A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141683939 | |||||||
chr7:141683953 | G | A | 1 | a0001c0001t0002g0112 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.527+1525C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141683953 | |||||||
chr7:141684041 | C | A | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.527+1437G>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141684041 | |||||||
chr7:141684142 | G | T | 1 | a0001c0002t0001g0210 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.527+1336C>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141684142 | |||||||
chr7:141684217 | G | A | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.527+1261C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141684217 | |||||||
chr7:141684438 | C | T | 3 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 |
3 | HG02723.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.527+1040G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141684438 | |||||||
chr7:141684585 | C | T | 1 | a0001c0001t0002g0097 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.527+893G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141684585 | |||||||
chr7:141684728 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.527+750G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141684728 | |||||||
chr7:141684765 | G | A | 61 | a0001c0001t0001g0057 a0001c0001t0002g0058 a0001c0001t0005g0017 others(58): Show |
82 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.527+713C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141684765 | |||||||
chr7:141684765 | G | T | 1 | a0001c0002t0001g0209 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.527+713C>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141684765 | |||||||
chr7:141684777 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.527+701C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141684777 | |||||||
chr7:141684884 | C | A | 2 | a0001c0001t0024g0238 a0001c0002t0003g0243 |
2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.527+594G>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141684884 | |||||||
chr7:141684917 | A | G | 2 | a0001c0001t0024g0238 a0001c0002t0003g0243 |
2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.527+561T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141684917 | |||||||
chr7:141684992 | T | C | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.527+486A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141684992 | |||||||
chr7:141685012 | C | CAA | 16 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0197 others(13): Show |
21 | HG00597.hp1 HG00673.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.527+464_527+465dup others(2): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685012 | |||||||
chr7:141685027 | A | AATATATA others(7): Show |
1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.527+450_527+451ins others(14): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685027 | |||||||
chr7:141685027 | AAAATATA others(3): Show |
A | 1 | a0001c0001t0008g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.527+441_527+450del others(10): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685027 | |||||||
chr7:141685029 | A | AAAAT | 15 | a0001c0001t0001g0059 a0001c0001t0001g0123 a0001c0001t0001g0125 others(12): Show |
21 | HG00140.hp1 HG00140.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.527+448_527+449ins others(4): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685029 | |||||||
chr7:141685029 | A | AAAATATA others(3): Show |
1 | a0001c0001t0002g0033 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.527+448_527+449ins others(10): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685029 | |||||||
chr7:141685029 | A | AAAT | 6 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0073 others(3): Show |
6 | HG00733.hp1 HG01516.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.527+448_527+449ins others(3): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685029 | |||||||
chr7:141685029 | A | AT | 3 | a0001c0001t0001g0044 a0001c0001t0001g0160 a0001c0001t0007g0257 |
4 | HG01257.hp2 HG02109.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.527+448_527+449ins others(1): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685029 | |||||||
chr7:141685029 | A | T | 10 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0104 others(7): Show |
10 | HG01433.hp2 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.527+449T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685029 | |||||||
chr7:141685029 | AAT | A | 63 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0081 others(60): Show |
82 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.527+447_527+448del others(2): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685029 | |||||||
chr7:141685029 | AATAT | A | 48 | a0001c0001t0001g0057 a0001c0001t0001g0091 a0001c0001t0005g0017 others(45): Show |
70 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.527+445_527+448del others(4): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685029 | |||||||
chr7:141685029 | AATATATA others(3): Show |
A | 2 | a0001c0001t0008g0054 a0001c0001t0008g0055 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.527+439_527+448del others(10): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685029 | |||||||
chr7:141685029 | AATATATA others(7): Show |
A | 1 | a0001c0001t0026g0144 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.527+435_527+448del others(14): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685029 | |||||||
chr7:141685030 | AT | A | 11 | a0001c0001t0002g0015 a0001c0001t0002g0080 a0001c0001t0002g0132 others(8): Show |
20 | HG01123.hp2 HG01256.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.527+447delA | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685030 | |||||||
chr7:141685030 | ATAT | A | 8 | a0001c0001t0001g0025 a0001c0001t0001g0085 a0001c0001t0002g0113 others(5): Show |
9 | HG00323.hp2 HG00738.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.527+445_527+447del others(3): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685030 | |||||||
chr7:141685031 | T | A | 40 | a0001c0001t0001g0006 a0001c0001t0001g0038 a0001c0001t0001g0043 others(37): Show |
52 | HG00280.hp1 HG00423.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.527+447A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685031 | |||||||
chr7:141685033 | T | A | 79 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0081 others(76): Show |
112 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.527+445A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685033 | |||||||
chr7:141685035 | T | A | 67 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(64): Show |
101 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.527+443A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685035 | |||||||
chr7:141685037 | T | A | 52 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0091 others(49): Show |
76 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.527+441A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685037 | |||||||
chr7:141685039 | T | A | 32 | a0001c0001t0005g0017 a0001c0001t0005g0042 a0001c0001t0011g0018 others(29): Show |
48 | HG00438.hp1 HG00621.hp2 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.527+439A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685039 | |||||||
chr7:141685056 | A | T | 1 | a0001c0001t0002g0058 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.527+422T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685056 | |||||||
chr7:141685058 | A | T | 2 | a0001c0001t0002g0058 a0001c0002t0003g0246 |
2 | HG02602.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.527+420T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685058 | |||||||
chr7:141685065 | A | G | 1 | a0001c0001t0011g0018 | 3 | HG01261.hp2 HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.527+413T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685065 | |||||||
chr7:141685154 | G | A | 1 | a0001c0001t0006g0096 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.527+324C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 3/8 | chr7 | 141685154 | |||||||
chr7:141685753 | G | A | 2 | a0001c0002t0017g0049 a0001c0002t0017g0056 |
2 | NA18949.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.369-117C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 2/8 | chr7 | 141685753 | |||||||
chr7:141685832 | G | A | 1 | a0001c0001t0002g0029 | 2 | NA18983.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.369-196C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 2/8 | chr7 | 141685832 | |||||||
chr7:141685952 | T | C | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.369-316A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 2/8 | chr7 | 141685952 | |||||||
chr7:141685982 | C | T | 1 | a0001c0002t0003g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.369-346G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 2/8 | chr7 | 141685982 | |||||||
chr7:141686464 | AC | A | 79 | a0001c0001t0001g0028 a0001c0001t0001g0059 a0001c0001t0001g0060 others(76): Show |
102 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.368+94delG | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 2/8 | chr7 | 141686464 | |||||||
chr7:141686493 | A | T | 1 | a0001c0001t0024g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.368+66T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 2/8 | chr7 | 141686493 | |||||||
chr7:141686547 | A | G | 1 | a0001c0002t0003g0247 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.368+12T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 2/8 | chr7 | 141686547 | |||||||
chr7:141686753 | C | T | 1 | a0001c0002t0001g0204 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.269-95G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141686753 | |||||||
chr7:141686910 | G | T | 7 | a0001c0001t0001g0157 a0001c0001t0001g0168 a0001c0001t0002g0032 others(4): Show |
8 | HG01243.hp1 HG01891.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.269-252C>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141686910 | |||||||
chr7:141687009 | T | C | 3 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 |
3 | HG02723.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.269-351A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141687009 | |||||||
chr7:141687333 | G | A | 1 | a0001c0001t0006g0191 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.269-675C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141687333 | |||||||
chr7:141687463 | A | AT | 8 | a0001c0001t0002g0118 a0001c0001t0002g0154 a0001c0001t0002g0161 others(5): Show |
8 | HG01993.hp1 HG02056.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.269-806dupA | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141687463 | |||||||
chr7:141687476 | T | C | 3 | a0001c0001t0002g0226 a0001c0001t0002g0227 a0001c0001t0002g0228 |
3 | HG00408.hp2 HG03831.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.269-818A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141687476 | |||||||
chr7:141687489 | A | T | 1 | a0001c0002t0001g0224 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.269-831T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141687489 | |||||||
chr7:141687532 | C | T | 2 | a0001c0001t0011g0018 a0001c0001t0014g0239 |
4 | HG01261.hp2 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.269-874G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141687532 | |||||||
chr7:141687576 | TGCCTCAG others(163): Show |
T | 2 | a0001c0001t0002g0106 a0001c0001t0002g0117 |
2 | NA18954.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.269-1088_269-919de others(1): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141687576 | |||||||
chr7:141687609 | C | T | 2 | a0001c0002t0017g0049 a0001c0002t0017g0056 |
2 | NA18949.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.269-951G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141687609 | |||||||
chr7:141687631 | A | AT | 29 | a0001c0001t0001g0057 a0001c0001t0001g0081 a0001c0001t0002g0058 others(26): Show |
35 | HG00408.hp1 HG02027.hp2 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.269-974dupA | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141687631 | |||||||
chr7:141687631 | A | ATTT | 6 | a0001c0001t0001g0061 a0001c0001t0002g0001 a0001c0001t0002g0119 others(3): Show |
6 | HG02056.hp1 HG02083.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-976_269-974dup others(3): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141687631 | |||||||
chr7:141687631 | A | ATTTT | 64 | a0001c0001t0001g0028 a0001c0001t0001g0059 a0001c0001t0001g0060 others(61): Show |
83 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.269-977_269-974dup others(4): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141687631 | |||||||
chr7:141687631 | A | ATTTTT | 10 | a0001c0001t0001g0133 a0001c0001t0002g0001 a0001c0001t0002g0005 others(7): Show |
10 | HG00438.hp1 HG00438.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.269-978_269-974dup others(5): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141687631 | |||||||
chr7:141687631 | AT | A | 5 | a0001c0001t0005g0017 a0001c0001t0011g0018 a0001c0001t0014g0239 others(2): Show |
7 | HG01070.hp2 HG01261.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.269-974delA | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141687631 | |||||||
chr7:141687654 | G | A | 2 | a0001c0001t0024g0238 a0001c0001t0035g0242 |
2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.269-996C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141687654 | |||||||
chr7:141687720 | C | T | 51 | a0001c0001t0001g0057 a0001c0001t0005g0017 a0001c0001t0005g0042 others(48): Show |
72 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.269-1062G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141687720 | |||||||
chr7:141687728 | A | G | 6 | a0001c0001t0001g0158 a0001c0001t0006g0096 a0001c0001t0006g0102 others(3): Show |
6 | HG00140.hp2 HG00733.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-1070T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141687728 | |||||||
chr7:141687747 | G | A | 3 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 |
3 | HG02723.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.269-1089C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141687747 | |||||||
chr7:141687832 | C | T | 1 | a0001c0002t0003g0225 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.269-1174G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141687832 | |||||||
chr7:141687909 | C | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0110 |
3 | HG00738.hp1 HG01243.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.269-1251G>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141687909 | |||||||
chr7:141687937 | C | T | 1 | a0001c0001t0013g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.269-1279G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141687937 | |||||||
chr7:141688161 | T | C | 1 | a0001c0001t0002g0058 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.269-1503A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141688161 | |||||||
chr7:141688311 | T | A | 51 | a0001c0001t0001g0057 a0001c0001t0005g0017 a0001c0001t0005g0042 others(48): Show |
72 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.269-1653A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141688311 | |||||||
chr7:141688386 | A | G | 80 | a0001c0001t0001g0028 a0001c0001t0001g0059 a0001c0001t0001g0060 others(77): Show |
103 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.269-1728T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141688386 | |||||||
chr7:141688447 | A | G | 2 | a0001c0002t0017g0049 a0001c0002t0017g0056 |
2 | NA18949.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.269-1789T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141688447 | |||||||
chr7:141688549 | G | T | 7 | a0001c0001t0001g0043 a0001c0001t0001g0071 a0001c0001t0001g0072 others(4): Show |
8 | HG00642.hp2 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.269-1891C>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141688549 | |||||||
chr7:141688945 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.269-2287C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141688945 | |||||||
chr7:141688987 | T | C | 1 | a0001c0008t0033g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.269-2329A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141688987 | |||||||
chr7:141689039 | G | A | 5 | a0001c0001t0001g0038 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
6 | HG00280.hp1 HG01081.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-2381C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141689039 | |||||||
chr7:141689054 | C | T | 1 | a0001c0002t0001g0203 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.269-2396G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141689054 | |||||||
chr7:141689193 | G | A | 2 | a0001c0001t0024g0238 a0001c0001t0035g0242 |
2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.269-2535C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141689193 | |||||||
chr7:141689284 | G | T | 1 | a0001c0002t0001g0202 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.269-2626C>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141689284 | |||||||
chr7:141689411 | A | G | 1 | a0001c0002t0001g0069 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.269-2753T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141689411 | |||||||
chr7:141689580 | T | A | 2 | a0001c0002t0003g0222 a0001c0002t0003g0252 |
2 | NA18997.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.269-2922A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141689580 | |||||||
chr7:141689596 | T | TGGAACTT others(317): Show |
1 | a0001c0002t0015g0241 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.269-2939_269-2938i others(326): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141689596 | |||||||
chr7:141689596 | T | TGGAACTT others(336): Show |
1 | a0001c0002t0015g0240 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.269-2939_269-2938i others(345): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141689596 | |||||||
chr7:141689840 | A | G | 143 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0059 others(140): Show |
189 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.269-3182T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141689840 | |||||||
chr7:141689908 | G | C | 2 | a0001c0001t0001g0046 a0001c0001t0001g0258 |
3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.269-3250C>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141689908 | |||||||
chr7:141689955 | A | G | 1 | a0001c0001t0002g0165 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.269-3297T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141689955 | |||||||
chr7:141690233 | T | A | 1 | a0001c0001t0001g0195 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.269-3575A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141690233 | |||||||
chr7:141690288 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.269-3630G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141690288 | |||||||
chr7:141690335 | A | G | 1 | a0003c0009t0002g0114 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.269-3677T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141690335 | |||||||
chr7:141690345 | G | A | 4 | a0001c0001t0011g0018 a0001c0001t0014g0239 a0001c0001t0024g0238 others(1): Show |
6 | HG01261.hp2 HG02258.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.269-3687C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141690345 | |||||||
chr7:141690346 | C | T | 2 | a0001c0003t0002g0067 a0001c0003t0002g0068 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.269-3688G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141690346 | |||||||
chr7:141690467 | A | C | 1 | a0001c0001t0001g0164 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.269-3809T>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141690467 | |||||||
chr7:141690571 | C | T | 50 | a0001c0001t0001g0057 a0001c0001t0005g0017 a0001c0001t0005g0042 others(47): Show |
71 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.269-3913G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141690571 | |||||||
chr7:141690820 | A | C | 4 | a0001c0001t0011g0018 a0001c0001t0014g0239 a0001c0001t0024g0238 others(1): Show |
6 | HG01261.hp2 HG02258.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.269-4162T>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141690820 | |||||||
chr7:141690867 | C | T | 2 | a0001c0001t0011g0018 a0001c0001t0014g0239 |
4 | HG01261.hp2 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.269-4209G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141690867 | |||||||
chr7:141690979 | T | A | 4 | a0001c0001t0002g0145 a0001c0001t0024g0238 a0001c0001t0035g0242 others(1): Show |
4 | HG01168.hp1 HG02258.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.269-4321A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141690979 | |||||||
chr7:141690980 | A | T | 1 | a0001c0002t0003g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.269-4322T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141690980 | |||||||
chr7:141691391 | T | A | 4 | a0001c0001t0011g0018 a0001c0001t0014g0239 a0001c0001t0024g0238 others(1): Show |
6 | HG01261.hp2 HG02258.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.269-4733A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141691391 | |||||||
chr7:141691406 | G | C | 1 | a0001c0001t0001g0044 | 2 | NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.269-4748C>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141691406 | |||||||
chr7:141691636 | T | C | 4 | a0001c0001t0001g0148 a0001c0001t0002g0147 a0001c0001t0002g0149 others(1): Show |
4 | HG02027.hp1 NA18977.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.269-4978A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141691636 | |||||||
chr7:141691687 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.269-5029C>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141691687 | |||||||
chr7:141691775 | T | C | 1 | a0001c0002t0003g0243 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.269-5117A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141691775 | |||||||
chr7:141691805 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.269-5147G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141691805 | |||||||
chr7:141691908 | T | TA | 4 | a0001c0001t0011g0018 a0001c0001t0014g0239 a0001c0001t0024g0238 others(1): Show |
6 | HG01261.hp2 HG02258.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.269-5251dupT | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141691908 | |||||||
chr7:141691909 | A | T | 80 | a0001c0001t0001g0028 a0001c0001t0001g0059 a0001c0001t0001g0060 others(77): Show |
103 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.269-5251T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141691909 | |||||||
chr7:141692228 | T | C | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | NA18942.hp2 NA19004.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.269-5570A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141692228 | |||||||
chr7:141692298 | A | G | 1 | a0001c0001t0002g0115 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.269-5640T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141692298 | |||||||
chr7:141692622 | T | G | 2 | a0001c0001t0011g0018 a0001c0001t0014g0239 |
4 | HG01261.hp2 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.269-5964A>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141692622 | |||||||
chr7:141692639 | T | C | 2 | a0001c0002t0015g0240 a0001c0002t0015g0241 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.269-5981A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141692639 | |||||||
chr7:141692663 | G | A | 2 | a0001c0001t0011g0018 a0001c0001t0014g0239 |
4 | HG01261.hp2 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.269-6005C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141692663 | |||||||
chr7:141693142 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0160 |
3 | HG02109.hp1 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.269-6484C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141693142 | |||||||
chr7:141693199 | G | T | 3 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 |
3 | HG02723.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.269-6541C>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141693199 | |||||||
chr7:141693281 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.269-6623G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141693281 | |||||||
chr7:141693575 | A | G | 2 | a0001c0001t0024g0238 a0001c0001t0035g0242 |
2 | HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.269-6917T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141693575 | |||||||
chr7:141693587 | A | C | 1 | a0003c0009t0002g0114 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.269-6929T>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141693587 | |||||||
chr7:141693692 | G | A | 3 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 |
3 | HG02723.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.269-7034C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141693692 | |||||||
chr7:141693720 | C | T | 80 | a0001c0001t0001g0028 a0001c0001t0001g0059 a0001c0001t0001g0060 others(77): Show |
103 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.269-7062G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141693720 | |||||||
chr7:141694109 | A | G | 51 | a0001c0001t0001g0057 a0001c0001t0005g0017 a0001c0001t0005g0042 others(48): Show |
72 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.269-7451T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141694109 | |||||||
chr7:141694134 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.269-7476G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141694134 | |||||||
chr7:141694297 | A | G | 256 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(253): Show |
342 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.268+7589T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141694297 | |||||||
chr7:141694399 | T | C | 1 | a0001c0001t0002g0098 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.268+7487A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141694399 | |||||||
chr7:141694400 | A | G | 1 | a0001c0002t0003g0159 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.268+7486T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141694400 | |||||||
chr7:141694410 | G | A | 2 | a0001c0002t0015g0240 a0001c0002t0015g0241 |
2 | HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.268+7476C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141694410 | |||||||
chr7:141694525 | T | C | 1 | a0001c0005t0001g0048 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.268+7361A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141694525 | |||||||
chr7:141694696 | G | T | 1 | a0001c0002t0003g0246 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.268+7190C>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141694696 | |||||||
chr7:141694741 | T | C | 4 | a0001c0001t0011g0018 a0001c0001t0014g0239 a0001c0001t0024g0238 others(1): Show |
6 | HG01261.hp2 HG02258.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+7145A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141694741 | |||||||
chr7:141694764 | CA | C | 77 | a0001c0001t0001g0028 a0001c0001t0001g0059 a0001c0001t0001g0060 others(74): Show |
99 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.268+7121delT | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141694764 | |||||||
chr7:141695096 | A | T | 9 | a0001c0001t0001g0060 a0001c0001t0002g0131 a0001c0001t0008g0053 others(6): Show |
9 | HG02723.hp1 HG02970.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.268+6790T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141695096 | |||||||
chr7:141695422 | A | AG | 136 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0059 others(133): Show |
181 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.268+6463_268+6464i others(3): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141695422 | |||||||
chr7:141695423 | C | A | 136 | a0001c0001t0001g0028 a0001c0001t0001g0057 a0001c0001t0001g0059 others(133): Show |
181 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.268+6463G>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141695423 | |||||||
chr7:141695458 | T | C | 1 | a0001c0001t0002g0154 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.268+6428A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141695458 | |||||||
chr7:141695495 | A | G | 3 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 |
3 | HG01175.hp2 HG01192.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.268+6391T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141695495 | |||||||
chr7:141696074 | C | G | 1 | a0001c0002t0003g0159 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.268+5812G>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141696074 | |||||||
chr7:141696095 | G | C | 3 | a0001c0001t0002g0026 a0001c0002t0001g0094 a0001c0002t0001g0095 |
4 | NA18979.hp1 NA18984.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+5791C>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141696095 | |||||||
chr7:141696146 | A | G | 2 | a0001c0002t0017g0049 a0001c0002t0017g0056 |
2 | NA18949.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.268+5740T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141696146 | |||||||
chr7:141696187 | C | A | 4 | a0001c0001t0011g0018 a0001c0001t0014g0239 a0001c0001t0024g0238 others(1): Show |
6 | HG01261.hp2 HG02258.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+5699G>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141696187 | |||||||
chr7:141696424 | A | C | 1 | a0001c0001t0001g0158 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.268+5462T>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141696424 | |||||||
chr7:141696623 | C | T | 1 | a0001c0002t0009g0201 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.268+5263G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141696623 | |||||||
chr7:141697346 | C | T | 1 | a0001c0001t0002g0232 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.268+4540G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141697346 | |||||||
chr7:141697399 | G | A | 1 | a0001c0001t0001g0046 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.268+4487C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141697399 | |||||||
chr7:141697473 | T | C | 2 | a0001c0002t0017g0049 a0001c0002t0017g0056 |
2 | NA18949.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.268+4413A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141697473 | |||||||
chr7:141697493 | C | T | 1 | a0001c0007t0001g0200 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.268+4393G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141697493 | |||||||
chr7:141697749 | A | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0254 |
3 | HG00642.hp2 HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.268+4137T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141697749 | |||||||
chr7:141697851 | C | T | 2 | a0001c0002t0017g0049 a0001c0002t0017g0056 |
2 | NA18949.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.268+4035G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141697851 | |||||||
chr7:141697972 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0196 a0001c0001t0001g0197 others(2): Show |
8 | HG00735.hp2 HG02055.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.268+3914C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141697972 | |||||||
chr7:141698045 | T | C | 1 | a0001c0001t0002g0155 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.268+3841A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141698045 | |||||||
chr7:141698210 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.268+3676C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141698210 | |||||||
chr7:141698218 | C | T | 5 | a0001c0001t0001g0110 a0001c0001t0002g0010 a0001c0001t0002g0108 others(2): Show |
7 | HG01167.hp2 HG01496.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.268+3668G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141698218 | |||||||
chr7:141698239 | C | T | 49 | a0001c0001t0001g0057 a0001c0001t0005g0017 a0001c0001t0005g0042 others(46): Show |
68 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.268+3647G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141698239 | |||||||
chr7:141698512 | C | G | 3 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 |
3 | HG02723.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.268+3374G>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141698512 | |||||||
chr7:141698648 | C | T | 45 | a0001c0001t0005g0017 a0001c0001t0005g0042 a0001c0002t0001g0003 others(42): Show |
63 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.268+3238G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141698648 | |||||||
chr7:141698761 | A | G | 5 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 others(2): Show |
7 | HG01261.hp2 HG02723.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.268+3125T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141698761 | |||||||
chr7:141698788 | A | T | 174 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(171): Show |
236 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.268+3098T>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141698788 | |||||||
chr7:141698863 | T | C | 1 | a0001c0001t0002g0156 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.268+3023A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141698863 | |||||||
chr7:141698892 | C | T | 1 | a0001c0001t0002g0106 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.268+2994G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141698892 | |||||||
chr7:141698907 | A | G | 117 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(114): Show |
156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.268+2979T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141698907 | |||||||
chr7:141698944 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.268+2942G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141698944 | |||||||
chr7:141698968 | T | G | 1 | a0001c0002t0001g0224 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.268+2918A>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141698968 | |||||||
chr7:141699052 | C | A | 1 | a0001c0001t0012g0052 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.268+2834G>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141699052 | |||||||
chr7:141699062 | T | G | 6 | a0001c0001t0011g0018 a0001c0001t0014g0239 a0001c0001t0024g0238 others(3): Show |
8 | HG01261.hp2 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.268+2824A>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141699062 | |||||||
chr7:141699142 | T | C | 169 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(166): Show |
229 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.268+2744A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141699142 | |||||||
chr7:141699394 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.268+2492T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141699394 | |||||||
chr7:141699454 | T | G | 15 | a0001c0001t0001g0007 a0001c0001t0002g0058 a0001c0001t0002g0244 others(12): Show |
22 | HG00408.hp1 HG02015.hp1 HG02155.hp2 others(19): Show |
intron_variant | MODIFIER | c.268+2432A>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141699454 | |||||||
chr7:141699648 | G | A | 2 | a0001c0002t0017g0049 a0001c0002t0017g0056 |
2 | NA18949.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.268+2238C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141699648 | |||||||
chr7:141699752 | C | A | 1 | a0001c0001t0005g0042 | 2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.268+2134G>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141699752 | |||||||
chr7:141699856 | A | G | 1 | a0001c0001t0023g0103 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.268+2030T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141699856 | |||||||
chr7:141699916 | T | TCA | 9 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0254 others(6): Show |
11 | HG00408.hp2 HG00642.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.268+1968_268+1969d others(4): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141699916 | |||||||
chr7:141699916 | T | TCACA | 2 | a0001c0001t0011g0018 a0001c0001t0014g0239 |
4 | HG01261.hp2 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+1966_268+1969d others(6): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141699916 | |||||||
chr7:141699916 | T | TCACACA | 6 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+1964_268+1969d others(8): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141699916 | |||||||
chr7:141699916 | T | TCACACAC others(5): Show |
1 | a0001c0001t0002g0058 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.268+1958_268+1969d others(14): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141699916 | |||||||
chr7:141699916 | T | TCACACAC others(7): Show |
2 | a0001c0002t0017g0049 a0001c0002t0017g0056 |
2 | NA18949.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.268+1956_268+1969d others(16): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141699916 | |||||||
chr7:141699916 | TCA | T | 6 | a0001c0001t0002g0063 a0001c0001t0002g0064 a0001c0001t0002g0101 others(3): Show |
6 | HG01257.hp1 HG01346.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.268+1968_268+1969d others(4): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141699916 | |||||||
chr7:141699946 | C | G | 28 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(25): Show |
39 | HG00408.hp1 HG00642.hp2 HG01261.hp2 others(36): Show |
intron_variant | MODIFIER | c.268+1940G>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141699946 | |||||||
chr7:141700188 | C | T | 51 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(48): Show |
72 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.268+1698G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141700188 | |||||||
chr7:141700195 | T | C | 3 | a0001c0001t0002g0058 a0001c0002t0017g0049 a0001c0002t0017g0056 |
3 | HG03225.hp1 NA18949.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.268+1691A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141700195 | |||||||
chr7:141700322 | T | A | 1 | a0001c0001t0001g0057 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.268+1564A>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141700322 | |||||||
chr7:141700351 | T | C | 1 | a0001c0001t0002g0231 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.268+1535A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141700351 | |||||||
chr7:141700389 | G | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | NA18974.hp1 NA18986.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.268+1497C>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141700389 | |||||||
chr7:141700476 | T | TC | 4 | a0001c0001t0002g0058 a0001c0001t0008g0053 a0001c0001t0008g0054 others(1): Show |
4 | HG02723.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+1409_268+1410i others(3): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141700476 | |||||||
chr7:141700476 | TG | T | 17 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
26 | HG00408.hp1 HG00642.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.268+1409delC | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141700476 | |||||||
chr7:141700477 | G | A | 5 | a0001c0001t0001g0057 a0001c0001t0002g0058 a0001c0001t0008g0053 others(2): Show |
5 | HG02723.hp1 HG02970.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.268+1409C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141700477 | |||||||
chr7:141700477 | G | C | 9 | a0001c0001t0011g0018 a0001c0001t0014g0239 a0001c0001t0024g0238 others(6): Show |
11 | HG01261.hp2 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.268+1409C>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141700477 | |||||||
chr7:141700477 | G | GA | 17 | a0001c0001t0001g0008 a0001c0001t0001g0092 a0001c0001t0001g0160 others(14): Show |
19 | HG00280.hp2 HG01081.hp2 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.268+1408dupT | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141700477 | |||||||
chr7:141700478 | A | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
26 | HG00408.hp1 HG00642.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.268+1408T>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141700478 | |||||||
chr7:141700494 | G | A | 2 | a0001c0001t0002g0232 a0001c0001t0002g0233 |
2 | NA18948.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.268+1392C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141700494 | |||||||
chr7:141700662 | A | G | 2 | a0001c0002t0017g0049 a0001c0002t0017g0056 |
2 | NA18949.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.268+1224T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141700662 | |||||||
chr7:141700814 | A | G | 31 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(28): Show |
42 | HG00408.hp1 HG00642.hp2 HG01261.hp2 others(39): Show |
intron_variant | MODIFIER | c.268+1072T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141700814 | |||||||
chr7:141700954 | G | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
26 | HG00408.hp1 HG00642.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.268+932C>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141700954 | |||||||
chr7:141700982 | C | T | 3 | a0001c0001t0008g0053 a0001c0001t0008g0054 a0001c0001t0008g0055 |
3 | HG02723.hp1 HG02970.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.268+904G>A | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141700982 | |||||||
chr7:141701100 | C | A | 1 | a0001c0001t0002g0234 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.268+786G>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141701100 | |||||||
chr7:141701162 | G | C | 1 | a0001c0001t0002g0235 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.268+724C>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141701162 | |||||||
chr7:141701176 | T | C | 1 | a0001c0002t0001g0236 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.268+710A>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141701176 | |||||||
chr7:141701305 | G | A | 1 | a0001c0002t0031g0237 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.268+581C>T | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141701305 | |||||||
chr7:141701350 | G | C | 23 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(20): Show |
34 | HG00408.hp1 HG00642.hp2 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.268+536C>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141701350 | |||||||
chr7:141701358 | A | AGGGCGAG others(23): Show |
3 | a0001c0001t0012g0051 a0001c0001t0012g0052 a0001c0008t0033g0050 |
3 | HG02622.hp1 HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.268+498_268+527dup others(30): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141701358 | |||||||
chr7:141701358 | AGGGCGAG others(23): Show |
A | 1 | a0001c0001t0012g0255 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.268+498_268+527del others(30): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141701358 | |||||||
chr7:141701404 | GGGGGACG others(22): Show |
G | 1 | a0001c0002t0017g0049 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.268+453_268+481del others(29): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141701404 | |||||||
chr7:141701414 | GTGGGGGG others(23): Show |
G | 1 | a0001c0002t0017g0056 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.268+442_268+471del others(30): Show |
DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141701414 | |||||||
chr7:141701444 | A | G | 1 | a0001c0002t0017g0049 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.268+442T>C | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141701444 | |||||||
chr7:141701691 | G | C | 5 | a0001c0001t0001g0046 a0001c0001t0001g0258 a0001c0001t0007g0045 others(2): Show |
7 | HG01070.hp1 HG01099.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.268+195C>G | DENND11 | ENSG00000257093.7 | transcript | ENST00000536163.6 | protein_coding | 1/8 | chr7 | 141701691 |