| geneid | 6764 |
|---|---|
| ensemblid | ENSG00000166444.19 |
| hgncid | 11350 |
| symbol | DENND2B |
| name | DENN domain containing 2B |
| refseq_nuc | NM_213618.2 |
| refseq_prot | NP_998783.1 |
| ensembl_nuc | ENST00000313726.11 |
| ensembl_prot | ENSP00000319678.6 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 8693352 |
| end | 8810674 |
| strand | - |
| ver | v1.2 |
| region | chr11:8693352-8810674 |
| region5000 | chr11:8688352-8815674 |
| regionname0 | DENND2B_chr11_8693352_8810674 |
| regionname5000 | DENND2B_chr11_8688352_8815674 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1137 | 141 | 72 | 14 | 41 | 2 | 11 | 29 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0002 | 0/1 | 1137 | 91 | 3 | 19 | 53 | 4 | 11 | 40 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0003 | 0/0 | 1137 | 90 | 12 | 19 | 42 | 7 | 10 | 31 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0004 | 0/0 | 1137 | 7 | 1 | 3 | 0 | 0 | 3 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0005 | 0/0 | 1137 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0006 | 0/0 | 1137 | 6 | 0 | 0 | 4 | 1 | 1 | 4 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0007 | 0/0 | 1137 | 3 | 0 | 1 | 2 | 0 | 0 | 2 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0008 | 0/0 | 1137 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0009 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0010 | 0/0 | 1137 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0011 | 0/0 | 1137 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0012 | 0/0 | 1137 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0013 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0014 | 0/0 | 1137 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 3414 | 134 | 67 | 13 | 41 | 2 | 10 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| c0002 | 0/0 | 3414 | 90 | 12 | 19 | 42 | 7 | 10 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| c0003 | 0/1 | 3414 | 89 | 3 | 17 | 53 | 4 | 11 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| c0004 | 0/0 | 3414 | 7 | 1 | 3 | 0 | 0 | 3 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| c0005 | 0/0 | 3414 | 6 | 0 | 0 | 4 | 1 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| c0006 | 0/0 | 3414 | 6 | 0 | 0 | 6 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| c0007 | 0/0 | 3414 | 6 | 5 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| c0008 | 0/0 | 3414 | 3 | 0 | 1 | 2 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| c0009 | 0/0 | 3414 | 2 | 0 | 0 | 2 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| c0010 | 0/0 | 3414 | 2 | 0 | 2 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| c0011 | 0/0 | 3414 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| c0012 | 0/0 | 3414 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| c0013 | 0/0 | 3414 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| c0014 | 0/0 | 3414 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| c0015 | 0/0 | 3414 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| c0016 | 0/0 | 3414 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| c0017 | 0/0 | 3414 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 928 | 207 | 56 | 38 | 87 | 9 | 15 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| t0002 | 0/0 | 932 | 117 | 28 | 18 | 54 | 4 | 13 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| t0003 | 0/0 | 928 | 15 | 1 | 1 | 6 | 1 | 6 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| t0004 | 0/0 | 928 | 3 | 0 | 1 | 0 | 0 | 2 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| t0005 | 0/0 | 936 | 3 | 3 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| t0006 | 0/0 | 928 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| t0007 | 0/0 | 928 | 2 | 0 | 0 | 2 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| t0008 | 0/0 | 928 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| t0009 | 0/0 | 932 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| t0010 | 0/0 | 932 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0014 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0174 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3414 | 134 | 67 | 13 | 41 | 2 | 10 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0001c0007 | 0/0 | 3414 | 6 | 5 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0001c0011 | 0/0 | 3414 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0002c0003 | 0/1 | 3414 | 89 | 3 | 17 | 53 | 4 | 11 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0002c0010 | 0/0 | 3414 | 2 | 0 | 2 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0003c0002 | 0/0 | 3414 | 90 | 12 | 19 | 42 | 7 | 10 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0004c0004 | 0/0 | 3414 | 7 | 1 | 3 | 0 | 0 | 3 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0005c0006 | 0/0 | 3414 | 6 | 0 | 0 | 6 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0006c0005 | 0/0 | 3414 | 6 | 0 | 0 | 4 | 1 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0007c0008 | 0/0 | 3414 | 3 | 0 | 1 | 2 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0008c0009 | 0/0 | 3414 | 2 | 0 | 0 | 2 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0009c0017 | 0/0 | 3414 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0010c0013 | 0/0 | 3414 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0011c0014 | 0/0 | 3414 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0012c0016 | 0/0 | 3414 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0013c0015 | 0/0 | 3414 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0014c0012 | 0/0 | 3414 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4341 | 83 | 45 | 11 | 21 | 2 | 3 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0001c0001t0002 | 0/0 | 4345 | 37 | 18 | 1 | 17 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0001c0001t0003 | 0/0 | 4341 | 9 | 1 | 1 | 2 | 0 | 5 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0001c0001t0004 | 0/0 | 4341 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0001c0001t0005 | 0/0 | 4349 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0001c0001t0006 | 0/0 | 4341 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0001c0001t0007 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0001c0007t0001 | 0/0 | 4341 | 3 | 2 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0001c0007t0002 | 0/0 | 4345 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0001c0007t0005 | 0/0 | 4349 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0001c0011t0002 | 0/0 | 4345 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0002c0003t0001 | 0/1 | 4341 | 40 | 1 | 10 | 23 | 3 | 2 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0002c0003t0002 | 0/0 | 4345 | 44 | 2 | 7 | 25 | 1 | 9 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0002c0003t0003 | 0/0 | 4341 | 2 | 0 | 0 | 2 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0002c0003t0007 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0002c0003t0009 | 0/0 | 4345 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0002c0003t0010 | 0/0 | 4345 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0002c0010t0002 | 0/0 | 4345 | 2 | 0 | 2 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0003c0002t0001 | 0/0 | 4341 | 54 | 6 | 11 | 27 | 4 | 6 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0003c0002t0002 | 0/0 | 4345 | 30 | 6 | 8 | 12 | 2 | 2 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0003c0002t0003 | 0/0 | 4341 | 4 | 0 | 0 | 2 | 1 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0003c0002t0004 | 0/0 | 4341 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0003c0002t0008 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0004c0004t0001 | 0/0 | 4341 | 7 | 1 | 3 | 0 | 0 | 3 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0005c0006t0001 | 0/0 | 4341 | 6 | 0 | 0 | 6 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0006c0005t0001 | 0/0 | 4341 | 5 | 0 | 0 | 4 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0006c0005t0002 | 0/0 | 4345 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0007c0008t0001 | 0/0 | 4341 | 3 | 0 | 1 | 2 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0008c0009t0001 | 0/0 | 4341 | 2 | 0 | 0 | 2 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0009c0017t0001 | 0/0 | 4341 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0010c0013t0001 | 0/0 | 4341 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0011c0014t0004 | 0/0 | 4341 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0012c0016t0002 | 0/0 | 4345 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0013c0015t0001 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| a0014c0012t0001 | 0/0 | 4341 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | copy fasta | chr11 | 8688352 | 8815674 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0014 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0003g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0001t0007g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0007t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0007t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0007t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0007t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0007t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0007t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0001c0011t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0174 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0007g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0009g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0003t0010g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0010t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0002c0010t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0003g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0004g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0003c0002t0008g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0004c0004t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0004c0004t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0004c0004t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0004c0004t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0004c0004t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0004c0004t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0004c0004t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0005c0006t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0005c0006t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0005c0006t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0005c0006t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0005c0006t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0005c0006t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0006c0005t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0006c0005t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0006c0005t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0006c0005t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0006c0005t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0006c0005t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0007c0008t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0007c0008t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0007c0008t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0008c0009t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0008c0009t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0009c0017t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0010c0013t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0011c0014t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0012c0016t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0013c0015t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| a0014c0012t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0002 | c0003 | t0001 | g0199 | EUR | FIN | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00280 | hp2 | a0003 | c0002 | t0001 | g0320 | EUR | FIN | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00323 | hp1 | a0003 | c0002 | t0003 | g0279 | EUR | FIN | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00323 | hp2 | a0002 | c0003 | t0002 | g0178 | EUR | FIN | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00408 | hp1 | a0003 | c0002 | t0001 | g0116 | EAS | CHS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00408 | hp2 | a0003 | c0002 | t0002 | g0289 | EAS | CHS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00438 | hp1 | a0013 | c0015 | t0001 | g0243 | EAS | CHS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00438 | hp2 | a0002 | c0003 | t0002 | g0189 | EAS | CHS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00544 | hp2 | a0002 | c0003 | t0002 | g0160 | EAS | CHS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | CHS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00558 | hp2 | a0002 | c0003 | t0001 | g0131 | EAS | CHS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00597 | hp1 | a0002 | c0003 | t0001 | g0158 | EAS | CHS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00597 | hp2 | a0003 | c0002 | t0002 | g0298 | EAS | CHS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00609 | hp1 | a0002 | c0003 | t0001 | g0244 | EAS | CHS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00609 | hp2 | a0003 | c0002 | t0001 | g0090 | EAS | CHS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00621 | hp1 | a0003 | c0002 | t0001 | g0124 | EAS | CHS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00621 | hp2 | a0002 | c0003 | t0002 | g0194 | EAS | CHS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0349 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00642 | hp1 | a0004 | c0004 | t0001 | g0339 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00642 | hp2 | a0002 | c0003 | t0002 | g0072 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00673 | hp1 | a0003 | c0002 | t0001 | g0100 | EAS | CHS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00733 | hp1 | a0002 | c0003 | t0002 | g0165 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00733 | hp2 | a0003 | c0002 | t0002 | g0332 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01069 | hp2 | a0003 | c0002 | t0002 | g0331 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01070 | hp1 | a0003 | c0002 | t0002 | g0316 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01074 | hp1 | a0002 | c0003 | t0001 | g0145 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01074 | hp2 | a0003 | c0002 | t0001 | g0317 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01099 | hp1 | a0002 | c0003 | t0002 | g0198 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01106 | hp1 | a0003 | c0002 | t0001 | g0313 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01109 | hp2 | a0002 | c0003 | t0002 | g0163 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01167 | hp2 | a0002 | c0003 | t0001 | g0205 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01168 | hp1 | a0003 | c0002 | t0002 | g0312 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01168 | hp2 | a0011 | c0014 | t0004 | g0222 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01169 | hp1 | a0002 | c0003 | t0001 | g0204 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01169 | hp2 | a0003 | c0002 | t0002 | g0309 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01175 | hp1 | a0007 | c0008 | t0001 | g0294 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01175 | hp2 | a0003 | c0002 | t0001 | g0314 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01192 | hp1 | a0003 | c0002 | t0001 | g0125 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01192 | hp2 | a0002 | c0003 | t0002 | g0148 | AMR | PUR | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01255 | hp1 | a0003 | c0002 | t0002 | g0321 | AMR | CLM | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01255 | hp2 | a0003 | c0002 | t0001 | g0139 | AMR | CLM | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01256 | hp1 | a0003 | c0002 | t0001 | g0327 | AMR | CLM | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01256 | hp2 | a0002 | c0010 | t0002 | g0040 | AMR | CLM | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01257 | hp1 | a0003 | c0002 | t0001 | g0037 | AMR | CLM | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01257 | hp2 | a0002 | c0003 | t0001 | g0208 | AMR | CLM | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01258 | hp1 | a0002 | c0010 | t0002 | g0039 | AMR | CLM | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01258 | hp2 | a0002 | c0003 | t0001 | g0209 | AMR | CLM | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01261 | hp1 | a0002 | c0003 | t0002 | g0142 | AMR | CLM | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01261 | hp2 | a0004 | c0004 | t0001 | g0335 | AMR | CLM | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01346 | hp2 | a0003 | c0002 | t0001 | g0127 | AMR | CLM | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01361 | hp1 | a0002 | c0003 | t0002 | g0213 | AMR | CLM | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01361 | hp2 | a0003 | c0002 | t0001 | g0326 | AMR | CLM | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01433 | hp1 | a0003 | c0002 | t0002 | g0322 | AMR | CLM | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01433 | hp2 | a0002 | c0003 | t0001 | g0143 | AMR | CLM | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0261 | EUR | IBS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01515 | hp2 | a0003 | c0002 | t0001 | g0318 | EUR | IBS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01516 | hp1 | a0003 | c0002 | t0002 | g0328 | EUR | IBS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01516 | hp2 | a0002 | c0003 | t0001 | g0212 | EUR | IBS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01517 | hp1 | a0003 | c0002 | t0002 | g0329 | EUR | IBS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0266 | EUR | IBS | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01891 | hp1 | a0009 | c0017 | t0001 | g0120 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01943 | hp1 | a0001 | c0007 | t0001 | g0345 | AMR | PEL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01943 | hp2 | a0003 | c0002 | t0001 | g0152 | AMR | PEL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01978 | hp1 | a0002 | c0003 | t0001 | g0215 | AMR | PEL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01978 | hp2 | a0010 | c0013 | t0001 | g0285 | AMR | PEL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01993 | hp1 | a0002 | c0003 | t0001 | g0176 | AMR | PEL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01993 | hp2 | a0003 | c0002 | t0002 | g0311 | AMR | PEL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02004 | hp1 | a0002 | c0003 | t0001 | g0001 | AMR | PEL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | KHV | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02015 | hp2 | a0002 | c0003 | t0003 | g0193 | EAS | KHV | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02040 | hp1 | a0003 | c0002 | t0002 | g0300 | EAS | KHV | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02055 | hp1 | a0002 | c0003 | t0002 | g0207 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02056 | hp1 | a0003 | c0002 | t0002 | g0292 | EAS | KHV | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02056 | hp2 | a0002 | c0003 | t0001 | g0136 | EAS | KHV | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02071 | hp1 | a0002 | c0003 | t0001 | g0216 | EAS | KHV | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | KHV | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02080 | hp2 | a0008 | c0009 | t0001 | g0134 | EAS | KHV | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02083 | hp2 | a0002 | c0003 | t0009 | g0161 | EAS | KHV | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02132 | hp1 | a0003 | c0002 | t0001 | g0087 | EAS | KHV | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02148 | hp1 | a0003 | c0002 | t0001 | g0306 | AMR | PEL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02148 | hp2 | a0002 | c0003 | t0001 | g0175 | AMR | PEL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02155 | hp1 | a0003 | c0002 | t0002 | g0284 | EAS | CDX | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02155 | hp2 | a0008 | c0009 | t0001 | g0133 | EAS | CDX | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02165 | hp1 | a0014 | c0012 | t0001 | g0236 | EAS | CDX | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02165 | hp2 | a0002 | c0003 | t0002 | g0192 | EAS | CDX | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02280 | hp1 | a0003 | c0002 | t0002 | g0310 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02451 | hp1 | a0001 | c0007 | t0001 | g0036 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | KHV | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02523 | hp2 | a0003 | c0002 | t0001 | g0122 | EAS | KHV | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02647 | hp1 | a0003 | c0002 | t0002 | g0340 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0343 | SAS | PJL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02683 | hp2 | a0003 | c0002 | t0001 | g0108 | SAS | PJL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02698 | hp1 | a0003 | c0002 | t0001 | g0308 | SAS | PJL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02698 | hp2 | a0002 | c0003 | t0002 | g0203 | SAS | PJL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02717 | hp2 | a0012 | c0016 | t0002 | g0304 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02738 | hp2 | a0002 | c0003 | t0001 | g0068 | SAS | PJL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02818 | hp2 | a0003 | c0002 | t0002 | g0301 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0296 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0347 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02896 | hp1 | a0003 | c0002 | t0001 | g0184 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02896 | hp2 | a0003 | c0002 | t0002 | g0030 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0348 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02897 | hp2 | a0003 | c0002 | t0001 | g0182 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02922 | hp1 | a0003 | c0002 | t0001 | g0007 | AFR | ESN | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | ESN | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | ESN | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | ESN | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0346 | AFR | ESN | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02976 | hp1 | a0001 | c0007 | t0005 | g0029 | AFR | ESN | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02976 | hp2 | a0001 | c0007 | t0001 | g0344 | AFR | ESN | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03017 | hp1 | a0002 | c0003 | t0002 | g0169 | SAS | PJL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03017 | hp2 | a0001 | c0011 | t0002 | g0250 | SAS | PJL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03041 | hp2 | a0003 | c0002 | t0002 | g0078 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03098 | hp1 | a0001 | c0007 | t0002 | g0034 | AFR | MSL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | MSL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ESN | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | ESN | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | MSL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0341 | AFR | MSL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03491 | hp1 | a0002 | c0003 | t0001 | g0050 | SAS | PJL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03491 | hp2 | a0004 | c0004 | t0001 | g0333 | SAS | PJL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03654 | hp1 | a0003 | c0002 | t0001 | g0315 | SAS | PJL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | PJL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0342 | SAS | PJL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03669 | hp2 | a0003 | c0002 | t0002 | g0103 | SAS | PJL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03688 | hp1 | a0002 | c0003 | t0002 | g0079 | SAS | STU | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0221 | SAS | STU | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03704 | hp1 | a0002 | c0003 | t0002 | g0202 | SAS | PJL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03704 | hp2 | a0003 | c0002 | t0002 | g0336 | SAS | PJL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03710 | hp1 | a0003 | c0002 | t0003 | g0338 | SAS | PJL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03710 | hp2 | a0002 | c0003 | t0002 | g0186 | SAS | PJL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | BEB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03831 | hp2 | a0002 | c0003 | t0002 | g0210 | SAS | BEB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03834 | hp1 | a0003 | c0002 | t0001 | g0084 | SAS | BEB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0255 | SAS | BEB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03927 | hp1 | a0006 | c0005 | t0001 | g0278 | SAS | BEB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03927 | hp2 | a0002 | c0003 | t0002 | g0170 | SAS | BEB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03942 | hp2 | a0003 | c0002 | t0004 | g0337 | SAS | BEB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG04115 | hp1 | a0002 | c0003 | t0002 | g0185 | SAS | STU | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG04115 | hp2 | a0004 | c0004 | t0001 | g0334 | SAS | STU | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG04184 | hp1 | a0002 | c0003 | t0002 | g0214 | SAS | BEB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG04184 | hp2 | a0004 | c0004 | t0001 | g0319 | SAS | BEB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0172 | SAS | STU | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG04204 | hp2 | a0003 | c0002 | t0001 | g0111 | SAS | STU | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG04228 | hp1 | a0003 | c0002 | t0001 | g0109 | SAS | STU | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0240 | SAS | STU | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18612 | hp1 | a0002 | c0003 | t0002 | g0069 | EAS | CHB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18612 | hp2 | a0002 | c0003 | t0003 | g0094 | EAS | CHB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | YRI | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | YRI | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18939 | hp1 | a0007 | c0008 | t0001 | g0297 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18939 | hp2 | a0002 | c0003 | t0002 | g0146 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18942 | hp1 | a0002 | c0003 | t0001 | g0154 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18942 | hp2 | a0003 | c0002 | t0001 | g0132 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18946 | hp1 | a0006 | c0005 | t0001 | g0112 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18946 | hp2 | a0002 | c0003 | t0002 | g0071 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18948 | hp1 | a0002 | c0003 | t0002 | g0153 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18950 | hp1 | a0003 | c0002 | t0001 | g0101 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18950 | hp2 | a0002 | c0003 | t0001 | g0190 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18951 | hp2 | a0003 | c0002 | t0001 | g0206 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18952 | hp1 | a0003 | c0002 | t0003 | g0102 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18952 | hp2 | a0003 | c0002 | t0001 | g0095 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18953 | hp1 | a0002 | c0003 | t0001 | g0218 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18954 | hp2 | a0005 | c0006 | t0001 | g0130 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18956 | hp1 | a0002 | c0003 | t0002 | g0141 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18956 | hp2 | a0003 | c0002 | t0002 | g0286 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18961 | hp1 | a0003 | c0002 | t0001 | g0256 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18961 | hp2 | a0002 | c0003 | t0001 | g0129 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18962 | hp1 | a0002 | c0003 | t0002 | g0149 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18966 | hp1 | a0002 | c0003 | t0010 | g0350 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18966 | hp2 | a0002 | c0003 | t0001 | g0166 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18968 | hp2 | a0005 | c0006 | t0001 | g0288 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18969 | hp1 | a0003 | c0002 | t0001 | g0110 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18969 | hp2 | a0002 | c0003 | t0002 | g0191 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18970 | hp2 | a0003 | c0002 | t0001 | g0099 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18975 | hp1 | a0003 | c0002 | t0001 | g0283 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18979 | hp1 | a0003 | c0002 | t0001 | g0106 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18980 | hp1 | a0003 | c0002 | t0001 | g0123 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18980 | hp2 | a0002 | c0003 | t0002 | g0159 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18982 | hp1 | a0003 | c0002 | t0001 | g0089 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18982 | hp2 | a0002 | c0003 | t0002 | g0157 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18983 | hp2 | a0002 | c0003 | t0001 | g0164 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18986 | hp1 | a0003 | c0002 | t0002 | g0290 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18988 | hp1 | a0005 | c0006 | t0001 | g0093 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18988 | hp2 | a0002 | c0003 | t0001 | g0144 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18990 | hp1 | a0003 | c0002 | t0001 | g0105 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18990 | hp2 | a0002 | c0003 | t0002 | g0156 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18992 | hp1 | a0002 | c0003 | t0002 | g0070 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18994 | hp1 | a0001 | c0001 | t0007 | g0351 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18994 | hp2 | a0002 | c0003 | t0002 | g0067 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18995 | hp1 | a0002 | c0003 | t0002 | g0179 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18995 | hp2 | a0003 | c0002 | t0001 | g0104 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18997 | hp1 | a0002 | c0003 | t0001 | g0188 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18997 | hp2 | a0005 | c0006 | t0001 | g0091 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18998 | hp1 | a0006 | c0005 | t0001 | g0113 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18999 | hp1 | a0003 | c0002 | t0001 | g0280 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18999 | hp2 | a0002 | c0003 | t0002 | g0155 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19004 | hp1 | a0002 | c0003 | t0002 | g0054 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19004 | hp2 | a0003 | c0002 | t0002 | g0291 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19005 | hp1 | a0003 | c0002 | t0001 | g0287 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19005 | hp2 | a0002 | c0003 | t0002 | g0031 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19007 | hp1 | a0002 | c0003 | t0001 | g0197 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19007 | hp2 | a0003 | c0002 | t0001 | g0083 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19009 | hp2 | a0003 | c0002 | t0002 | g0088 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19010 | hp1 | a0002 | c0003 | t0001 | g0211 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19011 | hp1 | a0002 | c0003 | t0002 | g0151 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19011 | hp2 | a0003 | c0002 | t0002 | g0138 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19012 | hp1 | a0002 | c0003 | t0001 | g0085 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19012 | hp2 | a0003 | c0002 | t0001 | g0098 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | LWK | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | LWK | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | LWK | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19057 | hp1 | a0002 | c0003 | t0002 | g0147 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19057 | hp2 | a0003 | c0002 | t0003 | g0097 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19060 | hp1 | a0002 | c0003 | t0001 | g0126 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19060 | hp2 | a0002 | c0003 | t0001 | g0259 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19062 | hp1 | a0007 | c0008 | t0001 | g0295 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19062 | hp2 | a0002 | c0003 | t0002 | g0196 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19063 | hp1 | a0003 | c0002 | t0001 | g0305 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19064 | hp1 | a0002 | c0003 | t0001 | g0181 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19064 | hp2 | a0003 | c0002 | t0001 | g0282 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19066 | hp2 | a0005 | c0006 | t0001 | g0092 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19067 | hp2 | a0006 | c0005 | t0001 | g0115 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19074 | hp2 | a0003 | c0002 | t0002 | g0107 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19079 | hp1 | a0002 | c0003 | t0001 | g0137 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19081 | hp1 | a0002 | c0003 | t0002 | g0195 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19081 | hp2 | a0006 | c0005 | t0001 | g0114 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19083 | hp1 | a0003 | c0002 | t0001 | g0082 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19083 | hp2 | a0002 | c0003 | t0001 | g0150 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19084 | hp2 | a0003 | c0002 | t0001 | g0128 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19085 | hp1 | a0002 | c0003 | t0007 | g0352 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19085 | hp2 | a0005 | c0006 | t0001 | g0086 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19086 | hp1 | a0003 | c0002 | t0008 | g0032 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19088 | hp1 | a0002 | c0003 | t0001 | g0135 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19088 | hp2 | a0002 | c0003 | t0002 | g0201 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA19090 | hp2 | a0002 | c0003 | t0001 | g0177 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ASW | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA20129 | hp2 | a0003 | c0002 | t0001 | g0008 | AFR | ASW | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA20752 | hp1 | a0003 | c0002 | t0001 | g0324 | EUR | TSI | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA20752 | hp2 | a0002 | c0003 | t0001 | g0173 | EUR | TSI | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA20805 | hp1 | a0003 | c0002 | t0001 | g0325 | EUR | TSI | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA20805 | hp2 | a0006 | c0005 | t0002 | g0180 | EUR | TSI | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG01123 | hp2 | a0004 | c0004 | t0001 | g0307 | AMR | CLM | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG02559 | hp2 | a0003 | c0002 | t0002 | g0058 | AFR | ACB | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03471 | hp1 | a0001 | c0007 | t0005 | g0024 | AFR | MSL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG06807 | hp1 | a0004 | c0004 | t0001 | g0323 | AFR | USA | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| HG06807 | hp2 | a0002 | c0003 | t0001 | g0075 | AFR | USA | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18955 | hp1 | a0003 | c0002 | t0002 | g0096 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | USA | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA20300 | hp2 | a0003 | c0002 | t0001 | g0183 | AFR | USA | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA21309 | hp1 | a0002 | c0003 | t0002 | g0217 | AFR | LWK | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| NA21309 | hp2 | a0003 | c0002 | t0001 | g0303 | AFR | LWK | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0003 | t0001 | g0174 | REF | REF | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0014 | REF | REF | DENND2B_chr11_8688352_8815674 | DENND2B | chr11 | 8688352 | 8815674 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:8707189
|
C | T | 4 | a0005a0007a0008others(1): Show | 12 | HG00438.hp1 HG01175.hp1 HG02080.hp2 others(9): Show |
missense_variant | MODERATE | c.2467G>A | p.Ala823Thr | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/20 | 2650/4341 | 2467/3414 | 823/1137 | chr11 | 8707189 | ||
| chr11:8730093
|
G | C | 7 | a0003a0004a0005others(4): Show | 114 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
missense_variant | MODERATE | c.1197C>G | p.Asp399Glu | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/20 | 1380/4341 | 1197/3414 | 399/1137 | chr11 | 8730093 | ||
| chr11:8730199
|
G | A | 1 | a0012 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.1091C>T | p.Thr364Ile | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/20 | 1274/4341 | 1091/3414 | 364/1137 | chr11 | 8730199 | ||
| chr11:8730342
|
C | G | 3 | a0002a0006a0008 | 99 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(96): Show |
missense_variant | MODERATE | c.948G>C | p.Lys316Asn | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/20 | 1131/4341 | 948/3414 | 316/1137 | chr11 | 8730342 | ||
| chr11:8730355
|
C | T | 1 | a0011 | 1 | HG01168.hp2 | missense_variant | MODERATE | c.935G>A | p.Arg312Gln | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/20 | 1118/4341 | 935/3414 | 312/1137 | chr11 | 8730355 | ||
| chr11:8730541
|
C | T | 2 | a0007a0010 | 4 | HG01175.hp1 HG01978.hp2 NA18939.hp1 others(1): Show |
missense_variant | MODERATE | c.749G>A | p.Arg250Gln | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/20 | 932/4341 | 749/3414 | 250/1137 | chr11 | 8730541 | ||
| chr11:8730621
|
C | G | 1 | a0014 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.669G>C | p.Lys223Asn | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/20 | 852/4341 | 669/3414 | 223/1137 | chr11 | 8730621 | ||
| chr11:8730818
|
G | C | 1 | a0009 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.472C>G | p.Arg158Gly | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/20 | 655/4341 | 472/3414 | 158/1137 | chr11 | 8730818 | ||
| chr11:8731051
|
G | C | 1 | a0004 | 7 | HG00642.hp1 HG01123.hp2 HG01261.hp2 others(4): Show |
missense_variant | MODERATE | c.239C>G | p.Pro80Arg | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/20 | 422/4341 | 239/3414 | 80/1137 | chr11 | 8731051 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:8712713
|
G | A | 1 | a0002c0010 | 2 | HG01256.hp2 HG01258.hp1 |
synonymous_variant | LOW | c.2010C>T | p.His670His | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 9/20 | 2193/4341 | 2010/3414 | 670/1137 | chr11 | 8712713 | ||
| chr11:8730030
|
A | G | 1 | a0011c0014 | 1 | HG01168.hp2 | synonymous_variant | LOW | c.1260T>C | p.Pro420Pro | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/20 | 1443/4341 | 1260/3414 | 420/1137 | chr11 | 8730030 | ||
| chr11:8730399
|
G | A | 1 | a0001c0007 | 6 | HG01943.hp1 HG02451.hp1 HG02976.hp1 others(3): Show |
synonymous_variant | LOW | c.891C>T | p.Gly297Gly | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/20 | 1074/4341 | 891/3414 | 297/1137 | chr11 | 8730399 | ||
| chr11:8730465
|
C | T | 1 | a0001c0011 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.825G>A | p.Arg275Arg | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/20 | 1008/4341 | 825/3414 | 275/1137 | chr11 | 8730465 | ||
| chr11:8730969
|
C | T | 1 | a0001c0011 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.321G>A | p.Ser107Ser | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/20 | 504/4341 | 321/3414 | 107/1137 | chr11 | 8730969 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:8693527
|
G | C | 3 | a0001c0001t0004a0003c0002t0004a0011c0014t0004 | 3 | HG01168.hp2 HG03942.hp2 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*569C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 20/20 | 569 | chr11 | 8693527 | |||||
| chr11:8693546
|
C | T | 1 | a0003c0002t0008 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*550G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 20/20 | 550 | chr11 | 8693546 | |||||
| chr11:8693696
|
G | A | 1 | a0002c0003t0009 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*400C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 20/20 | 400 | chr11 | 8693696 | |||||
| chr11:8693715
|
T | TCAGG | 10 | a0001c0001t0002a0001c0007t0002a0001c0011t0002others(7): Show | 119 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*377_*380dupCCTG | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 20/20 | 380 | chr11 | 8693715 | |||||
| chr11:8693715
|
T | TCAGGCAG others(1): Show |
2 | a0001c0001t0005a0001c0007t0005 | 3 | HG02145.hp1 HG02976.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*373_*380dupCCTGCC others(2): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 20/20 | 380 | chr11 | 8693715 | |||||
| chr11:8693728
|
C | A | 3 | a0001c0001t0003a0002c0003t0003a0003c0002t0003 | 15 | HG00323.hp1 HG01167.hp1 HG02015.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*368G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 20/20 | 368 | chr11 | 8693728 | |||||
| chr11:8693809
|
C | T | 1 | a0001c0001t0006 | 2 | HG02257.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*287G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 20/20 | 287 | chr11 | 8693809 | |||||
| chr11:8810669
|
C | A | 3 | a0001c0001t0007a0002c0003t0007a0002c0003t0010 | 3 | NA18966.hp1 NA18994.hp1 NA19085.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-178G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/20 | chr11 | 8810669 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:8694145
|
G | A | 1 | a0003c0002t0002g0289 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3380-15C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 19/19 | chr11 | 8694145 | ||||||
| chr11:8694332
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3380-202C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 19/19 | chr11 | 8694332 | ||||||
| chr11:8694345
|
C | T | 1 | a0003c0002t0001g0320 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3380-215G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 19/19 | chr11 | 8694345 | ||||||
| chr11:8694465
|
C | G | 1 | a0001c0001t0001g0006 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3380-335G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 19/19 | chr11 | 8694465 | ||||||
| chr11:8694482
|
A | G | 2 | a0001c0001t0001g0257a0001c0007t0002g0034 | 2 | HG03098.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.3380-352T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 19/19 | chr11 | 8694482 | ||||||
| chr11:8694524
|
G | C | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3380-394C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 19/19 | chr11 | 8694524 | ||||||
| chr11:8694618
|
A | T | 2 | a0003c0002t0001g0306a0003c0002t0002g0311 | 2 | HG01993.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.3380-488T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 19/19 | chr11 | 8694618 | ||||||
| chr11:8694738
|
G | A | 1 | a0001c0001t0003g0255 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3380-608C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 19/19 | chr11 | 8694738 | ||||||
| chr11:8694760
|
A | G | 1 | a0001c0001t0003g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3380-630T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 19/19 | chr11 | 8694760 | ||||||
| chr11:8695093
|
T | C | 1 | a0001c0001t0003g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3379+370A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 19/19 | chr11 | 8695093 | ||||||
| chr11:8695302
|
G | A | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3379+161C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 19/19 | chr11 | 8695302 | ||||||
| chr11:8695406
|
C | A | 1 | a0001c0007t0001g0345 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3379+57G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 19/19 | chr11 | 8695406 | ||||||
| chr11:8695421
|
T | A | 53 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0021others(50): Show | 53 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.3379+42A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 19/19 | chr11 | 8695421 | ||||||
| chr11:8695456
|
C | T | 122 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0060others(119): Show | 122 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(119): Show |
splice_region_variant&intron_variant | LOW | c.3379+7G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 19/19 | chr11 | 8695456 | ||||||
| chr11:8695852
|
G | A | 1 | a0002c0003t0001g0144 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.3293-303C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 18/19 | chr11 | 8695852 | ||||||
| chr11:8695950
|
T | TG | 56 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0019others(53): Show | 56 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.3293-402dupC | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 18/19 | chr11 | 8695950 | ||||||
| chr11:8695966
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3293-417G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 18/19 | chr11 | 8695966 | ||||||
| chr11:8696031
|
C | T | 1 | a0003c0002t0001g0124 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3292+396G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 18/19 | chr11 | 8696031 | ||||||
| chr11:8696054
|
T | C | 1 | a0002c0003t0010g0350 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3292+373A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 18/19 | chr11 | 8696054 | ||||||
| chr11:8696060
|
G | C | 213 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(210): Show | 213 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.3292+367C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 18/19 | chr11 | 8696060 | ||||||
| chr11:8696248
|
T | C | 1 | a0003c0002t0001g0111 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3292+179A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 18/19 | chr11 | 8696248 | ||||||
| chr11:8696252
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3292+175C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 18/19 | chr11 | 8696252 | ||||||
| chr11:8696327
|
G | C | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3292+100C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 18/19 | chr11 | 8696327 | ||||||
| chr11:8696371
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3292+56A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 18/19 | chr11 | 8696371 | ||||||
| chr11:8696767
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3053-101G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 17/19 | chr11 | 8696767 | ||||||
| chr11:8697028
|
A | G | 6 | a0001c0001t0002g0016a0001c0001t0002g0121a0001c0001t0002g0341others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3053-362T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 17/19 | chr11 | 8697028 | ||||||
| chr11:8697127
|
A | G | 12 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(9): Show | 12 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.3052+398T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 17/19 | chr11 | 8697127 | ||||||
| chr11:8697394
|
G | C | 2 | a0001c0001t0002g0021a0001c0001t0002g0296 | 2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3052+131C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 17/19 | chr11 | 8697394 | ||||||
| chr11:8697422
|
A | C | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3052+103T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 17/19 | chr11 | 8697422 | ||||||
| chr11:8697474
|
G | T | 2 | a0001c0001t0001g0241a0001c0001t0001g0269 | 2 | NA18955.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.3052+51C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 17/19 | chr11 | 8697474 | ||||||
| chr11:8697715
|
G | A | 5 | a0001c0001t0001g0261a0001c0001t0001g0264a0001c0001t0001g0265others(2): Show | 5 | HG01070.hp2 HG01099.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.2941-79C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8697715 | ||||||
| chr11:8697831
|
A | T | 1 | a0002c0003t0002g0202 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2941-195T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8697831 | ||||||
| chr11:8698068
|
C | G | 212 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0025others(209): Show | 212 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.2941-432G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698068 | ||||||
| chr11:8698137
|
C | CA | 43 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0026others(40): Show | 43 | HG00280.hp1 HG00673.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.2941-502dupT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698137 | ||||||
| chr11:8698137
|
C | CAA | 41 | a0001c0001t0001g0006a0001c0001t0001g0167a0001c0001t0001g0219others(38): Show | 41 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.2941-503_2941-502d others(4): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698137 | ||||||
| chr11:8698137
|
C | CAAA | 31 | a0001c0001t0001g0035a0001c0001t0001g0117a0001c0001t0001g0168others(28): Show | 31 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.2941-504_2941-502d others(5): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698137 | ||||||
| chr11:8698137
|
C | CAAAA | 26 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0001g0257others(23): Show | 26 | HG00323.hp2 HG00621.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.2941-505_2941-502d others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698137 | ||||||
| chr11:8698137
|
C | CAAAAA | 23 | a0001c0001t0001g0060a0001c0001t0001g0231a0001c0001t0001g0239others(20): Show | 23 | HG00642.hp2 HG01070.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.2941-506_2941-502d others(7): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698137 | ||||||
| chr11:8698137
|
C | CAAAAAA | 23 | a0001c0001t0001g0003a0001c0001t0001g0254a0001c0001t0002g0228others(20): Show | 23 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.2941-507_2941-502d others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698137 | ||||||
| chr11:8698137
|
C | CAAAAAAA | 14 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0242others(11): Show | 14 | HG00673.hp2 HG01099.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2941-508_2941-502d others(9): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698137 | ||||||
| chr11:8698137
|
C | CAAAAAAA others(1): Show |
12 | a0001c0001t0001g0245a0002c0003t0001g0259a0002c0003t0002g0151others(9): Show | 12 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.2941-509_2941-502d others(10): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698137 | ||||||
| chr11:8698137
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0002g0052 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2941-511_2941-502d others(12): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698137 | ||||||
| chr11:8698137
|
C | CAAAAAAA others(4): Show |
1 | a0002c0003t0002g0153 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2941-512_2941-502d others(13): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698137 | ||||||
| chr11:8698137
|
CA | C | 16 | a0001c0001t0002g0021a0001c0001t0002g0041a0001c0001t0002g0045others(13): Show | 16 | HG00558.hp1 HG00621.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.2941-502delT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698137 | ||||||
| chr11:8698137
|
CAA | C | 9 | a0001c0001t0001g0028a0001c0001t0001g0062a0001c0001t0001g0063others(6): Show | 9 | HG01109.hp1 HG01346.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2941-503_2941-502d others(4): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698137 | ||||||
| chr11:8698137
|
CAAA | C | 11 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0033others(8): Show | 11 | HG00639.hp1 HG01168.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.2941-504_2941-502d others(5): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698137 | ||||||
| chr11:8698137
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2941-511_2941-502d others(12): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698137 | ||||||
| chr11:8698137
|
CAAAAAAA others(7): Show |
C | 7 | a0001c0001t0001g0023a0001c0001t0001g0076a0001c0001t0001g0081others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.2941-515_2941-502d others(16): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698137 | ||||||
| chr11:8698166
|
A | AAG | 7 | a0001c0001t0003g0004a0001c0001t0003g0080a0002c0003t0002g0185others(4): Show | 7 | HG00438.hp2 HG01167.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2941-531_2941-530i others(4): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698166 | ||||||
| chr11:8698166
|
A | AG | 17 | a0001c0001t0001g0276a0001c0001t0002g0010a0001c0001t0003g0171others(14): Show | 17 | HG00323.hp1 HG01175.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.2941-531dupC | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698166 | ||||||
| chr11:8698166
|
A | G | 31 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0001g0119others(28): Show | 31 | HG00558.hp1 HG00621.hp2 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.2941-530T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698166 | ||||||
| chr11:8698167
|
G | A | 18 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0241others(15): Show | 18 | HG00544.hp2 HG00673.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.2941-531C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698167 | ||||||
| chr11:8698199
|
C | G | 1 | a0002c0003t0002g0214 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2941-563G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698199 | ||||||
| chr11:8698260
|
C | CCAGG | 11 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(8): Show | 11 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.2941-628_2941-625d others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698260 | ||||||
| chr11:8698408
|
T | C | 97 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0060others(94): Show | 97 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.2940+525A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698408 | ||||||
| chr11:8698450
|
C | T | 10 | a0003c0002t0001g0308a0003c0002t0001g0313a0003c0002t0001g0314others(7): Show | 10 | HG00280.hp2 HG01074.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.2940+483G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698450 | ||||||
| chr11:8698568
|
T | C | 3 | a0002c0003t0002g0071a0002c0003t0002g0179a0002c0003t0002g0191 | 3 | NA18946.hp2 NA18969.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.2940+365A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698568 | ||||||
| chr11:8698663
|
G | A | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2940+270C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 16/19 | chr11 | 8698663 | ||||||
| chr11:8699068
|
C | A | 69 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0060others(66): Show | 69 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.2899-94G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 15/19 | chr11 | 8699068 | ||||||
| chr11:8699175
|
T | C | 1 | a0001c0001t0001g0268 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2898+38A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 15/19 | chr11 | 8699175 | ||||||
| chr11:8699193
|
T | G | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0033others(7): Show | 10 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.2898+20A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 15/19 | chr11 | 8699193 | ||||||
| chr11:8699426
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | HG02717.hp1 HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2721-36G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8699426 | ||||||
| chr11:8699428
|
G | A | 1 | a0003c0002t0002g0096 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2721-38C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8699428 | ||||||
| chr11:8699535
|
G | C | 3 | a0001c0001t0005g0022a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02145.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2721-145C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8699535 | ||||||
| chr11:8699553
|
C | T | 1 | a0001c0001t0003g0255 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2721-163G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8699553 | ||||||
| chr11:8699558
|
C | T | 3 | a0001c0001t0005g0022a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02145.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2721-168G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8699558 | ||||||
| chr11:8699576
|
G | A | 5 | a0001c0001t0002g0016a0001c0001t0002g0121a0001c0001t0002g0341others(2): Show | 5 | HG02559.hp2 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2721-186C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8699576 | ||||||
| chr11:8699594
|
T | A | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2721-204A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8699594 | ||||||
| chr11:8699613
|
G | A | 3 | a0001c0001t0005g0022a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02145.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2721-223C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8699613 | ||||||
| chr11:8699631
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2721-241C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8699631 | ||||||
| chr11:8699688
|
A | C | 1 | a0003c0002t0002g0096 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2721-298T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8699688 | ||||||
| chr11:8699785
|
T | A | 1 | a0001c0001t0001g0117 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2721-395A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8699785 | ||||||
| chr11:8699850
|
G | C | 1 | a0003c0002t0001g0303 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2721-460C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8699850 | ||||||
| chr11:8699952
|
C | G | 1 | a0003c0002t0002g0096 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2721-562G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8699952 | ||||||
| chr11:8700064
|
TG | T | 131 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0035others(128): Show | 131 | HG00408.hp1 HG00544.hp2 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.2721-675delC | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8700064 | ||||||
| chr11:8700066
|
G | T | 29 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0047others(26): Show | 29 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.2721-676C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8700066 | ||||||
| chr11:8700067
|
G | C | 1 | a0001c0001t0001g0187 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2721-677C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8700067 | ||||||
| chr11:8700068
|
G | A | 1 | a0001c0001t0002g0045 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2721-678C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8700068 | ||||||
| chr11:8700068
|
G | T | 2 | a0002c0003t0002g0067a0002c0003t0002g0155 | 2 | NA18994.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.2721-678C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8700068 | ||||||
| chr11:8700069
|
G | A | 28 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0047others(25): Show | 28 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.2721-679C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8700069 | ||||||
| chr11:8700070
|
G | A | 1 | a0002c0003t0002g0170 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2721-680C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8700070 | ||||||
| chr11:8700070
|
G | T | 1 | a0003c0002t0001g0206 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2721-680C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8700070 | ||||||
| chr11:8700073
|
G | C | 1 | a0003c0002t0002g0096 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2721-683C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8700073 | ||||||
| chr11:8700074
|
C | A | 1 | a0003c0002t0002g0096 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2721-684G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8700074 | ||||||
| chr11:8700075
|
A | G | 1 | a0003c0002t0002g0096 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2721-685T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8700075 | ||||||
| chr11:8700449
|
T | G | 1 | a0003c0002t0002g0096 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2721-1059A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8700449 | ||||||
| chr11:8700462
|
C | T | 1 | a0003c0002t0002g0058 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2721-1072G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8700462 | ||||||
| chr11:8700517
|
G | C | 2 | a0002c0010t0002g0039a0002c0010t0002g0040 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2721-1127C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8700517 | ||||||
| chr11:8700613
|
C | G | 1 | a0002c0003t0002g0196 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2721-1223G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8700613 | ||||||
| chr11:8700639
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2721-1249A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8700639 | ||||||
| chr11:8700663
|
A | T | 1 | a0003c0002t0002g0096 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2721-1273T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8700663 | ||||||
| chr11:8700778
|
G | C | 197 | a0001c0001t0001g0006a0001c0001t0001g0025a0001c0001t0001g0027others(194): Show | 197 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.2721-1388C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8700778 | ||||||
| chr11:8700816
|
T | A | 1 | a0001c0001t0002g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2721-1426A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8700816 | ||||||
| chr11:8700892
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0252 | 2 | HG00741.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2721-1502C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8700892 | ||||||
| chr11:8700893
|
C | G | 8 | a0001c0001t0001g0187a0001c0001t0001g0263a0002c0003t0001g0001others(5): Show | 8 | HG01069.hp1 HG01433.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.2721-1503G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8700893 | ||||||
| chr11:8701074
|
A | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0242others(62): Show | 65 | HG00323.hp2 HG00544.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.2720+1498T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701074 | ||||||
| chr11:8701344
|
C | CAGGGGCG others(3): Show |
1 | a0001c0001t0001g0242 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2720+1227_2720+122 others(14): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701344 | ||||||
| chr11:8701344
|
C | CAGGGGGG others(1): Show |
3 | a0001c0001t0002g0021a0001c0001t0002g0055a0001c0001t0002g0296 | 3 | HG02886.hp2 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2720+1227_2720+122 others(12): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701344 | ||||||
| chr11:8701344
|
C | CAGGGGGG others(5): Show |
1 | a0001c0001t0002g0046 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2720+1227_2720+122 others(16): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701344 | ||||||
| chr11:8701344
|
C | CAGGGGGG others(7): Show |
1 | a0001c0001t0002g0043 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2720+1227_2720+122 others(18): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701344 | ||||||
| chr11:8701344
|
C | CAGGGGGG others(8): Show |
1 | a0001c0001t0002g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2720+1227_2720+122 others(19): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701344 | ||||||
| chr11:8701344
|
C | CG | 52 | a0001c0001t0001g0026a0001c0001t0001g0076a0001c0001t0001g0168others(49): Show | 52 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.2720+1227dupC | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701344 | ||||||
| chr11:8701344
|
C | CGG | 33 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0062others(30): Show | 33 | HG01070.hp2 HG01099.hp2 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.2720+1226_2720+122 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701344 | ||||||
| chr11:8701344
|
C | CGGGGGGG others(3): Show |
2 | a0001c0001t0002g0044a0003c0002t0002g0311 | 2 | HG01993.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.2720+1218_2720+122 others(14): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701344 | ||||||
| chr11:8701344
|
C | CGGGGGGG others(7): Show |
1 | a0003c0002t0001g0306 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2720+1214_2720+122 others(18): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701344 | ||||||
| chr11:8701344
|
C | CGGGGGGG others(9): Show |
1 | a0001c0001t0002g0041 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2720+1227_2720+122 others(20): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701344 | ||||||
| chr11:8701344
|
CG | C | 22 | a0001c0001t0001g0015a0001c0001t0001g0023a0001c0001t0001g0057others(19): Show | 22 | HG00642.hp1 HG01074.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.2720+1227delC | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701344 | ||||||
| chr11:8701345
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0002g0224others(1): Show | 4 | HG02572.hp1 HG03704.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.2720+1227C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701345 | ||||||
| chr11:8701345
|
G | C | 5 | a0001c0001t0005g0022a0001c0007t0005g0024a0001c0007t0005g0029others(2): Show | 5 | HG02145.hp1 HG02559.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2720+1227C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701345 | ||||||
| chr11:8701345
|
G | T | 1 | a0001c0001t0002g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2720+1227C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701345 | ||||||
| chr11:8701348
|
G | C | 2 | a0001c0007t0005g0024a0001c0007t0005g0029 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2720+1224C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701348 | ||||||
| chr11:8701349
|
G | T | 4 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(1): Show | 4 | HG02451.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2720+1223C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701349 | ||||||
| chr11:8701349
|
GGGGGGGG others(4): Show |
G | 2 | a0001c0001t0002g0010a0012c0016t0002g0304 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2720+1212_2720+122 others(15): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701349 | ||||||
| chr11:8701350
|
G | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | NA18979.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.2720+1222C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701350 | ||||||
| chr11:8701350
|
G | T | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2720+1222C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701350 | ||||||
| chr11:8701353
|
GGGGGGGA | G | 31 | a0001c0001t0001g0027a0001c0001t0001g0347a0001c0001t0001g0348others(28): Show | 31 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.2720+1212_2720+121 others(11): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701353 | ||||||
| chr11:8701354
|
GGGGGGA | G | 34 | a0001c0001t0001g0033a0001c0001t0001g0038a0001c0001t0001g0260others(31): Show | 34 | HG00733.hp1 HG01255.hp2 HG01256.hp2 others(31): Show |
intron_variant | MODIFIER | c.2720+1212_2720+121 others(10): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701354 | ||||||
| chr11:8701355
|
GGGGGA | G | 35 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0238others(32): Show | 35 | HG00408.hp1 HG00609.hp2 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.2720+1212_2720+121 others(9): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701355 | ||||||
| chr11:8701356
|
GGGGA | G | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0117others(26): Show | 29 | HG00597.hp1 HG00621.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.2720+1212_2720+121 others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701356 | ||||||
| chr11:8701359
|
GA | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0249a0001c0001t0002g0224others(1): Show | 4 | HG00741.hp1 HG02257.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.2720+1212delT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701359 | ||||||
| chr11:8701360
|
A | G | 31 | a0001c0001t0001g0047a0001c0001t0001g0062a0001c0001t0001g0066others(28): Show | 31 | HG00438.hp2 HG00558.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.2720+1212T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701360 | ||||||
| chr11:8701369
|
A | G | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(186): Show | 189 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(186): Show |
intron_variant | MODIFIER | c.2720+1203T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701369 | ||||||
| chr11:8701384
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0047 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2720+1188C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701384 | ||||||
| chr11:8701438
|
T | C | 1 | a0001c0001t0001g0277 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2720+1134A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701438 | ||||||
| chr11:8701511
|
T | G | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0033others(7): Show | 10 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.2720+1061A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701511 | ||||||
| chr11:8701884
|
C | G | 8 | a0001c0001t0001g0187a0001c0001t0001g0263a0002c0003t0001g0001others(5): Show | 8 | HG01069.hp1 HG01433.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.2720+688G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701884 | ||||||
| chr11:8701953
|
C | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0061a0001c0001t0001g0252 | 3 | HG00741.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2720+619G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8701953 | ||||||
| chr11:8702016
|
G | A | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(182): Show | 185 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(182): Show |
intron_variant | MODIFIER | c.2720+556C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8702016 | ||||||
| chr11:8702027
|
A | G | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(183): Show | 186 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.2720+545T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8702027 | ||||||
| chr11:8702161
|
C | T | 3 | a0003c0002t0002g0309a0003c0002t0002g0312a0003c0002t0002g0316 | 3 | HG01070.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2720+411G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8702161 | ||||||
| chr11:8702202
|
G | A | 3 | a0001c0001t0001g0230a0001c0001t0001g0330a0006c0005t0001g0278 | 3 | HG01106.hp2 HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.2720+370C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8702202 | ||||||
| chr11:8702279
|
C | T | 8 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0002g0048others(5): Show | 8 | HG01884.hp2 HG02622.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.2720+293G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8702279 | ||||||
| chr11:8702417
|
G | T | 1 | a0001c0001t0001g0263 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2720+155C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 14/19 | chr11 | 8702417 | ||||||
| chr11:8702732
|
CGAT | C | 9 | a0003c0002t0001g0308a0003c0002t0001g0313a0003c0002t0001g0314others(6): Show | 9 | HG00280.hp2 HG01074.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.2572-15_2572-13del others(3): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8702732 | ||||||
| chr11:8702778
|
G | T | 1 | a0001c0001t0001g0017 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2572-58C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8702778 | ||||||
| chr11:8702798
|
A | AG | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(202): Show | 205 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.2572-79dupC | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8702798 | ||||||
| chr11:8702806
|
T | C | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2572-86A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8702806 | ||||||
| chr11:8702908
|
G | A | 5 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0065others(2): Show | 5 | HG01109.hp1 HG01346.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2572-188C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8702908 | ||||||
| chr11:8703007
|
G | A | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0033others(7): Show | 10 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.2572-287C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8703007 | ||||||
| chr11:8703024
|
A | G | 150 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(147): Show | 150 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.2572-304T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8703024 | ||||||
| chr11:8703316
|
CAT | C | 5 | a0001c0001t0002g0016a0001c0001t0002g0121a0001c0001t0002g0341others(2): Show | 5 | HG02896.hp2 HG02970.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2572-598_2572-597d others(4): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8703316 | ||||||
| chr11:8703488
|
G | C | 1 | a0001c0001t0002g0229 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2572-768C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8703488 | ||||||
| chr11:8703721
|
A | G | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(208): Show | 211 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.2572-1001T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8703721 | ||||||
| chr11:8703925
|
G | C | 1 | a0001c0001t0001g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2572-1205C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8703925 | ||||||
| chr11:8703936
|
C | T | 1 | a0002c0003t0001g0001 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2572-1216G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8703936 | ||||||
| chr11:8704024
|
G | A | 1 | a0001c0007t0001g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2572-1304C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8704024 | ||||||
| chr11:8704036
|
A | G | 3 | a0001c0001t0004g0172a0003c0002t0004g0337a0011c0014t0004g0222 | 3 | HG01168.hp2 HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2572-1316T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8704036 | ||||||
| chr11:8704079
|
G | C | 63 | a0001c0001t0001g0258a0001c0001t0002g0052a0001c0001t0002g0053others(60): Show | 63 | HG00323.hp2 HG00544.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.2572-1359C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8704079 | ||||||
| chr11:8704469
|
T | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2572-1749A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8704469 | ||||||
| chr11:8704524
|
G | T | 21 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0033others(18): Show | 21 | HG00639.hp1 HG01109.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.2572-1804C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8704524 | ||||||
| chr11:8704556
|
C | G | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2572-1836G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8704556 | ||||||
| chr11:8704622
|
A | C | 1 | a0001c0007t0001g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2572-1902T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8704622 | ||||||
| chr11:8704728
|
C | T | 5 | a0001c0001t0001g0261a0001c0001t0001g0264a0001c0001t0001g0265others(2): Show | 5 | HG01070.hp2 HG01099.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.2572-2008G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8704728 | ||||||
| chr11:8704777
|
A | C | 1 | a0001c0001t0001g0230 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2572-2057T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8704777 | ||||||
| chr11:8704912
|
G | T | 66 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0060others(63): Show | 66 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.2571+2173C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8704912 | ||||||
| chr11:8705001
|
G | A | 1 | a0003c0002t0001g0109 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2571+2084C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8705001 | ||||||
| chr11:8705165
|
C | T | 1 | a0003c0002t0002g0301 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2571+1920G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8705165 | ||||||
| chr11:8705419
|
G | A | 8 | a0002c0003t0001g0216a0003c0002t0001g0037a0003c0002t0001g0123others(5): Show | 8 | HG01192.hp1 HG01255.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2571+1666C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8705419 | ||||||
| chr11:8705627
|
G | A | 6 | a0001c0001t0002g0016a0001c0001t0002g0121a0001c0001t0002g0341others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2571+1458C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8705627 | ||||||
| chr11:8705657
|
TCTC | T | 14 | a0001c0001t0003g0080a0001c0001t0003g0171a0001c0001t0003g0221others(11): Show | 14 | HG00323.hp1 HG01167.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.2571+1425_2571+142 others(7): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8705657 | ||||||
| chr11:8705780
|
A | C | 1 | a0002c0003t0002g0170 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2571+1305T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8705780 | ||||||
| chr11:8705982
|
C | T | 11 | a0001c0001t0002g0074a0001c0001t0002g0162a0001c0001t0002g0200others(8): Show | 11 | HG00597.hp2 HG02040.hp1 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.2571+1103G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8705982 | ||||||
| chr11:8706062
|
G | C | 2 | a0002c0003t0002g0163a0002c0003t0002g0217 | 2 | HG01109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2571+1023C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8706062 | ||||||
| chr11:8706150
|
C | T | 213 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0013others(210): Show | 213 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(210): Show |
intron_variant | MODIFIER | c.2571+935G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8706150 | ||||||
| chr11:8706280
|
A | G | 7 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(4): Show | 7 | HG00639.hp1 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2571+805T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8706280 | ||||||
| chr11:8706376
|
A | G | 3 | a0001c0001t0005g0022a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02145.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2571+709T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8706376 | ||||||
| chr11:8706412
|
C | T | 5 | a0002c0003t0002g0054a0002c0003t0002g0141a0002c0003t0002g0151others(2): Show | 5 | HG02056.hp1 HG02083.hp2 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.2571+673G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8706412 | ||||||
| chr11:8706682
|
A | G | 6 | a0001c0001t0001g0261a0001c0001t0001g0264a0001c0001t0001g0265others(3): Show | 6 | HG01070.hp2 HG01099.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.2571+403T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8706682 | ||||||
| chr11:8706787
|
A | G | 2 | a0002c0003t0001g0181a0002c0003t0001g0190 | 2 | NA18950.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.2571+298T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8706787 | ||||||
| chr11:8706919
|
A | G | 3 | a0002c0003t0002g0071a0002c0003t0002g0179a0002c0003t0002g0191 | 3 | NA18946.hp2 NA18969.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.2571+166T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 13/19 | chr11 | 8706919 | ||||||
| chr11:8707322
|
T | A | 3 | a0001c0001t0004g0172a0003c0002t0004g0337a0011c0014t0004g0222 | 3 | HG01168.hp2 HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2431-97A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 12/19 | chr11 | 8707322 | ||||||
| chr11:8707510
|
A | G | 36 | a0001c0001t0001g0006a0001c0001t0002g0010a0001c0001t0002g0019others(33): Show | 36 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.2430+267T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 12/19 | chr11 | 8707510 | ||||||
| chr11:8707525
|
C | T | 1 | a0003c0002t0002g0284 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2430+252G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 12/19 | chr11 | 8707525 | ||||||
| chr11:8707729
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0004g0172others(2): Show | 5 | HG01168.hp2 HG02622.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.2430+48C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 12/19 | chr11 | 8707729 | ||||||
| chr11:8707874
|
A | G | 3 | a0001c0001t0005g0022a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02145.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2353-20T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8707874 | ||||||
| chr11:8708078
|
G | C | 10 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0033others(7): Show | 10 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.2353-224C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8708078 | ||||||
| chr11:8708188
|
T | C | 1 | a0001c0001t0002g0227 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2353-334A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8708188 | ||||||
| chr11:8708197
|
GGCTGGGA others(3): Show |
G | 1 | a0003c0002t0001g0206 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2353-353_2353-344d others(12): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8708197 | ||||||
| chr11:8708436
|
A | G | 9 | a0005c0006t0001g0086a0005c0006t0001g0091a0005c0006t0001g0092others(6): Show | 9 | HG00438.hp1 HG01175.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.2353-582T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8708436 | ||||||
| chr11:8708463
|
G | T | 1 | a0003c0002t0002g0286 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2353-609C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8708463 | ||||||
| chr11:8708620
|
T | C | 1 | a0001c0001t0002g0270 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2353-766A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8708620 | ||||||
| chr11:8708663
|
T | A | 1 | a0003c0002t0002g0138 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2353-809A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8708663 | ||||||
| chr11:8708772
|
A | G | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2353-918T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8708772 | ||||||
| chr11:8708878
|
G | A | 1 | a0003c0002t0002g0286 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2353-1024C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8708878 | ||||||
| chr11:8708910
|
C | A | 1 | a0003c0002t0002g0286 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2353-1056G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8708910 | ||||||
| chr11:8708938
|
A | C | 1 | a0003c0002t0002g0286 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2353-1084T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8708938 | ||||||
| chr11:8708952
|
CA | C | 130 | a0001c0001t0001g0006a0001c0001t0001g0025a0001c0001t0001g0027others(127): Show | 130 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.2353-1099delT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8708952 | ||||||
| chr11:8708952
|
CAA | C | 55 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0231others(52): Show | 55 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.2353-1100_2353-109 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8708952 | ||||||
| chr11:8709086
|
G | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(174): Show | 177 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(174): Show |
intron_variant | MODIFIER | c.2353-1232C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8709086 | ||||||
| chr11:8709107
|
G | A | 2 | a0001c0001t0004g0172a0003c0002t0004g0337 | 2 | HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2353-1253C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8709107 | ||||||
| chr11:8709344
|
G | A | 1 | a0003c0002t0001g0283 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2353-1490C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8709344 | ||||||
| chr11:8709661
|
T | C | 2 | a0001c0001t0001g0063a0001c0001t0001g0065 | 2 | HG01109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2352+1184A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8709661 | ||||||
| chr11:8709673
|
G | A | 1 | a0001c0001t0003g0343 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2352+1172C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8709673 | ||||||
| chr11:8710205
|
G | C | 5 | a0003c0002t0002g0321a0003c0002t0002g0322a0003c0002t0002g0331others(2): Show | 5 | HG00733.hp2 HG01069.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.2352+640C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8710205 | ||||||
| chr11:8710541
|
G | A | 1 | a0001c0001t0005g0022 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2352+304C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8710541 | ||||||
| chr11:8710569
|
T | G | 1 | a0003c0002t0001g0124 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2352+276A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8710569 | ||||||
| chr11:8710738
|
TAAAATTG others(3): Show |
T | 1 | a0002c0003t0002g0196 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2352+97_2352+106de others(11): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8710738 | ||||||
| chr11:8710753
|
G | GCA | 37 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0026others(34): Show | 37 | HG00558.hp2 HG00609.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.2352+90_2352+91dup others(2): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8710753 | ||||||
| chr11:8710753
|
G | GCACA | 11 | a0001c0001t0001g0005a0001c0001t0001g0233a0001c0001t0001g0252others(8): Show | 11 | HG00558.hp1 HG00621.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.2352+88_2352+91dup others(4): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8710753 | ||||||
| chr11:8710753
|
G | GCACACA | 10 | a0001c0001t0002g0016a0001c0001t0002g0019a0001c0001t0002g0021others(7): Show | 10 | HG00438.hp2 HG01256.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.2352+86_2352+91dup others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8710753 | ||||||
| chr11:8710753
|
G | GCACACAC others(1): Show |
11 | a0001c0001t0002g0041a0001c0001t0002g0043a0001c0001t0002g0044others(8): Show | 11 | HG01361.hp2 HG02015.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.2352+84_2352+91dup others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8710753 | ||||||
| chr11:8710753
|
G | GCACACAC others(3): Show |
1 | a0003c0002t0002g0058 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2352+82_2352+91dup others(10): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8710753 | ||||||
| chr11:8710753
|
G | GCACACAC others(5): Show |
3 | a0001c0001t0002g0045a0003c0002t0002g0328a0003c0002t0002g0329 | 3 | HG01516.hp1 HG01517.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.2352+80_2352+91dup others(12): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8710753 | ||||||
| chr11:8710753
|
G | GCACACAC others(7): Show |
1 | a0001c0007t0001g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2352+78_2352+91dup others(14): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8710753 | ||||||
| chr11:8710753
|
GCA | G | 26 | a0001c0001t0001g0006a0001c0001t0001g0258a0001c0007t0001g0344others(23): Show | 26 | HG00642.hp1 HG00733.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.2352+90_2352+91del others(2): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8710753 | ||||||
| chr11:8710753
|
GCACA | G | 47 | a0001c0001t0001g0028a0001c0001t0001g0230a0001c0001t0002g0052others(44): Show | 47 | HG00323.hp2 HG00544.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.2352+88_2352+91del others(4): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8710753 | ||||||
| chr11:8710753
|
GCACACA | G | 16 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0002g0074others(13): Show | 16 | HG02165.hp1 HG02523.hp1 HG03209.hp2 others(13): Show |
intron_variant | MODIFIER | c.2352+86_2352+91del others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8710753 | ||||||
| chr11:8710753
|
GCACACAC others(1): Show |
G | 65 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0060others(62): Show | 65 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.2352+84_2352+91del others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8710753 | ||||||
| chr11:8710753
|
GCACACAC others(3): Show |
G | 18 | a0001c0001t0001g0027a0001c0001t0001g0033a0001c0001t0001g0042others(15): Show | 18 | HG00639.hp1 HG01109.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.2352+82_2352+91del others(10): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8710753 | ||||||
| chr11:8710781
|
A | G | 1 | a0003c0002t0003g0338 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2352+64T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8710781 | ||||||
| chr11:8710793
|
A | C | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2352+52T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8710793 | ||||||
| chr11:8710794
|
C | CACACACA others(10): Show |
1 | a0001c0001t0002g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2352+50_2352+51ins others(17): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 11/19 | chr11 | 8710794 | ||||||
| chr11:8711016
|
T | C | 2 | a0003c0002t0001g0122a0003c0002t0001g0256 | 2 | HG02523.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.2283-102A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 10/19 | chr11 | 8711016 | ||||||
| chr11:8711418
|
G | A | 3 | a0001c0001t0004g0172a0003c0002t0004g0337a0011c0014t0004g0222 | 3 | HG01168.hp2 HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2173-187C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 9/19 | chr11 | 8711418 | ||||||
| chr11:8711456
|
G | A | 1 | a0008c0009t0001g0133 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2173-225C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 9/19 | chr11 | 8711456 | ||||||
| chr11:8711518
|
C | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2173-287G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 9/19 | chr11 | 8711518 | ||||||
| chr11:8711688
|
A | G | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2173-457T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 9/19 | chr11 | 8711688 | ||||||
| chr11:8711696
|
C | A | 1 | a0003c0002t0002g0331 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2173-465G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 9/19 | chr11 | 8711696 | ||||||
| chr11:8711782
|
G | A | 1 | a0002c0003t0002g0169 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2173-551C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 9/19 | chr11 | 8711782 | ||||||
| chr11:8711855
|
G | GA | 15 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0028others(12): Show | 15 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.2173-625dupT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 9/19 | chr11 | 8711855 | ||||||
| chr11:8712092
|
G | A | 1 | a0001c0001t0005g0022 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2172+459C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 9/19 | chr11 | 8712092 | ||||||
| chr11:8712191
|
G | A | 1 | a0001c0001t0005g0022 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2172+360C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 9/19 | chr11 | 8712191 | ||||||
| chr11:8712216
|
C | T | 330 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(327): Show | 330 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(327): Show |
intron_variant | MODIFIER | c.2172+335G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 9/19 | chr11 | 8712216 | ||||||
| chr11:8712257
|
CTG | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0004g0172others(2): Show | 5 | HG01168.hp2 HG02622.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.2172+292_2172+293d others(4): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 9/19 | chr11 | 8712257 | ||||||
| chr11:8712383
|
C | T | 1 | a0001c0007t0001g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2172+168G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 9/19 | chr11 | 8712383 | ||||||
| chr11:8712422
|
G | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2172+129C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 9/19 | chr11 | 8712422 | ||||||
| chr11:8712738
|
G | A | 1 | a0001c0001t0005g0022 | 1 | HG02145.hp1 | splice_region_variant&intron_variant | LOW | c.1988-3C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 8/19 | chr11 | 8712738 | ||||||
| chr11:8713094
|
C | T | 1 | a0001c0001t0007g0351 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1988-359G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 8/19 | chr11 | 8713094 | ||||||
| chr11:8713103
|
A | ACTTGAGC others(6): Show |
219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(216): Show | 219 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(216): Show |
intron_variant | MODIFIER | c.1988-369_1988-368i others(15): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 8/19 | chr11 | 8713103 | ||||||
| chr11:8713103
|
A | ACTTTGAG others(7): Show |
1 | a0002c0003t0002g0153 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1988-369_1988-368i others(16): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 8/19 | chr11 | 8713103 | ||||||
| chr11:8713288
|
G | C | 1 | a0001c0001t0002g0224 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1988-553C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 8/19 | chr11 | 8713288 | ||||||
| chr11:8713360
|
A | T | 1 | a0002c0003t0002g0153 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1988-625T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 8/19 | chr11 | 8713360 | ||||||
| chr11:8713361
|
C | A | 1 | a0002c0003t0002g0153 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1988-626G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 8/19 | chr11 | 8713361 | ||||||
| chr11:8713387
|
A | G | 2 | a0002c0003t0001g0075a0002c0003t0001g0145 | 2 | HG01074.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1987+611T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 8/19 | chr11 | 8713387 | ||||||
| chr11:8713529
|
G | A | 1 | a0001c0001t0002g0051 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1987+469C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 8/19 | chr11 | 8713529 | ||||||
| chr11:8713901
|
G | A | 1 | a0002c0003t0001g0166 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1987+97C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 8/19 | chr11 | 8713901 | ||||||
| chr11:8714115
|
G | A | 212 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(209): Show | 212 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(209): Show |
intron_variant | MODIFIER | c.1943-73C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 7/19 | chr11 | 8714115 | ||||||
| chr11:8714373
|
A | G | 1 | a0001c0001t0002g0227 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1942+237T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 7/19 | chr11 | 8714373 | ||||||
| chr11:8714494
|
T | G | 1 | a0001c0001t0001g0330 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1942+116A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 7/19 | chr11 | 8714494 | ||||||
| chr11:8714499
|
C | T | 346 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(343): Show | 346 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(343): Show |
intron_variant | MODIFIER | c.1942+111G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 7/19 | chr11 | 8714499 | ||||||
| chr11:8715119
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0002g0019others(1): Show | 4 | HG02572.hp2 HG02622.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1846-413C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 6/19 | chr11 | 8715119 | ||||||
| chr11:8715136
|
C | T | 1 | a0003c0002t0001g0109 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1846-430G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 6/19 | chr11 | 8715136 | ||||||
| chr11:8715148
|
T | C | 99 | a0001c0001t0001g0057a0001c0001t0001g0226a0001c0001t0001g0258others(96): Show | 99 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1846-442A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 6/19 | chr11 | 8715148 | ||||||
| chr11:8715201
|
T | G | 23 | a0001c0001t0001g0057a0001c0001t0002g0073a0002c0003t0001g0085others(20): Show | 23 | HG00558.hp2 HG00597.hp1 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.1845+402A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 6/19 | chr11 | 8715201 | ||||||
| chr11:8715293
|
G | A | 1 | a0003c0002t0002g0286 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1845+310C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 6/19 | chr11 | 8715293 | ||||||
| chr11:8715318
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1845+285G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 6/19 | chr11 | 8715318 | ||||||
| chr11:8715461
|
T | G | 1 | a0001c0001t0003g0171 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1845+142A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 6/19 | chr11 | 8715461 | ||||||
| chr11:8715824
|
G | A | 1 | a0001c0001t0002g0235 | 1 | NA18989.hp2 | splice_region_variant&intron_variant | LOW | c.1630-6C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 5/19 | chr11 | 8715824 | ||||||
| chr11:8715838
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1630-20C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 5/19 | chr11 | 8715838 | ||||||
| chr11:8715842
|
G | A | 3 | a0001c0001t0005g0022a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02145.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1630-24C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 5/19 | chr11 | 8715842 | ||||||
| chr11:8715898
|
A | G | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1630-80T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 5/19 | chr11 | 8715898 | ||||||
| chr11:8715934
|
C | G | 8 | a0003c0002t0002g0309a0003c0002t0002g0312a0003c0002t0002g0316others(5): Show | 8 | HG00733.hp2 HG01069.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.1630-116G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 5/19 | chr11 | 8715934 | ||||||
| chr11:8716048
|
C | T | 47 | a0001c0001t0001g0057a0001c0001t0002g0010a0001c0001t0002g0016others(44): Show | 47 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.1630-230G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 5/19 | chr11 | 8716048 | ||||||
| chr11:8716117
|
G | A | 1 | a0002c0003t0001g0244 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1630-299C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 5/19 | chr11 | 8716117 | ||||||
| chr11:8716124
|
C | T | 54 | a0001c0001t0001g0006a0001c0001t0001g0057a0001c0001t0001g0219others(51): Show | 54 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1630-306G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 5/19 | chr11 | 8716124 | ||||||
| chr11:8716177
|
C | T | 87 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0027others(84): Show | 87 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.1630-359G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 5/19 | chr11 | 8716177 | ||||||
| chr11:8716191
|
C | T | 1 | a0001c0001t0007g0351 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1630-373G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 5/19 | chr11 | 8716191 | ||||||
| chr11:8716203
|
A | G | 72 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0033others(69): Show | 72 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.1630-385T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 5/19 | chr11 | 8716203 | ||||||
| chr11:8716285
|
C | T | 1 | a0001c0001t0002g0044 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1630-467G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 5/19 | chr11 | 8716285 | ||||||
| chr11:8716461
|
G | A | 1 | a0001c0001t0001g0262 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1630-643C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 5/19 | chr11 | 8716461 | ||||||
| chr11:8716650
|
CT | C | 153 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0035others(150): Show | 153 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.1630-833delA | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 5/19 | chr11 | 8716650 | ||||||
| chr11:8716797
|
G | A | 1 | a0002c0003t0002g0072 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1629+944C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 5/19 | chr11 | 8716797 | ||||||
| chr11:8716818
|
T | C | 2 | a0001c0007t0005g0024a0001c0007t0005g0029 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1629+923A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 5/19 | chr11 | 8716818 | ||||||
| chr11:8716835
|
A | T | 2 | a0001c0001t0002g0224a0001c0001t0002g0225 | 2 | HG02572.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1629+906T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 5/19 | chr11 | 8716835 | ||||||
| chr11:8716985
|
G | C | 233 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0033others(230): Show | 233 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.1629+756C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 5/19 | chr11 | 8716985 | ||||||
| chr11:8717296
|
T | C | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0035others(159): Show | 162 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1629+445A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 5/19 | chr11 | 8717296 | ||||||
| chr11:8717596
|
G | T | 1 | a0002c0003t0001g0068 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1629+145C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 5/19 | chr11 | 8717596 | ||||||
| chr11:8717613
|
C | T | 4 | a0001c0001t0006g0018a0001c0001t0006g0020a0003c0002t0003g0097others(1): Show | 4 | HG02257.hp1 HG02965.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1629+128G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 5/19 | chr11 | 8717613 | ||||||
| chr11:8717991
|
A | G | 1 | a0002c0003t0001g0150 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1478-99T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8717991 | ||||||
| chr11:8718092
|
A | AG | 5 | a0001c0001t0001g0081a0001c0001t0001g0302a0002c0003t0001g0085others(2): Show | 5 | HG00642.hp1 HG02055.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1478-201_1478-200i others(3): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718092 | ||||||
| chr11:8718092
|
A | AGCCCACC others(2): Show |
333 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(330): Show | 333 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.1478-201_1478-200i others(11): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718092 | ||||||
| chr11:8718092
|
A | AGCCCACC others(3): Show |
2 | a0001c0001t0001g0281a0001c0001t0001g0293 | 2 | HG02083.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1478-201_1478-200i others(12): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718092 | ||||||
| chr11:8718092
|
A | AGCCCACC others(10): Show |
3 | a0002c0003t0001g0126a0002c0003t0001g0211a0002c0003t0001g0218 | 3 | NA18953.hp1 NA19010.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1478-201_1478-200i others(19): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718092 | ||||||
| chr11:8718092
|
A | AGCCCACC others(18): Show |
3 | a0001c0001t0001g0258a0001c0001t0004g0172a0004c0004t0001g0334 | 3 | HG03471.hp2 HG04115.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1478-201_1478-200i others(27): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718092 | ||||||
| chr11:8718092
|
A | AGCCCACC others(19): Show |
4 | a0001c0001t0001g0042a0001c0001t0001g0253a0002c0003t0002g0142others(1): Show | 4 | HG01168.hp2 HG01261.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.1478-201_1478-200i others(28): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718092 | ||||||
| chr11:8718095
|
C | G | 7 | a0001c0001t0001g0260a0001c0001t0001g0262a0001c0001t0002g0267others(4): Show | 7 | HG00408.hp2 HG00558.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.1478-203G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718095 | ||||||
| chr11:8718096
|
A | AC | 15 | a0001c0001t0002g0043a0001c0001t0002g0162a0001c0001t0002g0223others(12): Show | 15 | HG00642.hp2 HG01175.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1478-205dupG | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718096 | ||||||
| chr11:8718097
|
C | A | 3 | a0001c0001t0001g0042a0002c0003t0002g0142a0011c0014t0004g0222 | 3 | HG01168.hp2 HG01261.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1478-205G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718097 | ||||||
| chr11:8718103
|
C | G | 1 | a0002c0003t0001g0085 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1478-211G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718103 | ||||||
| chr11:8718104
|
A | AC | 43 | a0001c0001t0001g0009a0001c0001t0001g0062a0001c0001t0001g0231others(40): Show | 43 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.1478-213dupG | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718104 | ||||||
| chr11:8718104
|
A | ACCCCCCC others(3): Show |
3 | a0001c0001t0001g0081a0001c0001t0001g0302a0003c0002t0001g0095 | 3 | HG02055.hp2 HG02145.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1478-213_1478-212i others(12): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718104 | ||||||
| chr11:8718104
|
A | ACCCCCCC others(4): Show |
1 | a0004c0004t0001g0339 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1478-213_1478-212i others(13): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718104 | ||||||
| chr11:8718106
|
C | A | 1 | a0002c0003t0001g0001 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1478-214G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718106 | ||||||
| chr11:8718110
|
C | T | 1 | a0003c0002t0002g0088 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1478-218G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718110 | ||||||
| chr11:8718123
|
C | A | 2 | a0001c0001t0001g0272a0001c0007t0001g0036 | 2 | HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1478-231G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718123 | ||||||
| chr11:8718274
|
A | G | 47 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0238others(44): Show | 47 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1478-382T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718274 | ||||||
| chr11:8718297
|
G | C | 1 | a0001c0001t0005g0022 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1478-405C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718297 | ||||||
| chr11:8718381
|
A | T | 1 | a0002c0003t0002g0159 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1478-489T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718381 | ||||||
| chr11:8718389
|
A | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0026a0001c0001t0001g0349others(4): Show | 7 | HG00639.hp1 HG00639.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1478-497T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718389 | ||||||
| chr11:8718409
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1478-517G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718409 | ||||||
| chr11:8718410
|
G | A | 1 | a0002c0003t0001g0259 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1478-518C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718410 | ||||||
| chr11:8718490
|
G | A | 1 | a0007c0008t0001g0294 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1478-598C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718490 | ||||||
| chr11:8718540
|
G | A | 2 | a0003c0002t0001g0087a0003c0002t0002g0301 | 2 | HG02132.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1478-648C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718540 | ||||||
| chr11:8718542
|
T | C | 1 | a0001c0007t0001g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1478-650A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718542 | ||||||
| chr11:8718547
|
C | A | 1 | a0003c0002t0001g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1478-655G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718547 | ||||||
| chr11:8718575
|
C | T | 1 | a0002c0003t0002g0214 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1478-683G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718575 | ||||||
| chr11:8718755
|
T | C | 1 | a0009c0017t0001g0120 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1478-863A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718755 | ||||||
| chr11:8718845
|
C | T | 1 | a0003c0002t0002g0103 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1478-953G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718845 | ||||||
| chr11:8718893
|
C | T | 1 | a0002c0003t0001g0050 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1478-1001G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8718893 | ||||||
| chr11:8719017
|
C | T | 5 | a0003c0002t0001g0007a0003c0002t0001g0008a0003c0002t0001g0182others(2): Show | 5 | HG02896.hp1 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1478-1125G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8719017 | ||||||
| chr11:8719036
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1478-1144G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8719036 | ||||||
| chr11:8719270
|
T | C | 1 | a0001c0001t0002g0121 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1478-1378A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8719270 | ||||||
| chr11:8719379
|
G | A | 3 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02451.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1478-1487C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8719379 | ||||||
| chr11:8719553
|
G | A | 1 | a0003c0002t0001g0313 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1478-1661C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8719553 | ||||||
| chr11:8719927
|
C | T | 2 | a0001c0007t0005g0024a0001c0007t0005g0029 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1478-2035G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8719927 | ||||||
| chr11:8719956
|
T | C | 28 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0027others(25): Show | 28 | HG00558.hp1 HG02015.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1478-2064A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8719956 | ||||||
| chr11:8720125
|
C | G | 5 | a0001c0001t0001g0261a0001c0001t0001g0264a0001c0001t0001g0265others(2): Show | 5 | HG01070.hp2 HG01099.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1478-2233G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8720125 | ||||||
| chr11:8720222
|
T | C | 1 | a0002c0003t0002g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1478-2330A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8720222 | ||||||
| chr11:8720525
|
C | G | 1 | a0003c0002t0003g0338 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1478-2633G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8720525 | ||||||
| chr11:8720587
|
C | T | 1 | a0001c0001t0002g0225 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1478-2695G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8720587 | ||||||
| chr11:8720974
|
A | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0347a0001c0001t0001g0348others(1): Show | 4 | HG00639.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1478-3082T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8720974 | ||||||
| chr11:8721038
|
A | G | 28 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0027others(25): Show | 28 | HG00558.hp1 HG02015.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1478-3146T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8721038 | ||||||
| chr11:8721055
|
T | C | 1 | a0003c0002t0001g0325 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1478-3163A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8721055 | ||||||
| chr11:8721277
|
C | G | 1 | a0003c0002t0001g0256 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1478-3385G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8721277 | ||||||
| chr11:8721318
|
TC | T | 91 | a0001c0001t0002g0162a0002c0003t0001g0001a0002c0003t0001g0050others(88): Show | 91 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.1478-3427delG | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8721318 | ||||||
| chr11:8721508
|
CTCCG | C | 309 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(306): Show | 309 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.1478-3620_1478-361 others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8721508 | ||||||
| chr11:8721599
|
T | A | 1 | a0001c0001t0001g0230 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1478-3707A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8721599 | ||||||
| chr11:8721643
|
T | G | 1 | a0001c0001t0001g0187 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1478-3751A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8721643 | ||||||
| chr11:8721853
|
C | G | 1 | a0002c0003t0002g0148 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1478-3961G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8721853 | ||||||
| chr11:8721872
|
G | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(1): Show | 4 | HG02145.hp2 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1478-3980C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8721872 | ||||||
| chr11:8722032
|
G | T | 327 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(324): Show | 327 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(324): Show |
intron_variant | MODIFIER | c.1477+4041C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8722032 | ||||||
| chr11:8722166
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0003g0004 | 2 | HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1477+3907A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8722166 | ||||||
| chr11:8722178
|
C | G | 1 | a0001c0001t0001g0023 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1477+3895G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8722178 | ||||||
| chr11:8722213
|
C | T | 5 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0117others(2): Show | 5 | HG02622.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1477+3860G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8722213 | ||||||
| chr11:8722478
|
AG | A | 4 | a0001c0007t0001g0036a0001c0007t0002g0034a0001c0007t0005g0024others(1): Show | 4 | HG02451.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1477+3594delC | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8722478 | ||||||
| chr11:8722672
|
C | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.1477+3401G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8722672 | ||||||
| chr11:8722725
|
C | T | 2 | a0003c0002t0002g0328a0003c0002t0002g0329 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1477+3348G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8722725 | ||||||
| chr11:8722753
|
T | G | 3 | a0001c0001t0004g0172a0003c0002t0004g0337a0011c0014t0004g0222 | 3 | HG01168.hp2 HG03942.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1477+3320A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8722753 | ||||||
| chr11:8722828
|
T | C | 1 | a0002c0003t0002g0165 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1477+3245A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8722828 | ||||||
| chr11:8722854
|
C | G | 4 | a0001c0007t0001g0036a0001c0007t0002g0034a0001c0007t0005g0024others(1): Show | 4 | HG02451.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1477+3219G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8722854 | ||||||
| chr11:8722950
|
G | A | 4 | a0001c0007t0001g0036a0001c0007t0002g0034a0001c0007t0005g0024others(1): Show | 4 | HG02451.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1477+3123C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8722950 | ||||||
| chr11:8723101
|
T | G | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(75): Show | 78 | HG00438.hp1 HG00544.hp1 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.1477+2972A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8723101 | ||||||
| chr11:8723461
|
G | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0027others(1): Show | 4 | HG02109.hp2 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1477+2612C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8723461 | ||||||
| chr11:8723476
|
G | A | 1 | a0002c0003t0001g0173 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1477+2597C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8723476 | ||||||
| chr11:8723508
|
G | T | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(299): Show | 302 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.1477+2565C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8723508 | ||||||
| chr11:8723534
|
T | C | 229 | a0001c0001t0001g0025a0001c0001t0001g0060a0001c0001t0001g0062others(226): Show | 229 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.1477+2539A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8723534 | ||||||
| chr11:8723602
|
C | T | 343 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(340): Show | 343 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(340): Show |
intron_variant | MODIFIER | c.1477+2471G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8723602 | ||||||
| chr11:8723656
|
A | G | 2 | a0003c0002t0001g0111a0003c0002t0002g0336 | 2 | HG03704.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1477+2417T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8723656 | ||||||
| chr11:8723961
|
T | G | 4 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0007t0001g0344others(1): Show | 4 | HG01943.hp1 HG02976.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1477+2112A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8723961 | ||||||
| chr11:8724092
|
G | A | 24 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0027others(21): Show | 24 | HG00558.hp1 HG02015.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.1477+1981C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8724092 | ||||||
| chr11:8724164
|
C | T | 64 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0064others(61): Show | 64 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.1477+1909G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8724164 | ||||||
| chr11:8724623
|
A | C | 1 | a0012c0016t0002g0304 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1477+1450T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8724623 | ||||||
| chr11:8724703
|
G | A | 1 | a0001c0001t0004g0172 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1477+1370C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8724703 | ||||||
| chr11:8724902
|
C | A | 1 | a0003c0002t0001g0303 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1477+1171G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8724902 | ||||||
| chr11:8724926
|
T | C | 2 | a0001c0007t0001g0344a0001c0007t0001g0345 | 2 | HG01943.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1477+1147A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8724926 | ||||||
| chr11:8724927
|
G | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1477+1146C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8724927 | ||||||
| chr11:8724977
|
T | C | 3 | a0003c0002t0001g0122a0003c0002t0001g0123a0003c0002t0001g0132 | 3 | HG02523.hp2 NA18942.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1477+1096A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8724977 | ||||||
| chr11:8725100
|
G | T | 1 | a0001c0001t0001g0257 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1477+973C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8725100 | ||||||
| chr11:8725104
|
A | G | 4 | a0001c0001t0001g0033a0001c0001t0001g0119a0001c0001t0002g0118others(1): Show | 4 | HG01884.hp2 HG02486.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1477+969T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8725104 | ||||||
| chr11:8725137
|
G | A | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(167): Show | 170 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.1477+936C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8725137 | ||||||
| chr11:8725369
|
A | ATAT | 332 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(329): Show | 332 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(329): Show |
intron_variant | MODIFIER | c.1477+701_1477+703d others(5): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8725369 | ||||||
| chr11:8725374
|
A | ATTAC | 7 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0257others(4): Show | 7 | HG02145.hp1 HG02257.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.1477+698_1477+699i others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8725374 | ||||||
| chr11:8725375
|
C | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0257others(9): Show | 12 | HG00733.hp1 HG01943.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1477+698G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8725375 | ||||||
| chr11:8725376
|
T | TAC | 5 | a0001c0001t0001g0347a0001c0007t0001g0344a0001c0007t0001g0345others(2): Show | 5 | HG00733.hp1 HG01943.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1477+696_1477+697i others(4): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8725376 | ||||||
| chr11:8725410
|
T | C | 1 | a0003c0002t0002g0336 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1477+663A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8725410 | ||||||
| chr11:8725848
|
C | G | 25 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0027others(22): Show | 25 | HG00558.hp1 HG02015.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1477+225G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 4/19 | chr11 | 8725848 | ||||||
| chr11:8726275
|
T | A | 2 | a0002c0003t0002g0178a0002c0003t0002g0207 | 2 | HG00323.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1341-66A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8726275 | ||||||
| chr11:8726430
|
G | A | 1 | a0002c0003t0002g0178 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1341-221C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8726430 | ||||||
| chr11:8726498
|
C | T | 1 | a0002c0003t0001g0068 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1341-289G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8726498 | ||||||
| chr11:8726564
|
T | C | 1 | a0003c0002t0001g0090 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1341-355A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8726564 | ||||||
| chr11:8726704
|
T | G | 2 | a0002c0010t0002g0039a0002c0010t0002g0040 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1341-495A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8726704 | ||||||
| chr11:8726943
|
G | A | 331 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(328): Show | 331 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.1341-734C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8726943 | ||||||
| chr11:8726999
|
T | C | 2 | a0001c0007t0001g0344a0001c0007t0001g0345 | 2 | HG01943.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1341-790A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8726999 | ||||||
| chr11:8727000
|
G | C | 1 | a0001c0001t0001g0258 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1341-791C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8727000 | ||||||
| chr11:8727227
|
T | A | 1 | a0001c0001t0003g0171 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1341-1018A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8727227 | ||||||
| chr11:8727302
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1341-1093T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8727302 | ||||||
| chr11:8727460
|
C | A | 1 | a0002c0003t0003g0193 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1341-1251G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8727460 | ||||||
| chr11:8727475
|
T | C | 1 | a0002c0003t0002g0148 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1341-1266A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8727475 | ||||||
| chr11:8727896
|
C | T | 1 | a0001c0001t0002g0346 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1341-1687G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8727896 | ||||||
| chr11:8727900
|
G | GT | 121 | a0001c0001t0001g0081a0001c0001t0001g0258a0001c0001t0001g0330others(118): Show | 121 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1341-1692dupA | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8727900 | ||||||
| chr11:8727900
|
G | GTT | 11 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0117others(8): Show | 11 | HG01123.hp2 HG01175.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.1341-1693_1341-169 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8727900 | ||||||
| chr11:8727900
|
GT | G | 7 | a0001c0007t0001g0344a0001c0007t0001g0345a0002c0003t0001g0085others(4): Show | 7 | HG00544.hp2 HG01943.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1341-1692delA | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8727900 | ||||||
| chr11:8727964
|
AAC | A | 4 | a0001c0001t0001g0047a0001c0001t0002g0010a0001c0001t0002g0019others(1): Show | 4 | HG02486.hp1 HG02622.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1341-1757_1341-175 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8727964 | ||||||
| chr11:8727964
|
AACAC | A | 8 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(5): Show | 8 | HG00639.hp2 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1341-1759_1341-175 others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8727964 | ||||||
| chr11:8727964
|
AACACAC | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0042a0001c0001t0001g0140others(3): Show | 6 | HG01123.hp1 HG01943.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1341-1761_1341-175 others(10): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8727964 | ||||||
| chr11:8727964
|
AACACACA others(1): Show |
A | 3 | a0001c0001t0001g0117a0001c0001t0002g0227a0003c0002t0001g0326 | 3 | HG01361.hp2 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1341-1763_1341-175 others(12): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8727964 | ||||||
| chr11:8727964
|
AACACACA others(3): Show |
A | 37 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029others(34): Show | 37 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1341-1765_1341-175 others(14): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8727964 | ||||||
| chr11:8727964
|
AACACACA others(5): Show |
A | 4 | a0001c0001t0001g0219a0001c0001t0001g0220a0003c0002t0002g0300others(1): Show | 4 | HG02040.hp1 HG03209.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1341-1767_1341-175 others(16): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8727964 | ||||||
| chr11:8727964
|
AACACACA others(7): Show |
A | 69 | a0002c0003t0001g0174a0002c0003t0002g0148a0002c0003t0002g0163others(66): Show | 69 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.1341-1769_1341-175 others(18): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8727964 | ||||||
| chr11:8727964
|
AACACACA others(9): Show |
A | 40 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0027others(37): Show | 40 | HG00544.hp1 HG00558.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1341-1771_1341-175 others(20): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8727964 | ||||||
| chr11:8727964
|
AACACACA others(11): Show |
A | 98 | a0001c0001t0001g0033a0001c0001t0001g0076a0001c0001t0001g0119others(95): Show | 98 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1341-1773_1341-175 others(22): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8727964 | ||||||
| chr11:8727964
|
AACACACA others(13): Show |
A | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(77): Show | 80 | HG00438.hp1 HG00639.hp1 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.1341-1775_1341-175 others(24): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8727964 | ||||||
| chr11:8727964
|
AACACACA others(15): Show |
A | 1 | a0001c0001t0002g0229 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1341-1777_1341-175 others(26): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8727964 | ||||||
| chr11:8727972
|
CACACACA others(8): Show |
C | 1 | a0001c0001t0002g0044 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1341-1778_1341-176 others(19): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8727972 | ||||||
| chr11:8728008
|
C | T | 2 | a0001c0001t0001g0140a0001c0001t0002g0225 | 2 | HG02257.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1341-1799G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8728008 | ||||||
| chr11:8728189
|
A | C | 6 | a0001c0001t0001g0245a0001c0001t0001g0249a0001c0001t0001g0254others(3): Show | 6 | HG02080.hp1 HG03834.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.1340+1761T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8728189 | ||||||
| chr11:8728314
|
T | A | 1 | a0001c0001t0001g0119 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1340+1636A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8728314 | ||||||
| chr11:8728408
|
G | A | 1 | a0002c0003t0002g0194 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1340+1542C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8728408 | ||||||
| chr11:8728593
|
TC | T | 351 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(348): Show | 351 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(348): Show |
intron_variant | MODIFIER | c.1340+1356delG | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8728593 | ||||||
| chr11:8729006
|
C | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(78): Show | 81 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.1340+944G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8729006 | ||||||
| chr11:8729030
|
A | C | 26 | a0003c0002t0001g0007a0003c0002t0001g0008a0003c0002t0001g0182others(23): Show | 26 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.1340+920T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8729030 | ||||||
| chr11:8729122
|
C | T | 1 | a0001c0001t0005g0022 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1340+828G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8729122 | ||||||
| chr11:8729135
|
C | T | 1 | a0001c0001t0003g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1340+815G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8729135 | ||||||
| chr11:8729148
|
C | A | 1 | a0002c0003t0001g0136 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1340+802G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8729148 | ||||||
| chr11:8729248
|
C | T | 1 | a0002c0003t0002g0031 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1340+702G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8729248 | ||||||
| chr11:8729268
|
T | G | 1 | a0002c0003t0002g0203 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1340+682A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8729268 | ||||||
| chr11:8729295
|
G | A | 1 | a0002c0003t0002g0185 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1340+655C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8729295 | ||||||
| chr11:8729324
|
A | G | 1 | a0001c0001t0002g0346 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1340+626T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8729324 | ||||||
| chr11:8729401
|
A | G | 1 | a0001c0001t0002g0073 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1340+549T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8729401 | ||||||
| chr11:8729633
|
A | G | 4 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0117others(1): Show | 4 | HG02622.hp1 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1340+317T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8729633 | ||||||
| chr11:8729719
|
A | G | 2 | a0001c0007t0001g0344a0001c0007t0001g0345 | 2 | HG01943.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1340+231T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8729719 | ||||||
| chr11:8729781
|
A | T | 2 | a0001c0007t0001g0344a0001c0007t0001g0345 | 2 | HG01943.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1340+169T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8729781 | ||||||
| chr11:8729932
|
C | T | 2 | a0002c0003t0001g0204a0002c0003t0001g0205 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1340+18G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 3/19 | chr11 | 8729932 | ||||||
| chr11:8731414
|
G | T | 4 | a0006c0005t0001g0112a0006c0005t0001g0113a0006c0005t0001g0114others(1): Show | 4 | NA18946.hp1 NA18998.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-205C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8731414 | ||||||
| chr11:8731452
|
T | C | 1 | a0001c0001t0001g0330 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.81-243A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8731452 | ||||||
| chr11:8731908
|
C | A | 6 | a0003c0002t0001g0007a0003c0002t0001g0008a0003c0002t0001g0182others(3): Show | 6 | HG02896.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.81-699G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8731908 | ||||||
| chr11:8732005
|
A | G | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(193): Show | 196 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.81-796T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8732005 | ||||||
| chr11:8732006
|
C | T | 1 | a0002c0003t0001g0131 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.81-797G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8732006 | ||||||
| chr11:8732095
|
C | G | 1 | a0003c0002t0001g0101 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.81-886G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8732095 | ||||||
| chr11:8732101
|
T | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0347a0001c0001t0001g0348others(1): Show | 4 | HG00639.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-892A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8732101 | ||||||
| chr11:8732170
|
C | T | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(84): Show | 87 | HG00438.hp1 HG00544.hp1 HG00673.hp2 others(84): Show |
intron_variant | MODIFIER | c.81-961G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8732170 | ||||||
| chr11:8732182
|
A | G | 96 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0002g0162others(93): Show | 96 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.81-973T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8732182 | ||||||
| chr11:8732360
|
A | T | 1 | a0001c0007t0001g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.81-1151T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8732360 | ||||||
| chr11:8732369
|
G | A | 3 | a0003c0002t0001g0182a0003c0002t0001g0183a0003c0002t0001g0184 | 3 | HG02896.hp1 HG02897.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.81-1160C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8732369 | ||||||
| chr11:8732385
|
T | C | 1 | a0002c0003t0002g0054 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.81-1176A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8732385 | ||||||
| chr11:8732400
|
C | T | 5 | a0001c0001t0001g0231a0001c0001t0001g0238a0001c0001t0001g0239others(2): Show | 5 | HG00673.hp2 HG02040.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.81-1191G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8732400 | ||||||
| chr11:8732454
|
C | T | 4 | a0001c0007t0001g0036a0001c0007t0002g0034a0001c0007t0005g0024others(1): Show | 4 | HG02451.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-1245G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8732454 | ||||||
| chr11:8732484
|
A | G | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(193): Show | 196 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.81-1275T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8732484 | ||||||
| chr11:8732537
|
G | GT | 3 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0005g0022 | 3 | HG02145.hp1 HG02257.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.81-1329dupA | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8732537 | ||||||
| chr11:8732601
|
A | G | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(193): Show | 196 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.81-1392T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8732601 | ||||||
| chr11:8732635
|
GA | G | 112 | a0003c0002t0001g0007a0003c0002t0001g0008a0003c0002t0001g0037others(109): Show | 112 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.81-1427delT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8732635 | ||||||
| chr11:8733012
|
A | G | 53 | a0003c0002t0001g0037a0003c0002t0001g0082a0003c0002t0001g0083others(50): Show | 53 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.81-1803T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8733012 | ||||||
| chr11:8733393
|
A | G | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.81-2184T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8733393 | ||||||
| chr11:8733523
|
T | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.81-2314A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8733523 | ||||||
| chr11:8734041
|
T | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0140a0001c0001t0002g0225others(2): Show | 5 | HG02145.hp1 HG02257.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.81-2832A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8734041 | ||||||
| chr11:8734321
|
G | GT | 6 | a0001c0001t0001g0140a0001c0001t0001g0167a0001c0001t0001g0249others(3): Show | 6 | HG01261.hp2 HG02145.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.81-3113dupA | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8734321 | ||||||
| chr11:8734390
|
G | A | 1 | a0014c0012t0001g0236 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.81-3181C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8734390 | ||||||
| chr11:8734422
|
T | C | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.81-3213A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8734422 | ||||||
| chr11:8734483
|
G | C | 1 | a0001c0001t0003g0171 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.81-3274C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8734483 | ||||||
| chr11:8734594
|
C | CCTGCGTA others(29): Show |
1 | a0001c0001t0002g0296 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.81-3386_81-3385ins others(36): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8734594 | ||||||
| chr11:8734721
|
G | A | 2 | a0002c0003t0001g0208a0002c0003t0001g0209 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.81-3512C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8734721 | ||||||
| chr11:8734738
|
G | A | 1 | a0001c0007t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.81-3529C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8734738 | ||||||
| chr11:8734791
|
C | CA | 86 | a0001c0001t0001g0234a0001c0001t0002g0162a0001c0001t0003g0251others(83): Show | 86 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.81-3583dupT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8734791 | ||||||
| chr11:8734791
|
CA | C | 129 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0027others(126): Show | 129 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.81-3583delT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8734791 | ||||||
| chr11:8734791
|
CAA | C | 20 | a0001c0001t0001g0064a0001c0001t0001g0140a0001c0001t0001g0347others(17): Show | 20 | HG00639.hp1 HG01070.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.81-3584_81-3583del others(2): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8734791 | ||||||
| chr11:8734910
|
T | A | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.81-3701A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8734910 | ||||||
| chr11:8734985
|
T | C | 2 | a0001c0007t0001g0344a0001c0007t0001g0345 | 2 | HG01943.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.81-3776A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8734985 | ||||||
| chr11:8735006
|
G | C | 4 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(1): Show | 4 | HG02145.hp2 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.81-3797C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8735006 | ||||||
| chr11:8735113
|
C | T | 1 | a0001c0007t0001g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.81-3904G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8735113 | ||||||
| chr11:8735309
|
G | A | 94 | a0001c0001t0002g0162a0002c0003t0001g0001a0002c0003t0001g0050others(91): Show | 94 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.81-4100C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8735309 | ||||||
| chr11:8735532
|
G | A | 1 | a0002c0003t0002g0072 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.81-4323C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8735532 | ||||||
| chr11:8735856
|
A | G | 2 | a0001c0007t0001g0344a0001c0007t0001g0345 | 2 | HG01943.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.81-4647T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8735856 | ||||||
| chr11:8736021
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.81-4812G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8736021 | ||||||
| chr11:8736353
|
C | T | 3 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349 | 3 | HG00639.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.81-5144G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8736353 | ||||||
| chr11:8736366
|
G | GA | 124 | a0001c0001t0001g0258a0001c0001t0002g0235a0001c0001t0003g0080others(121): Show | 124 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.81-5158dupT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8736366 | ||||||
| chr11:8736407
|
C | T | 1 | a0011c0014t0004g0222 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.81-5198G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8736407 | ||||||
| chr11:8736567
|
T | C | 99 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0117others(96): Show | 99 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.81-5358A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8736567 | ||||||
| chr11:8736644
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.81-5435C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8736644 | ||||||
| chr11:8736748
|
T | C | 3 | a0002c0003t0002g0071a0002c0003t0002g0179a0002c0003t0002g0191 | 3 | NA18946.hp2 NA18969.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.81-5539A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8736748 | ||||||
| chr11:8736762
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.81-5553C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8736762 | ||||||
| chr11:8736766
|
T | C | 1 | a0003c0002t0003g0279 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.81-5557A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8736766 | ||||||
| chr11:8736797
|
G | A | 6 | a0003c0002t0002g0321a0003c0002t0002g0322a0003c0002t0002g0331others(3): Show | 6 | HG00733.hp2 HG01069.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.81-5588C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8736797 | ||||||
| chr11:8736818
|
C | A | 2 | a0001c0007t0005g0024a0001c0007t0005g0029 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81-5609G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8736818 | ||||||
| chr11:8737020
|
A | G | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.81-5811T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8737020 | ||||||
| chr11:8737024
|
G | C | 2 | a0001c0007t0001g0344a0001c0007t0001g0345 | 2 | HG01943.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.81-5815C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8737024 | ||||||
| chr11:8737162
|
A | C | 1 | a0002c0003t0002g0203 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.81-5953T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8737162 | ||||||
| chr11:8737192
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0015 | 2 | HG00639.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.81-5983A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8737192 | ||||||
| chr11:8737518
|
C | T | 4 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0117others(1): Show | 4 | HG02622.hp1 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.81-6309G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8737518 | ||||||
| chr11:8737616
|
G | A | 30 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0027others(27): Show | 30 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.81-6407C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8737616 | ||||||
| chr11:8737643
|
G | A | 1 | a0003c0002t0001g0303 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.81-6434C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8737643 | ||||||
| chr11:8737653
|
TTCTC | T | 30 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0027others(27): Show | 30 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.81-6448_81-6445del others(4): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8737653 | ||||||
| chr11:8737673
|
T | TTCTC | 103 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0117others(100): Show | 103 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.81-6468_81-6465dup others(4): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8737673 | ||||||
| chr11:8737854
|
C | T | 2 | a0001c0001t0006g0018a0001c0001t0006g0020 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.81-6645G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8737854 | ||||||
| chr11:8737914
|
A | AT | 108 | a0001c0001t0001g0023a0001c0001t0001g0042a0001c0001t0001g0047others(105): Show | 108 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.81-6706dupA | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8737914 | ||||||
| chr11:8738000
|
T | C | 3 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0005g0022 | 3 | HG02145.hp1 HG02257.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.81-6791A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8738000 | ||||||
| chr11:8738063
|
G | C | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.81-6854C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8738063 | ||||||
| chr11:8738248
|
A | G | 31 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0027others(28): Show | 31 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.81-7039T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8738248 | ||||||
| chr11:8738400
|
C | T | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.81-7191G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8738400 | ||||||
| chr11:8738531
|
T | C | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.81-7322A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8738531 | ||||||
| chr11:8738609
|
G | A | 138 | a0001c0001t0001g0140a0001c0001t0002g0162a0001c0001t0002g0225others(135): Show | 138 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.81-7400C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8738609 | ||||||
| chr11:8738802
|
C | T | 1 | a0003c0002t0001g0326 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.81-7593G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8738802 | ||||||
| chr11:8739306
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.81-8097A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8739306 | ||||||
| chr11:8739325
|
G | C | 1 | a0001c0001t0001g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.81-8116C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8739325 | ||||||
| chr11:8739434
|
G | A | 1 | a0002c0003t0002g0189 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.81-8225C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8739434 | ||||||
| chr11:8739934
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.81-8725G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8739934 | ||||||
| chr11:8740164
|
G | A | 3 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227 | 3 | HG02257.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.81-8955C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8740164 | ||||||
| chr11:8740195
|
TA | T | 10 | a0001c0001t0001g0265a0001c0001t0001g0347a0001c0001t0001g0348others(7): Show | 10 | HG01070.hp1 HG01255.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.81-8987delT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8740195 | ||||||
| chr11:8740235
|
A | G | 97 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0219others(94): Show | 97 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.81-9026T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8740235 | ||||||
| chr11:8740252
|
T | A | 1 | a0001c0007t0005g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.81-9043A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8740252 | ||||||
| chr11:8740516
|
T | C | 2 | a0003c0002t0003g0097a0003c0002t0003g0102 | 2 | NA18952.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.81-9307A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8740516 | ||||||
| chr11:8740615
|
T | G | 30 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0038others(27): Show | 30 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.81-9406A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8740615 | ||||||
| chr11:8740703
|
C | G | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.81-9494G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8740703 | ||||||
| chr11:8740711
|
T | A | 2 | a0003c0002t0001g0306a0003c0002t0002g0311 | 2 | HG01993.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.81-9502A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8740711 | ||||||
| chr11:8740751
|
G | A | 2 | a0002c0003t0002g0179a0002c0003t0002g0191 | 2 | NA18969.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.81-9542C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8740751 | ||||||
| chr11:8740775
|
TCTA | T | 8 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227others(5): Show | 8 | HG01168.hp2 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.81-9569_81-9567del others(3): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8740775 | ||||||
| chr11:8740850
|
G | A | 3 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02451.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81-9641C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8740850 | ||||||
| chr11:8740948
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0003g0004 | 2 | HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.80+9673C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8740948 | ||||||
| chr11:8741096
|
G | A | 1 | a0003c0002t0003g0279 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.80+9525C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8741096 | ||||||
| chr11:8741562
|
C | T | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG00673.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+9059G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8741562 | ||||||
| chr11:8741565
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0047 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.80+9056C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8741565 | ||||||
| chr11:8741601
|
A | C | 1 | a0001c0001t0006g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.80+9020T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8741601 | ||||||
| chr11:8741708
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0003g0004 | 2 | HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.80+8913A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8741708 | ||||||
| chr11:8741746
|
C | T | 6 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227others(3): Show | 6 | HG02257.hp2 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.80+8875G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8741746 | ||||||
| chr11:8741826
|
G | A | 3 | a0001c0001t0001g0245a0001c0001t0001g0249a0001c0001t0001g0254 | 3 | NA19009.hp1 NA19074.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.80+8795C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8741826 | ||||||
| chr11:8741868
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.80+8753G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8741868 | ||||||
| chr11:8741918
|
GTCT | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(76): Show | 79 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.80+8700_80+8702del others(3): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8741918 | ||||||
| chr11:8741922
|
C | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(76): Show | 79 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.80+8699G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8741922 | ||||||
| chr11:8742014
|
G | A | 339 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(336): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.80+8607C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8742014 | ||||||
| chr11:8742268
|
T | A | 125 | a0001c0001t0001g0035a0001c0001t0001g0258a0001c0001t0001g0293others(122): Show | 125 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.80+8353A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8742268 | ||||||
| chr11:8742455
|
A | G | 28 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(25): Show | 28 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.80+8166T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8742455 | ||||||
| chr11:8742493
|
C | G | 1 | a0001c0001t0002g0228 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.80+8128G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8742493 | ||||||
| chr11:8742694
|
C | T | 1 | a0003c0002t0001g0122 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.80+7927G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8742694 | ||||||
| chr11:8742807
|
G | C | 1 | a0001c0001t0002g0041 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.80+7814C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8742807 | ||||||
| chr11:8742868
|
C | T | 1 | a0002c0003t0001g0135 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.80+7753G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8742868 | ||||||
| chr11:8743200
|
C | A | 1 | a0001c0001t0001g0268 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.80+7421G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8743200 | ||||||
| chr11:8743263
|
A | C | 4 | a0001c0001t0001g0005a0001c0001t0003g0004a0001c0007t0001g0344others(1): Show | 4 | HG01943.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.80+7358T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8743263 | ||||||
| chr11:8743357
|
C | T | 1 | a0002c0003t0002g0202 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.80+7264G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8743357 | ||||||
| chr11:8743379
|
G | A | 4 | a0002c0003t0001g0085a0002c0003t0001g0150a0002c0003t0001g0181others(1): Show | 4 | NA18950.hp2 NA19012.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+7242C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8743379 | ||||||
| chr11:8743411
|
G | A | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+7210C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8743411 | ||||||
| chr11:8743551
|
A | G | 3 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227 | 3 | HG02257.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.80+7070T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8743551 | ||||||
| chr11:8743560
|
A | T | 125 | a0001c0001t0001g0035a0001c0001t0001g0258a0001c0001t0001g0293others(122): Show | 125 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.80+7061T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8743560 | ||||||
| chr11:8743561
|
T | A | 1 | a0002c0003t0002g0214 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.80+7060A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8743561 | ||||||
| chr11:8743570
|
T | A | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(162): Show | 165 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.80+7051A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8743570 | ||||||
| chr11:8743578
|
T | A | 1 | a0001c0001t0001g0268 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.80+7043A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8743578 | ||||||
| chr11:8743655
|
C | T | 3 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227 | 3 | HG02257.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.80+6966G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8743655 | ||||||
| chr11:8743686
|
A | T | 1 | a0001c0001t0001g0268 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.80+6935T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8743686 | ||||||
| chr11:8743753
|
C | T | 8 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227others(5): Show | 8 | HG01168.hp2 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+6868G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8743753 | ||||||
| chr11:8743827
|
G | T | 3 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02451.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.80+6794C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8743827 | ||||||
| chr11:8744071
|
T | G | 3 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02451.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.80+6550A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8744071 | ||||||
| chr11:8744113
|
T | C | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.80+6508A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8744113 | ||||||
| chr11:8744132
|
G | GT | 19 | a0001c0001t0001g0012a0001c0001t0001g0262a0001c0001t0001g0268others(16): Show | 19 | HG00639.hp2 HG00642.hp1 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.80+6488dupA | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8744132 | ||||||
| chr11:8744148
|
T | G | 26 | a0001c0001t0001g0027a0001c0001t0001g0057a0001c0001t0001g0060others(23): Show | 26 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.80+6473A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8744148 | ||||||
| chr11:8744149
|
G | T | 178 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0023others(175): Show | 178 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.80+6472C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8744149 | ||||||
| chr11:8744195
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0002g0021 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.80+6426C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8744195 | ||||||
| chr11:8744385
|
C | T | 23 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(20): Show | 23 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.80+6236G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8744385 | ||||||
| chr11:8744386
|
G | A | 1 | a0003c0002t0002g0078 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.80+6235C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8744386 | ||||||
| chr11:8744796
|
T | C | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+5825A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8744796 | ||||||
| chr11:8744806
|
G | A | 2 | a0002c0003t0002g0169a0002c0003t0002g0186 | 2 | HG03017.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.80+5815C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8744806 | ||||||
| chr11:8744924
|
A | AT | 278 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(275): Show | 278 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(275): Show |
intron_variant | MODIFIER | c.80+5696dupA | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8744924 | ||||||
| chr11:8744924
|
A | ATT | 10 | a0001c0001t0001g0140a0001c0001t0001g0249a0001c0001t0002g0225others(7): Show | 10 | HG02257.hp2 HG02451.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.80+5695_80+5696dup others(2): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8744924 | ||||||
| chr11:8745206
|
C | A | 2 | a0001c0007t0005g0024a0001c0007t0005g0029 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.80+5415G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8745206 | ||||||
| chr11:8745480
|
A | C | 7 | a0001c0001t0001g0226a0001c0001t0002g0073a0001c0001t0002g0074others(4): Show | 7 | HG00438.hp1 HG02523.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.80+5141T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8745480 | ||||||
| chr11:8745616
|
C | G | 9 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0047others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.80+5005G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8745616 | ||||||
| chr11:8745754
|
T | C | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.80+4867A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8745754 | ||||||
| chr11:8746103
|
GGCCACAG others(19): Show |
G | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(74): Show | 77 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.80+4492_80+4517del others(26): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8746103 | ||||||
| chr11:8746122
|
G | A | 118 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(115): Show | 118 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.80+4499C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8746122 | ||||||
| chr11:8746134
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.80+4487G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8746134 | ||||||
| chr11:8746201
|
G | A | 12 | a0001c0001t0001g0140a0001c0001t0001g0347a0001c0001t0001g0348others(9): Show | 12 | HG00639.hp1 HG01168.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.80+4420C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8746201 | ||||||
| chr11:8746489
|
TA | T | 3 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227 | 3 | HG02257.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.80+4131delT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8746489 | ||||||
| chr11:8746569
|
A | C | 1 | a0011c0014t0004g0222 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.80+4052T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8746569 | ||||||
| chr11:8746655
|
A | G | 1 | a0002c0003t0002g0214 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.80+3966T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8746655 | ||||||
| chr11:8746659
|
T | G | 1 | a0001c0001t0001g0042 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.80+3962A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8746659 | ||||||
| chr11:8746677
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.80+3944A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8746677 | ||||||
| chr11:8746863
|
G | A | 1 | a0006c0005t0001g0278 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.80+3758C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8746863 | ||||||
| chr11:8747095
|
T | C | 1 | a0001c0001t0001g0241 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.80+3526A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8747095 | ||||||
| chr11:8747100
|
G | A | 1 | a0002c0003t0002g0165 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.80+3521C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8747100 | ||||||
| chr11:8747230
|
TCA | T | 3 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227 | 3 | HG02257.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.80+3389_80+3390del others(2): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8747230 | ||||||
| chr11:8747251
|
ACC | A | 14 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0047others(11): Show | 14 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.80+3368_80+3369del others(2): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8747251 | ||||||
| chr11:8747357
|
A | G | 1 | a0001c0007t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.80+3264T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8747357 | ||||||
| chr11:8747438
|
G | A | 1 | a0003c0002t0002g0058 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.80+3183C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8747438 | ||||||
| chr11:8747550
|
A | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(173): Show | 176 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.80+3071T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8747550 | ||||||
| chr11:8747660
|
T | C | 8 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227others(5): Show | 8 | HG01168.hp2 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+2961A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8747660 | ||||||
| chr11:8747726
|
A | G | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.80+2895T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8747726 | ||||||
| chr11:8747751
|
A | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0252 | 2 | HG00741.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.80+2870T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8747751 | ||||||
| chr11:8747893
|
C | T | 5 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(2): Show | 5 | HG02145.hp2 HG02818.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.80+2728G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8747893 | ||||||
| chr11:8747979
|
T | C | 28 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(25): Show | 28 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.80+2642A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8747979 | ||||||
| chr11:8748046
|
A | C | 344 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(341): Show | 344 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(341): Show |
intron_variant | MODIFIER | c.80+2575T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8748046 | ||||||
| chr11:8748268
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.80+2353A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8748268 | ||||||
| chr11:8748276
|
T | G | 3 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02451.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.80+2345A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8748276 | ||||||
| chr11:8748411
|
C | T | 2 | a0003c0002t0003g0097a0003c0002t0003g0102 | 2 | NA18952.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.80+2210G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8748411 | ||||||
| chr11:8748566
|
A | G | 12 | a0001c0001t0001g0140a0001c0001t0001g0347a0001c0001t0001g0348others(9): Show | 12 | HG00639.hp1 HG01168.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.80+2055T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8748566 | ||||||
| chr11:8748584
|
C | T | 1 | a0003c0002t0001g0122 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.80+2037G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8748584 | ||||||
| chr11:8748592
|
C | T | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.80+2029G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8748592 | ||||||
| chr11:8748624
|
G | GGGAGGGA others(31): Show |
4 | a0001c0001t0001g0005a0001c0001t0003g0004a0001c0007t0001g0344others(1): Show | 4 | HG01943.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.80+1996_80+1997ins others(38): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8748624 | ||||||
| chr11:8749008
|
A | G | 1 | a0002c0003t0001g0068 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.80+1613T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8749008 | ||||||
| chr11:8749268
|
C | A | 1 | a0003c0002t0001g0128 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.80+1353G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8749268 | ||||||
| chr11:8749290
|
C | G | 8 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227others(5): Show | 8 | HG01168.hp2 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+1331G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8749290 | ||||||
| chr11:8749507
|
G | C | 8 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227others(5): Show | 8 | HG01168.hp2 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.80+1114C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8749507 | ||||||
| chr11:8749540
|
C | G | 3 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349 | 3 | HG00639.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.80+1081G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8749540 | ||||||
| chr11:8749657
|
C | A | 1 | a0001c0001t0003g0255 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.80+964G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8749657 | ||||||
| chr11:8750116
|
C | A | 2 | a0001c0001t0001g0023a0001c0001t0002g0021 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.80+505G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8750116 | ||||||
| chr11:8750130
|
G | A | 1 | a0003c0002t0001g0083 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.80+491C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 2/19 | chr11 | 8750130 | ||||||
| chr11:8750820
|
T | G | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-25-95A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8750820 | ||||||
| chr11:8750822
|
T | C | 3 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02451.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-25-97A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8750822 | ||||||
| chr11:8751026
|
A | G | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-301T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8751026 | ||||||
| chr11:8751027
|
T | C | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-302A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8751027 | ||||||
| chr11:8751039
|
C | T | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-25-314G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8751039 | ||||||
| chr11:8751212
|
G | T | 2 | a0001c0007t0001g0344a0001c0007t0001g0345 | 2 | HG01943.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-25-487C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8751212 | ||||||
| chr11:8751265
|
T | C | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(195): Show | 198 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.-25-540A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8751265 | ||||||
| chr11:8751306
|
C | A | 3 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227 | 3 | HG02257.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-25-581G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8751306 | ||||||
| chr11:8751391
|
G | A | 1 | a0001c0001t0002g0296 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-25-666C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8751391 | ||||||
| chr11:8751401
|
G | A | 1 | a0002c0003t0002g0153 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-25-676C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8751401 | ||||||
| chr11:8751432
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0002g0021 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-25-707T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8751432 | ||||||
| chr11:8751484
|
C | T | 23 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(20): Show | 23 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.-25-759G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8751484 | ||||||
| chr11:8751556
|
G | A | 3 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02451.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-25-831C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8751556 | ||||||
| chr11:8751589
|
G | A | 3 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349 | 3 | HG00639.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-25-864C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8751589 | ||||||
| chr11:8751598
|
CG | C | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(75): Show | 78 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-25-874delC | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8751598 | ||||||
| chr11:8751658
|
G | A | 2 | a0003c0002t0001g0108a0003c0002t0002g0103 | 2 | HG02683.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-25-933C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8751658 | ||||||
| chr11:8751712
|
G | A | 1 | a0002c0003t0002g0186 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-25-987C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8751712 | ||||||
| chr11:8751867
|
A | T | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-25-1142T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8751867 | ||||||
| chr11:8751991
|
C | G | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-1266G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8751991 | ||||||
| chr11:8751992
|
G | A | 1 | a0003c0002t0003g0338 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-25-1267C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8751992 | ||||||
| chr11:8752008
|
T | C | 12 | a0001c0001t0001g0140a0001c0001t0001g0347a0001c0001t0001g0348others(9): Show | 12 | HG00639.hp1 HG01168.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-25-1283A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8752008 | ||||||
| chr11:8752322
|
G | A | 8 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227others(5): Show | 8 | HG01168.hp2 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25-1597C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8752322 | ||||||
| chr11:8752429
|
G | A | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-1704C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8752429 | ||||||
| chr11:8752451
|
C | CA | 118 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(115): Show | 118 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-25-1727dupT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8752451 | ||||||
| chr11:8752551
|
G | A | 1 | a0005c0006t0001g0288 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-25-1826C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8752551 | ||||||
| chr11:8752666
|
G | C | 8 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227others(5): Show | 8 | HG01168.hp2 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25-1941C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8752666 | ||||||
| chr11:8752675
|
G | A | 6 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227others(3): Show | 6 | HG02257.hp2 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25-1950C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8752675 | ||||||
| chr11:8752677
|
C | A | 4 | a0002c0003t0002g0071a0002c0003t0002g0160a0002c0003t0002g0179others(1): Show | 4 | HG00544.hp2 NA18946.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-1952G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8752677 | ||||||
| chr11:8752791
|
G | A | 6 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227others(3): Show | 6 | HG02257.hp2 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25-2066C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8752791 | ||||||
| chr11:8752918
|
G | A | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-2193C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8752918 | ||||||
| chr11:8753279
|
C | T | 3 | a0001c0007t0005g0024a0001c0007t0005g0029a0002c0003t0002g0202 | 3 | HG02976.hp1 HG03471.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-25-2554G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8753279 | ||||||
| chr11:8753280
|
G | A | 1 | a0001c0001t0003g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-25-2555C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8753280 | ||||||
| chr11:8753311
|
T | G | 1 | a0002c0003t0002g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-25-2586A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8753311 | ||||||
| chr11:8753376
|
G | A | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(79): Show | 82 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.-25-2651C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8753376 | ||||||
| chr11:8753628
|
G | T | 6 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227others(3): Show | 6 | HG02257.hp2 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25-2903C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8753628 | ||||||
| chr11:8753636
|
ACT | A | 22 | a0001c0001t0001g0226a0001c0001t0001g0245a0001c0001t0001g0249others(19): Show | 22 | HG00438.hp1 HG01167.hp1 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.-25-2913_-25-2912d others(4): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8753636 | ||||||
| chr11:8753872
|
G | A | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(185): Show | 188 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.-25-3147C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8753872 | ||||||
| chr11:8753953
|
C | T | 1 | a0004c0004t0001g0335 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-25-3228G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8753953 | ||||||
| chr11:8754026
|
C | T | 3 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349 | 3 | HG00639.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-25-3301G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754026 | ||||||
| chr11:8754029
|
G | A | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-25-3304C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCACACAC others(1): Show |
3 | a0001c0001t0002g0051a0001c0001t0002g0224a0001c0001t0002g0246 | 3 | HG02572.hp1 NA18951.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-25-3312_-25-3305d others(10): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCACACAC others(3): Show |
6 | a0001c0001t0001g0057a0001c0001t0001g0060a0001c0001t0001g0167others(3): Show | 6 | HG01891.hp2 HG02015.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25-3314_-25-3305d others(12): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCACACAC others(5): Show |
2 | a0001c0001t0001g0062a0001c0001t0001g0168 | 2 | HG01346.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-25-3316_-25-3305d others(14): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCACACAC others(7): Show |
7 | a0001c0001t0001g0026a0001c0001t0001g0063a0001c0001t0001g0065others(4): Show | 7 | HG01109.hp1 HG02109.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-25-3318_-25-3305d others(16): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCACACAC others(9): Show |
4 | a0001c0001t0001g0027a0001c0001t0001g0064a0001c0001t0001g0066others(1): Show | 4 | HG02258.hp2 HG02559.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-3320_-25-3305d others(18): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCCGCACA others(14): Show |
1 | a0001c0001t0001g0261 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-25-3305_-25-3304i others(23): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCGCACA | 4 | a0001c0001t0001g0249a0001c0001t0001g0258a0001c0007t0005g0024others(1): Show | 4 | HG02976.hp1 HG03471.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-3305_-25-3304i others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCGCACAC others(1): Show |
16 | a0001c0001t0001g0025a0001c0001t0001g0226a0001c0001t0001g0234others(13): Show | 16 | HG00639.hp1 HG01167.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-25-3305_-25-3304i others(10): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCGCACAC others(3): Show |
20 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0241others(17): Show | 20 | HG00438.hp1 HG00673.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.-25-3305_-25-3304i others(12): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCGCACAC others(5): Show |
14 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0076others(11): Show | 14 | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-25-3305_-25-3304i others(14): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCGCACAC others(7): Show |
14 | a0001c0001t0001g0033a0001c0001t0001g0038a0001c0001t0001g0081others(11): Show | 14 | HG00558.hp1 HG01099.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.-25-3305_-25-3304i others(16): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCGCACAC others(9): Show |
10 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0061others(7): Show | 10 | HG00741.hp1 HG00741.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-25-3305_-25-3304i others(18): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCGCACAC others(11): Show |
7 | a0001c0001t0001g0023a0001c0001t0001g0042a0001c0001t0001g0047others(4): Show | 7 | HG00544.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-25-3305_-25-3304i others(20): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCGCACAC others(13): Show |
2 | a0001c0001t0001g0266a0009c0017t0001g0120 | 2 | HG01517.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.-25-3305_-25-3304i others(22): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCGCACAC others(15): Show |
3 | a0001c0001t0001g0119a0003c0002t0001g0007a0003c0002t0001g0008 | 3 | HG02922.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-25-3305_-25-3304i others(24): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCGCGCAC others(1): Show |
48 | a0002c0003t0001g0129a0002c0003t0001g0131a0002c0003t0001g0135others(45): Show | 48 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.-25-3305_-25-3304i others(10): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCGCGCAC others(3): Show |
90 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0003g0221others(87): Show | 90 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.-25-3305_-25-3304i others(12): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCGCGCAC others(5): Show |
32 | a0001c0001t0001g0035a0001c0001t0001g0277a0001c0001t0001g0293others(29): Show | 32 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.-25-3305_-25-3304i others(14): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCGCGCAC others(7): Show |
11 | a0002c0003t0001g0068a0002c0003t0001g0126a0002c0003t0001g0208others(8): Show | 11 | HG01192.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-25-3305_-25-3304i others(16): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCGCGCAC others(9): Show |
2 | a0002c0003t0002g0079a0004c0004t0001g0333 | 2 | HG03491.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-25-3305_-25-3304i others(18): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCGCGCAC others(11): Show |
1 | a0003c0002t0002g0336 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-25-3305_-25-3304i others(20): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCGCGCGC others(1): Show |
14 | a0003c0002t0001g0037a0003c0002t0001g0125a0003c0002t0001g0127others(11): Show | 14 | HG00597.hp2 HG01192.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.-25-3305_-25-3304i others(10): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCGCGCGC others(3): Show |
8 | a0002c0003t0001g0144a0002c0003t0002g0142a0002c0010t0002g0039others(5): Show | 8 | HG01256.hp2 HG01258.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25-3305_-25-3304i others(12): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCGCGCGC others(5): Show |
1 | a0001c0001t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-25-3305_-25-3304i others(14): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCGCGCGC others(7): Show |
3 | a0003c0002t0001g0182a0003c0002t0001g0183a0003c0002t0001g0184 | 3 | HG02896.hp1 HG02897.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-25-3305_-25-3304i others(16): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCGCGCGC others(11): Show |
1 | a0001c0001t0003g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-25-3305_-25-3304i others(20): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GCGCGCGC others(15): Show |
2 | a0001c0007t0001g0344a0001c0007t0001g0345 | 2 | HG01943.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-25-3305_-25-3304i others(24): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754029
|
G | GTGCACAC others(5): Show |
1 | a0001c0001t0001g0187 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-25-3305_-25-3304i others(14): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754029 | ||||||
| chr11:8754031
|
A | G | 7 | a0001c0001t0001g0140a0001c0001t0001g0231a0001c0001t0001g0263others(4): Show | 7 | HG02071.hp2 HG02257.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-25-3306T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754031 | ||||||
| chr11:8754063
|
A | AC | 6 | a0002c0003t0001g0068a0002c0003t0002g0148a0002c0003t0002g0185others(3): Show | 6 | HG01192.hp2 HG01261.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25-3339_-25-3338i others(3): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754063 | ||||||
| chr11:8754063
|
A | ACACACAC others(8): Show |
3 | a0001c0001t0001g0231a0001c0001t0001g0263a0001c0001t0002g0229 | 3 | HG02071.hp2 HG02738.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-25-3339_-25-3338i others(17): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754063 | ||||||
| chr11:8754064
|
A | C | 4 | a0001c0001t0001g0033a0001c0001t0001g0119a0001c0001t0002g0118others(1): Show | 4 | HG01884.hp2 HG02486.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-3339T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754064 | ||||||
| chr11:8754226
|
A | G | 1 | a0001c0001t0006g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-25-3501T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754226 | ||||||
| chr11:8754460
|
TC | T | 4 | a0001c0001t0001g0005a0001c0001t0003g0004a0001c0007t0001g0344others(1): Show | 4 | HG01943.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-3736delG | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754460 | ||||||
| chr11:8754596
|
A | G | 2 | a0001c0001t0002g0041a0001c0001t0002g0045 | 2 | NA18948.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-25-3871T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8754596 | ||||||
| chr11:8755146
|
G | T | 23 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(20): Show | 23 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.-25-4421C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8755146 | ||||||
| chr11:8755153
|
C | T | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(176): Show | 179 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.-25-4428G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8755153 | ||||||
| chr11:8755247
|
T | A | 8 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227others(5): Show | 8 | HG01168.hp2 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25-4522A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8755247 | ||||||
| chr11:8755681
|
T | A | 4 | a0001c0001t0001g0005a0001c0001t0003g0004a0001c0007t0001g0344others(1): Show | 4 | HG01943.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-4956A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8755681 | ||||||
| chr11:8755846
|
T | C | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-5121A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8755846 | ||||||
| chr11:8755861
|
T | C | 121 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(118): Show | 121 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.-25-5136A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8755861 | ||||||
| chr11:8756202
|
T | TA | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-5478dupT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8756202 | ||||||
| chr11:8756242
|
A | G | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(176): Show | 179 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.-25-5517T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8756242 | ||||||
| chr11:8756331
|
G | C | 28 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(25): Show | 28 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.-25-5606C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8756331 | ||||||
| chr11:8756530
|
G | A | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(192): Show | 195 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.-25-5805C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8756530 | ||||||
| chr11:8756639
|
T | C | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(75): Show | 78 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-25-5914A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8756639 | ||||||
| chr11:8756805
|
A | G | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(197): Show | 200 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(197): Show |
intron_variant | MODIFIER | c.-25-6080T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8756805 | ||||||
| chr11:8756865
|
C | T | 1 | a0003c0002t0001g0305 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-25-6140G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8756865 | ||||||
| chr11:8757213
|
A | G | 1 | a0003c0002t0001g0306 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-25-6488T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8757213 | ||||||
| chr11:8757240
|
G | A | 9 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0047others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25-6515C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8757240 | ||||||
| chr11:8757434
|
C | T | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-25-6709G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8757434 | ||||||
| chr11:8757438
|
G | C | 2 | a0002c0003t0002g0169a0002c0003t0002g0186 | 2 | HG03017.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-25-6713C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8757438 | ||||||
| chr11:8757625
|
T | C | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(183): Show | 186 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.-25-6900A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8757625 | ||||||
| chr11:8757881
|
G | A | 1 | a0002c0003t0002g0207 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-25-7156C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8757881 | ||||||
| chr11:8758212
|
A | G | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-7487T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8758212 | ||||||
| chr11:8758397
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-25-7672C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8758397 | ||||||
| chr11:8758691
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-25-7966T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8758691 | ||||||
| chr11:8758844
|
T | C | 1 | a0001c0001t0002g0227 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-25-8119A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8758844 | ||||||
| chr11:8758917
|
C | G | 1 | a0003c0002t0004g0337 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-25-8192G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8758917 | ||||||
| chr11:8759085
|
G | A | 21 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0038others(18): Show | 21 | HG00544.hp1 HG00558.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-25-8360C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8759085 | ||||||
| chr11:8759248
|
C | T | 1 | a0002c0003t0001g0085 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-25-8523G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8759248 | ||||||
| chr11:8759330
|
G | T | 1 | a0003c0002t0001g0095 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-25-8605C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8759330 | ||||||
| chr11:8759379
|
T | C | 1 | a0003c0002t0002g0096 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-25-8654A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8759379 | ||||||
| chr11:8759438
|
T | C | 2 | a0001c0001t0001g0261a0001c0001t0001g0266 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-25-8713A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8759438 | ||||||
| chr11:8759473
|
T | C | 3 | a0001c0001t0001g0245a0001c0001t0001g0249a0001c0001t0001g0254 | 3 | NA19009.hp1 NA19074.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-25-8748A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8759473 | ||||||
| chr11:8759617
|
G | A | 1 | a0002c0003t0002g0170 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-25-8892C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8759617 | ||||||
| chr11:8759705
|
T | C | 4 | a0001c0001t0001g0005a0001c0001t0002g0162a0001c0001t0003g0004others(1): Show | 4 | HG02723.hp2 HG03139.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-8980A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8759705 | ||||||
| chr11:8759710
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-25-8985G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8759710 | ||||||
| chr11:8759931
|
A | T | 1 | a0003c0002t0001g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-25-9206T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8759931 | ||||||
| chr11:8760181
|
C | T | 1 | a0002c0003t0002g0159 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-25-9456G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8760181 | ||||||
| chr11:8760219
|
C | A | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-25-9494G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8760219 | ||||||
| chr11:8760355
|
C | T | 3 | a0003c0002t0001g0182a0003c0002t0001g0183a0003c0002t0001g0184 | 3 | HG02896.hp1 HG02897.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-25-9630G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8760355 | ||||||
| chr11:8760648
|
A | G | 12 | a0001c0001t0001g0140a0001c0001t0001g0347a0001c0001t0001g0348others(9): Show | 12 | HG00639.hp1 HG01168.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-25-9923T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8760648 | ||||||
| chr11:8760723
|
T | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-25-9998A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8760723 | ||||||
| chr11:8760732
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-25-10007A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8760732 | ||||||
| chr11:8760804
|
G | C | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-25-10079C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8760804 | ||||||
| chr11:8760882
|
C | T | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-25-10157G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8760882 | ||||||
| chr11:8760897
|
T | C | 121 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(118): Show | 121 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.-25-10172A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8760897 | ||||||
| chr11:8760973
|
A | G | 94 | a0001c0001t0001g0330a0001c0001t0003g0080a0002c0003t0001g0129others(91): Show | 94 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.-25-10248T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8760973 | ||||||
| chr11:8761023
|
T | TC | 94 | a0001c0001t0001g0330a0001c0001t0003g0080a0002c0003t0001g0129others(91): Show | 94 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.-25-10299dupG | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8761023 | ||||||
| chr11:8761181
|
T | C | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-10456A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8761181 | ||||||
| chr11:8761311
|
T | C | 2 | a0001c0001t0001g0226a0001c0001t0002g0073 | 2 | NA18747.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-25-10586A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8761311 | ||||||
| chr11:8761491
|
C | T | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-25-10766G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8761491 | ||||||
| chr11:8761497
|
C | A | 1 | a0001c0001t0001g0025 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-25-10772G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8761497 | ||||||
| chr11:8761558
|
C | T | 1 | a0001c0007t0001g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-25-10833G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8761558 | ||||||
| chr11:8761636
|
G | C | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-25-10911C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8761636 | ||||||
| chr11:8761698
|
C | T | 1 | a0003c0002t0001g0089 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-25-10973G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8761698 | ||||||
| chr11:8761796
|
T | C | 3 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02451.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-25-11071A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8761796 | ||||||
| chr11:8761798
|
ATAAAGGC | A | 8 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227others(5): Show | 8 | HG01168.hp2 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25-11080_-25-1107 others(11): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8761798 | ||||||
| chr11:8762166
|
A | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(192): Show | 195 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.-25-11441T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8762166 | ||||||
| chr11:8762332
|
C | T | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-11607G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8762332 | ||||||
| chr11:8762371
|
T | C | 8 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227others(5): Show | 8 | HG01168.hp2 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25-11646A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8762371 | ||||||
| chr11:8762651
|
G | A | 1 | a0003c0002t0002g0291 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-25-11926C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8762651 | ||||||
| chr11:8762678
|
T | G | 10 | a0003c0002t0002g0078a0003c0002t0003g0279a0003c0002t0003g0338others(7): Show | 10 | HG00323.hp1 HG00642.hp1 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25-11953A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8762678 | ||||||
| chr11:8762784
|
C | T | 3 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02451.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-25-12059G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8762784 | ||||||
| chr11:8762814
|
C | T | 1 | a0002c0003t0002g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-25-12089G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8762814 | ||||||
| chr11:8762815
|
G | A | 2 | a0002c0003t0001g0208a0002c0003t0001g0209 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-25-12090C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8762815 | ||||||
| chr11:8763093
|
T | G | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-25-12368A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8763093 | ||||||
| chr11:8763100
|
G | C | 93 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0002g0162others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-25-12375C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8763100 | ||||||
| chr11:8763111
|
C | A | 1 | a0002c0003t0001g0150 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-25-12386G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8763111 | ||||||
| chr11:8763222
|
T | A | 1 | a0002c0003t0001g0150 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-25-12497A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8763222 | ||||||
| chr11:8763223
|
G | T | 1 | a0002c0003t0001g0150 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-25-12498C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8763223 | ||||||
| chr11:8763224
|
A | G | 1 | a0002c0003t0001g0150 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-25-12499T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8763224 | ||||||
| chr11:8763322
|
G | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(175): Show | 178 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.-25-12597C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8763322 | ||||||
| chr11:8763445
|
A | G | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-12720T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8763445 | ||||||
| chr11:8763747
|
A | G | 9 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0047others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25-13022T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8763747 | ||||||
| chr11:8763817
|
C | T | 2 | a0001c0007t0001g0344a0001c0007t0001g0345 | 2 | HG01943.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-25-13092G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8763817 | ||||||
| chr11:8763946
|
AG | A | 3 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02451.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-25-13222delC | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8763946 | ||||||
| chr11:8764052
|
C | T | 3 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349 | 3 | HG00639.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-25-13327G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764052 | ||||||
| chr11:8764085
|
A | C | 3 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02451.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-25-13360T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764085 | ||||||
| chr11:8764097
|
G | A | 1 | a0001c0001t0002g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-25-13372C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764097 | ||||||
| chr11:8764143
|
C | A | 1 | a0001c0001t0002g0228 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-25-13418G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764143 | ||||||
| chr11:8764157
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-25-13432A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764157 | ||||||
| chr11:8764195
|
G | A | 1 | a0002c0003t0002g0054 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-25-13470C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764195 | ||||||
| chr11:8764205
|
G | A | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-13480C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764205 | ||||||
| chr11:8764219
|
CA | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(179): Show | 182 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.-25-13495delT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764219 | ||||||
| chr11:8764230
|
C | A | 1 | a0003c0002t0003g0279 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-25-13505G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764230 | ||||||
| chr11:8764311
|
A | G | 4 | a0007c0008t0001g0294a0007c0008t0001g0295a0007c0008t0001g0297others(1): Show | 4 | HG01175.hp1 HG01978.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-13586T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764311 | ||||||
| chr11:8764331
|
C | A | 1 | a0001c0007t0001g0344 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-25-13606G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764331 | ||||||
| chr11:8764427
|
T | C | 1 | a0001c0001t0001g0187 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-25-13702A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764427 | ||||||
| chr11:8764463
|
T | A | 5 | a0002c0003t0001g0129a0002c0003t0001g0131a0002c0003t0001g0135others(2): Show | 5 | HG00558.hp2 HG02056.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25-13738A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764463 | ||||||
| chr11:8764511
|
C | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(175): Show | 178 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.-25-13786G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764511 | ||||||
| chr11:8764539
|
A | G | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-13814T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764539 | ||||||
| chr11:8764726
|
T | C | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-25-14001A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764726 | ||||||
| chr11:8764757
|
C | A | 1 | a0006c0005t0002g0180 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-25-14032G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764757 | ||||||
| chr11:8764942
|
C | CA | 113 | a0001c0001t0001g0035a0001c0001t0001g0302a0001c0001t0001g0330others(110): Show | 113 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.-25-14218dupT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764942 | ||||||
| chr11:8764942
|
C | CAA | 7 | a0001c0001t0001g0293a0001c0001t0001g0299a0003c0002t0001g0095others(4): Show | 7 | HG03516.hp2 NA18952.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-25-14219_-25-1421 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764942 | ||||||
| chr11:8764942
|
CA | C | 93 | a0001c0001t0001g0167a0001c0001t0001g0219a0001c0001t0001g0220others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-25-14218delT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764942 | ||||||
| chr11:8764942
|
CAAAAAAA others(1): Show |
C | 71 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(68): Show | 71 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.-25-14225_-25-1421 others(12): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764942 | ||||||
| chr11:8764954
|
A | G | 1 | a0003c0002t0001g0256 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-25-14229T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8764954 | ||||||
| chr11:8765422
|
T | C | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-25-14697A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8765422 | ||||||
| chr11:8765455
|
C | T | 1 | a0003c0002t0001g0152 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-25-14730G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8765455 | ||||||
| chr11:8765691
|
A | AT | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(169): Show | 172 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.-25-14967dupA | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8765691 | ||||||
| chr11:8765716
|
T | C | 9 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0047others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25-14991A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8765716 | ||||||
| chr11:8765735
|
C | T | 339 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(336): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.-25-15010G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8765735 | ||||||
| chr11:8765809
|
G | A | 1 | a0003c0002t0002g0058 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-25-15084C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8765809 | ||||||
| chr11:8765836
|
G | A | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-25-15111C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8765836 | ||||||
| chr11:8765856
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-25-15131C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8765856 | ||||||
| chr11:8765921
|
C | T | 1 | a0002c0003t0003g0193 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-25-15196G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8765921 | ||||||
| chr11:8766025
|
T | C | 3 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02451.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-25-15300A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8766025 | ||||||
| chr11:8766073
|
A | C | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(186): Show | 189 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.-25-15348T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8766073 | ||||||
| chr11:8766160
|
T | A | 1 | a0001c0001t0001g0077 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-25-15435A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8766160 | ||||||
| chr11:8766376
|
GCTCCCAG others(6): Show |
G | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-15664_-25-1565 others(17): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8766376 | ||||||
| chr11:8766557
|
C | T | 2 | a0002c0003t0002g0031a0003c0002t0001g0206 | 2 | NA18951.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-25-15832G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8766557 | ||||||
| chr11:8766621
|
A | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(174): Show | 177 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.-25-15896T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8766621 | ||||||
| chr11:8766628
|
C | T | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-25-15903G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8766628 | ||||||
| chr11:8766653
|
G | C | 1 | a0002c0003t0002g0147 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-25-15928C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8766653 | ||||||
| chr11:8766678
|
A | C | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(186): Show | 189 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.-25-15953T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8766678 | ||||||
| chr11:8766679
|
C | G | 1 | a0001c0001t0001g0268 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-25-15954G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8766679 | ||||||
| chr11:8766710
|
G | A | 1 | a0003c0002t0002g0284 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-25-15985C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8766710 | ||||||
| chr11:8766750
|
G | A | 1 | a0001c0001t0001g0269 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-25-16025C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8766750 | ||||||
| chr11:8766761
|
G | T | 1 | a0002c0003t0001g0174 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-25-16036C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8766761 | ||||||
| chr11:8766887
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-25-16162C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8766887 | ||||||
| chr11:8767050
|
G | A | 3 | a0001c0001t0001g0245a0001c0001t0001g0249a0001c0001t0001g0254 | 3 | NA19009.hp1 NA19074.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-25-16325C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8767050 | ||||||
| chr11:8767073
|
C | G | 9 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0047others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25-16348G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8767073 | ||||||
| chr11:8767133
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0003g0004a0001c0007t0001g0344others(1): Show | 4 | HG01943.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-16408C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8767133 | ||||||
| chr11:8767333
|
G | A | 1 | a0001c0001t0002g0224 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-25-16608C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8767333 | ||||||
| chr11:8767424
|
TGAA | T | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(176): Show | 179 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.-25-16702_-25-1670 others(7): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8767424 | ||||||
| chr11:8767618
|
G | C | 57 | a0002c0003t0001g0129a0002c0003t0001g0131a0002c0003t0001g0135others(54): Show | 57 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.-25-16893C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8767618 | ||||||
| chr11:8768142
|
T | G | 3 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349 | 3 | HG00639.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-25-17417A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8768142 | ||||||
| chr11:8768248
|
T | C | 4 | a0001c0001t0001g0005a0001c0001t0003g0004a0001c0007t0001g0344others(1): Show | 4 | HG01943.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-17523A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8768248 | ||||||
| chr11:8768284
|
T | G | 2 | a0001c0007t0005g0024a0001c0007t0005g0029 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-25-17559A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8768284 | ||||||
| chr11:8768398
|
A | AACCATAG others(6): Show |
1 | a0002c0003t0001g0150 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-25-17686_-25-1767 others(17): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8768398 | ||||||
| chr11:8768410
|
C | A | 1 | a0002c0003t0001g0212 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-25-17685G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8768410 | ||||||
| chr11:8768533
|
G | A | 1 | a0003c0002t0001g0206 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-25-17808C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8768533 | ||||||
| chr11:8768623
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-25-17898C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8768623 | ||||||
| chr11:8768853
|
T | G | 1 | a0001c0001t0002g0074 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-25-18128A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8768853 | ||||||
| chr11:8768879
|
T | C | 1 | a0002c0003t0010g0350 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-25-18154A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8768879 | ||||||
| chr11:8769239
|
C | CT | 172 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(169): Show | 172 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.-25-18515dupA | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8769239 | ||||||
| chr11:8769239
|
C | CTT | 6 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(3): Show | 6 | HG00597.hp1 HG00639.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25-18516_-25-1851 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8769239 | ||||||
| chr11:8769301
|
G | A | 3 | a0002c0003t0001g0173a0002c0003t0001g0204a0002c0003t0001g0205 | 3 | HG01167.hp2 HG01169.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-25-18576C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8769301 | ||||||
| chr11:8769325
|
C | T | 1 | a0003c0002t0001g0124 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-25-18600G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8769325 | ||||||
| chr11:8769358
|
C | T | 1 | a0001c0001t0002g0010 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-25-18633G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8769358 | ||||||
| chr11:8769491
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0003g0004 | 2 | HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-25-18766G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8769491 | ||||||
| chr11:8769591
|
T | C | 4 | a0001c0001t0001g0005a0001c0001t0003g0004a0001c0007t0001g0344others(1): Show | 4 | HG01943.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-18866A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8769591 | ||||||
| chr11:8769595
|
G | A | 9 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0047others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25-18870C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8769595 | ||||||
| chr11:8769680
|
C | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(173): Show | 176 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.-25-18955G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8769680 | ||||||
| chr11:8769694
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0003g0004a0001c0007t0001g0344others(1): Show | 4 | HG01943.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-18969C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8769694 | ||||||
| chr11:8769912
|
C | A | 3 | a0002c0003t0001g0154a0002c0003t0001g0164a0002c0003t0002g0192 | 3 | HG02165.hp2 NA18942.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-25-19187G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8769912 | ||||||
| chr11:8769991
|
G | C | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-19266C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8769991 | ||||||
| chr11:8770003
|
T | C | 1 | a0002c0003t0002g0203 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-25-19278A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8770003 | ||||||
| chr11:8770165
|
T | G | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-25-19440A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8770165 | ||||||
| chr11:8770179
|
A | G | 1 | a0003c0002t0001g0206 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-25-19454T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8770179 | ||||||
| chr11:8770189
|
C | T | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-19464G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8770189 | ||||||
| chr11:8770434
|
A | G | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(193): Show | 196 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.-25-19709T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8770434 | ||||||
| chr11:8770746
|
C | G | 9 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0047others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25-20021G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8770746 | ||||||
| chr11:8771075
|
C | T | 115 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(112): Show | 115 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-25-20350G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771075 | ||||||
| chr11:8771085
|
T | C | 1 | a0001c0007t0001g0036 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-25-20360A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771085 | ||||||
| chr11:8771103
|
G | C | 2 | a0002c0003t0001g0204a0002c0003t0001g0205 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-25-20378C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771103 | ||||||
| chr11:8771116
|
G | A | 1 | a0002c0003t0001g0177 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-25-20391C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771116 | ||||||
| chr11:8771182
|
G | A | 1 | a0002c0003t0001g0215 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-25-20457C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771182 | ||||||
| chr11:8771226
|
A | C | 1 | a0001c0001t0001g0119 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-25-20501T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771226 | ||||||
| chr11:8771256
|
T | C | 3 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227 | 3 | HG02257.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-25-20531A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771256 | ||||||
| chr11:8771378
|
T | G | 1 | a0001c0001t0001g0230 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-25-20653A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771378 | ||||||
| chr11:8771529
|
C | CAGAG | 31 | a0001c0001t0001g0330a0003c0002t0001g0108a0003c0002t0001g0306others(28): Show | 31 | HG00280.hp2 HG00642.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.-25-20808_-25-2080 others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771529 | ||||||
| chr11:8771529
|
C | CAGAGAG | 50 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0035others(47): Show | 50 | HG00323.hp1 HG00609.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.-25-20810_-25-2080 others(10): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771529 | ||||||
| chr11:8771529
|
C | CAGAGAGA others(1): Show |
24 | a0001c0001t0001g0299a0001c0001t0002g0048a0001c0001t0002g0049others(21): Show | 24 | HG00558.hp2 HG00621.hp1 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.-25-20812_-25-2080 others(12): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771529 | ||||||
| chr11:8771529
|
C | CAGAGAGA others(3): Show |
25 | a0001c0001t0001g0005a0001c0001t0003g0004a0001c0007t0005g0029others(22): Show | 25 | HG00408.hp1 HG00408.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.-25-20814_-25-2080 others(14): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771529 | ||||||
| chr11:8771529
|
C | CAGAGAGA others(5): Show |
9 | a0001c0007t0005g0024a0003c0002t0001g0082a0003c0002t0001g0089others(6): Show | 9 | HG03471.hp1 NA18968.hp2 NA18975.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25-20816_-25-2080 others(16): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771529 | ||||||
| chr11:8771529
|
C | CAGAGAGA others(7): Show |
2 | a0003c0002t0001g0100a0003c0002t0003g0102 | 2 | HG00673.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-25-20818_-25-2080 others(18): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771529 | ||||||
| chr11:8771529
|
C | CAGAGAGA others(9): Show |
5 | a0001c0001t0001g0348a0001c0001t0001g0349a0003c0002t0001g0104others(2): Show | 5 | HG00639.hp1 HG02897.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25-20820_-25-2080 others(20): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771529 | ||||||
| chr11:8771529
|
C | CAGAGAGA others(11): Show |
3 | a0001c0001t0001g0347a0003c0002t0001g0101a0003c0002t0001g0110 | 3 | HG02895.hp1 NA18950.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-25-20822_-25-2080 others(22): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771529 | ||||||
| chr11:8771529
|
C | CAGAGAGA others(17): Show |
1 | a0001c0001t0001g0257 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-25-20828_-25-2080 others(28): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771529 | ||||||
| chr11:8771529
|
C | CAGAGAGA others(31): Show |
1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-25-20842_-25-2080 others(42): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771529 | ||||||
| chr11:8771529
|
CAG | C | 5 | a0001c0001t0001g0009a0001c0001t0002g0019a0002c0003t0001g0208others(2): Show | 5 | HG01257.hp2 HG01258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25-20806_-25-2080 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771529 | ||||||
| chr11:8771529
|
CAGAG | C | 8 | a0001c0001t0001g0219a0001c0001t0001g0220a0002c0003t0001g0085others(5): Show | 8 | HG03209.hp2 NA18950.hp2 NA18992.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25-20808_-25-2080 others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771529 | ||||||
| chr11:8771529
|
CAGAGAG | C | 84 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0117others(81): Show | 84 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-25-20810_-25-2080 others(10): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771529 | ||||||
| chr11:8771529
|
CAGAGAGA others(3): Show |
C | 2 | a0002c0003t0001g0174a0002c0003t0002g0031 | 2 | NA19005.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-25-20814_-25-2080 others(14): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771529 | ||||||
| chr11:8771529
|
CAGAGAGA others(5): Show |
C | 4 | a0001c0001t0001g0033a0001c0001t0001g0119a0001c0001t0002g0118others(1): Show | 4 | HG01884.hp2 HG02486.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-20816_-25-2080 others(16): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771529 | ||||||
| chr11:8771533
|
G | C | 1 | a0002c0003t0001g0150 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-25-20808C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771533 | ||||||
| chr11:8771560
|
A | AGAGAGAG others(21): Show |
1 | a0011c0014t0004g0222 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-25-20836_-25-2083 others(32): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771560 | ||||||
| chr11:8771560
|
A | AGAGAGAG others(11): Show |
1 | a0001c0001t0004g0172 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-25-20836_-25-2083 others(22): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771560 | ||||||
| chr11:8771566
|
A | AGAGAGAG others(39): Show |
1 | a0003c0002t0001g0007 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-25-20842_-25-2084 others(50): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771566 | ||||||
| chr11:8771566
|
A | AGAGAGAG others(37): Show |
1 | a0001c0001t0001g0061 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-25-20842_-25-2084 others(48): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771566 | ||||||
| chr11:8771566
|
A | AGAGAGAG others(35): Show |
2 | a0001c0001t0001g0028a0001c0001t0001g0252 | 2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-25-20842_-25-2084 others(46): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771566 | ||||||
| chr11:8771566
|
A | AGAGAGAG others(37): Show |
1 | a0003c0002t0001g0008 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-25-20842_-25-2084 others(48): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771566 | ||||||
| chr11:8771566
|
A | AGAGAGAG others(36): Show |
1 | a0001c0001t0001g0263 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-25-20842_-25-2084 others(47): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771566 | ||||||
| chr11:8771566
|
A | AGAGAGAG others(31): Show |
2 | a0001c0001t0001g0187a0001c0001t0002g0270 | 2 | HG00741.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.-25-20842_-25-2084 others(42): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771566 | ||||||
| chr11:8771566
|
A | AGAGAGAG others(29): Show |
6 | a0001c0001t0001g0003a0001c0001t0001g0232a0001c0001t0001g0233others(3): Show | 6 | HG00544.hp1 HG01884.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25-20842_-25-2084 others(40): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771566 | ||||||
| chr11:8771566
|
A | AGAGAGAG others(27): Show |
3 | a0001c0001t0001g0265a0001c0001t0001g0281a0006c0005t0001g0278 | 3 | HG02004.hp2 HG02083.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-25-20842_-25-2084 others(38): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771566 | ||||||
| chr11:8771566
|
A | AGAGAGAG others(25): Show |
7 | a0001c0001t0001g0234a0001c0001t0001g0247a0001c0001t0001g0248others(4): Show | 7 | HG01099.hp2 HG02818.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-25-20842_-25-2084 others(36): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771566 | ||||||
| chr11:8771566
|
A | AGAGAGAG others(23): Show |
9 | a0001c0001t0001g0239a0001c0001t0001g0245a0001c0001t0001g0249others(6): Show | 9 | HG02080.hp1 HG02132.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25-20842_-25-2084 others(34): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771566 | ||||||
| chr11:8771566
|
A | AGAGAGAG others(21): Show |
9 | a0001c0001t0001g0038a0001c0001t0001g0076a0001c0001t0001g0262others(6): Show | 9 | HG00438.hp1 HG01517.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25-20842_-25-2084 others(32): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771566 | ||||||
| chr11:8771566
|
A | AGAGAGAG others(19): Show |
7 | a0001c0001t0001g0081a0001c0001t0001g0226a0001c0001t0001g0238others(4): Show | 7 | HG01515.hp1 HG02040.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-25-20842_-25-2084 others(30): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771566 | ||||||
| chr11:8771566
|
A | AGAGAGAG others(17): Show |
5 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0241others(2): Show | 5 | HG01167.hp1 HG02071.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25-20842_-25-2084 others(28): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771566 | ||||||
| chr11:8771566
|
A | AGAGAGAG others(15): Show |
4 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0269others(1): Show | 4 | HG02717.hp1 HG03834.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-20842_-25-2084 others(26): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771566 | ||||||
| chr11:8771566
|
A | AGAGAGAG others(13): Show |
2 | a0001c0001t0001g0242a0003c0002t0002g0030 | 2 | HG00673.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-25-20842_-25-2084 others(24): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771566 | ||||||
| chr11:8771566
|
A | AGAGAGAG others(11): Show |
2 | a0001c0001t0001g0275a0001c0001t0002g0228 | 2 | HG02451.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.-25-20842_-25-2084 others(22): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771566 | ||||||
| chr11:8771566
|
A | AGAGAGAG others(9): Show |
3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG02615.hp2 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-25-20842_-25-2084 others(20): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771566 | ||||||
| chr11:8771566
|
A | AGAGAGAG others(7): Show |
6 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0002g0021others(3): Show | 6 | HG01070.hp2 HG02109.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25-20842_-25-2084 others(18): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771566 | ||||||
| chr11:8771566
|
A | AGAGAGAG others(5): Show |
1 | a0001c0001t0001g0025 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-25-20842_-25-2084 others(16): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771566 | ||||||
| chr11:8771566
|
A | AGAGAGAG others(3): Show |
2 | a0001c0001t0001g0023a0001c0001t0002g0346 | 2 | HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-25-20842_-25-2084 others(14): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771566 | ||||||
| chr11:8771664
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0002g0021 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-25-20939A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771664 | ||||||
| chr11:8771702
|
T | C | 1 | a0002c0003t0002g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-25-20977A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771702 | ||||||
| chr11:8771991
|
G | A | 8 | a0001c0001t0001g0187a0001c0001t0001g0261a0001c0001t0001g0263others(5): Show | 8 | HG00741.hp2 HG01069.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.-25-21266C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771991 | ||||||
| chr11:8771996
|
T | G | 12 | a0001c0001t0001g0140a0001c0001t0001g0347a0001c0001t0001g0348others(9): Show | 12 | HG00639.hp1 HG01168.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-25-21271A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8771996 | ||||||
| chr11:8772066
|
C | T | 1 | a0001c0001t0002g0045 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-25-21341G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8772066 | ||||||
| chr11:8772128
|
T | TAC | 117 | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0230others(114): Show | 117 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-25-21405_-25-2140 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8772128 | ||||||
| chr11:8772128
|
T | TACAC | 14 | a0001c0001t0001g0025a0001c0001t0001g0272a0001c0001t0001g0273others(11): Show | 14 | HG00642.hp1 HG02109.hp1 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.-25-21407_-25-2140 others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8772128 | ||||||
| chr11:8772128
|
T | TACACAC | 10 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0007t0001g0036others(7): Show | 10 | HG00280.hp2 HG00558.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25-21409_-25-2140 others(10): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8772128 | ||||||
| chr11:8772128
|
T | TACACACA others(1): Show |
3 | a0003c0002t0001g0008a0008c0009t0001g0133a0008c0009t0001g0134 | 3 | HG02080.hp2 HG02155.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-25-21411_-25-2140 others(12): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8772128 | ||||||
| chr11:8772128
|
TAC | T | 98 | a0001c0001t0001g0005a0001c0001t0001g0033a0001c0001t0001g0042others(95): Show | 98 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.-25-21405_-25-2140 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8772128 | ||||||
| chr11:8772128
|
TACAC | T | 5 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227others(2): Show | 5 | HG01168.hp2 HG02257.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25-21407_-25-2140 others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8772128 | ||||||
| chr11:8772332
|
G | A | 1 | a0002c0003t0002g0214 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-25-21607C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8772332 | ||||||
| chr11:8772429
|
A | G | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(244): Show | 247 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.-25-21704T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8772429 | ||||||
| chr11:8772444
|
G | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-25-21719C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8772444 | ||||||
| chr11:8772589
|
T | C | 1 | a0001c0001t0003g0004 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-25-21864A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8772589 | ||||||
| chr11:8772644
|
A | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(70): Show | 73 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.-25-21919T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8772644 | ||||||
| chr11:8772811
|
G | A | 2 | a0003c0002t0001g0100a0003c0002t0001g0116 | 2 | HG00408.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.-25-22086C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8772811 | ||||||
| chr11:8773063
|
C | T | 1 | a0003c0002t0001g0124 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-25-22338G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8773063 | ||||||
| chr11:8773255
|
G | A | 2 | a0002c0003t0001g0208a0002c0003t0001g0209 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-25-22530C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8773255 | ||||||
| chr11:8773276
|
C | T | 71 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(68): Show | 71 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.-25-22551G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8773276 | ||||||
| chr11:8773298
|
C | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-25-22573G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8773298 | ||||||
| chr11:8773377
|
C | T | 12 | a0001c0001t0001g0140a0001c0001t0001g0347a0001c0001t0001g0348others(9): Show | 12 | HG00639.hp1 HG01168.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-25-22652G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8773377 | ||||||
| chr11:8773533
|
G | A | 93 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0002g0162others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-25-22808C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8773533 | ||||||
| chr11:8773579
|
G | A | 2 | a0003c0002t0001g0326a0003c0002t0001g0327 | 2 | HG01256.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.-25-22854C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8773579 | ||||||
| chr11:8774236
|
C | G | 4 | a0001c0001t0001g0005a0001c0001t0003g0004a0001c0007t0001g0344others(1): Show | 4 | HG01943.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-23511G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8774236 | ||||||
| chr11:8774240
|
C | T | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-25-23515G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8774240 | ||||||
| chr11:8774283
|
A | T | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-25-23558T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8774283 | ||||||
| chr11:8774285
|
C | T | 1 | a0002c0003t0001g0181 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-25-23560G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8774285 | ||||||
| chr11:8774474
|
A | G | 1 | a0003c0002t0002g0078 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-25-23749T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8774474 | ||||||
| chr11:8774493
|
C | T | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-25-23768G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8774493 | ||||||
| chr11:8774859
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0003g0004 | 2 | HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-25-24134A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8774859 | ||||||
| chr11:8774863
|
G | GT | 10 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0140others(7): Show | 10 | HG02055.hp2 HG02257.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25-24139dupA | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8774863 | ||||||
| chr11:8774863
|
G | T | 1 | a0001c0001t0001g0057 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-25-24138C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8774863 | ||||||
| chr11:8774868
|
T | G | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-25-24143A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8774868 | ||||||
| chr11:8774875
|
TA | T | 5 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(2): Show | 5 | HG00639.hp1 HG01168.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25-24151delT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8774875 | ||||||
| chr11:8774876
|
A | T | 11 | a0001c0001t0001g0005a0001c0001t0001g0140a0001c0001t0002g0225others(8): Show | 11 | HG01943.hp1 HG02257.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-25-24151T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8774876 | ||||||
| chr11:8774877
|
A | T | 16 | a0001c0001t0001g0005a0001c0001t0001g0140a0001c0001t0001g0347others(13): Show | 16 | HG00639.hp1 HG01168.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.-25-24152T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8774877 | ||||||
| chr11:8774880
|
A | T | 3 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02451.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-25-24155T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8774880 | ||||||
| chr11:8774883
|
A | T | 3 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02451.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-25-24158T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8774883 | ||||||
| chr11:8774929
|
G | A | 3 | a0003c0002t0001g0182a0003c0002t0001g0183a0003c0002t0001g0184 | 3 | HG02896.hp1 HG02897.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-25-24204C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8774929 | ||||||
| chr11:8775008
|
G | A | 93 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0002g0162others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-25-24283C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8775008 | ||||||
| chr11:8775236
|
G | T | 1 | a0002c0003t0002g0072 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-25-24511C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8775236 | ||||||
| chr11:8775412
|
A | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0140a0001c0001t0001g0347others(13): Show | 16 | HG00639.hp1 HG01168.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.-25-24687T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8775412 | ||||||
| chr11:8775790
|
G | T | 1 | a0003c0002t0001g0282 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-25-25065C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8775790 | ||||||
| chr11:8775920
|
A | C | 2 | a0002c0003t0002g0031a0003c0002t0001g0206 | 2 | NA18951.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.-25-25195T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8775920 | ||||||
| chr11:8776102
|
A | G | 2 | a0001c0001t0001g0042a0001c0001t0001g0047 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-25-25377T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776102 | ||||||
| chr11:8776131
|
G | GAC | 16 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0081others(13): Show | 16 | HG02055.hp2 HG02071.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.-25-25408_-25-2540 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776131 | ||||||
| chr11:8776134
|
A | ACACG | 3 | a0001c0001t0001g0028a0001c0001t0001g0237a0001c0001t0001g0281 | 3 | HG00544.hp1 HG02083.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-25-25410_-25-2540 others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776134 | ||||||
| chr11:8776134
|
A | ACG | 3 | a0002c0003t0001g0001a0002c0003t0001g0143a0002c0003t0001g0175 | 3 | HG01433.hp2 HG02004.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-25-25411_-25-2541 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776134 | ||||||
| chr11:8776134
|
A | ACGCG | 4 | a0002c0003t0001g0075a0002c0003t0001g0145a0002c0003t0001g0211others(1): Show | 4 | HG01074.hp1 HG01516.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-25410_-25-2540 others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776134 | ||||||
| chr11:8776134
|
ACG | A | 27 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0038others(24): Show | 27 | HG00558.hp1 HG00673.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.-25-25411_-25-2541 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776134 | ||||||
| chr11:8776134
|
ACGCACGT others(5): Show |
A | 3 | a0001c0001t0001g0187a0001c0001t0001g0263a0001c0001t0002g0270 | 3 | HG00741.hp2 HG01069.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-25-25421_-25-2541 others(16): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776134 | ||||||
| chr11:8776136
|
G | A | 19 | a0001c0001t0001g0006a0001c0001t0001g0061a0001c0001t0001g0076others(16): Show | 19 | HG00438.hp1 HG00741.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.-25-25411C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776136 | ||||||
| chr11:8776137
|
C | T | 1 | a0002c0003t0002g0214 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-25-25412G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776137 | ||||||
| chr11:8776137
|
CACGT | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0061a0001c0001t0001g0232others(3): Show | 6 | HG00741.hp1 HG01099.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25-25416_-25-2541 others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776137 | ||||||
| chr11:8776138
|
A | G | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0028others(131): Show | 134 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.-25-25413T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776138 | ||||||
| chr11:8776139
|
CGT | C | 28 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(25): Show | 28 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.-25-25416_-25-2541 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776139 | ||||||
| chr11:8776141
|
T | C | 162 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(159): Show | 162 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.-25-25416A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776141 | ||||||
| chr11:8776142
|
G | A | 1 | a0001c0001t0003g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-25-25417C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776142 | ||||||
| chr11:8776144
|
G | A | 2 | a0001c0001t0002g0229a0001c0001t0003g0343 | 2 | HG02683.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-25-25419C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776144 | ||||||
| chr11:8776144
|
GCGCA | G | 4 | a0001c0007t0001g0036a0001c0007t0002g0034a0001c0007t0005g0024others(1): Show | 4 | HG02451.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-25423_-25-2542 others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776144 | ||||||
| chr11:8776146
|
G | GCACACAC others(15): Show |
1 | a0001c0001t0005g0022 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-25-25422_-25-2542 others(26): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776146 | ||||||
| chr11:8776146
|
G | GCGCA | 3 | a0001c0001t0001g0042a0001c0001t0003g0004a0002c0003t0001g0176 | 3 | HG01993.hp1 HG02723.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-25-25422_-25-2542 others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776146 | ||||||
| chr11:8776146
|
G | GCGCACAC others(7): Show |
2 | a0001c0001t0001g0117a0001c0001t0002g0118 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-25-25422_-25-2542 others(18): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776146 | ||||||
| chr11:8776146
|
G | GCGCACAC others(9): Show |
2 | a0001c0001t0001g0119a0009c0017t0001g0120 | 2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-25-25422_-25-2542 others(20): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776146 | ||||||
| chr11:8776146
|
G | GCGCACAC others(13): Show |
1 | a0001c0001t0001g0033 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-25-25422_-25-2542 others(24): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776146 | ||||||
| chr11:8776146
|
G | GCGCACAC others(23): Show |
1 | a0001c0001t0002g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-25-25422_-25-2542 others(34): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776146 | ||||||
| chr11:8776146
|
G | GCGCGCAC others(1): Show |
18 | a0002c0003t0001g0126a0002c0003t0001g0188a0002c0003t0001g0197others(15): Show | 18 | HG01167.hp2 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.-25-25422_-25-2542 others(12): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776146 | ||||||
| chr11:8776146
|
G | GCGCGCAC others(3): Show |
12 | a0001c0001t0002g0162a0002c0003t0001g0173a0002c0003t0001g0204others(9): Show | 12 | HG00323.hp2 HG00438.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-25-25422_-25-2542 others(14): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776146 | ||||||
| chr11:8776146
|
G | GCGCGCAC others(5): Show |
4 | a0002c0003t0001g0177a0002c0003t0001g0190a0002c0003t0002g0194others(1): Show | 4 | HG00621.hp2 NA18950.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-25422_-25-2542 others(16): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776146 | ||||||
| chr11:8776146
|
G | GCGCGCAC others(7): Show |
5 | a0002c0003t0001g0085a0002c0003t0002g0185a0002c0003t0002g0195others(2): Show | 5 | HG01099.hp1 HG04115.hp1 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25-25422_-25-2542 others(18): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776146 | ||||||
| chr11:8776146
|
G | GCGCGCAC others(9): Show |
2 | a0002c0003t0002g0142a0002c0003t0002g0159 | 2 | HG01261.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-25-25422_-25-2542 others(20): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776146 | ||||||
| chr11:8776146
|
GCA | G | 3 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349 | 3 | HG00639.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-25-25423_-25-2542 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776146 | ||||||
| chr11:8776148
|
A | ACG | 38 | a0002c0003t0001g0129a0002c0003t0001g0135a0002c0003t0001g0136others(35): Show | 38 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.-25-25425_-25-2542 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776148 | ||||||
| chr11:8776148
|
A | ACGCG | 3 | a0003c0002t0001g0111a0003c0002t0002g0298a0008c0009t0001g0133 | 3 | HG00597.hp2 HG02155.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-25-25427_-25-2542 others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776148 | ||||||
| chr11:8776148
|
A | G | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(113): Show | 116 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.-25-25423T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776148 | ||||||
| chr11:8776149
|
C | T | 5 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227others(2): Show | 5 | HG01168.hp2 HG02257.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25-25424G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776149 | ||||||
| chr11:8776150
|
G | A | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(76): Show | 79 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-25-25425C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776150 | ||||||
| chr11:8776151
|
C | A | 1 | a0001c0001t0001g0299 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-25-25426G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776151 | ||||||
| chr11:8776151
|
C | T | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-25426G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776151 | ||||||
| chr11:8776152
|
G | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(91): Show | 94 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-25-25427C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776152 | ||||||
| chr11:8776152
|
G | GCACACA | 6 | a0002c0003t0001g0144a0002c0003t0001g0174a0002c0003t0002g0072others(3): Show | 6 | HG00642.hp2 HG03831.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25-25428_-25-2542 others(10): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776152 | ||||||
| chr11:8776152
|
G | GCACACAC others(1): Show |
11 | a0002c0003t0001g0050a0002c0003t0001g0154a0002c0003t0001g0158others(8): Show | 11 | HG00597.hp1 HG00733.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-25-25428_-25-2542 others(12): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776152 | ||||||
| chr11:8776152
|
G | GCACACAC others(3): Show |
7 | a0002c0003t0001g0164a0002c0003t0001g0216a0002c0003t0002g0069others(4): Show | 7 | HG01256.hp2 HG01258.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.-25-25428_-25-2542 others(14): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776152 | ||||||
| chr11:8776152
|
G | GCACACAC others(5): Show |
3 | a0002c0003t0002g0031a0002c0003t0002g0054a0002c0003t0002g0207 | 3 | HG02055.hp1 NA19004.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-25-25428_-25-2542 others(16): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776152 | ||||||
| chr11:8776152
|
G | GCACACAC others(7): Show |
3 | a0002c0003t0001g0181a0002c0003t0001g0244a0002c0003t0002g0203 | 3 | HG00609.hp1 HG02698.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-25-25428_-25-2542 others(18): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776152 | ||||||
| chr11:8776153
|
C | T | 4 | a0001c0007t0001g0036a0001c0007t0002g0034a0001c0007t0005g0024others(1): Show | 4 | HG02451.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-25428G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776153 | ||||||
| chr11:8776154
|
G | A | 156 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(153): Show | 156 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.-25-25429C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776154 | ||||||
| chr11:8776154
|
G | GCACACAC others(3): Show |
4 | a0001c0001t0001g0219a0001c0001t0001g0220a0002c0003t0002g0070others(1): Show | 4 | HG00544.hp2 HG03209.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-25430_-25-2542 others(14): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776154 | ||||||
| chr11:8776154
|
G | GCACACAC others(9): Show |
1 | a0002c0003t0002g0186 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-25-25430_-25-2542 others(20): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776154 | ||||||
| chr11:8776154
|
GCGCGCGC others(1): Show |
G | 28 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(25): Show | 28 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.-25-25437_-25-2543 others(12): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776154 | ||||||
| chr11:8776156
|
G | A | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(166): Show | 169 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.-25-25431C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776156 | ||||||
| chr11:8776156
|
G | GCACACAC others(3): Show |
1 | a0002c0003t0002g0191 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-25-25432_-25-2543 others(14): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776156 | ||||||
| chr11:8776156
|
G | GCACACAC others(5): Show |
1 | a0002c0003t0001g0068 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-25-25432_-25-2543 others(16): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776156 | ||||||
| chr11:8776156
|
GCGCGCAC others(3): Show |
G | 1 | a0010c0013t0001g0285 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-25-25441_-25-2543 others(14): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776156 | ||||||
| chr11:8776158
|
G | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(170): Show | 173 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.-25-25433C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776158 | ||||||
| chr11:8776158
|
G | GCACACAC others(5): Show |
1 | a0002c0003t0002g0170 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-25-25434_-25-2543 others(16): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776158 | ||||||
| chr11:8776160
|
G | A | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(177): Show | 180 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.-25-25435C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776160 | ||||||
| chr11:8776160
|
GCA | G | 15 | a0001c0001t0001g0035a0001c0001t0001g0187a0001c0001t0001g0263others(12): Show | 15 | HG00741.hp2 HG01069.hp1 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.-25-25437_-25-2543 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776160 | ||||||
| chr11:8776160
|
GCACA | G | 23 | a0001c0001t0001g0330a0003c0002t0001g0308a0003c0002t0001g0314others(20): Show | 23 | HG00280.hp2 HG00642.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.-25-25439_-25-2543 others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776160 | ||||||
| chr11:8776160
|
GCACACA | G | 14 | a0001c0001t0001g0017a0003c0002t0001g0306a0003c0002t0001g0313others(11): Show | 14 | HG00323.hp1 HG00733.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.-25-25441_-25-2543 others(10): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776160 | ||||||
| chr11:8776162
|
A | G | 76 | a0001c0001t0001g0009a0001c0001t0001g0293a0001c0001t0001g0299others(73): Show | 76 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.-25-25437T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776162 | ||||||
| chr11:8776164
|
A | G | 82 | a0001c0001t0001g0035a0001c0001t0001g0187a0001c0001t0001g0263others(79): Show | 82 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.-25-25439T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776164 | ||||||
| chr11:8776166
|
A | G | 48 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(45): Show | 48 | HG00280.hp2 HG00408.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.-25-25441T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776166 | ||||||
| chr11:8776168
|
A | G | 36 | a0001c0001t0001g0330a0003c0002t0001g0306a0003c0002t0001g0308others(33): Show | 36 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.-25-25443T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776168 | ||||||
| chr11:8776170
|
A | G | 36 | a0001c0001t0001g0330a0003c0002t0001g0306a0003c0002t0001g0308others(33): Show | 36 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.-25-25445T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776170 | ||||||
| chr11:8776172
|
A | ACACACAC others(6): Show |
1 | a0002c0003t0001g0150 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-25-25448_-25-2544 others(17): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776172 | ||||||
| chr11:8776186
|
A | ACACACAC others(3): Show |
2 | a0001c0007t0001g0344a0001c0007t0001g0345 | 2 | HG01943.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-25-25462_-25-2546 others(14): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776186 | ||||||
| chr11:8776474
|
C | T | 3 | a0002c0003t0002g0146a0002c0003t0002g0147a0002c0003t0002g0201 | 3 | NA18939.hp2 NA19057.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-25-25749G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776474 | ||||||
| chr11:8776520
|
G | C | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-25795C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776520 | ||||||
| chr11:8776539
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-25-25814T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8776539 | ||||||
| chr11:8777151
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-25-26426T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8777151 | ||||||
| chr11:8777277
|
C | G | 339 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(336): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.-25-26552G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8777277 | ||||||
| chr11:8777306
|
G | C | 38 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(35): Show | 38 | HG00639.hp1 HG01109.hp1 HG01346.hp1 others(35): Show |
intron_variant | MODIFIER | c.-25-26581C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8777306 | ||||||
| chr11:8777417
|
T | A | 1 | a0002c0003t0002g0169 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-25-26692A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8777417 | ||||||
| chr11:8777759
|
C | T | 2 | a0003c0002t0001g0007a0003c0002t0001g0008 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-25-27034G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8777759 | ||||||
| chr11:8777764
|
A | G | 3 | a0001c0001t0001g0234a0001c0001t0001g0248a0001c0001t0001g0253 | 3 | HG01884.hp1 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-25-27039T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8777764 | ||||||
| chr11:8777836
|
A | T | 1 | a0001c0001t0002g0074 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-25-27111T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8777836 | ||||||
| chr11:8777853
|
T | C | 1 | a0001c0001t0001g0231 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-25-27128A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8777853 | ||||||
| chr11:8777997
|
A | C | 3 | a0002c0003t0002g0169a0002c0003t0002g0170a0002c0003t0002g0186 | 3 | HG03017.hp1 HG03710.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-25-27272T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8777997 | ||||||
| chr11:8778176
|
G | A | 1 | a0002c0003t0002g0072 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-25-27451C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8778176 | ||||||
| chr11:8778200
|
T | C | 3 | a0001c0001t0001g0038a0001c0001t0001g0260a0001c0001t0001g0262 | 3 | NA18954.hp1 NA18975.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-25-27475A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8778200 | ||||||
| chr11:8778202
|
G | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(70): Show | 73 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.-25-27477C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8778202 | ||||||
| chr11:8778503
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-25-27778G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8778503 | ||||||
| chr11:8778604
|
G | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-25-27879C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8778604 | ||||||
| chr11:8778665
|
G | A | 2 | a0001c0007t0005g0024a0001c0007t0005g0029 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-25-27940C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8778665 | ||||||
| chr11:8778779
|
G | A | 1 | a0003c0002t0002g0284 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-25-28054C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8778779 | ||||||
| chr11:8778806
|
C | T | 1 | a0002c0003t0001g0173 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-25-28081G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8778806 | ||||||
| chr11:8778870
|
T | C | 3 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02451.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-25-28145A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8778870 | ||||||
| chr11:8778957
|
A | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(84): Show | 87 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.-25-28232T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8778957 | ||||||
| chr11:8779044
|
C | T | 10 | a0001c0001t0001g0140a0001c0001t0001g0347a0001c0001t0001g0348others(7): Show | 10 | HG00639.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-25-28319G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8779044 | ||||||
| chr11:8779087
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-25-28362A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8779087 | ||||||
| chr11:8779183
|
C | T | 4 | a0001c0001t0001g0005a0001c0001t0003g0004a0001c0007t0001g0344others(1): Show | 4 | HG01943.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-28458G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8779183 | ||||||
| chr11:8779184
|
G | T | 1 | a0005c0006t0001g0091 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-25-28459C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8779184 | ||||||
| chr11:8779202
|
G | A | 1 | a0001c0001t0003g0221 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-25-28477C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8779202 | ||||||
| chr11:8779332
|
C | T | 342 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(339): Show | 342 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.-25-28607G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8779332 | ||||||
| chr11:8779467
|
G | T | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25-28742C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8779467 | ||||||
| chr11:8779494
|
T | TTTTC | 6 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0001t0001g0063others(3): Show | 6 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25-28773_-25-2877 others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8779494 | ||||||
| chr11:8779509
|
TCTTTC | T | 4 | a0001c0001t0001g0005a0001c0001t0003g0004a0001c0007t0001g0344others(1): Show | 4 | HG01943.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25-28789_-25-2878 others(9): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8779509 | ||||||
| chr11:8779513
|
TC | T | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(164): Show | 167 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.-25-28789delG | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8779513 | ||||||
| chr11:8779514
|
C | T | 17 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0042others(14): Show | 17 | HG01106.hp2 HG01168.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.-25-28789G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8779514 | ||||||
| chr11:8779517
|
T | C | 10 | a0001c0001t0001g0140a0001c0001t0001g0347a0001c0001t0001g0348others(7): Show | 10 | HG00639.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-25-28792A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8779517 | ||||||
| chr11:8779572
|
G | C | 2 | a0001c0007t0001g0344a0001c0007t0001g0345 | 2 | HG01943.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-25-28847C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8779572 | ||||||
| chr11:8779588
|
C | A | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(172): Show | 175 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.-25-28863G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8779588 | ||||||
| chr11:8779784
|
G | A | 3 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227 | 3 | HG02257.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-25-29059C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8779784 | ||||||
| chr11:8779999
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-25-29274G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8779999 | ||||||
| chr11:8780065
|
G | A | 3 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | HG01109.hp1 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-25-29340C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8780065 | ||||||
| chr11:8780071
|
A | T | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(70): Show | 73 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.-25-29346T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8780071 | ||||||
| chr11:8780113
|
C | T | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-25-29388G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8780113 | ||||||
| chr11:8780243
|
G | C | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(170): Show | 173 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.-25-29518C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8780243 | ||||||
| chr11:8780250
|
C | G | 10 | a0001c0001t0001g0140a0001c0001t0001g0347a0001c0001t0001g0348others(7): Show | 10 | HG00639.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-25-29525G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8780250 | ||||||
| chr11:8780800
|
G | T | 4 | a0001c0001t0001g0005a0001c0001t0003g0004a0001c0007t0001g0344others(1): Show | 4 | HG01943.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+29717C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8780800 | ||||||
| chr11:8780875
|
A | G | 339 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(336): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.-26+29642T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8780875 | ||||||
| chr11:8780884
|
G | A | 5 | a0002c0003t0002g0069a0002c0003t0002g0070a0002c0003t0002g0146others(2): Show | 5 | NA18612.hp1 NA18939.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26+29633C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8780884 | ||||||
| chr11:8780923
|
G | A | 10 | a0001c0001t0001g0140a0001c0001t0001g0347a0001c0001t0001g0348others(7): Show | 10 | HG00639.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26+29594C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8780923 | ||||||
| chr11:8781005
|
A | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0140a0001c0001t0001g0347others(13): Show | 16 | HG00639.hp1 HG01168.hp2 HG01943.hp1 others(13): Show |
intron_variant | MODIFIER | c.-26+29512T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8781005 | ||||||
| chr11:8781018
|
G | A | 10 | a0001c0001t0001g0140a0001c0001t0001g0347a0001c0001t0001g0348others(7): Show | 10 | HG00639.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26+29499C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8781018 | ||||||
| chr11:8781058
|
G | C | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-26+29459C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8781058 | ||||||
| chr11:8781102
|
A | G | 339 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(336): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.-26+29415T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8781102 | ||||||
| chr11:8781131
|
G | A | 1 | a0002c0003t0001g0068 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-26+29386C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8781131 | ||||||
| chr11:8781228
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0003g0004a0001c0007t0001g0344others(1): Show | 4 | HG01943.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+29289C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8781228 | ||||||
| chr11:8781248
|
C | T | 2 | a0001c0007t0001g0344a0001c0007t0001g0345 | 2 | HG01943.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-26+29269G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8781248 | ||||||
| chr11:8781301
|
G | T | 9 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0047others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-26+29216C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8781301 | ||||||
| chr11:8781424
|
C | T | 1 | a0002c0003t0002g0141 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-26+29093G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8781424 | ||||||
| chr11:8781483
|
T | C | 4 | a0001c0001t0001g0005a0001c0001t0003g0004a0001c0007t0001g0344others(1): Show | 4 | HG01943.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+29034A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8781483 | ||||||
| chr11:8781615
|
T | TAC | 4 | a0001c0001t0002g0073a0001c0001t0004g0172a0003c0002t0002g0289others(1): Show | 4 | HG00408.hp2 HG01168.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26+28900_-26+2890 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8781615 | ||||||
| chr11:8781615
|
TAC | T | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(196): Show | 199 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(196): Show |
intron_variant | MODIFIER | c.-26+28900_-26+2890 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8781615 | ||||||
| chr11:8781615
|
TACAC | T | 3 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02451.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-26+28898_-26+2890 others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8781615 | ||||||
| chr11:8781615
|
TACACAC | T | 3 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227 | 3 | HG02257.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-26+28896_-26+2890 others(10): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8781615 | ||||||
| chr11:8781615
|
TACACACA others(1): Show |
T | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26+28894_-26+2890 others(12): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8781615 | ||||||
| chr11:8781645
|
A | T | 10 | a0001c0001t0001g0140a0001c0001t0001g0347a0001c0001t0001g0348others(7): Show | 10 | HG00639.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26+28872T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8781645 | ||||||
| chr11:8781855
|
G | T | 4 | a0001c0001t0001g0005a0001c0001t0003g0004a0001c0007t0001g0344others(1): Show | 4 | HG01943.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+28662C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8781855 | ||||||
| chr11:8781944
|
A | G | 10 | a0001c0001t0001g0140a0001c0001t0001g0347a0001c0001t0001g0348others(7): Show | 10 | HG00639.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26+28573T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8781944 | ||||||
| chr11:8781965
|
T | C | 1 | a0003c0002t0002g0078 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-26+28552A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8781965 | ||||||
| chr11:8782056
|
C | T | 4 | a0001c0001t0001g0033a0001c0001t0001g0119a0001c0001t0002g0118others(1): Show | 4 | HG01884.hp2 HG02486.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+28461G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8782056 | ||||||
| chr11:8782140
|
C | T | 1 | a0001c0001t0003g0251 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-26+28377G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8782140 | ||||||
| chr11:8782189
|
T | G | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-26+28328A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8782189 | ||||||
| chr11:8782214
|
G | A | 12 | a0001c0001t0001g0140a0001c0001t0001g0347a0001c0001t0001g0348others(9): Show | 12 | HG00639.hp1 HG01168.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-26+28303C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8782214 | ||||||
| chr11:8782564
|
C | T | 311 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(308): Show | 311 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.-26+27953G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8782564 | ||||||
| chr11:8782703
|
G | A | 3 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227 | 3 | HG02257.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-26+27814C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8782703 | ||||||
| chr11:8782752
|
G | T | 1 | a0010c0013t0001g0285 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-26+27765C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8782752 | ||||||
| chr11:8782816
|
A | G | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(191): Show | 194 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.-26+27701T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8782816 | ||||||
| chr11:8782886
|
C | CA | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(83): Show | 86 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(83): Show |
intron_variant | MODIFIER | c.-26+27630dupT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8782886 | ||||||
| chr11:8782886
|
C | CAA | 11 | a0001c0001t0001g0061a0001c0001t0001g0140a0001c0001t0001g0237others(8): Show | 11 | HG00544.hp1 HG00741.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.-26+27629_-26+2763 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8782886 | ||||||
| chr11:8782886
|
CAAAA | C | 116 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(113): Show | 116 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-26+27627_-26+2763 others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8782886 | ||||||
| chr11:8783046
|
C | CT | 122 | a0001c0001t0001g0035a0001c0001t0001g0042a0001c0001t0001g0047others(119): Show | 122 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.-26+27470dupA | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8783046 | ||||||
| chr11:8783046
|
C | CTT | 55 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0025others(52): Show | 55 | HG00438.hp1 HG00741.hp1 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.-26+27469_-26+2747 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8783046 | ||||||
| chr11:8783046
|
C | CTTT | 34 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(31): Show | 34 | HG00544.hp1 HG00558.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.-26+27468_-26+2747 others(7): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8783046 | ||||||
| chr11:8783046
|
C | CTTTT | 6 | a0001c0001t0001g0230a0001c0001t0001g0238a0001c0001t0001g0257others(3): Show | 6 | HG02040.hp2 HG02738.hp1 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-26+27467_-26+2747 others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8783046 | ||||||
| chr11:8783066
|
T | TC | 6 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0055others(3): Show | 6 | HG02572.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-26+27450dupG | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8783066 | ||||||
| chr11:8783336
|
C | G | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26+27181G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8783336 | ||||||
| chr11:8783469
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0047 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-26+27048C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8783469 | ||||||
| chr11:8783685
|
A | G | 9 | a0003c0002t0003g0279a0003c0002t0003g0338a0004c0004t0001g0307others(6): Show | 9 | HG00323.hp1 HG00642.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.-26+26832T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8783685 | ||||||
| chr11:8783704
|
C | G | 3 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02451.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-26+26813G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8783704 | ||||||
| chr11:8783714
|
A | G | 117 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(114): Show | 117 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-26+26803T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8783714 | ||||||
| chr11:8783734
|
TAGC | T | 3 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227 | 3 | HG02257.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-26+26780_-26+2678 others(7): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8783734 | ||||||
| chr11:8783760
|
C | T | 12 | a0001c0001t0001g0140a0001c0001t0001g0347a0001c0001t0001g0348others(9): Show | 12 | HG00639.hp1 HG01168.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-26+26757G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8783760 | ||||||
| chr11:8783761
|
G | A | 1 | a0001c0001t0003g0240 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-26+26756C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8783761 | ||||||
| chr11:8783827
|
G | A | 10 | a0001c0001t0001g0140a0001c0001t0001g0347a0001c0001t0001g0348others(7): Show | 10 | HG00639.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26+26690C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8783827 | ||||||
| chr11:8783835
|
A | T | 1 | a0001c0001t0001g0025 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-26+26682T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8783835 | ||||||
| chr11:8784037
|
G | T | 2 | a0001c0001t0001g0023a0001c0001t0002g0021 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-26+26480C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784037 | ||||||
| chr11:8784141
|
G | C | 28 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(25): Show | 28 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.-26+26376C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784141 | ||||||
| chr11:8784217
|
T | G | 3 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0258 | 3 | HG02055.hp2 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-26+26300A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784217 | ||||||
| chr11:8784221
|
C | G | 1 | a0001c0007t0002g0034 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-26+26296G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784221 | ||||||
| chr11:8784252
|
G | GA | 23 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0047others(20): Show | 23 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.-26+26264dupT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784252 | ||||||
| chr11:8784252
|
GA | G | 165 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0011others(162): Show | 165 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.-26+26264delT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784252 | ||||||
| chr11:8784269
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-26+26248T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784269 | ||||||
| chr11:8784360
|
G | A | 2 | a0002c0003t0001g0208a0002c0003t0001g0209 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-26+26157C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784360 | ||||||
| chr11:8784408
|
T | C | 3 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02451.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-26+26109A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784408 | ||||||
| chr11:8784425
|
A | T | 336 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(333): Show | 336 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.-26+26092T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784425 | ||||||
| chr11:8784426
|
C | A | 3 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02451.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-26+26091G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784426 | ||||||
| chr11:8784426
|
C | CA | 17 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0047others(14): Show | 17 | HG00639.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.-26+26090dupT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784426 | ||||||
| chr11:8784607
|
G | A | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(166): Show | 169 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.-26+25910C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784607 | ||||||
| chr11:8784608
|
C | T | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-26+25909G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784608 | ||||||
| chr11:8784626
|
T | A | 1 | a0002c0003t0001g0050 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-26+25891A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784626 | ||||||
| chr11:8784641
|
C | A | 9 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0047others(6): Show | 9 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-26+25876G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784641 | ||||||
| chr11:8784693
|
C | T | 10 | a0001c0001t0001g0140a0001c0001t0001g0347a0001c0001t0001g0348others(7): Show | 10 | HG00639.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26+25824G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784693 | ||||||
| chr11:8784698
|
C | T | 1 | a0002c0003t0001g0244 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-26+25819G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784698 | ||||||
| chr11:8784837
|
C | CA | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(107): Show | 110 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.-26+25679dupT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784837 | ||||||
| chr11:8784837
|
CA | C | 11 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0047others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-26+25679delT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784837 | ||||||
| chr11:8784837
|
CAA | C | 10 | a0001c0001t0001g0140a0001c0001t0001g0347a0001c0001t0001g0348others(7): Show | 10 | HG00639.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26+25678_-26+2567 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784837 | ||||||
| chr11:8784967
|
T | C | 1 | a0002c0003t0002g0163 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-26+25550A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8784967 | ||||||
| chr11:8785162
|
G | T | 117 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(114): Show | 117 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-26+25355C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8785162 | ||||||
| chr11:8785247
|
C | T | 4 | a0001c0001t0001g0005a0001c0001t0003g0004a0001c0007t0001g0344others(1): Show | 4 | HG01943.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+25270G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8785247 | ||||||
| chr11:8785249
|
T | C | 3 | a0002c0003t0002g0146a0002c0003t0002g0147a0002c0003t0002g0201 | 3 | NA18939.hp2 NA19057.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-26+25268A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8785249 | ||||||
| chr11:8785295
|
T | C | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-26+25222A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8785295 | ||||||
| chr11:8785575
|
C | T | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG02280.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-26+24942G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8785575 | ||||||
| chr11:8785632
|
A | C | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(177): Show | 180 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.-26+24885T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8785632 | ||||||
| chr11:8785639
|
G | A | 28 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(25): Show | 28 | HG01109.hp1 HG01346.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.-26+24878C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8785639 | ||||||
| chr11:8785652
|
A | G | 7 | a0001c0001t0001g0245a0001c0001t0001g0249a0001c0001t0001g0254others(4): Show | 7 | HG02080.hp1 HG03834.hp2 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.-26+24865T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8785652 | ||||||
| chr11:8786001
|
C | T | 311 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(308): Show | 311 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.-26+24516G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8786001 | ||||||
| chr11:8786097
|
A | T | 2 | a0003c0002t0001g0182a0003c0002t0001g0184 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-26+24420T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8786097 | ||||||
| chr11:8786278
|
G | C | 6 | a0001c0001t0001g0025a0001c0001t0001g0272a0001c0001t0001g0273others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-26+24239C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8786278 | ||||||
| chr11:8786331
|
T | A | 3 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02451.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-26+24186A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8786331 | ||||||
| chr11:8786637
|
C | A | 17 | a0003c0002t0001g0282a0003c0002t0001g0283a0003c0002t0001g0287others(14): Show | 17 | HG00408.hp2 HG00597.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.-26+23880G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8786637 | ||||||
| chr11:8786705
|
G | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(175): Show | 178 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.-26+23812C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8786705 | ||||||
| chr11:8786766
|
T | C | 3 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227 | 3 | HG02257.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-26+23751A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8786766 | ||||||
| chr11:8786830
|
A | G | 1 | a0003c0002t0002g0088 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-26+23687T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8786830 | ||||||
| chr11:8787040
|
A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(175): Show | 178 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.-26+23477T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8787040 | ||||||
| chr11:8787085
|
A | C | 58 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0025others(55): Show | 58 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.-26+23432T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8787085 | ||||||
| chr11:8787274
|
G | T | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-26+23243C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8787274 | ||||||
| chr11:8787285
|
A | G | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-26+23232T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8787285 | ||||||
| chr11:8787300
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0003g0004 | 2 | HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-26+23217A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8787300 | ||||||
| chr11:8787347
|
AT | A | 311 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(308): Show | 311 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.-26+23169delA | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8787347 | ||||||
| chr11:8787413
|
C | A | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26+23104G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8787413 | ||||||
| chr11:8787461
|
C | T | 3 | a0001c0007t0001g0036a0001c0007t0005g0024a0001c0007t0005g0029 | 3 | HG02451.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-26+23056G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8787461 | ||||||
| chr11:8787469
|
C | A | 93 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0002g0162others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-26+23048G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8787469 | ||||||
| chr11:8787599
|
C | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0252 | 2 | HG00741.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-26+22918G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8787599 | ||||||
| chr11:8787599
|
C | G | 337 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(334): Show | 337 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.-26+22918G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8787599 | ||||||
| chr11:8787655
|
C | T | 3 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227 | 3 | HG02257.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-26+22862G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8787655 | ||||||
| chr11:8787656
|
G | T | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-26+22861C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8787656 | ||||||
| chr11:8787862
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-26+22655G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8787862 | ||||||
| chr11:8787920
|
C | A | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-26+22597G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8787920 | ||||||
| chr11:8788013
|
A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(175): Show | 178 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.-26+22504T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8788013 | ||||||
| chr11:8788071
|
G | A | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-26+22446C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8788071 | ||||||
| chr11:8788128
|
G | A | 2 | a0002c0003t0007g0352a0002c0003t0010g0350 | 2 | NA18966.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-26+22389C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8788128 | ||||||
| chr11:8788172
|
G | C | 1 | a0001c0001t0001g0117 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-26+22345C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8788172 | ||||||
| chr11:8788297
|
A | G | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(191): Show | 194 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.-26+22220T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8788297 | ||||||
| chr11:8788345
|
C | A | 1 | a0001c0001t0001g0277 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-26+22172G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8788345 | ||||||
| chr11:8788445
|
G | A | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-26+22072C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8788445 | ||||||
| chr11:8788461
|
C | T | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-26+22056G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8788461 | ||||||
| chr11:8788485
|
C | A | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-26+22032G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8788485 | ||||||
| chr11:8788618
|
G | A | 4 | a0001c0001t0004g0172a0001c0007t0001g0344a0001c0007t0001g0345others(1): Show | 4 | HG01168.hp2 HG01943.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+21899C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8788618 | ||||||
| chr11:8788638
|
T | G | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-26+21879A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8788638 | ||||||
| chr11:8788840
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0002g0021 | 2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-26+21677A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8788840 | ||||||
| chr11:8789207
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-26+21310T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8789207 | ||||||
| chr11:8789367
|
G | A | 1 | a0002c0003t0002g0070 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-26+21150C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8789367 | ||||||
| chr11:8789753
|
CACA | C | 70 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(67): Show | 70 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.-26+20761_-26+2076 others(7): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8789753 | ||||||
| chr11:8789775
|
C | CA | 95 | a0001c0001t0001g0005a0001c0001t0001g0219a0001c0001t0001g0220others(92): Show | 95 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.-26+20741dupT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8789775 | ||||||
| chr11:8789782
|
T | A | 8 | a0001c0001t0001g0005a0001c0001t0003g0004a0001c0007t0001g0036others(5): Show | 8 | HG01943.hp1 HG02451.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-26+20735A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8789782 | ||||||
| chr11:8789783
|
A | T | 1 | a0002c0003t0001g0188 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-26+20734T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8789783 | ||||||
| chr11:8789784
|
A | AT | 5 | a0001c0007t0001g0036a0001c0007t0001g0344a0001c0007t0001g0345others(2): Show | 5 | HG01943.hp1 HG02451.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26+20732_-26+2073 others(5): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8789784 | ||||||
| chr11:8789897
|
G | A | 1 | a0003c0002t0002g0030 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-26+20620C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8789897 | ||||||
| chr11:8790069
|
G | A | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(76): Show | 79 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.-26+20448C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8790069 | ||||||
| chr11:8790100
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0258 | 2 | HG02055.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-26+20417G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8790100 | ||||||
| chr11:8790121
|
T | C | 1 | a0002c0003t0001g0131 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-26+20396A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8790121 | ||||||
| chr11:8790142
|
C | T | 3 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227 | 3 | HG02257.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-26+20375G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8790142 | ||||||
| chr11:8790342
|
T | G | 1 | a0001c0001t0001g0330 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-26+20175A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8790342 | ||||||
| chr11:8790732
|
G | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(77): Show | 80 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-26+19785C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8790732 | ||||||
| chr11:8790807
|
G | A | 2 | a0002c0003t0001g0166a0002c0003t0002g0153 | 2 | NA18948.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.-26+19710C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8790807 | ||||||
| chr11:8790970
|
T | C | 3 | a0003c0002t0001g0108a0003c0002t0001g0111a0003c0002t0002g0103 | 3 | HG02683.hp2 HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-26+19547A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8790970 | ||||||
| chr11:8791055
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-26+19462T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8791055 | ||||||
| chr11:8791365
|
G | C | 1 | a0001c0001t0003g0080 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-26+19152C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8791365 | ||||||
| chr11:8791611
|
C | A | 4 | a0001c0001t0001g0033a0001c0001t0001g0119a0001c0001t0002g0118others(1): Show | 4 | HG01884.hp2 HG02486.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+18906G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8791611 | ||||||
| chr11:8791765
|
C | CA | 35 | a0001c0001t0001g0226a0001c0001t0001g0230a0001c0001t0001g0231others(32): Show | 35 | HG00438.hp1 HG00639.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.-26+18751dupT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8791765 | ||||||
| chr11:8791765
|
C | CAA | 77 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0002g0162others(74): Show | 77 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-26+18750_-26+1875 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8791765 | ||||||
| chr11:8791765
|
C | CAAA | 16 | a0002c0003t0001g0144a0002c0003t0001g0154a0002c0003t0001g0164others(13): Show | 16 | HG00544.hp2 HG00733.hp1 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.-26+18749_-26+1875 others(7): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8791765 | ||||||
| chr11:8791765
|
CA | C | 117 | a0001c0001t0001g0015a0001c0001t0001g0035a0001c0001t0001g0293others(114): Show | 117 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-26+18751delT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8791765 | ||||||
| chr11:8791850
|
A | G | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(79): Show | 82 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.-26+18667T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8791850 | ||||||
| chr11:8791871
|
T | C | 2 | a0001c0001t0004g0172a0011c0014t0004g0222 | 2 | HG01168.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-26+18646A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8791871 | ||||||
| chr11:8791981
|
G | A | 116 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(113): Show | 116 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-26+18536C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8791981 | ||||||
| chr11:8791994
|
CA | C | 310 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(307): Show | 310 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.-26+18522delT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8791994 | ||||||
| chr11:8792105
|
T | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(82): Show | 85 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.-26+18412A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8792105 | ||||||
| chr11:8792110
|
CA | C | 116 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(113): Show | 116 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.-26+18406delT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8792110 | ||||||
| chr11:8792342
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-26+18175T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8792342 | ||||||
| chr11:8792409
|
G | A | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(204): Show | 207 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.-26+18108C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8792409 | ||||||
| chr11:8792718
|
A | G | 4 | a0001c0001t0001g0252a0001c0007t0001g0036a0001c0007t0005g0024others(1): Show | 4 | HG02451.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26+17799T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8792718 | ||||||
| chr11:8792750
|
G | A | 2 | a0003c0002t0001g0108a0003c0002t0002g0103 | 2 | HG02683.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-26+17767C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8792750 | ||||||
| chr11:8792947
|
G | C | 4 | a0001c0001t0002g0041a0001c0001t0002g0045a0001c0001t0002g0052others(1): Show | 4 | NA18948.hp2 NA18953.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+17570C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8792947 | ||||||
| chr11:8793356
|
G | T | 4 | a0001c0001t0001g0252a0001c0007t0001g0036a0001c0007t0005g0024others(1): Show | 4 | HG02451.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26+17161C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8793356 | ||||||
| chr11:8793568
|
T | C | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(205): Show | 208 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.-26+16949A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8793568 | ||||||
| chr11:8793731
|
G | C | 5 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(2): Show | 5 | HG02145.hp2 HG02818.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-26+16786C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8793731 | ||||||
| chr11:8793906
|
T | C | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(205): Show | 208 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.-26+16611A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8793906 | ||||||
| chr11:8793923
|
A | G | 93 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0002g0162others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-26+16594T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8793923 | ||||||
| chr11:8794052
|
G | C | 117 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(114): Show | 117 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-26+16465C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8794052 | ||||||
| chr11:8794085
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0252a0001c0001t0003g0004others(5): Show | 8 | HG01943.hp1 HG02451.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-26+16432C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8794085 | ||||||
| chr11:8794157
|
A | G | 143 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(140): Show | 143 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.-26+16360T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8794157 | ||||||
| chr11:8794195
|
A | G | 1 | a0002c0003t0002g0170 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-26+16322T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8794195 | ||||||
| chr11:8794278
|
C | A | 97 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0347others(94): Show | 97 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-26+16239G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8794278 | ||||||
| chr11:8794431
|
A | G | 1 | a0001c0001t0001g0330 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-26+16086T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8794431 | ||||||
| chr11:8794694
|
C | A | 6 | a0003c0002t0001g0082a0003c0002t0001g0083a0003c0002t0001g0089others(3): Show | 6 | NA18970.hp2 NA18982.hp1 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.-26+15823G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8794694 | ||||||
| chr11:8794703
|
T | A | 1 | a0001c0001t0002g0296 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-26+15814A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8794703 | ||||||
| chr11:8794948
|
T | C | 97 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0001g0347others(94): Show | 97 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.-26+15569A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8794948 | ||||||
| chr11:8794962
|
T | C | 3 | a0003c0002t0001g0116a0003c0002t0001g0122a0003c0002t0001g0123 | 3 | HG00408.hp1 HG02523.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.-26+15555A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8794962 | ||||||
| chr11:8795000
|
T | TGGCTGTC others(17): Show |
1 | a0006c0005t0001g0278 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-26+15493_-26+1551 others(28): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8795000 | ||||||
| chr11:8795148
|
G | A | 101 | a0001c0001t0001g0005a0001c0001t0001g0219a0001c0001t0001g0220others(98): Show | 101 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.-26+15369C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8795148 | ||||||
| chr11:8795422
|
T | G | 1 | a0001c0001t0001g0231 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-26+15095A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8795422 | ||||||
| chr11:8795532
|
G | A | 1 | a0003c0002t0001g0314 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-26+14985C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8795532 | ||||||
| chr11:8795659
|
A | G | 115 | a0001c0001t0001g0005a0001c0001t0001g0033a0001c0001t0001g0042others(112): Show | 115 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-26+14858T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8795659 | ||||||
| chr11:8795729
|
A | T | 115 | a0001c0001t0001g0005a0001c0001t0001g0033a0001c0001t0001g0042others(112): Show | 115 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.-26+14788T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8795729 | ||||||
| chr11:8795762
|
T | C | 1 | a0001c0001t0005g0022 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-26+14755A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8795762 | ||||||
| chr11:8795768
|
G | A | 93 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0002g0162others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-26+14749C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8795768 | ||||||
| chr11:8795967
|
G | A | 1 | a0003c0002t0002g0058 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-26+14550C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8795967 | ||||||
| chr11:8796033
|
T | C | 124 | a0001c0001t0001g0035a0001c0001t0001g0252a0001c0001t0001g0293others(121): Show | 124 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-26+14484A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8796033 | ||||||
| chr11:8796123
|
T | C | 1 | a0001c0001t0002g0341 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-26+14394A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8796123 | ||||||
| chr11:8796197
|
T | A | 3 | a0001c0001t0002g0074a0001c0001t0002g0200a0001c0001t0002g0228 | 3 | HG02523.hp1 NA18970.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-26+14320A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8796197 | ||||||
| chr11:8796261
|
A | G | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(183): Show | 186 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.-26+14256T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8796261 | ||||||
| chr11:8796264
|
G | A | 6 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0055others(3): Show | 6 | HG02572.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-26+14253C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8796264 | ||||||
| chr11:8796293
|
G | A | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(183): Show | 186 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.-26+14224C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8796293 | ||||||
| chr11:8796336
|
G | A | 71 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(68): Show | 71 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.-26+14181C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8796336 | ||||||
| chr11:8796367
|
C | T | 1 | a0003c0002t0001g0087 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-26+14150G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8796367 | ||||||
| chr11:8796473
|
C | T | 123 | a0001c0001t0001g0035a0001c0001t0001g0252a0001c0001t0001g0293others(120): Show | 123 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.-26+14044G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8796473 | ||||||
| chr11:8796570
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0003g0004a0001c0007t0001g0344others(1): Show | 4 | HG01943.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+13947C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8796570 | ||||||
| chr11:8796705
|
CT | C | 4 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349others(1): Show | 4 | HG00639.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26+13811delA | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8796705 | ||||||
| chr11:8796839
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-26+13678A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8796839 | ||||||
| chr11:8797285
|
C | T | 4 | a0001c0001t0001g0005a0001c0001t0003g0004a0001c0007t0001g0344others(1): Show | 4 | HG01943.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+13232G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8797285 | ||||||
| chr11:8797286
|
G | A | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(166): Show | 169 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.-26+13231C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8797286 | ||||||
| chr11:8797408
|
C | T | 1 | a0011c0014t0004g0222 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-26+13109G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8797408 | ||||||
| chr11:8797430
|
C | CCTTCCCC others(3): Show |
1 | a0002c0003t0001g0199 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-26+13077_-26+1308 others(14): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8797430 | ||||||
| chr11:8797434
|
C | A | 14 | a0001c0001t0001g0057a0001c0001t0002g0041a0001c0001t0002g0043others(11): Show | 14 | HG02922.hp2 HG03130.hp2 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.-26+13083G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8797434 | ||||||
| chr11:8797434
|
C | CCCCCTTC others(3): Show |
3 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227 | 3 | HG02257.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-26+13082_-26+1308 others(14): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8797434 | ||||||
| chr11:8797456
|
T | C | 95 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0002g0162others(92): Show | 95 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.-26+13061A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8797456 | ||||||
| chr11:8797468
|
T | C | 96 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0002g0162others(93): Show | 96 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.-26+13049A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8797468 | ||||||
| chr11:8797532
|
C | CT | 4 | a0002c0003t0001g0154a0002c0003t0001g0188a0002c0003t0002g0195others(1): Show | 4 | NA18942.hp1 NA18997.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+12984dupA | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8797532 | ||||||
| chr11:8797567
|
A | G | 1 | a0002c0003t0009g0161 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-26+12950T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8797567 | ||||||
| chr11:8797596
|
A | C | 47 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(44): Show | 47 | HG00741.hp1 HG01109.hp1 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.-26+12921T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8797596 | ||||||
| chr11:8797820
|
C | T | 64 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(61): Show | 64 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.-26+12697G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8797820 | ||||||
| chr11:8797856
|
A | C | 6 | a0003c0002t0001g0082a0003c0002t0001g0083a0003c0002t0001g0089others(3): Show | 6 | NA18970.hp2 NA18982.hp1 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.-26+12661T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8797856 | ||||||
| chr11:8797992
|
C | T | 2 | a0001c0007t0001g0344a0001c0007t0001g0345 | 2 | HG01943.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-26+12525G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8797992 | ||||||
| chr11:8798003
|
C | T | 13 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0047others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-26+12514G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8798003 | ||||||
| chr11:8798136
|
T | A | 128 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(125): Show | 128 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.-26+12381A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8798136 | ||||||
| chr11:8798192
|
A | G | 5 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-26+12325T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8798192 | ||||||
| chr11:8798204
|
A | C | 1 | a0002c0003t0010g0350 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-26+12313T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8798204 | ||||||
| chr11:8798236
|
C | T | 2 | a0001c0007t0001g0344a0001c0007t0001g0345 | 2 | HG01943.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-26+12281G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8798236 | ||||||
| chr11:8798250
|
G | C | 1 | a0003c0002t0001g0152 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-26+12267C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8798250 | ||||||
| chr11:8798261
|
A | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(73): Show | 76 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.-26+12256T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8798261 | ||||||
| chr11:8798392
|
T | C | 1 | a0002c0003t0002g0165 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-26+12125A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8798392 | ||||||
| chr11:8798607
|
C | T | 3 | a0001c0001t0001g0140a0001c0001t0002g0225a0001c0001t0002g0227 | 3 | HG02257.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-26+11910G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8798607 | ||||||
| chr11:8798702
|
A | G | 1 | a0001c0001t0001g0272 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-26+11815T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8798702 | ||||||
| chr11:8798750
|
G | A | 3 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349 | 3 | HG00639.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26+11767C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8798750 | ||||||
| chr11:8798828
|
C | CT | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(205): Show | 208 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.-26+11688dupA | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8798828 | ||||||
| chr11:8798884
|
A | C | 2 | a0001c0001t0003g0221a0011c0014t0004g0222 | 2 | HG01168.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-26+11633T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8798884 | ||||||
| chr11:8798914
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0003g0004 | 2 | HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-26+11603C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8798914 | ||||||
| chr11:8798988
|
C | T | 4 | a0001c0001t0001g0330a0003c0002t0001g0111a0003c0002t0002g0331others(1): Show | 4 | HG01069.hp2 HG01106.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+11529G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8798988 | ||||||
| chr11:8799042
|
G | T | 71 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(68): Show | 71 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.-26+11475C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799042 | ||||||
| chr11:8799107
|
C | T | 2 | a0001c0007t0001g0344a0001c0007t0001g0345 | 2 | HG01943.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-26+11410G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799107 | ||||||
| chr11:8799130
|
T | C | 2 | a0001c0001t0003g0342a0001c0001t0003g0343 | 2 | HG02683.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-26+11387A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799130 | ||||||
| chr11:8799435
|
A | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(73): Show | 76 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.-26+11082T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799435 | ||||||
| chr11:8799458
|
G | C | 2 | a0001c0001t0003g0221a0011c0014t0004g0222 | 2 | HG01168.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-26+11059C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799458 | ||||||
| chr11:8799533
|
C | G | 3 | a0001c0001t0001g0033a0001c0001t0002g0118a0001c0001t0002g0223 | 3 | HG01884.hp2 HG02486.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-26+10984G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799533 | ||||||
| chr11:8799561
|
C | CT | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(107): Show | 110 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.-26+10955dupA | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799561 | ||||||
| chr11:8799561
|
CT | C | 140 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(137): Show | 140 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.-26+10955delA | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799561 | ||||||
| chr11:8799561
|
CTT | C | 21 | a0001c0001t0001g0219a0001c0001t0002g0049a0001c0001t0007g0351others(18): Show | 21 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.-26+10954_-26+1095 others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799561 | ||||||
| chr11:8799561
|
CTTTTTTT others(5): Show |
C | 15 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0047others(12): Show | 15 | HG01168.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-26+10944_-26+1095 others(16): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799561 | ||||||
| chr11:8799651
|
G | A | 2 | a0001c0001t0003g0221a0011c0014t0004g0222 | 2 | HG01168.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-26+10866C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799651 | ||||||
| chr11:8799918
|
T | TTTA | 4 | a0001c0001t0001g0015a0001c0001t0002g0016a0001c0001t0006g0018others(1): Show | 4 | HG01123.hp1 HG02257.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26+10596_-26+1059 others(7): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799918 | ||||||
| chr11:8799918
|
T | TTTATTA | 3 | a0001c0001t0001g0017a0001c0001t0001g0060a0001c0001t0002g0045 | 3 | HG01891.hp2 HG03453.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.-26+10593_-26+1059 others(10): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799918 | ||||||
| chr11:8799918
|
TTTA | T | 19 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(16): Show | 19 | HG00741.hp1 HG01168.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.-26+10596_-26+1059 others(7): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799918 | ||||||
| chr11:8799918
|
TTTATTA | T | 48 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0027others(45): Show | 48 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.-26+10593_-26+1059 others(10): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799918 | ||||||
| chr11:8799918
|
TTTATTAT others(2): Show |
T | 31 | a0002c0003t0001g0085a0002c0003t0001g0144a0002c0003t0001g0154others(28): Show | 31 | HG00280.hp1 HG00544.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.-26+10590_-26+1059 others(13): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799918 | ||||||
| chr11:8799918
|
TTTATTAT others(5): Show |
T | 58 | a0001c0001t0002g0162a0001c0001t0004g0172a0002c0003t0001g0001others(55): Show | 58 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-26+10587_-26+1059 others(16): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799918 | ||||||
| chr11:8799918
|
TTTATTAT others(8): Show |
T | 3 | a0001c0001t0001g0005a0001c0001t0003g0004a0003c0002t0001g0100 | 3 | HG00673.hp1 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-26+10584_-26+1059 others(19): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799918 | ||||||
| chr11:8799918
|
TTTATTAT others(11): Show |
T | 10 | a0001c0001t0001g0276a0001c0001t0001g0347a0001c0001t0001g0348others(7): Show | 10 | HG00639.hp1 HG01943.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26+10581_-26+1059 others(22): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799918 | ||||||
| chr11:8799918
|
TTTATTAT others(14): Show |
T | 142 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(139): Show | 142 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.-26+10578_-26+1059 others(25): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799918 | ||||||
| chr11:8799930
|
A | T | 2 | a0002c0003t0007g0352a0002c0003t0010g0350 | 2 | NA18966.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-26+10587T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799930 | ||||||
| chr11:8799957
|
A | G | 60 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.-26+10560T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8799957 | ||||||
| chr11:8800094
|
C | T | 2 | a0001c0007t0001g0344a0001c0007t0001g0345 | 2 | HG01943.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-26+10423G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8800094 | ||||||
| chr11:8800190
|
A | G | 339 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(336): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.-26+10327T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8800190 | ||||||
| chr11:8800425
|
C | T | 75 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(72): Show | 75 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.-26+10092G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8800425 | ||||||
| chr11:8800485
|
A | G | 74 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0042others(71): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.-26+10032T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8800485 | ||||||
| chr11:8800701
|
T | C | 1 | a0001c0001t0006g0018 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-26+9816A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8800701 | ||||||
| chr11:8800967
|
G | T | 3 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349 | 3 | HG00639.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26+9550C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8800967 | ||||||
| chr11:8801054
|
G | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(69): Show | 72 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.-26+9463C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801054 | ||||||
| chr11:8801109
|
A | C | 2 | a0001c0001t0003g0221a0011c0014t0004g0222 | 2 | HG01168.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-26+9408T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801109 | ||||||
| chr11:8801126
|
C | T | 9 | a0003c0002t0001g0082a0003c0002t0001g0083a0003c0002t0001g0089others(6): Show | 9 | NA18952.hp2 NA18955.hp1 NA18970.hp2 others(6): Show |
intron_variant | MODIFIER | c.-26+9391G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801126 | ||||||
| chr11:8801196
|
G | A | 15 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0047others(12): Show | 15 | HG01168.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-26+9321C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801196 | ||||||
| chr11:8801626
|
G | A | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(206): Show | 209 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.-26+8891C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801626 | ||||||
| chr11:8801640
|
T | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(206): Show | 209 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.-26+8877A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801640 | ||||||
| chr11:8801689
|
A | AAAAAAGA others(3): Show |
4 | a0001c0001t0001g0140a0001c0001t0001g0241a0001c0001t0002g0225others(1): Show | 4 | HG02257.hp2 HG02647.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+8827_-26+8828i others(12): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801689 | ||||||
| chr11:8801689
|
A | AAAAAAGA others(7): Show |
12 | a0001c0001t0001g0033a0001c0001t0001g0042a0001c0001t0001g0047others(9): Show | 12 | HG01168.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.-26+8827_-26+8828i others(16): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801689 | ||||||
| chr11:8801689
|
A | AAAAAGAA others(2): Show |
183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(180): Show | 183 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.-26+8827_-26+8828i others(11): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801689 | ||||||
| chr11:8801689
|
A | AAAAGAAA others(1): Show |
10 | a0001c0001t0001g0232a0001c0001t0001g0260a0001c0001t0001g0261others(7): Show | 10 | HG01515.hp1 HG01943.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.-26+8820_-26+8827d others(10): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801689 | ||||||
| chr11:8801689
|
A | AG | 89 | a0001c0001t0002g0162a0001c0001t0004g0172a0002c0003t0001g0001others(86): Show | 89 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.-26+8827_-26+8828i others(3): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801689 | ||||||
| chr11:8801689
|
A | G | 38 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0027others(35): Show | 38 | HG00741.hp1 HG01109.hp1 HG01257.hp2 others(35): Show |
intron_variant | MODIFIER | c.-26+8828T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801689 | ||||||
| chr11:8801701
|
G | C | 6 | a0001c0001t0001g0257a0001c0001t0001g0272a0001c0001t0001g0274others(3): Show | 6 | HG02109.hp1 HG02132.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-26+8816C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801701 | ||||||
| chr11:8801705
|
C | G | 219 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(216): Show | 219 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.-26+8812G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801705 | ||||||
| chr11:8801768
|
C | G | 31 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(28): Show | 31 | HG00741.hp1 HG01109.hp1 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.-26+8749G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801768 | ||||||
| chr11:8801906
|
C | G | 31 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0057others(28): Show | 31 | HG00741.hp1 HG01109.hp1 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.-26+8611G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801906 | ||||||
| chr11:8801917
|
G | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(69): Show | 72 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.-26+8600C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801917 | ||||||
| chr11:8801946
|
C | T | 157 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(154): Show | 157 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.-26+8571G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801946 | ||||||
| chr11:8801991
|
TG | T | 73 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0023others(70): Show | 73 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.-26+8525delC | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801991 | ||||||
| chr11:8801994
|
GGA | G | 58 | a0001c0001t0001g0033a0001c0001t0001g0047a0001c0001t0001g0117others(55): Show | 58 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.-26+8521_-26+8522d others(4): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801994 | ||||||
| chr11:8801995
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0081a0001c0001t0001g0140others(6): Show | 9 | HG00741.hp2 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-26+8522C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801995 | ||||||
| chr11:8801995
|
G | GA | 24 | a0001c0001t0001g0005a0001c0001t0001g0060a0001c0001t0001g0065others(21): Show | 24 | HG00597.hp1 HG00621.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-26+8521dupT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801995 | ||||||
| chr11:8801995
|
GA | G | 60 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0330others(57): Show | 60 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.-26+8521delT | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8801995 | ||||||
| chr11:8802043
|
A | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(206): Show | 209 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.-26+8474T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8802043 | ||||||
| chr11:8802116
|
T | A | 1 | a0001c0001t0002g0228 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-26+8401A>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8802116 | ||||||
| chr11:8802250
|
G | A | 1 | a0003c0002t0001g0303 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-26+8267C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8802250 | ||||||
| chr11:8802280
|
G | A | 1 | a0011c0014t0004g0222 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-26+8237C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8802280 | ||||||
| chr11:8802299
|
G | GAA | 137 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0042others(134): Show | 137 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.-26+8216_-26+8217d others(4): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8802299 | ||||||
| chr11:8802299
|
G | GAAA | 73 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(70): Show | 73 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.-26+8215_-26+8217d others(5): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8802299 | ||||||
| chr11:8802415
|
A | T | 1 | a0001c0001t0002g0296 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-26+8102T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8802415 | ||||||
| chr11:8802580
|
A | G | 1 | a0001c0001t0001g0245 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-26+7937T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8802580 | ||||||
| chr11:8802689
|
T | C | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(100): Show | 103 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.-26+7828A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8802689 | ||||||
| chr11:8802841
|
C | T | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(237): Show | 240 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-26+7676G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8802841 | ||||||
| chr11:8802871
|
A | C | 64 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(61): Show | 64 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.-26+7646T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8802871 | ||||||
| chr11:8803367
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0003g0004 | 2 | HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-26+7150G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8803367 | ||||||
| chr11:8803449
|
A | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(236): Show | 239 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-26+7068T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8803449 | ||||||
| chr11:8803529
|
A | G | 3 | a0002c0003t0002g0146a0002c0003t0002g0147a0002c0003t0002g0201 | 3 | NA18939.hp2 NA19057.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-26+6988T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8803529 | ||||||
| chr11:8803820
|
G | A | 2 | a0001c0001t0003g0221a0011c0014t0004g0222 | 2 | HG01168.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-26+6697C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8803820 | ||||||
| chr11:8804047
|
C | T | 2 | a0001c0007t0001g0344a0001c0007t0001g0345 | 2 | HG01943.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-26+6470G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8804047 | ||||||
| chr11:8804219
|
A | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0025others(96): Show | 99 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.-26+6298T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8804219 | ||||||
| chr11:8804227
|
A | G | 100 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0042others(97): Show | 100 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.-26+6290T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8804227 | ||||||
| chr11:8804254
|
G | A | 2 | a0002c0003t0001g0211a0002c0003t0001g0218 | 2 | NA18953.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.-26+6263C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8804254 | ||||||
| chr11:8804318
|
T | C | 154 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0027others(151): Show | 154 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.-26+6199A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8804318 | ||||||
| chr11:8804369
|
TGGG | T | 133 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(130): Show | 133 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-26+6145_-26+6147d others(5): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8804369 | ||||||
| chr11:8804419
|
G | A | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(203): Show | 206 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.-26+6098C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8804419 | ||||||
| chr11:8804524
|
G | A | 56 | a0002c0003t0001g0085a0002c0003t0001g0129a0002c0003t0001g0131others(53): Show | 56 | HG00408.hp1 HG00558.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.-26+5993C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8804524 | ||||||
| chr11:8804547
|
C | CTTTT | 11 | a0001c0001t0001g0006a0001c0001t0001g0066a0001c0001t0001g0349others(8): Show | 11 | HG00639.hp1 HG01515.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-26+5966_-26+5969d others(6): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8804547 | ||||||
| chr11:8804547
|
C | CTTTTT | 283 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0025others(280): Show | 283 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.-26+5965_-26+5969d others(7): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8804547 | ||||||
| chr11:8804547
|
C | CTTTTTT | 40 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0038others(37): Show | 40 | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.-26+5964_-26+5969d others(8): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8804547 | ||||||
| chr11:8804608
|
G | A | 2 | a0002c0003t0001g0197a0002c0003t0001g0216 | 2 | HG02071.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-26+5909C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8804608 | ||||||
| chr11:8804670
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0003g0004 | 2 | HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-26+5847C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8804670 | ||||||
| chr11:8804706
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-26+5811C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8804706 | ||||||
| chr11:8804772
|
G | A | 2 | a0001c0007t0001g0344a0001c0007t0001g0345 | 2 | HG01943.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-26+5745C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8804772 | ||||||
| chr11:8804944
|
T | C | 3 | a0001c0001t0002g0223a0001c0001t0002g0225a0001c0001t0002g0227 | 3 | HG02572.hp2 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-26+5573A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8804944 | ||||||
| chr11:8804961
|
G | T | 2 | a0001c0001t0002g0074a0001c0001t0002g0200 | 2 | NA18970.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-26+5556C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8804961 | ||||||
| chr11:8804968
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-26+5549A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8804968 | ||||||
| chr11:8805012
|
C | A | 96 | a0001c0001t0001g0006a0001c0001t0001g0140a0001c0001t0001g0167others(93): Show | 96 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.-26+5505G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8805012 | ||||||
| chr11:8805027
|
T | C | 2 | a0001c0001t0003g0221a0011c0014t0004g0222 | 2 | HG01168.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-26+5490A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8805027 | ||||||
| chr11:8805141
|
C | T | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(271): Show | 274 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.-26+5376G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8805141 | ||||||
| chr11:8805153
|
G | T | 102 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0026others(99): Show | 102 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-26+5364C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8805153 | ||||||
| chr11:8805232
|
A | G | 114 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0033others(111): Show | 114 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.-26+5285T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8805232 | ||||||
| chr11:8805299
|
T | C | 3 | a0002c0003t0002g0185a0002c0003t0002g0198a0002c0003t0002g0213 | 3 | HG01099.hp1 HG01361.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-26+5218A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8805299 | ||||||
| chr11:8805300
|
TG | T | 3 | a0002c0003t0002g0169a0002c0003t0002g0170a0002c0003t0002g0186 | 3 | HG03017.hp1 HG03710.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-26+5216delC | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8805300 | ||||||
| chr11:8805773
|
G | A | 3 | a0001c0001t0001g0140a0001c0001t0003g0221a0011c0014t0004g0222 | 3 | HG01168.hp2 HG02257.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-26+4744C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8805773 | ||||||
| chr11:8805783
|
A | T | 1 | a0003c0002t0001g0306 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-26+4734T>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8805783 | ||||||
| chr11:8805965
|
C | T | 1 | a0010c0013t0001g0285 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-26+4552G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8805965 | ||||||
| chr11:8806080
|
G | C | 1 | a0001c0001t0001g0117 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-26+4437C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806080 | ||||||
| chr11:8806189
|
G | A | 4 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0258others(1): Show | 4 | HG02055.hp2 HG02895.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+4328C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806189 | ||||||
| chr11:8806203
|
A | C | 60 | a0001c0001t0001g0035a0001c0001t0001g0293a0001c0001t0001g0299others(57): Show | 60 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-26+4314T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806203 | ||||||
| chr11:8806470
|
T | C | 71 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0117others(68): Show | 71 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.-26+4047A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806470 | ||||||
| chr11:8806507
|
T | C | 71 | a0001c0001t0001g0033a0001c0001t0001g0035a0001c0001t0001g0117others(68): Show | 71 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.-26+4010A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806507 | ||||||
| chr11:8806590
|
C | T | 1 | a0002c0003t0001g0199 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-26+3927G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806590 | ||||||
| chr11:8806603
|
A | AACACACA others(11): Show |
1 | a0001c0001t0001g0330 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-26+3913_-26+3914i others(20): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806603 | ||||||
| chr11:8806603
|
A | AACACACA others(15): Show |
1 | a0002c0003t0002g0159 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-26+3913_-26+3914i others(24): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806603 | ||||||
| chr11:8806605
|
A | AACACACA others(1): Show |
9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(6): Show | 9 | HG00741.hp1 HG01109.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.-26+3904_-26+3911d others(10): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806605 | ||||||
| chr11:8806605
|
A | AACACACA others(3): Show |
2 | a0001c0001t0001g0277a0006c0005t0001g0278 | 2 | HG01070.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-26+3902_-26+3911d others(12): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806605 | ||||||
| chr11:8806605
|
A | AACACACA others(5): Show |
28 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(25): Show | 28 | HG00558.hp1 HG00741.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.-26+3900_-26+3911d others(14): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806605 | ||||||
| chr11:8806605
|
A | AACACACA others(7): Show |
29 | a0001c0001t0001g0081a0001c0001t0001g0237a0001c0001t0001g0238others(26): Show | 29 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.-26+3898_-26+3911d others(16): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806605 | ||||||
| chr11:8806605
|
A | AACACACA others(9): Show |
33 | a0001c0001t0001g0035a0001c0001t0001g0076a0001c0001t0001g0220others(30): Show | 33 | HG00408.hp1 HG01256.hp2 HG01258.hp1 others(30): Show |
intron_variant | MODIFIER | c.-26+3896_-26+3911d others(18): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806605 | ||||||
| chr11:8806605
|
A | AACACACA others(11): Show |
39 | a0001c0001t0001g0028a0001c0001t0001g0226a0001c0001t0001g0299others(36): Show | 39 | HG00280.hp1 HG00673.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.-26+3894_-26+3911d others(20): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806605 | ||||||
| chr11:8806605
|
A | AACACACA others(13): Show |
48 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(45): Show | 48 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.-26+3892_-26+3911d others(22): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806605 | ||||||
| chr11:8806605
|
A | AACACACA others(15): Show |
46 | a0001c0001t0001g0119a0001c0001t0001g0293a0001c0001t0002g0051others(43): Show | 46 | HG00280.hp2 HG00323.hp2 HG01175.hp1 others(43): Show |
intron_variant | MODIFIER | c.-26+3890_-26+3911d others(24): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806605 | ||||||
| chr11:8806605
|
A | AACACACA others(17): Show |
41 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0117others(38): Show | 41 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-26+3888_-26+3911d others(26): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806605 | ||||||
| chr11:8806605
|
A | AACACACA others(19): Show |
19 | a0001c0001t0001g0219a0001c0001t0002g0043a0001c0001t0002g0044others(16): Show | 19 | HG00597.hp1 HG02145.hp1 HG02148.hp1 others(16): Show |
intron_variant | MODIFIER | c.-26+3886_-26+3911d others(28): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806605 | ||||||
| chr11:8806605
|
A | AACACACA others(21): Show |
16 | a0001c0001t0001g0042a0001c0001t0002g0021a0001c0001t0002g0041others(13): Show | 16 | HG01074.hp1 HG01192.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.-26+3884_-26+3911d others(30): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806605 | ||||||
| chr11:8806605
|
A | AACACACA others(23): Show |
4 | a0001c0001t0001g0033a0002c0003t0001g0143a0002c0003t0001g0144others(1): Show | 4 | HG01261.hp1 HG01433.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+3882_-26+3911d others(32): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806605 | ||||||
| chr11:8806605
|
A | ACACACAC others(6): Show |
1 | a0006c0005t0001g0112 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-26+3911_-26+3912i others(15): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806605 | ||||||
| chr11:8806605
|
A | ACACACAC others(8): Show |
1 | a0001c0001t0002g0228 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-26+3911_-26+3912i others(17): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806605 | ||||||
| chr11:8806605
|
A | ACACACAC others(12): Show |
1 | a0002c0003t0002g0072 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-26+3911_-26+3912i others(21): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806605 | ||||||
| chr11:8806605
|
A | ACACACAC others(14): Show |
1 | a0004c0004t0001g0319 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-26+3911_-26+3912i others(23): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806605 | ||||||
| chr11:8806605
|
A | ACACACAC others(18): Show |
1 | a0002c0003t0002g0067 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-26+3911_-26+3912i others(27): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806605 | ||||||
| chr11:8806605
|
A | ACACACAC others(22): Show |
1 | a0003c0002t0001g0082 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-26+3911_-26+3912i others(31): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806605 | ||||||
| chr11:8806605
|
A | C | 2 | a0001c0001t0001g0330a0002c0003t0002g0159 | 2 | HG01106.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.-26+3912T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806605 | ||||||
| chr11:8806638
|
A | ACACACAC others(11): Show |
1 | a0001c0001t0001g0140 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-26+3878_-26+3879i others(20): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806638 | ||||||
| chr11:8806639
|
C | CACACACA others(14): Show |
4 | a0002c0003t0001g0216a0003c0002t0001g0139a0003c0002t0002g0138others(1): Show | 4 | HG01255.hp2 HG02071.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26+3877_-26+3878i others(23): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806639 | ||||||
| chr11:8806639
|
C | CACACACA others(16): Show |
1 | a0004c0004t0001g0339 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-26+3877_-26+3878i others(25): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806639 | ||||||
| chr11:8806639
|
C | CACACACA others(20): Show |
2 | a0002c0003t0001g0215a0003c0002t0001g0305 | 2 | HG01978.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-26+3877_-26+3878i others(29): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806639 | ||||||
| chr11:8806744
|
T | C | 1 | a0003c0002t0002g0030 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-26+3773A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806744 | ||||||
| chr11:8806838
|
G | A | 1 | a0003c0002t0003g0279 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-26+3679C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806838 | ||||||
| chr11:8806867
|
T | C | 335 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(332): Show | 335 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-26+3650A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806867 | ||||||
| chr11:8806908
|
C | CT | 334 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(331): Show | 334 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.-26+3608dupA | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8806908 | ||||||
| chr11:8807134
|
C | A | 4 | a0001c0001t0001g0140a0001c0001t0003g0221a0002c0003t0002g0217others(1): Show | 4 | HG01168.hp2 HG02257.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26+3383G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8807134 | ||||||
| chr11:8807259
|
C | T | 2 | a0001c0007t0001g0344a0001c0007t0001g0345 | 2 | HG01943.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-26+3258G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8807259 | ||||||
| chr11:8807558
|
G | T | 71 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0038others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.-26+2959C>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8807558 | ||||||
| chr11:8807616
|
A | G | 335 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(332): Show | 335 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-26+2901T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8807616 | ||||||
| chr11:8807621
|
A | G | 207 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0025others(204): Show | 207 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.-26+2896T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8807621 | ||||||
| chr11:8807869
|
G | A | 91 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0187others(88): Show | 91 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.-26+2648C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8807869 | ||||||
| chr11:8807916
|
C | T | 337 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(334): Show | 337 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(334): Show |
intron_variant | MODIFIER | c.-26+2601G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8807916 | ||||||
| chr11:8807947
|
C | G | 262 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(259): Show | 262 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.-26+2570G>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8807947 | ||||||
| chr11:8808055
|
T | C | 19 | a0002c0003t0001g0126a0002c0003t0001g0129a0002c0003t0001g0131others(16): Show | 19 | HG00558.hp2 HG00621.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-26+2462A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8808055 | ||||||
| chr11:8808172
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-26+2345C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8808172 | ||||||
| chr11:8808404
|
AAACACAT others(7): Show |
A | 1 | a0001c0001t0001g0038 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-26+2099_-26+2112d others(16): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8808404 | ||||||
| chr11:8808420
|
T | G | 37 | a0001c0001t0001g0330a0002c0010t0002g0039a0002c0010t0002g0040others(34): Show | 37 | HG00280.hp2 HG00642.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.-26+2097A>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8808420 | ||||||
| chr11:8808645
|
G | A | 1 | a0002c0003t0001g0218 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-26+1872C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8808645 | ||||||
| chr11:8808838
|
G | A | 26 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0057others(23): Show | 26 | HG00741.hp1 HG01109.hp1 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.-26+1679C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8808838 | ||||||
| chr11:8808901
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-26+1616A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8808901 | ||||||
| chr11:8808907
|
AC | A | 93 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0187others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-26+1609delG | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8808907 | ||||||
| chr11:8808923
|
G | C | 335 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(332): Show | 335 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(332): Show |
intron_variant | MODIFIER | c.-26+1594C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8808923 | ||||||
| chr11:8809126
|
G | A | 2 | a0001c0001t0001g0219a0001c0001t0001g0220 | 2 | HG03209.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-26+1391C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8809126 | ||||||
| chr11:8809194
|
T | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | NA18979.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-26+1323A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8809194 | ||||||
| chr11:8809254
|
G | C | 93 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0187others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-26+1263C>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8809254 | ||||||
| chr11:8809532
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-26+985G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8809532 | ||||||
| chr11:8810049
|
CT | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0076others(151): Show | 154 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.-26+467delA | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8810049 | ||||||
| chr11:8810049
|
CTT | C | 66 | a0001c0001t0001g0003a0001c0001t0001g0226a0001c0001t0001g0230others(63): Show | 66 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.-26+466_-26+467del others(2): Show |
DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8810049 | ||||||
| chr11:8810067
|
T | C | 2 | a0001c0001t0002g0341a0001c0001t0002g0346 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-26+450A>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8810067 | ||||||
| chr11:8810067
|
T | TC | 59 | a0001c0001t0001g0293a0001c0001t0001g0299a0001c0001t0001g0302others(56): Show | 59 | HG00280.hp2 HG00408.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-26+449dupG | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8810067 | ||||||
| chr11:8810125
|
C | A | 2 | a0001c0001t0003g0342a0001c0001t0003g0343 | 2 | HG02683.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.-26+392G>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8810125 | ||||||
| chr11:8810180
|
G | A | 2 | a0001c0007t0001g0344a0001c0007t0001g0345 | 2 | HG01943.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-26+337C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8810180 | ||||||
| chr11:8810294
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0003g0004 | 2 | HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-26+223G>A | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8810294 | ||||||
| chr11:8810373
|
G | A | 1 | a0001c0001t0002g0346 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-26+144C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8810373 | ||||||
| chr11:8810380
|
A | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | NA18979.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-26+137T>C | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8810380 | ||||||
| chr11:8810383
|
G | A | 3 | a0001c0001t0001g0347a0001c0001t0001g0348a0001c0001t0001g0349 | 3 | HG00639.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26+134C>T | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8810383 | ||||||
| chr11:8810399
|
A | C | 1 | a0002c0003t0001g0001 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-26+118T>G | DENND2B | ENSG00000166444.19 | transcript | ENST00000313726.11 | protein_coding | 1/19 | chr11 | 8810399 |