geneid | 163259 |
---|---|
ensemblid | ENSG00000175984.16 |
hgncid | 24748 |
symbol | DENND2C |
name | DENN domain containing 2C |
refseq_nuc | NM_001256404.2 |
refseq_prot | NP_001243333.1 |
ensembl_nuc | ENST00000393274.6 |
ensembl_prot | ENSP00000376955.1 |
mane_status | MANE Select |
chr | chr1 |
start | 114582850 |
end | 114670049 |
strand | - |
ver | v1.2 |
region | chr1:114582850-114670049 |
region5000 | chr1:114577850-114675049 |
regionname0 | DENND2C_chr1_114582850_114670049 |
regionname5000 | DENND2C_chr1_114577850_114675049 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 928 | 219 | 62 | 36 | 105 | 2 | 13 | 79 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0002 | 0/0 | 928 | 36 | 2 | 12 | 10 | 6 | 6 | 5 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0003 | 0/0 | 928 | 23 | 1 | 12 | 0 | 1 | 9 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0004 | 0/1 | 928 | 15 | 4 | 4 | 1 | 1 | 4 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0005 | 0/0 | 928 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0006 | 0/0 | 928 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0007 | 0/0 | 928 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0008 | 0/0 | 928 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0009 | 0/0 | 928 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2787 | 213 | 61 | 35 | 103 | 1 | 12 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
c0002 | 0/0 | 2787 | 35 | 2 | 12 | 10 | 6 | 5 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
c0003 | 0/0 | 2787 | 22 | 1 | 11 | 0 | 1 | 9 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
c0004 | 0/1 | 2787 | 15 | 4 | 4 | 1 | 1 | 4 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
c0005 | 0/0 | 2787 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
c0006 | 0/0 | 2787 | 2 | 0 | 0 | 1 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
c0007 | 0/0 | 2787 | 2 | 0 | 2 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
c0008 | 0/0 | 2787 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
c0009 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
c0010 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
c0011 | 0/0 | 2787 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
c0012 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
c0013 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
c0014 | 0/0 | 2787 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
c0015 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
c0016 | 0/0 | 2787 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3393 | 109 | 22 | 21 | 51 | 4 | 11 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0002 | 1/0 | 3391 | 63 | 0 | 12 | 47 | 0 | 3 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0003 | 0/0 | 3390 | 17 | 1 | 8 | 0 | 1 | 7 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0004 | 0/1 | 3391 | 17 | 4 | 4 | 2 | 1 | 5 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0005 | 0/0 | 3392 | 7 | 0 | 2 | 5 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0006 | 0/0 | 3397 | 6 | 1 | 2 | 0 | 1 | 2 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0007 | 0/0 | 3391 | 6 | 1 | 3 | 0 | 0 | 2 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0008 | 0/0 | 3395 | 5 | 3 | 0 | 1 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0009 | 0/0 | 3401 | 5 | 5 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0010 | 0/0 | 3393 | 4 | 0 | 2 | 2 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0011 | 0/0 | 3404 | 4 | 4 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0012 | 0/0 | 3398 | 4 | 3 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0013 | 0/0 | 3396 | 3 | 0 | 2 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0014 | 0/0 | 3393 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0015 | 0/0 | 3393 | 2 | 1 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0016 | 0/0 | 3393 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0017 | 0/0 | 3397 | 2 | 0 | 0 | 2 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0018 | 0/0 | 3394 | 2 | 0 | 0 | 2 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0019 | 0/0 | 3403 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0020 | 0/0 | 3409 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0021 | 0/0 | 3401 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0022 | 0/0 | 3396 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0023 | 0/0 | 3392 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0024 | 0/0 | 3399 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0025 | 0/0 | 3408 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0026 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0027 | 0/0 | 3393 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0028 | 0/0 | 3393 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0029 | 0/0 | 3395 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0030 | 0/0 | 3395 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0031 | 0/0 | 3392 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0032 | 0/0 | 3394 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0033 | 0/0 | 3392 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0034 | 0/0 | 3396 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0035 | 0/0 | 3399 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0036 | 0/0 | 3394 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0037 | 0/0 | 3399 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0038 | 0/0 | 3394 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0039 | 0/0 | 3392 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0040 | 0/0 | 3395 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0041 | 0/0 | 3393 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0042 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0043 | 0/0 | 3391 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0044 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0045 | 0/0 | 3395 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0046 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0047 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0048 | 0/0 | 3395 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0049 | 0/0 | 3393 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0050 | 0/0 | 3391 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0051 | 0/0 | 3398 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
t0052 | 0/0 | 3391 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0051 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0173 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2787 | 213 | 61 | 35 | 103 | 1 | 12 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0006 | 0/0 | 2787 | 2 | 0 | 0 | 1 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0011 | 0/0 | 2787 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0012 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0013 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0014 | 0/0 | 2787 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0002c0002 | 0/0 | 2787 | 35 | 2 | 12 | 10 | 6 | 5 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0002c0016 | 0/0 | 2787 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0003c0003 | 0/0 | 2787 | 22 | 1 | 11 | 0 | 1 | 9 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0003c0008 | 0/0 | 2787 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0004c0004 | 0/1 | 2787 | 15 | 4 | 4 | 1 | 1 | 4 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0005c0007 | 0/0 | 2787 | 2 | 0 | 2 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0006c0005 | 0/0 | 2787 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0007c0010 | 0/0 | 2787 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0008c0015 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0009c0009 | 0/0 | 2787 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6179 | 81 | 22 | 11 | 42 | 1 | 5 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0002 | 1/0 | 6177 | 62 | 0 | 12 | 46 | 0 | 3 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0005 | 0/0 | 6178 | 7 | 0 | 2 | 5 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0006 | 0/0 | 6183 | 3 | 1 | 0 | 0 | 0 | 2 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0008 | 0/0 | 6181 | 3 | 2 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0009 | 0/0 | 6187 | 4 | 4 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0010 | 0/0 | 6179 | 3 | 0 | 2 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0011 | 0/0 | 6190 | 4 | 4 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0012 | 0/0 | 6184 | 4 | 3 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0013 | 0/0 | 6182 | 3 | 0 | 2 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0014 | 0/0 | 6179 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0016 | 0/0 | 6179 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0017 | 0/0 | 6183 | 2 | 0 | 0 | 2 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0018 | 0/0 | 6180 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0019 | 0/0 | 6189 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0020 | 0/0 | 6195 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0021 | 0/0 | 6187 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0023 | 0/0 | 6178 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0024 | 0/0 | 6185 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0025 | 0/0 | 6194 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0026 | 0/0 | 6179 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0027 | 0/0 | 6179 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0028 | 0/0 | 6179 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0029 | 0/0 | 6181 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0031 | 0/0 | 6178 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0032 | 0/0 | 6180 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0033 | 0/0 | 6178 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0034 | 0/0 | 6182 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0036 | 0/0 | 6180 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0037 | 0/0 | 6185 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0040 | 0/0 | 6181 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0042 | 0/0 | 6177 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0043 | 0/0 | 6177 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0045 | 0/0 | 6181 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0046 | 0/0 | 6184 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0047 | 0/0 | 6176 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0048 | 0/0 | 6181 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0049 | 0/0 | 6179 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0050 | 0/0 | 6177 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0051 | 0/0 | 6184 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0001t0052 | 0/0 | 6177 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0006t0004 | 0/0 | 6177 | 2 | 0 | 0 | 1 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0011t0044 | 0/0 | 6179 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0012t0010 | 0/0 | 6179 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0013t0009 | 0/0 | 6187 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0001c0014t0006 | 0/0 | 6183 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0002c0002t0001 | 0/0 | 6179 | 26 | 0 | 10 | 8 | 3 | 5 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0002c0002t0008 | 0/0 | 6181 | 2 | 1 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0002c0002t0015 | 0/0 | 6179 | 2 | 1 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0002c0002t0018 | 0/0 | 6180 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0002c0002t0030 | 0/0 | 6181 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0002c0002t0035 | 0/0 | 6185 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0002c0002t0038 | 0/0 | 6180 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0002c0002t0041 | 0/0 | 6179 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0002c0016t0001 | 0/0 | 6179 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0003c0003t0003 | 0/0 | 6176 | 17 | 1 | 8 | 0 | 1 | 7 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0003c0003t0007 | 0/0 | 6177 | 4 | 0 | 2 | 0 | 0 | 2 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0003c0003t0039 | 0/0 | 6178 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0003c0008t0007 | 0/0 | 6177 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0004c0004t0004 | 0/1 | 6177 | 15 | 4 | 4 | 1 | 1 | 4 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0005c0007t0006 | 0/0 | 6183 | 2 | 0 | 2 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0006c0005t0022 | 0/0 | 6182 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0007c0010t0007 | 0/0 | 6177 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0008c0015t0001 | 0/0 | 6179 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
a0009c0009t0002 | 0/0 | 6177 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | copy fasta | chr1 | 114577850 | 114675049 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0173 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0005g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0006g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0008g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0008g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0009g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0009g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0009g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0009g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0010g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0010g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0010g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0011g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0011g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0011g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0012g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0012g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0012g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0012g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0013g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0013g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0013g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0014g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0014g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0016g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0016g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0017g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0017g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0018g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0019g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0019g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0020g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0020g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0021g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0021g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0023g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0023g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0024g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0024g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0025g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0026g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0027g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0028g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0029g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0031g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0032g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0033g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0034g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0036g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0037g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0040g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0042g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0043g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0045g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0046g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0047g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0048g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0049g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0050g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0051g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0001t0052g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0006t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0006t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0011t0044g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0012t0010g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0013t0009g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0001c0014t0006g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0008g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0008g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0015g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0015g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0018g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0030g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0035g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0038g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0002t0041g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0002c0016t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0007g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0007g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0007g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0007g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0003t0039g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0003c0008t0007g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0051 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0004c0004t0004g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0005c0007t0006g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0005c0007t0006g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0006c0005t0022g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0006c0005t0022g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0007c0010t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0008c0015t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
a0009c0009t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0246 | EUR | GBR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00099 | hp2 | a0003 | c0003 | t0003 | g0283 | EUR | GBR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00140 | hp1 | a0002 | c0002 | t0035 | g0248 | EUR | GBR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00140 | hp2 | a0002 | c0002 | t0041 | g0258 | EUR | GBR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0257 | EUR | FIN | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00323 | hp2 | a0001 | c0014 | t0006 | g0026 | EUR | FIN | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00558 | hp2 | a0002 | c0002 | t0030 | g0240 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00642 | hp1 | a0001 | c0001 | t0050 | g0194 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | CHS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00733 | hp1 | a0002 | c0002 | t0015 | g0245 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00733 | hp2 | a0003 | c0003 | t0003 | g0007 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0259 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00735 | hp2 | a0003 | c0003 | t0003 | g0289 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00738 | hp2 | a0003 | c0003 | t0039 | g0285 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00741 | hp1 | a0003 | c0003 | t0003 | g0271 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG00741 | hp2 | a0001 | c0011 | t0044 | g0227 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0268 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0242 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0267 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01081 | hp2 | a0003 | c0003 | t0003 | g0290 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01099 | hp1 | a0001 | c0001 | t0012 | g0054 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01099 | hp2 | a0003 | c0003 | t0003 | g0275 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01106 | hp1 | a0003 | c0008 | t0007 | g0282 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0263 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01109 | hp2 | a0003 | c0003 | t0003 | g0270 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01167 | hp1 | a0001 | c0001 | t0013 | g0025 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01168 | hp2 | a0005 | c0007 | t0006 | g0030 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01169 | hp1 | a0005 | c0007 | t0006 | g0029 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0247 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01175 | hp2 | a0001 | c0001 | t0013 | g0034 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01192 | hp1 | a0004 | c0004 | t0004 | g0066 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01192 | hp2 | a0002 | c0002 | t0038 | g0254 | AMR | PUR | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01257 | hp1 | a0004 | c0004 | t0004 | g0061 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01257 | hp2 | a0001 | c0001 | t0005 | g0161 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01261 | hp1 | a0004 | c0004 | t0004 | g0063 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01261 | hp2 | a0001 | c0001 | t0049 | g0181 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01346 | hp1 | a0001 | c0001 | t0048 | g0160 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01346 | hp2 | a0003 | c0003 | t0007 | g0274 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0249 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01433 | hp1 | a0004 | c0004 | t0004 | g0049 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01496 | hp1 | a0001 | c0001 | t0031 | g0136 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | IBS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0256 | EUR | IBS | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01884 | hp2 | a0001 | c0001 | t0019 | g0012 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01891 | hp1 | a0004 | c0004 | t0004 | g0072 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01891 | hp2 | a0001 | c0001 | t0020 | g0008 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01928 | hp2 | a0001 | c0001 | t0032 | g0141 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0041 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01952 | hp2 | a0003 | c0003 | t0007 | g0288 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0166 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01978 | hp2 | a0001 | c0001 | t0010 | g0137 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01993 | hp1 | a0001 | c0001 | t0010 | g0105 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0251 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02004 | hp2 | a0003 | c0003 | t0003 | g0007 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02055 | hp2 | a0007 | c0010 | t0007 | g0058 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02056 | hp2 | a0001 | c0001 | t0005 | g0165 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02083 | hp1 | a0008 | c0015 | t0001 | g0074 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02145 | hp1 | a0001 | c0001 | t0045 | g0082 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02145 | hp2 | a0001 | c0001 | t0042 | g0015 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | CDX | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | CDX | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0243 | EAS | CDX | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | CDX | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02257 | hp1 | a0006 | c0005 | t0022 | g0068 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02257 | hp2 | a0004 | c0004 | t0004 | g0071 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02258 | hp1 | a0001 | c0001 | t0021 | g0019 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02258 | hp2 | a0001 | c0001 | t0023 | g0048 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02280 | hp1 | a0001 | c0001 | t0011 | g0002 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02280 | hp2 | a0001 | c0001 | t0043 | g0010 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0250 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02451 | hp1 | a0001 | c0001 | t0029 | g0055 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02451 | hp2 | a0001 | c0001 | t0024 | g0056 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02572 | hp2 | a0001 | c0001 | t0020 | g0009 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02602 | hp2 | a0003 | c0003 | t0003 | g0287 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02615 | hp1 | a0001 | c0001 | t0016 | g0238 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02622 | hp1 | a0001 | c0001 | t0009 | g0016 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02622 | hp2 | a0001 | c0001 | t0008 | g0147 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02698 | hp1 | a0003 | c0003 | t0003 | g0276 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02698 | hp2 | a0001 | c0006 | t0004 | g0059 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02723 | hp1 | a0001 | c0001 | t0011 | g0002 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02818 | hp2 | a0003 | c0003 | t0003 | g0277 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02886 | hp1 | a0001 | c0001 | t0009 | g0018 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02886 | hp2 | a0001 | c0001 | t0046 | g0053 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02896 | hp1 | a0001 | c0001 | t0014 | g0078 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02896 | hp2 | a0001 | c0001 | t0040 | g0057 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02897 | hp1 | a0001 | c0001 | t0012 | g0046 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02897 | hp2 | a0001 | c0001 | t0014 | g0079 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02922 | hp1 | a0001 | c0001 | t0009 | g0017 | AFR | ESN | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02922 | hp2 | a0004 | c0004 | t0004 | g0070 | AFR | ESN | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02976 | hp1 | a0001 | c0001 | t0051 | g0073 | AFR | ESN | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03017 | hp1 | a0003 | c0003 | t0003 | g0281 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03041 | hp1 | a0001 | c0001 | t0021 | g0021 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03098 | hp2 | a0004 | c0004 | t0004 | g0050 | AFR | MSL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03195 | hp1 | a0001 | c0001 | t0011 | g0045 | AFR | ESN | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03209 | hp1 | a0001 | c0001 | t0011 | g0043 | AFR | MSL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03209 | hp2 | a0001 | c0001 | t0026 | g0264 | AFR | MSL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03225 | hp1 | a0001 | c0001 | t0009 | g0014 | AFR | MSL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03225 | hp2 | a0001 | c0001 | t0016 | g0237 | AFR | MSL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03239 | hp1 | a0003 | c0003 | t0003 | g0279 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03453 | hp2 | a0001 | c0001 | t0012 | g0052 | AFR | MSL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03490 | hp1 | a0004 | c0004 | t0004 | g0087 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0291 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0292 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03540 | hp1 | a0001 | c0001 | t0036 | g0023 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03540 | hp2 | a0002 | c0002 | t0008 | g0265 | AFR | GWD | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03654 | hp1 | a0004 | c0004 | t0004 | g0221 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03654 | hp2 | a0003 | c0003 | t0003 | g0280 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03669 | hp2 | a0004 | c0004 | t0004 | g0062 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0261 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03704 | hp2 | a0003 | c0003 | t0003 | g0273 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03710 | hp1 | a0003 | c0003 | t0003 | g0278 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03834 | hp1 | a0001 | c0001 | t0013 | g0028 | SAS | BEB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03834 | hp2 | a0003 | c0003 | t0007 | g0284 | SAS | BEB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03927 | hp1 | a0004 | c0004 | t0004 | g0065 | SAS | BEB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0266 | SAS | BEB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG04115 | hp1 | a0001 | c0001 | t0027 | g0100 | SAS | STU | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | STU | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG04184 | hp1 | a0001 | c0001 | t0006 | g0032 | SAS | BEB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG04184 | hp2 | a0003 | c0003 | t0007 | g0286 | SAS | BEB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG04199 | hp2 | a0002 | c0002 | t0001 | g0255 | SAS | STU | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18612 | hp2 | a0001 | c0001 | t0017 | g0022 | EAS | CHB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0239 | EAS | CHB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | CHB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18906 | hp1 | a0001 | c0001 | t0012 | g0224 | AFR | YRI | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18957 | hp2 | a0001 | c0001 | t0017 | g0020 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18960 | hp1 | a0001 | c0001 | t0008 | g0134 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18960 | hp2 | a0009 | c0009 | t0002 | g0209 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18961 | hp2 | a0001 | c0001 | t0005 | g0220 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18962 | hp2 | a0001 | c0001 | t0010 | g0106 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18964 | hp2 | a0004 | c0004 | t0004 | g0067 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18966 | hp1 | a0001 | c0001 | t0052 | g0198 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18967 | hp1 | a0001 | c0001 | t0018 | g0111 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18967 | hp2 | a0001 | c0001 | t0005 | g0162 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18969 | hp1 | a0001 | c0001 | t0047 | g0206 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18986 | hp1 | a0001 | c0006 | t0004 | g0060 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18989 | hp1 | a0001 | c0001 | t0005 | g0168 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19010 | hp2 | a0002 | c0002 | t0018 | g0236 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19011 | hp1 | a0001 | c0012 | t0010 | g0092 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19055 | hp1 | a0001 | c0001 | t0033 | g0024 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19055 | hp2 | a0001 | c0001 | t0034 | g0139 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19060 | hp1 | a0001 | c0001 | t0005 | g0170 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19240 | hp1 | a0001 | c0001 | t0023 | g0047 | AFR | YRI | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0027 | AFR | ASW | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA20129 | hp2 | a0001 | c0001 | t0019 | g0011 | AFR | ASW | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA20752 | hp1 | a0002 | c0002 | t0008 | g0241 | EUR | TSI | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA20752 | hp2 | a0004 | c0004 | t0004 | g0064 | EUR | TSI | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA20905 | hp1 | a0002 | c0016 | t0001 | g0262 | SAS | GIH | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA20905 | hp2 | a0001 | c0001 | t0006 | g0031 | SAS | GIH | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG01123 | hp2 | a0003 | c0003 | t0003 | g0272 | AMR | CLM | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02109 | hp1 | a0001 | c0001 | t0024 | g0223 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02109 | hp2 | a0001 | c0013 | t0009 | g0013 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02486 | hp1 | a0001 | c0001 | t0008 | g0143 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02559 | hp1 | a0002 | c0002 | t0015 | g0244 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG06807 | hp1 | a0001 | c0001 | t0028 | g0269 | AFR | USA | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
HG06807 | hp2 | a0001 | c0001 | t0025 | g0044 | AFR | USA | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA18955 | hp2 | a0001 | c0001 | t0037 | g0033 | EAS | JPT | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | USA | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | USA | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA21309 | hp1 | a0006 | c0005 | t0022 | g0069 | AFR | LWK | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
homoSapiens_chm13v2 | hp1 | a0004 | c0004 | t0004 | g0051 | REF | REF | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0173 | REF | REF | DENND2C_chr1_114577850_114675049 | DENND2C | chr1 | 114577850 | 114675049 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:114600249
|
G | A | 1 | a0005 | 2 | HG01168.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.2060C>T | p.Ser687Phe | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 15/21 | 2700/6177 | 2060/2787 | 687/928 | chr1 | 114600249 | ||
chr1:114621933
|
C | T | 1 | a0004 | 15 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(12): Show |
missense_variant | MODERATE | c.1189G>A | p.Gly397Ser | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 7/21 | 1829/6177 | 1189/2787 | 397/928 | chr1 | 114621933 | ||
chr1:114622040
|
T | C | 1 | a0008 | 1 | HG02083.hp1 | missense_variant | MODERATE | c.1082A>G | p.His361Arg | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 7/21 | 1722/6177 | 1082/2787 | 361/928 | chr1 | 114622040 | ||
chr1:114625318
|
A | G | 1 | a0007 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.667T>C | p.Ser223Pro | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/21 | 1307/6177 | 667/2787 | 223/928 | chr1 | 114625318 | ||
chr1:114625378
|
A | T | 1 | a0009 | 1 | NA18960.hp2 | missense_variant | MODERATE | c.607T>A | p.Cys203Ser | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/21 | 1247/6177 | 607/2787 | 203/928 | chr1 | 114625378 | ||
chr1:114625476
|
T | C | 1 | a0002 | 36 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(33): Show |
missense_variant | MODERATE | c.509A>G | p.Asp170Gly | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/21 | 1149/6177 | 509/2787 | 170/928 | chr1 | 114625476 | ||
chr1:114625605
|
C | T | 1 | a0006 | 2 | HG02257.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.380G>A | p.Cys127Tyr | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/21 | 1020/6177 | 380/2787 | 127/928 | chr1 | 114625605 | ||
chr1:114625979
|
A | T | 1 | a0003 | 23 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(20): Show |
missense_variant | MODERATE | c.6T>A | p.Asp2Glu | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/21 | 646/6177 | 6/2787 | 2/928 | chr1 | 114625979 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:114587732
|
C | T | 2 | a0001c0006a0004c0004 | 17 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(14): Show |
synonymous_variant | LOW | c.2652G>A | p.Arg884Arg | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 19/21 | 3292/6177 | 2652/2787 | 884/928 | chr1 | 114587732 | ||
chr1:114587804
|
A | G | 1 | a0001c0014 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.2580T>C | p.Ser860Ser | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 19/21 | 3220/6177 | 2580/2787 | 860/928 | chr1 | 114587804 | ||
chr1:114587852
|
C | T | 1 | a0001c0013 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.2532G>A | p.Glu844Glu | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 19/21 | 3172/6177 | 2532/2787 | 844/928 | chr1 | 114587852 | ||
chr1:114605011
|
C | T | 1 | a0001c0012 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.1578G>A | p.Gln526Gln | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 11/21 | 2218/6177 | 1578/2787 | 526/928 | chr1 | 114605011 | ||
chr1:114608752
|
C | T | 1 | a0001c0011 | 1 | HG00741.hp2 | synonymous_variant | LOW | c.1491G>A | p.Val497Val | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/21 | 2131/6177 | 1491/2787 | 497/928 | chr1 | 114608752 | ||
chr1:114611101
|
G | A | 1 | a0003c0008 | 1 | HG01106.hp1 | synonymous_variant | LOW | c.1341C>T | p.Asn447Asn | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 9/21 | 1981/6177 | 1341/2787 | 447/928 | chr1 | 114611101 | ||
chr1:114622015
|
G | A | 1 | a0002c0016 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.1107C>T | p.Asn369Asn | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 7/21 | 1747/6177 | 1107/2787 | 369/928 | chr1 | 114622015 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:114582859
|
T | G | 1 | a0001c0001t0046 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2741A>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 2741 | chr1 | 114582859 | |||||
chr1:114582904
|
A | T | 1 | a0001c0001t0050 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2696T>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 2696 | chr1 | 114582904 | |||||
chr1:114582970
|
A | G | 1 | a0001c0011t0044 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2630T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 2630 | chr1 | 114582970 | |||||
chr1:114583349
|
T | TA | 8 | a0001c0001t0006a0001c0001t0013a0001c0001t0017others(5): Show | 14 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2250dupT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 2250 | chr1 | 114583349 | |||||
chr1:114583433
|
C | G | 1 | a0001c0001t0040 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2167G>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 2167 | chr1 | 114583433 | |||||
chr1:114583493
|
A | AAAACACA others(3): Show |
2 | a0001c0001t0009a0001c0013t0009 | 5 | HG02109.hp2 HG02622.hp1 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2106_*2107insGTGT others(6): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 2106 | chr1 | 114583493 | |||||
chr1:114583493
|
A | AAAACACA others(5): Show |
1 | a0001c0001t0019 | 2 | HG01884.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2106_*2107insGTGT others(8): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 2106 | chr1 | 114583493 | |||||
chr1:114583493
|
A | AAC | 13 | a0001c0001t0006a0001c0001t0008a0001c0001t0013others(10): Show | 22 | HG00140.hp2 HG00323.hp2 HG00558.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2105_*2106dupGT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 2106 | chr1 | 114583493 | |||||
chr1:114583493
|
A | AACAC | 6 | a0001c0001t0029a0001c0001t0037a0001c0001t0040others(3): Show | 7 | HG01346.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2103_*2106dupGTGT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 2106 | chr1 | 114583493 | |||||
chr1:114583493
|
A | AACACAC | 5 | a0001c0001t0012a0001c0001t0024a0001c0001t0046others(2): Show | 9 | HG00140.hp1 HG01099.hp1 HG02109.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2101_*2106dupGTGT others(2): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 2106 | chr1 | 114583493 | |||||
chr1:114583493
|
A | AACACACA others(3): Show |
1 | a0001c0001t0021 | 2 | HG02258.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2097_*2106dupGTGT others(6): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 2106 | chr1 | 114583493 | |||||
chr1:114583493
|
A | AACACACA others(7): Show |
1 | a0001c0001t0011 | 4 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2093_*2106dupGTGT others(10): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 2106 | chr1 | 114583493 | |||||
chr1:114583493
|
A | AACACACA others(11): Show |
2 | a0001c0001t0020a0001c0001t0025 | 3 | HG01891.hp2 HG02572.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2089_*2106dupGTGT others(14): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 2106 | chr1 | 114583493 | |||||
chr1:114583684
|
A | G | 2 | a0002c0002t0015a0002c0002t0038 | 3 | HG00733.hp1 HG01192.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1916T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 1916 | chr1 | 114583684 | |||||
chr1:114583761
|
C | T | 1 | a0001c0001t0042 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1839G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 1839 | chr1 | 114583761 | |||||
chr1:114583768
|
T | C | 1 | a0001c0001t0016 | 2 | HG02615.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1832A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 1832 | chr1 | 114583768 | |||||
chr1:114583794
|
C | T | 5 | a0001c0001t0017a0001c0001t0034a0001c0001t0037others(2): Show | 21 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1806G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 1806 | chr1 | 114583794 | |||||
chr1:114583807
|
C | CA | 11 | a0001c0001t0005a0001c0001t0006a0001c0001t0017others(8): Show | 22 | HG00323.hp2 HG01168.hp2 HG01169.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1792dupT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 1792 | chr1 | 114583807 | |||||
chr1:114583807
|
CA | C | 7 | a0001c0001t0011a0001c0001t0025a0001c0001t0031others(4): Show | 26 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1792delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 1792 | chr1 | 114583807 | |||||
chr1:114583835
|
A | AAC | 30 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(27): Show | 149 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*1763_*1764dupGT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 1764 | chr1 | 114583835 | |||||
chr1:114583863
|
A | C | 1 | a0001c0001t0014 | 2 | HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1737T>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 1737 | chr1 | 114583863 | |||||
chr1:114583974
|
A | G | 1 | a0001c0001t0033 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1626T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 1626 | chr1 | 114583974 | |||||
chr1:114584025
|
A | G | 4 | a0001c0001t0010a0001c0001t0031a0001c0001t0032others(1): Show | 6 | HG01496.hp1 HG01928.hp2 HG01978.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1575T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 1575 | chr1 | 114584025 | |||||
chr1:114584090
|
C | T | 1 | a0002c0002t0030 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1510G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 1510 | chr1 | 114584090 | |||||
chr1:114584204
|
A | T | 1 | a0001c0001t0029 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1396T>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 1396 | chr1 | 114584204 | |||||
chr1:114584333
|
G | A | 6 | a0001c0001t0009a0001c0001t0020a0001c0001t0021others(3): Show | 11 | HG01891.hp2 HG02109.hp2 HG02145.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1267C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 1267 | chr1 | 114584333 | |||||
chr1:114584438
|
A | G | 1 | a0001c0001t0028 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1162T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 1162 | chr1 | 114584438 | |||||
chr1:114584630
|
G | A | 1 | a0001c0011t0044 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*970C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 970 | chr1 | 114584630 | |||||
chr1:114585161
|
G | A | 1 | a0001c0001t0045 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*439C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 439 | chr1 | 114585161 | |||||
chr1:114585192
|
A | G | 1 | a0001c0001t0027 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*408T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 408 | chr1 | 114585192 | |||||
chr1:114585278
|
C | G | 1 | a0001c0001t0026 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*322G>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 322 | chr1 | 114585278 | |||||
chr1:114585367
|
T | TA | 6 | a0001c0001t0012a0001c0001t0023a0001c0001t0024others(3): Show | 12 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*232dupT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 232 | chr1 | 114585367 | |||||
chr1:114585466
|
A | G | 57 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(54): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*134T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 134 | chr1 | 114585466 | |||||
chr1:114585478
|
C | T | 1 | a0001c0001t0025 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*122G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 122 | chr1 | 114585478 | |||||
chr1:114585485
|
T | C | 1 | a0001c0001t0052 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*115A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 21/21 | 115 | chr1 | 114585485 | |||||
chr1:114626118
|
T | C | 1 | a0001c0001t0051 | 1 | HG02976.hp1 | 5_prime_UTR_variant | MODIFIER | c.-134A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/21 | 134 | chr1 | 114626118 | |||||
chr1:114645514
|
T | C | 1 | a0001c0001t0052 | 1 | NA18966.hp1 | 5_prime_UTR_variant | MODIFIER | c.-271A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/21 | 19530 | chr1 | 114645514 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:114585828
|
C | T | 1 | a0001c0001t0051g0073 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2756-197G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 20/20 | chr1 | 114585828 | ||||||
chr1:114586005
|
T | C | 1 | a0001c0001t0002g0212 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2756-374A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 20/20 | chr1 | 114586005 | ||||||
chr1:114586117
|
G | A | 2 | a0004c0004t0004g0071a0004c0004t0004g0072 | 2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.2756-486C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 20/20 | chr1 | 114586117 | ||||||
chr1:114586325
|
G | A | 1 | a0001c0001t0019g0012 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2756-694C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 20/20 | chr1 | 114586325 | ||||||
chr1:114586502
|
G | A | 38 | a0001c0001t0012g0046a0001c0001t0012g0052a0001c0001t0012g0054others(35): Show | 39 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.2756-871C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 20/20 | chr1 | 114586502 | ||||||
chr1:114586684
|
CATTTATT others(10): Show |
C | 2 | a0001c0001t0014g0078a0001c0001t0014g0079 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2755+686_2755+702d others(19): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 20/20 | chr1 | 114586684 | ||||||
chr1:114586696
|
ATTTTTAT others(4): Show |
A | 1 | a0001c0001t0002g0172 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2755+680_2755+690d others(13): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 20/20 | chr1 | 114586696 | ||||||
chr1:114586830
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2755+557C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 20/20 | chr1 | 114586830 | ||||||
chr1:114586898
|
A | AT | 20 | a0001c0001t0001g0126a0001c0001t0002g0210a0001c0001t0006g0027others(17): Show | 20 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.2755+488dupA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 20/20 | chr1 | 114586898 | ||||||
chr1:114586975
|
G | A | 1 | a0001c0001t0024g0223 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2755+412C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 20/20 | chr1 | 114586975 | ||||||
chr1:114587074
|
T | A | 1 | a0008c0015t0001g0074 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2755+313A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 20/20 | chr1 | 114587074 | ||||||
chr1:114587088
|
G | A | 7 | a0002c0002t0001g0242a0002c0002t0001g0259a0002c0002t0008g0241others(4): Show | 7 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.2755+299C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 20/20 | chr1 | 114587088 | ||||||
chr1:114587122
|
G | A | 1 | a0001c0001t0002g0177 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2755+265C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 20/20 | chr1 | 114587122 | ||||||
chr1:114587203
|
T | C | 3 | a0001c0001t0016g0237a0001c0001t0016g0238a0001c0001t0026g0264 | 3 | HG02615.hp1 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2755+184A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 20/20 | chr1 | 114587203 | ||||||
chr1:114587478
|
A | G | 1 | a0002c0002t0030g0240 | 1 | HG00558.hp2 | splice_region_variant&intron_variant | LOW | c.2669-5T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 19/20 | chr1 | 114587478 | ||||||
chr1:114587628
|
C | G | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2668+88G>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 19/20 | chr1 | 114587628 | ||||||
chr1:114587638
|
T | C | 1 | a0001c0001t0040g0057 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2668+78A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 19/20 | chr1 | 114587638 | ||||||
chr1:114587713
|
G | A | 1 | a0003c0003t0003g0273 | 1 | HG03704.hp2 | splice_region_variant&intron_variant | LOW | c.2668+3C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 19/20 | chr1 | 114587713 | ||||||
chr1:114588036
|
G | A | 1 | a0001c0001t0002g0186 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2432-84C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114588036 | ||||||
chr1:114588407
|
T | A | 3 | a0001c0001t0016g0237a0001c0001t0016g0238a0001c0001t0026g0264 | 3 | HG02615.hp1 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2432-455A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114588407 | ||||||
chr1:114588666
|
A | G | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2432-714T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114588666 | ||||||
chr1:114588714
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2432-762G>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114588714 | ||||||
chr1:114588723
|
T | C | 1 | a0007c0010t0007g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2432-771A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114588723 | ||||||
chr1:114588819
|
T | C | 3 | a0001c0001t0016g0237a0001c0001t0016g0238a0001c0001t0026g0264 | 3 | HG02615.hp1 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2432-867A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114588819 | ||||||
chr1:114588877
|
G | A | 1 | a0001c0011t0044g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2432-925C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114588877 | ||||||
chr1:114589219
|
T | C | 10 | a0003c0003t0003g0275a0003c0003t0003g0276a0003c0003t0003g0280others(7): Show | 10 | HG00738.hp2 HG01099.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.2432-1267A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114589219 | ||||||
chr1:114589358
|
T | A | 1 | a0001c0011t0044g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2432-1406A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114589358 | ||||||
chr1:114589432
|
A | G | 1 | a0001c0001t0043g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2432-1480T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114589432 | ||||||
chr1:114589449
|
T | C | 17 | a0001c0006t0004g0059a0001c0006t0004g0060a0004c0004t0004g0049others(14): Show | 17 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.2432-1497A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114589449 | ||||||
chr1:114589600
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2432-1648A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114589600 | ||||||
chr1:114589638
|
A | G | 22 | a0003c0003t0003g0007a0003c0003t0003g0270a0003c0003t0003g0271others(19): Show | 23 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.2432-1686T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114589638 | ||||||
chr1:114589769
|
T | C | 7 | a0002c0002t0001g0242a0002c0002t0001g0259a0002c0002t0008g0241others(4): Show | 7 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.2432-1817A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114589769 | ||||||
chr1:114589888
|
A | T | 3 | a0001c0001t0024g0056a0006c0005t0022g0068a0006c0005t0022g0069 | 3 | HG02257.hp1 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2432-1936T>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114589888 | ||||||
chr1:114589989
|
C | T | 1 | a0001c0001t0002g0182 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2432-2037G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114589989 | ||||||
chr1:114590059
|
C | T | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2432-2107G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114590059 | ||||||
chr1:114590205
|
G | A | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2432-2253C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114590205 | ||||||
chr1:114590261
|
A | C | 1 | a0001c0001t0001g0096 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2432-2309T>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114590261 | ||||||
chr1:114590484
|
A | G | 1 | a0002c0002t0001g0239 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2432-2532T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114590484 | ||||||
chr1:114590706
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.2432-2754T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114590706 | ||||||
chr1:114590773
|
C | T | 39 | a0001c0001t0012g0046a0001c0001t0012g0052a0001c0001t0012g0054others(36): Show | 40 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.2432-2821G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114590773 | ||||||
chr1:114590778
|
C | CA | 160 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(157): Show | 164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.2432-2827dupT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114590778 | ||||||
chr1:114590778
|
C | CAA | 33 | a0001c0001t0001g0084a0001c0001t0001g0116a0001c0001t0001g0123others(30): Show | 34 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.2432-2828_2432-282 others(6): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114590778 | ||||||
chr1:114590778
|
CA | C | 18 | a0001c0001t0002g0192a0001c0001t0002g0215a0001c0001t0002g0217others(15): Show | 18 | HG01884.hp2 HG01891.hp2 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.2432-2827delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114590778 | ||||||
chr1:114590863
|
A | C | 1 | a0004c0004t0004g0065 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2432-2911T>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114590863 | ||||||
chr1:114591063
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2432-3111G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114591063 | ||||||
chr1:114591186
|
T | C | 2 | a0001c0001t0016g0237a0001c0001t0016g0238 | 2 | HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2432-3234A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114591186 | ||||||
chr1:114591598
|
C | T | 1 | a0001c0001t0002g0201 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2431+2875G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114591598 | ||||||
chr1:114591701
|
T | C | 14 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0032others(11): Show | 14 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.2431+2772A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114591701 | ||||||
chr1:114591860
|
TTTA | T | 23 | a0001c0001t0011g0043a0003c0003t0003g0007a0003c0003t0003g0270others(20): Show | 24 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.2431+2610_2431+261 others(7): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114591860 | ||||||
chr1:114591881
|
T | A | 2 | a0001c0001t0002g0172a0001c0001t0002g0195 | 2 | HG00544.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.2431+2592A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114591881 | ||||||
chr1:114592031
|
C | T | 4 | a0001c0001t0001g0086a0001c0001t0001g0131a0001c0001t0001g0159others(1): Show | 4 | HG02486.hp1 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2431+2442G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114592031 | ||||||
chr1:114592057
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2431+2416C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114592057 | ||||||
chr1:114592181
|
G | A | 1 | a0002c0002t0001g0233 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2431+2292C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114592181 | ||||||
chr1:114592187
|
A | G | 17 | a0001c0006t0004g0059a0001c0006t0004g0060a0004c0004t0004g0049others(14): Show | 17 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.2431+2286T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114592187 | ||||||
chr1:114592291
|
G | T | 1 | a0001c0001t0005g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2431+2182C>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114592291 | ||||||
chr1:114592414
|
T | G | 1 | a0002c0002t0015g0244 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2431+2059A>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114592414 | ||||||
chr1:114592434
|
A | G | 1 | a0001c0011t0044g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2431+2039T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114592434 | ||||||
chr1:114592453
|
C | A | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2431+2020G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114592453 | ||||||
chr1:114592762
|
A | G | 1 | a0004c0004t0004g0067 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2431+1711T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114592762 | ||||||
chr1:114592778
|
C | G | 12 | a0001c0001t0012g0046a0001c0001t0012g0052a0001c0001t0012g0054others(9): Show | 12 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2431+1695G>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114592778 | ||||||
chr1:114592888
|
C | T | 9 | a0001c0001t0001g0226a0002c0002t0001g0233a0002c0002t0001g0235others(6): Show | 9 | HG02155.hp2 HG02165.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.2431+1585G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114592888 | ||||||
chr1:114593097
|
T | C | 1 | a0001c0001t0002g0200 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2431+1376A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114593097 | ||||||
chr1:114593121
|
C | T | 1 | a0001c0001t0045g0082 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2431+1352G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114593121 | ||||||
chr1:114593188
|
T | C | 2 | a0001c0001t0001g0075a0001c0001t0018g0111 | 2 | NA18967.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.2431+1285A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114593188 | ||||||
chr1:114593474
|
T | A | 35 | a0002c0002t0001g0041a0002c0002t0001g0233a0002c0002t0001g0234others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(32): Show |
intron_variant | MODIFIER | c.2431+999A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114593474 | ||||||
chr1:114594010
|
G | A | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2431+463C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114594010 | ||||||
chr1:114594150
|
A | G | 81 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(78): Show | 84 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.2431+323T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114594150 | ||||||
chr1:114594242
|
T | C | 2 | a0001c0001t0001g0149a0001c0001t0001g0156 | 2 | HG03195.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2431+231A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114594242 | ||||||
chr1:114594245
|
A | G | 2 | a0001c0001t0020g0008a0001c0001t0020g0009 | 2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.2431+228T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114594245 | ||||||
chr1:114594317
|
C | T | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2431+156G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114594317 | ||||||
chr1:114594360
|
G | A | 3 | a0002c0002t0001g0246a0002c0002t0001g0251a0002c0002t0001g0257 | 3 | HG00099.hp1 HG00323.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.2431+113C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114594360 | ||||||
chr1:114594436
|
C | A | 15 | a0004c0004t0004g0049a0004c0004t0004g0050a0004c0004t0004g0051others(12): Show | 15 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.2431+37G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 18/20 | chr1 | 114594436 | ||||||
chr1:114594611
|
T | C | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2326-33A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 17/20 | chr1 | 114594611 | ||||||
chr1:114594626
|
G | A | 17 | a0001c0006t0004g0059a0001c0006t0004g0060a0004c0004t0004g0049others(14): Show | 17 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.2326-48C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 17/20 | chr1 | 114594626 | ||||||
chr1:114594784
|
G | T | 1 | a0001c0001t0045g0082 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2326-206C>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 17/20 | chr1 | 114594784 | ||||||
chr1:114594877
|
G | C | 1 | a0001c0011t0044g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2326-299C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 17/20 | chr1 | 114594877 | ||||||
chr1:114595203
|
G | C | 1 | a0001c0001t0052g0198 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2326-625C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 17/20 | chr1 | 114595203 | ||||||
chr1:114595371
|
T | G | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2325+461A>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 17/20 | chr1 | 114595371 | ||||||
chr1:114595494
|
A | G | 17 | a0001c0006t0004g0059a0001c0006t0004g0060a0004c0004t0004g0049others(14): Show | 17 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.2325+338T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 17/20 | chr1 | 114595494 | ||||||
chr1:114596734
|
G | A | 2 | a0002c0002t0001g0261a0002c0016t0001g0262 | 2 | HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2284-861C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 16/20 | chr1 | 114596734 | ||||||
chr1:114596750
|
GT | G | 22 | a0003c0003t0003g0007a0003c0003t0003g0270a0003c0003t0003g0271others(19): Show | 23 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.2284-878delA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 16/20 | chr1 | 114596750 | ||||||
chr1:114596759
|
T | A | 2 | a0002c0002t0015g0245a0002c0002t0030g0240 | 2 | HG00558.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.2284-886A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 16/20 | chr1 | 114596759 | ||||||
chr1:114596838
|
G | A | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.2284-965C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 16/20 | chr1 | 114596838 | ||||||
chr1:114597031
|
C | T | 3 | a0001c0001t0016g0237a0001c0001t0016g0238a0001c0001t0026g0264 | 3 | HG02615.hp1 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2284-1158G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 16/20 | chr1 | 114597031 | ||||||
chr1:114597219
|
G | A | 1 | a0001c0013t0009g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2284-1346C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 16/20 | chr1 | 114597219 | ||||||
chr1:114597273
|
G | A | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2284-1400C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 16/20 | chr1 | 114597273 | ||||||
chr1:114598294
|
G | A | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2283+980C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 16/20 | chr1 | 114598294 | ||||||
chr1:114598322
|
T | C | 1 | a0001c0001t0005g0170 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2283+952A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 16/20 | chr1 | 114598322 | ||||||
chr1:114598337
|
G | C | 1 | a0001c0006t0004g0059 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2283+937C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 16/20 | chr1 | 114598337 | ||||||
chr1:114598443
|
A | G | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2283+831T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 16/20 | chr1 | 114598443 | ||||||
chr1:114598513
|
C | T | 1 | a0001c0011t0044g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2283+761G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 16/20 | chr1 | 114598513 | ||||||
chr1:114598538
|
CAGAA | C | 9 | a0004c0004t0004g0051a0004c0004t0004g0061a0004c0004t0004g0062others(6): Show | 9 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.2283+732_2283+735d others(6): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 16/20 | chr1 | 114598538 | ||||||
chr1:114599140
|
T | G | 1 | a0001c0001t0023g0048 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2283+134A>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 16/20 | chr1 | 114599140 | ||||||
chr1:114599769
|
G | A | 9 | a0004c0004t0004g0051a0004c0004t0004g0061a0004c0004t0004g0062others(6): Show | 9 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.2106-318C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 15/20 | chr1 | 114599769 | ||||||
chr1:114599822
|
T | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(145): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.2106-371A>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 15/20 | chr1 | 114599822 | ||||||
chr1:114599924
|
A | G | 1 | a0003c0003t0003g0276 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2105+280T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 15/20 | chr1 | 114599924 | ||||||
chr1:114599937
|
G | A | 2 | a0001c0001t0014g0078a0001c0001t0014g0079 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2105+267C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 15/20 | chr1 | 114599937 | ||||||
chr1:114599986
|
G | C | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2105+218C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 15/20 | chr1 | 114599986 | ||||||
chr1:114600567
|
C | A | 1 | a0001c0001t0021g0021 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1957-215G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 14/20 | chr1 | 114600567 | ||||||
chr1:114600567
|
C | T | 1 | a0007c0010t0007g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1957-215G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 14/20 | chr1 | 114600567 | ||||||
chr1:114601316
|
G | T | 3 | a0001c0001t0002g0169a0001c0001t0002g0199a0001c0001t0002g0203 | 3 | HG00438.hp1 HG02135.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.1815+192C>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 13/20 | chr1 | 114601316 | ||||||
chr1:114601414
|
G | A | 4 | a0002c0002t0001g0259a0002c0002t0015g0244a0002c0002t0015g0245others(1): Show | 4 | HG00733.hp1 HG00735.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1815+94C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 13/20 | chr1 | 114601414 | ||||||
chr1:114601609
|
C | A | 1 | a0004c0004t0004g0067 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1738-24G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 12/20 | chr1 | 114601609 | ||||||
chr1:114601683
|
C | T | 22 | a0003c0003t0003g0007a0003c0003t0003g0270a0003c0003t0003g0271others(19): Show | 23 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1738-98G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 12/20 | chr1 | 114601683 | ||||||
chr1:114601850
|
C | T | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1738-265G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 12/20 | chr1 | 114601850 | ||||||
chr1:114601948
|
G | A | 1 | a0001c0001t0005g0161 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1737+177C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 12/20 | chr1 | 114601948 | ||||||
chr1:114602082
|
A | G | 290 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(287): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1737+43T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 12/20 | chr1 | 114602082 | ||||||
chr1:114602273
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1668-79A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 11/20 | chr1 | 114602273 | ||||||
chr1:114602367
|
A | G | 1 | a0002c0002t0001g0255 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1668-173T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 11/20 | chr1 | 114602367 | ||||||
chr1:114602400
|
T | C | 1 | a0001c0011t0044g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1668-206A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 11/20 | chr1 | 114602400 | ||||||
chr1:114602673
|
C | G | 2 | a0001c0001t0020g0008a0001c0001t0020g0009 | 2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1668-479G>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 11/20 | chr1 | 114602673 | ||||||
chr1:114602876
|
T | C | 1 | a0002c0002t0008g0241 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1668-682A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 11/20 | chr1 | 114602876 | ||||||
chr1:114602992
|
G | A | 1 | a0001c0001t0002g0203 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1668-798C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 11/20 | chr1 | 114602992 | ||||||
chr1:114603065
|
T | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(144): Show | 150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.1668-871A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 11/20 | chr1 | 114603065 | ||||||
chr1:114603142
|
AT | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1668-949delA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 11/20 | chr1 | 114603142 | ||||||
chr1:114603269
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1668-1075A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 11/20 | chr1 | 114603269 | ||||||
chr1:114603579
|
C | A | 1 | a0001c0011t0044g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1667+1343G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 11/20 | chr1 | 114603579 | ||||||
chr1:114603671
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0142 | 4 | NA18941.hp2 NA18964.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.1667+1251G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 11/20 | chr1 | 114603671 | ||||||
chr1:114603672
|
G | A | 4 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0192others(1): Show | 4 | NA18951.hp2 NA18953.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1667+1250C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 11/20 | chr1 | 114603672 | ||||||
chr1:114603867
|
C | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(129): Show | 135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1667+1055G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 11/20 | chr1 | 114603867 | ||||||
chr1:114604030
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1667+892T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 11/20 | chr1 | 114604030 | ||||||
chr1:114604057
|
A | G | 1 | a0001c0001t0021g0021 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1667+865T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 11/20 | chr1 | 114604057 | ||||||
chr1:114604166
|
G | C | 1 | a0001c0001t0023g0048 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1667+756C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 11/20 | chr1 | 114604166 | ||||||
chr1:114604659
|
C | CT | 132 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(129): Show | 135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1667+262dupA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 11/20 | chr1 | 114604659 | ||||||
chr1:114605086
|
G | A | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1558-55C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114605086 | ||||||
chr1:114605169
|
T | A | 3 | a0001c0001t0020g0008a0001c0001t0020g0009a0001c0001t0021g0021 | 3 | HG01891.hp2 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1558-138A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114605169 | ||||||
chr1:114605494
|
G | T | 1 | a0001c0011t0044g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1558-463C>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114605494 | ||||||
chr1:114605689
|
G | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1558-658C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114605689 | ||||||
chr1:114605949
|
A | G | 1 | a0001c0001t0002g0036 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1558-918T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114605949 | ||||||
chr1:114606355
|
G | A | 1 | a0001c0001t0010g0106 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1558-1324C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114606355 | ||||||
chr1:114606449
|
G | A | 9 | a0004c0004t0004g0051a0004c0004t0004g0061a0004c0004t0004g0062others(6): Show | 9 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558-1418C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114606449 | ||||||
chr1:114606504
|
T | C | 1 | a0002c0002t0008g0241 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1558-1473A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114606504 | ||||||
chr1:114606614
|
G | T | 2 | a0004c0004t0004g0050a0004c0004t0004g0070 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1558-1583C>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114606614 | ||||||
chr1:114607160
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1557+1526G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114607160 | ||||||
chr1:114607351
|
A | C | 1 | a0001c0011t0044g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1557+1335T>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114607351 | ||||||
chr1:114607393
|
C | G | 5 | a0001c0001t0002g0215a0001c0001t0002g0217a0001c0001t0002g0218others(2): Show | 5 | HG01261.hp2 HG01928.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1557+1293G>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114607393 | ||||||
chr1:114607663
|
C | A | 1 | a0001c0001t0021g0021 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1557+1023G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114607663 | ||||||
chr1:114607844
|
C | G | 1 | a0001c0001t0001g0144 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1557+842G>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114607844 | ||||||
chr1:114607959
|
T | C | 19 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(16): Show | 19 | HG00544.hp1 HG01081.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.1557+727A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114607959 | ||||||
chr1:114608149
|
C | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(161): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1557+537G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114608149 | ||||||
chr1:114608172
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1557+514C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114608172 | ||||||
chr1:114608264
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1557+422T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114608264 | ||||||
chr1:114608291
|
A | G | 1 | a0004c0004t0004g0065 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1557+395T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114608291 | ||||||
chr1:114608513
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1557+173A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114608513 | ||||||
chr1:114608596
|
T | G | 1 | a0001c0001t0001g0132 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1557+90A>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114608596 | ||||||
chr1:114608662
|
G | A | 1 | a0001c0001t0002g0208 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1557+24C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 10/20 | chr1 | 114608662 | ||||||
chr1:114608881
|
G | A | 1 | a0001c0001t0001g0097 | 1 | NA19085.hp1 | splice_region_variant&intron_variant | LOW | c.1370-8C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 9/20 | chr1 | 114608881 | ||||||
chr1:114608924
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1370-51A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 9/20 | chr1 | 114608924 | ||||||
chr1:114608939
|
G | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0156 | 2 | HG03195.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1370-66C>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 9/20 | chr1 | 114608939 | ||||||
chr1:114608961
|
T | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1370-88A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 9/20 | chr1 | 114608961 | ||||||
chr1:114609218
|
C | T | 3 | a0002c0002t0001g0246a0002c0002t0001g0251a0002c0002t0001g0257 | 3 | HG00099.hp1 HG00323.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1370-345G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 9/20 | chr1 | 114609218 | ||||||
chr1:114609267
|
G | C | 1 | a0002c0002t0001g0256 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1370-394C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 9/20 | chr1 | 114609267 | ||||||
chr1:114609317
|
T | G | 1 | a0007c0010t0007g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1370-444A>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 9/20 | chr1 | 114609317 | ||||||
chr1:114609859
|
A | G | 1 | a0001c0001t0002g0205 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1370-986T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 9/20 | chr1 | 114609859 | ||||||
chr1:114610193
|
C | T | 38 | a0001c0001t0012g0046a0001c0001t0012g0052a0001c0001t0012g0054others(35): Show | 39 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1369+880G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 9/20 | chr1 | 114610193 | ||||||
chr1:114610207
|
C | T | 2 | a0001c0001t0020g0008a0001c0001t0020g0009 | 2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1369+866G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 9/20 | chr1 | 114610207 | ||||||
chr1:114610443
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG02559.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1369+630C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 9/20 | chr1 | 114610443 | ||||||
chr1:114610470
|
G | A | 17 | a0001c0006t0004g0059a0001c0006t0004g0060a0004c0004t0004g0049others(14): Show | 17 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.1369+603C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 9/20 | chr1 | 114610470 | ||||||
chr1:114610471
|
C | T | 17 | a0001c0006t0004g0059a0001c0006t0004g0060a0004c0004t0004g0049others(14): Show | 17 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.1369+602G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 9/20 | chr1 | 114610471 | ||||||
chr1:114610472
|
A | G | 17 | a0001c0006t0004g0059a0001c0006t0004g0060a0004c0004t0004g0049others(14): Show | 17 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.1369+601T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 9/20 | chr1 | 114610472 | ||||||
chr1:114610536
|
C | T | 6 | a0001c0001t0002g0005a0001c0001t0002g0171a0001c0001t0002g0176others(3): Show | 7 | HG00621.hp1 NA18941.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.1369+537G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 9/20 | chr1 | 114610536 | ||||||
chr1:114610560
|
C | T | 2 | a0001c0001t0020g0008a0001c0001t0020g0009 | 2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1369+513G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 9/20 | chr1 | 114610560 | ||||||
chr1:114610699
|
C | CA | 34 | a0001c0001t0001g0121a0001c0001t0001g0135a0001c0001t0002g0187others(31): Show | 34 | HG00323.hp2 HG01167.hp1 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.1369+373dupT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 9/20 | chr1 | 114610699 | ||||||
chr1:114611179
|
G | A | 1 | a0002c0002t0001g0246 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1325-62C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114611179 | ||||||
chr1:114611199
|
C | T | 4 | a0001c0001t0001g0086a0001c0001t0001g0131a0001c0001t0001g0159others(1): Show | 4 | HG02486.hp1 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325-82G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114611199 | ||||||
chr1:114611211
|
G | A | 2 | a0002c0002t0001g0267a0002c0002t0001g0268 | 2 | HG01070.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1325-94C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114611211 | ||||||
chr1:114611363
|
C | T | 1 | a0002c0002t0015g0244 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1325-246G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114611363 | ||||||
chr1:114611407
|
G | GA | 164 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(161): Show | 168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.1325-291dupT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114611407 | ||||||
chr1:114611625
|
T | C | 1 | a0007c0010t0007g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1325-508A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114611625 | ||||||
chr1:114611699
|
C | A | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1325-582G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114611699 | ||||||
chr1:114611778
|
A | AAC | 20 | a0001c0001t0002g0212a0001c0001t0005g0161a0001c0001t0005g0170others(17): Show | 20 | HG00099.hp2 HG01099.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.1325-663_1325-662d others(4): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114611778 | ||||||
chr1:114611778
|
A | AACAC | 30 | a0001c0001t0009g0017a0001c0001t0012g0052a0001c0001t0023g0047others(27): Show | 31 | HG00733.hp2 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1325-665_1325-662d others(6): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114611778 | ||||||
chr1:114611778
|
A | AACACAC | 5 | a0001c0001t0013g0028a0001c0001t0020g0008a0001c0001t0036g0023others(2): Show | 5 | HG01891.hp2 HG02698.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1325-667_1325-662d others(8): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114611778 | ||||||
chr1:114611778
|
A | AACACACA others(1): Show |
20 | a0001c0001t0006g0027a0001c0001t0006g0032a0001c0001t0009g0016others(17): Show | 20 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1325-669_1325-662d others(10): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114611778 | ||||||
chr1:114611778
|
A | AACACACA others(3): Show |
3 | a0001c0001t0021g0021a0001c0001t0037g0033a0003c0003t0003g0273 | 3 | HG03041.hp1 HG03704.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.1325-671_1325-662d others(12): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114611778 | ||||||
chr1:114611778
|
A | AACACACA others(5): Show |
2 | a0001c0001t0009g0014a0001c0001t0013g0034 | 2 | HG01175.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1325-673_1325-662d others(14): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114611778 | ||||||
chr1:114611778
|
AAC | A | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02055.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1325-663_1325-662d others(4): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114611778 | ||||||
chr1:114611778
|
AACAC | A | 4 | a0001c0001t0002g0035a0001c0001t0002g0038a0001c0001t0002g0039others(1): Show | 4 | HG00741.hp2 HG01358.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1325-665_1325-662d others(6): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114611778 | ||||||
chr1:114611778
|
AACACACA others(3): Show |
A | 7 | a0001c0001t0001g0096a0001c0001t0001g0158a0002c0002t0001g0247others(4): Show | 7 | HG00733.hp1 HG01175.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.1325-671_1325-662d others(12): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114611778 | ||||||
chr1:114611778
|
AACACACA others(5): Show |
A | 120 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(117): Show | 123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.1325-673_1325-662d others(14): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114611778 | ||||||
chr1:114611806
|
CACACACA others(4): Show |
C | 3 | a0001c0001t0001g0097a0002c0002t0001g0041a0002c0002t0001g0233 | 3 | HG01934.hp1 NA18940.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1325-700_1325-690d others(13): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114611806 | ||||||
chr1:114611818
|
A | C | 1 | a0001c0001t0047g0206 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1325-701T>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114611818 | ||||||
chr1:114611881
|
C | G | 2 | a0001c0006t0004g0059a0001c0006t0004g0060 | 2 | HG02698.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.1325-764G>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114611881 | ||||||
chr1:114612166
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1325-1049G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114612166 | ||||||
chr1:114612351
|
A | AT | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(114): Show | 120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.1325-1235dupA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114612351 | ||||||
chr1:114612520
|
A | AT | 17 | a0001c0001t0002g0213a0001c0006t0004g0059a0001c0006t0004g0060others(14): Show | 17 | HG00738.hp1 HG01192.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1325-1404dupA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114612520 | ||||||
chr1:114612548
|
C | G | 1 | a0001c0001t0001g0113 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1325-1431G>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114612548 | ||||||
chr1:114613022
|
T | C | 17 | a0001c0006t0004g0059a0001c0006t0004g0060a0004c0004t0004g0049others(14): Show | 17 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.1325-1905A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114613022 | ||||||
chr1:114613254
|
A | T | 1 | a0001c0001t0013g0028 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1325-2137T>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114613254 | ||||||
chr1:114613441
|
C | T | 1 | a0001c0001t0040g0057 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1325-2324G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114613441 | ||||||
chr1:114613506
|
A | G | 1 | a0001c0001t0002g0214 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1325-2389T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114613506 | ||||||
chr1:114613549
|
T | G | 22 | a0003c0003t0003g0007a0003c0003t0003g0270a0003c0003t0003g0271others(19): Show | 23 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1325-2432A>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114613549 | ||||||
chr1:114613741
|
T | C | 2 | a0002c0002t0001g0291a0002c0002t0001g0292 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1325-2624A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114613741 | ||||||
chr1:114613826
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1325-2709C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114613826 | ||||||
chr1:114613991
|
C | T | 10 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1325-2874G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114613991 | ||||||
chr1:114614056
|
A | G | 1 | a0001c0001t0021g0021 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1325-2939T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114614056 | ||||||
chr1:114614158
|
G | A | 2 | a0001c0001t0020g0008a0001c0001t0020g0009 | 2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1325-3041C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114614158 | ||||||
chr1:114614232
|
GA | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(90): Show | 96 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.1325-3116delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114614232 | ||||||
chr1:114614266
|
T | C | 17 | a0001c0006t0004g0059a0001c0006t0004g0060a0004c0004t0004g0049others(14): Show | 17 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.1325-3149A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114614266 | ||||||
chr1:114614293
|
G | A | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1325-3176C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114614293 | ||||||
chr1:114614440
|
T | C | 2 | a0001c0001t0001g0091a0007c0010t0007g0058 | 2 | HG02055.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1325-3323A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114614440 | ||||||
chr1:114614579
|
A | AT | 9 | a0004c0004t0004g0051a0004c0004t0004g0061a0004c0004t0004g0062others(6): Show | 9 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.1325-3463dupA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114614579 | ||||||
chr1:114614907
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1324+3479C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114614907 | ||||||
chr1:114615179
|
C | T | 1 | a0001c0001t0011g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1324+3207G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114615179 | ||||||
chr1:114615264
|
A | C | 2 | a0001c0001t0001g0155a0001c0001t0001g0157 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1324+3122T>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114615264 | ||||||
chr1:114615324
|
C | T | 3 | a0001c0001t0001g0075a0001c0001t0001g0085a0001c0001t0001g0091 | 3 | NA18986.hp2 NA19002.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1324+3062G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114615324 | ||||||
chr1:114615509
|
C | T | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1324+2877G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114615509 | ||||||
chr1:114615640
|
G | T | 1 | a0003c0003t0007g0286 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1324+2746C>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114615640 | ||||||
chr1:114615649
|
C | T | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1324+2737G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114615649 | ||||||
chr1:114615797
|
C | T | 1 | a0001c0013t0009g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1324+2589G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114615797 | ||||||
chr1:114615798
|
G | A | 1 | a0001c0011t0044g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1324+2588C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114615798 | ||||||
chr1:114615903
|
G | A | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1324+2483C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114615903 | ||||||
chr1:114615967
|
C | T | 17 | a0001c0006t0004g0059a0001c0006t0004g0060a0004c0004t0004g0049others(14): Show | 17 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.1324+2419G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114615967 | ||||||
chr1:114616178
|
T | C | 1 | a0007c0010t0007g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1324+2208A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114616178 | ||||||
chr1:114616274
|
C | T | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1324+2112G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114616274 | ||||||
chr1:114617066
|
C | T | 10 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(7): Show | 10 | HG01891.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1324+1320G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114617066 | ||||||
chr1:114617078
|
T | A | 3 | a0004c0004t0004g0049a0004c0004t0004g0050a0004c0004t0004g0070 | 3 | HG01433.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1324+1308A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114617078 | ||||||
chr1:114617081
|
C | G | 1 | a0001c0001t0008g0147 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1324+1305G>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114617081 | ||||||
chr1:114617212
|
C | T | 4 | a0001c0001t0024g0056a0001c0006t0004g0060a0006c0005t0022g0068others(1): Show | 4 | HG02257.hp1 HG02451.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324+1174G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114617212 | ||||||
chr1:114617307
|
CTTA | C | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1324+1076_1324+107 others(7): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114617307 | ||||||
chr1:114617609
|
GA | G | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1324+776delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114617609 | ||||||
chr1:114617657
|
C | CA | 25 | a0001c0001t0001g0124a0001c0001t0001g0230a0001c0001t0001g0231others(22): Show | 26 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1324+728dupT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114617657 | ||||||
chr1:114617736
|
GA | G | 7 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(4): Show | 7 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1324+649delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114617736 | ||||||
chr1:114617946
|
T | C | 1 | a0001c0001t0023g0047 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1324+440A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114617946 | ||||||
chr1:114617990
|
AT | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(129): Show | 135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1324+395delA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114617990 | ||||||
chr1:114618050
|
G | C | 13 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0032others(10): Show | 13 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.1324+336C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114618050 | ||||||
chr1:114618052
|
G | A | 12 | a0001c0001t0012g0046a0001c0001t0012g0052a0001c0001t0012g0054others(9): Show | 12 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1324+334C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114618052 | ||||||
chr1:114618337
|
C | G | 1 | a0001c0001t0045g0082 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1324+49G>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 8/20 | chr1 | 114618337 | ||||||
chr1:114618519
|
C | T | 22 | a0003c0003t0003g0007a0003c0003t0003g0270a0003c0003t0003g0271others(19): Show | 23 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1228-37G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 7/20 | chr1 | 114618519 | ||||||
chr1:114618880
|
T | C | 1 | a0001c0001t0002g0218 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1228-398A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 7/20 | chr1 | 114618880 | ||||||
chr1:114619118
|
T | C | 1 | a0001c0001t0002g0188 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1228-636A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 7/20 | chr1 | 114619118 | ||||||
chr1:114619248
|
G | A | 1 | a0004c0004t0004g0087 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1228-766C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 7/20 | chr1 | 114619248 | ||||||
chr1:114619331
|
TTAAG | T | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1228-853_1228-850d others(6): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 7/20 | chr1 | 114619331 | ||||||
chr1:114619894
|
C | G | 1 | a0001c0001t0002g0195 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1228-1412G>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 7/20 | chr1 | 114619894 | ||||||
chr1:114620202
|
C | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(66): Show | 72 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1227+1693G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 7/20 | chr1 | 114620202 | ||||||
chr1:114620224
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1227+1671A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 7/20 | chr1 | 114620224 | ||||||
chr1:114620228
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1227+1667T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 7/20 | chr1 | 114620228 | ||||||
chr1:114620636
|
G | C | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1227+1259C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 7/20 | chr1 | 114620636 | ||||||
chr1:114620767
|
A | G | 22 | a0003c0003t0003g0007a0003c0003t0003g0270a0003c0003t0003g0271others(19): Show | 23 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.1227+1128T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 7/20 | chr1 | 114620767 | ||||||
chr1:114620820
|
A | G | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1227+1075T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 7/20 | chr1 | 114620820 | ||||||
chr1:114621173
|
C | T | 15 | a0004c0004t0004g0049a0004c0004t0004g0050a0004c0004t0004g0051others(12): Show | 15 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.1227+722G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 7/20 | chr1 | 114621173 | ||||||
chr1:114621235
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1227+660G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 7/20 | chr1 | 114621235 | ||||||
chr1:114621251
|
T | C | 6 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0013g0025others(3): Show | 6 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1227+644A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 7/20 | chr1 | 114621251 | ||||||
chr1:114621788
|
A | T | 4 | a0001c0001t0001g0086a0001c0001t0001g0131a0001c0001t0001g0159others(1): Show | 4 | HG02486.hp1 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+107T>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 7/20 | chr1 | 114621788 | ||||||
chr1:114622185
|
C | G | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1057-120G>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 6/20 | chr1 | 114622185 | ||||||
chr1:114622219
|
T | A | 1 | a0001c0001t0036g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1057-154A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 6/20 | chr1 | 114622219 | ||||||
chr1:114622489
|
A | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1057-424T>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 6/20 | chr1 | 114622489 | ||||||
chr1:114622651
|
G | A | 2 | a0001c0001t0009g0014a0001c0001t0009g0016 | 2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1056+336C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 6/20 | chr1 | 114622651 | ||||||
chr1:114622851
|
T | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1056+136A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 6/20 | chr1 | 114622851 | ||||||
chr1:114623248
|
T | C | 3 | a0002c0002t0001g0246a0002c0002t0001g0251a0002c0002t0001g0257 | 3 | HG00099.hp1 HG00323.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.944-149A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 5/20 | chr1 | 114623248 | ||||||
chr1:114623729
|
ATTGT | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.807-90_807-87delAC others(2): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/20 | chr1 | 114623729 | ||||||
chr1:114623898
|
A | G | 37 | a0001c0001t0012g0046a0001c0001t0012g0052a0001c0001t0012g0054others(34): Show | 38 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.807-255T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/20 | chr1 | 114623898 | ||||||
chr1:114623924
|
T | G | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.807-281A>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/20 | chr1 | 114623924 | ||||||
chr1:114623942
|
G | A | 3 | a0001c0001t0002g0169a0001c0001t0002g0199a0001c0001t0002g0203 | 3 | HG00438.hp1 HG02135.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.807-299C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/20 | chr1 | 114623942 | ||||||
chr1:114624035
|
T | C | 8 | a0003c0003t0003g0007a0003c0003t0003g0270a0003c0003t0003g0271others(5): Show | 9 | HG00733.hp2 HG00741.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.807-392A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/20 | chr1 | 114624035 | ||||||
chr1:114624068
|
A | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0156 | 2 | HG03195.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.807-425T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/20 | chr1 | 114624068 | ||||||
chr1:114624193
|
T | C | 7 | a0001c0001t0012g0046a0001c0001t0012g0052a0001c0001t0012g0054others(4): Show | 7 | HG01099.hp1 HG02886.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.807-550A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/20 | chr1 | 114624193 | ||||||
chr1:114624468
|
C | CT | 146 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(143): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.806+710dupA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/20 | chr1 | 114624468 | ||||||
chr1:114624550
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.806+629G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/20 | chr1 | 114624550 | ||||||
chr1:114624624
|
CT | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(201): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.806+554delA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/20 | chr1 | 114624624 | ||||||
chr1:114624653
|
G | A | 2 | a0001c0001t0020g0008a0001c0001t0020g0009 | 2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.806+526C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/20 | chr1 | 114624653 | ||||||
chr1:114624725
|
G | A | 1 | a0002c0002t0001g0234 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.806+454C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/20 | chr1 | 114624725 | ||||||
chr1:114624779
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.806+400C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/20 | chr1 | 114624779 | ||||||
chr1:114624852
|
C | A | 1 | a0001c0001t0029g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.806+327G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/20 | chr1 | 114624852 | ||||||
chr1:114624903
|
G | A | 2 | a0001c0001t0002g0179a0001c0001t0002g0189 | 2 | NA19007.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.806+276C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/20 | chr1 | 114624903 | ||||||
chr1:114625104
|
T | C | 6 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(3): Show | 6 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.806+75A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/20 | chr1 | 114625104 | ||||||
chr1:114625118
|
A | C | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.806+61T>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/20 | chr1 | 114625118 | ||||||
chr1:114625145
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.806+34G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 4/20 | chr1 | 114625145 | ||||||
chr1:114626201
|
C | T | 22 | a0003c0003t0003g0007a0003c0003t0003g0270a0003c0003t0003g0271others(19): Show | 23 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.-204-13G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114626201 | ||||||
chr1:114626311
|
G | A | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-204-123C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114626311 | ||||||
chr1:114626447
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-204-259A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114626447 | ||||||
chr1:114626510
|
C | CT | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(136): Show | 142 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.-204-323dupA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114626510 | ||||||
chr1:114626510
|
C | CTT | 21 | a0001c0001t0001g0122a0001c0001t0001g0127a0001c0001t0001g0128others(18): Show | 22 | HG01358.hp2 HG01884.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-204-324_-204-323d others(4): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114626510 | ||||||
chr1:114626511
|
T | C | 1 | a0003c0003t0039g0285 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-204-323A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114626511 | ||||||
chr1:114627134
|
C | T | 1 | a0001c0001t0013g0034 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-204-946G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114627134 | ||||||
chr1:114627245
|
G | A | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(204): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-204-1057C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114627245 | ||||||
chr1:114627582
|
C | CA | 12 | a0001c0001t0002g0004a0001c0001t0002g0190a0001c0001t0002g0191others(9): Show | 13 | HG01346.hp1 HG01928.hp1 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.-204-1395dupT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114627582 | ||||||
chr1:114627582
|
CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0001g0081a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 6 | HG02486.hp2 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-204-1402_-204-139 others(12): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114627582 | ||||||
chr1:114627582
|
CAAAAAAA others(2): Show |
C | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(198): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.-204-1403_-204-139 others(13): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114627582 | ||||||
chr1:114627930
|
A | G | 1 | a0007c0010t0007g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-204-1742T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114627930 | ||||||
chr1:114627976
|
A | G | 1 | a0001c0001t0012g0224 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-204-1788T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114627976 | ||||||
chr1:114628279
|
C | A | 10 | a0001c0001t0001g0081a0001c0001t0001g0088a0001c0001t0001g0089others(7): Show | 10 | HG01496.hp1 HG01928.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.-204-2091G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114628279 | ||||||
chr1:114628306
|
C | T | 3 | a0001c0001t0020g0008a0001c0001t0020g0009a0001c0001t0021g0021 | 3 | HG01891.hp2 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-204-2118G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114628306 | ||||||
chr1:114628319
|
C | CA | 15 | a0001c0001t0001g0151a0001c0001t0001g0225a0001c0001t0009g0014others(12): Show | 15 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.-204-2132dupT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114628319 | ||||||
chr1:114628319
|
CA | C | 28 | a0001c0001t0001g0091a0001c0001t0001g0107a0001c0001t0001g0121others(25): Show | 29 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.-204-2132delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114628319 | ||||||
chr1:114628665
|
C | T | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-204-2477G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114628665 | ||||||
chr1:114628771
|
T | C | 1 | a0001c0013t0009g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-204-2583A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114628771 | ||||||
chr1:114628847
|
C | T | 1 | a0001c0013t0009g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-204-2659G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114628847 | ||||||
chr1:114628924
|
A | G | 1 | a0001c0001t0001g0133 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-204-2736T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114628924 | ||||||
chr1:114629028
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-204-2840G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114629028 | ||||||
chr1:114630052
|
C | T | 1 | a0007c0010t0007g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-204-3864G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114630052 | ||||||
chr1:114630053
|
G | A | 2 | a0004c0004t0004g0071a0004c0004t0004g0072 | 2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-204-3865C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114630053 | ||||||
chr1:114630094
|
C | A | 1 | a0004c0004t0004g0064 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-204-3906G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114630094 | ||||||
chr1:114630155
|
A | G | 1 | a0001c0001t0027g0100 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-204-3967T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114630155 | ||||||
chr1:114630170
|
T | G | 1 | a0001c0001t0002g0211 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-204-3982A>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114630170 | ||||||
chr1:114630216
|
G | A | 2 | a0002c0002t0001g0242a0002c0002t0041g0258 | 2 | HG00140.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-204-4028C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114630216 | ||||||
chr1:114630295
|
A | G | 2 | a0001c0006t0004g0059a0001c0006t0004g0060 | 2 | HG02698.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-204-4107T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114630295 | ||||||
chr1:114630378
|
G | A | 1 | a0001c0001t0029g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-204-4190C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114630378 | ||||||
chr1:114630513
|
CAG | C | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-204-4327_-204-432 others(6): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114630513 | ||||||
chr1:114630516
|
G | C | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-204-4328C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114630516 | ||||||
chr1:114630517
|
T | C | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-204-4329A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114630517 | ||||||
chr1:114630518
|
C | T | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-204-4330G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114630518 | ||||||
chr1:114630735
|
T | C | 1 | a0001c0001t0024g0223 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-204-4547A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114630735 | ||||||
chr1:114630924
|
A | G | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-204-4736T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114630924 | ||||||
chr1:114630936
|
C | T | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-204-4748G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114630936 | ||||||
chr1:114631037
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-204-4849T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114631037 | ||||||
chr1:114631474
|
G | A | 1 | a0001c0011t0044g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-204-5286C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114631474 | ||||||
chr1:114631579
|
C | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(144): Show | 150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.-204-5391G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114631579 | ||||||
chr1:114631580
|
G | A | 1 | a0001c0013t0009g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-204-5392C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114631580 | ||||||
chr1:114631692
|
G | T | 12 | a0001c0001t0012g0046a0001c0001t0012g0052a0001c0001t0012g0054others(9): Show | 12 | HG01099.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-204-5504C>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114631692 | ||||||
chr1:114632047
|
G | C | 1 | a0001c0001t0002g0193 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-204-5859C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114632047 | ||||||
chr1:114632087
|
C | CT | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-204-5900dupA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114632087 | ||||||
chr1:114632222
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-204-6034G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114632222 | ||||||
chr1:114632223
|
G | C | 2 | a0002c0002t0001g0243a0002c0002t0001g0252 | 2 | HG02155.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.-204-6035C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114632223 | ||||||
chr1:114632417
|
A | T | 4 | a0001c0001t0002g0215a0001c0001t0002g0217a0001c0001t0002g0218others(1): Show | 4 | HG01928.hp1 HG01934.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-6229T>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114632417 | ||||||
chr1:114632642
|
T | A | 1 | a0001c0011t0044g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-204-6454A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114632642 | ||||||
chr1:114632734
|
G | GT | 10 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-204-6547dupA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114632734 | ||||||
chr1:114632794
|
G | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(131): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.-204-6606C>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114632794 | ||||||
chr1:114633119
|
T | G | 1 | a0001c0001t0040g0057 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-204-6931A>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114633119 | ||||||
chr1:114633201
|
CT | C | 3 | a0001c0001t0020g0008a0001c0001t0020g0009a0001c0001t0021g0021 | 3 | HG01891.hp2 HG02572.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-204-7014delA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114633201 | ||||||
chr1:114633274
|
G | A | 4 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0228others(1): Show | 4 | HG02622.hp2 HG02818.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-7086C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114633274 | ||||||
chr1:114633319
|
C | A | 17 | a0001c0006t0004g0059a0001c0006t0004g0060a0004c0004t0004g0049others(14): Show | 17 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.-204-7131G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114633319 | ||||||
chr1:114633422
|
AGAGT | A | 11 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0032others(8): Show | 11 | HG00323.hp2 HG01167.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.-204-7238_-204-723 others(8): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114633422 | ||||||
chr1:114633439
|
C | CA | 14 | a0001c0001t0001g0109a0001c0001t0001g0144a0001c0001t0001g0145others(11): Show | 14 | HG00642.hp1 HG00741.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.-204-7252dupT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114633439 | ||||||
chr1:114633439
|
C | CAAAA | 7 | a0001c0001t0012g0046a0001c0001t0012g0052a0001c0001t0012g0054others(4): Show | 7 | HG01099.hp1 HG02258.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-204-7255_-204-725 others(8): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114633439 | ||||||
chr1:114633439
|
CA | C | 32 | a0001c0001t0001g0080a0001c0001t0001g0104a0001c0001t0001g0125others(29): Show | 32 | HG00323.hp2 HG00544.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-204-7252delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114633439 | ||||||
chr1:114633456
|
A | AG | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-204-7269_-204-726 others(5): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114633456 | ||||||
chr1:114633457
|
A | G | 1 | a0001c0001t0021g0021 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-204-7269T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114633457 | ||||||
chr1:114633467
|
A | G | 1 | a0001c0001t0016g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-204-7279T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114633467 | ||||||
chr1:114633468
|
AGAAG | A | 4 | a0001c0001t0001g0148a0001c0001t0001g0228a0001c0001t0008g0147others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-204-7284_-204-728 others(8): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114633468 | ||||||
chr1:114633469
|
G | A | 1 | a0001c0001t0016g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-204-7281C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114633469 | ||||||
chr1:114633472
|
G | A | 1 | a0001c0001t0016g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-204-7284C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114633472 | ||||||
chr1:114633485
|
G | A | 1 | a0007c0010t0007g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-204-7297C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114633485 | ||||||
chr1:114633838
|
GCAAAGAT others(3): Show |
G | 1 | a0001c0001t0002g0176 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-204-7660_-204-765 others(14): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114633838 | ||||||
chr1:114633965
|
G | A | 1 | a0007c0010t0007g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-204-7777C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114633965 | ||||||
chr1:114634105
|
T | C | 5 | a0001c0001t0001g0109a0001c0001t0001g0117a0001c0001t0001g0230others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.-204-7917A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114634105 | ||||||
chr1:114634164
|
A | C | 17 | a0001c0006t0004g0059a0001c0006t0004g0060a0004c0004t0004g0049others(14): Show | 17 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.-204-7976T>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114634164 | ||||||
chr1:114634263
|
T | C | 2 | a0001c0001t0001g0155a0001c0001t0001g0157 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-204-8075A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114634263 | ||||||
chr1:114634402
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-204-8214G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114634402 | ||||||
chr1:114634745
|
C | T | 1 | a0001c0001t0013g0025 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-204-8557G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114634745 | ||||||
chr1:114634894
|
G | A | 1 | a0001c0001t0037g0033 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-204-8706C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114634894 | ||||||
chr1:114635002
|
T | C | 1 | a0002c0002t0001g0253 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-204-8814A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114635002 | ||||||
chr1:114635026
|
T | TA | 24 | a0001c0001t0001g0080a0001c0001t0001g0119a0002c0002t0001g0233others(21): Show | 24 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.-204-8839dupT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114635026 | ||||||
chr1:114635026
|
T | TAA | 9 | a0002c0002t0001g0041a0002c0002t0001g0242a0002c0002t0001g0259others(6): Show | 9 | HG00140.hp2 HG00733.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.-204-8840_-204-883 others(6): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114635026 | ||||||
chr1:114635041
|
A | G | 13 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0032others(10): Show | 13 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.-204-8853T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114635041 | ||||||
chr1:114635083
|
A | G | 1 | a0002c0002t0035g0248 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-204-8895T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114635083 | ||||||
chr1:114635150
|
T | C | 3 | a0002c0002t0015g0244a0002c0002t0015g0245a0002c0002t0038g0254 | 3 | HG00733.hp1 HG01192.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-204-8962A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114635150 | ||||||
chr1:114635380
|
C | CA | 22 | a0003c0003t0003g0007a0003c0003t0003g0270a0003c0003t0003g0271others(19): Show | 23 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.-204-9193dupT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114635380 | ||||||
chr1:114635420
|
T | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-204-9232A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114635420 | ||||||
chr1:114635433
|
C | T | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-204-9245G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114635433 | ||||||
chr1:114635649
|
A | G | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-204-9461T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114635649 | ||||||
chr1:114635695
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-204-9507C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114635695 | ||||||
chr1:114635805
|
G | A | 3 | a0001c0001t0001g0075a0001c0001t0001g0085a0001c0001t0001g0091 | 3 | NA18986.hp2 NA19002.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-204-9617C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114635805 | ||||||
chr1:114635834
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG02559.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-205+9614C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114635834 | ||||||
chr1:114635867
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-205+9581T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114635867 | ||||||
chr1:114635875
|
G | A | 1 | a0001c0001t0036g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-205+9573C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114635875 | ||||||
chr1:114635948
|
T | C | 1 | a0001c0001t0048g0160 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-205+9500A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114635948 | ||||||
chr1:114636151
|
T | C | 1 | a0001c0001t0024g0056 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-205+9297A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114636151 | ||||||
chr1:114636354
|
T | C | 4 | a0001c0001t0002g0205a0001c0001t0002g0207a0001c0001t0002g0208others(1): Show | 4 | NA18747.hp2 NA18945.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.-205+9094A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114636354 | ||||||
chr1:114636472
|
C | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0132 | 3 | HG01884.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-205+8976G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114636472 | ||||||
chr1:114636658
|
C | A | 1 | a0002c0002t0001g0246 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-205+8790G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114636658 | ||||||
chr1:114636750
|
GT | G | 13 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0032others(10): Show | 13 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.-205+8697delA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114636750 | ||||||
chr1:114636839
|
T | C | 9 | a0004c0004t0004g0051a0004c0004t0004g0061a0004c0004t0004g0062others(6): Show | 9 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.-205+8609A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114636839 | ||||||
chr1:114636880
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-205+8568G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114636880 | ||||||
chr1:114636945
|
A | G | 1 | a0001c0011t0044g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-205+8503T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114636945 | ||||||
chr1:114637105
|
C | CA | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(213): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.-205+8342dupT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114637105 | ||||||
chr1:114637309
|
T | C | 1 | a0001c0001t0002g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-205+8139A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114637309 | ||||||
chr1:114637369
|
CA | C | 30 | a0001c0001t0002g0176a0001c0001t0009g0014a0001c0001t0009g0016others(27): Show | 30 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(27): Show |
intron_variant | MODIFIER | c.-205+8078delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114637369 | ||||||
chr1:114637369
|
CAAAAAA | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(145): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.-205+8073_-205+807 others(10): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114637369 | ||||||
chr1:114637384
|
A | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(145): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.-205+8064T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114637384 | ||||||
chr1:114637864
|
C | G | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-205+7584G>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114637864 | ||||||
chr1:114638005
|
C | T | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-205+7443G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114638005 | ||||||
chr1:114638027
|
T | C | 1 | a0001c0001t0036g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-205+7421A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114638027 | ||||||
chr1:114638051
|
T | C | 37 | a0001c0001t0012g0046a0001c0001t0012g0052a0001c0001t0012g0054others(34): Show | 38 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.-205+7397A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114638051 | ||||||
chr1:114638247
|
C | T | 1 | a0001c0001t0002g0178 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-205+7201G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114638247 | ||||||
chr1:114638254
|
C | T | 1 | a0001c0011t0044g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-205+7194G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114638254 | ||||||
chr1:114638507
|
C | T | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-205+6941G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114638507 | ||||||
chr1:114638511
|
C | T | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-205+6937G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114638511 | ||||||
chr1:114638628
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-205+6820G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114638628 | ||||||
chr1:114638762
|
CA | C | 94 | a0001c0001t0001g0091a0001c0001t0001g0094a0001c0001t0001g0095others(91): Show | 96 | HG00099.hp2 HG00323.hp2 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.-205+6685delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114638762 | ||||||
chr1:114638778
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-205+6670T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114638778 | ||||||
chr1:114638958
|
TA | T | 14 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0032others(11): Show | 14 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.-205+6489delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114638958 | ||||||
chr1:114638986
|
T | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-205+6462A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114638986 | ||||||
chr1:114639222
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-205+6226G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114639222 | ||||||
chr1:114639310
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-205+6138C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114639310 | ||||||
chr1:114639346
|
T | C | 1 | a0001c0001t0051g0073 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-205+6102A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114639346 | ||||||
chr1:114639463
|
T | A | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-205+5985A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114639463 | ||||||
chr1:114639583
|
GA | G | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(145): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.-205+5864delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114639583 | ||||||
chr1:114639689
|
C | T | 1 | a0002c0002t0015g0244 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-205+5759G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114639689 | ||||||
chr1:114639712
|
A | AT | 7 | a0001c0001t0001g0232a0001c0001t0010g0105a0001c0001t0010g0106others(4): Show | 7 | HG01496.hp1 HG01928.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.-205+5735dupA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114639712 | ||||||
chr1:114639778
|
C | T | 2 | a0001c0001t0014g0078a0001c0001t0014g0079 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-205+5670G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114639778 | ||||||
chr1:114640246
|
G | A | 2 | a0003c0003t0003g0275a0003c0003t0007g0288 | 2 | HG01099.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.-205+5202C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114640246 | ||||||
chr1:114640265
|
C | T | 1 | a0001c0001t0002g0175 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-205+5183G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114640265 | ||||||
chr1:114640554
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-205+4894G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114640554 | ||||||
chr1:114640562
|
G | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-205+4886C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114640562 | ||||||
chr1:114640589
|
G | A | 3 | a0001c0001t0001g0148a0001c0001t0001g0228a0001c0001t0008g0147 | 3 | HG02622.hp2 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-205+4859C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114640589 | ||||||
chr1:114640657
|
C | T | 2 | a0001c0001t0014g0078a0001c0001t0014g0079 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-205+4791G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114640657 | ||||||
chr1:114641103
|
C | T | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-205+4345G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114641103 | ||||||
chr1:114641211
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(220): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.-205+4237A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114641211 | ||||||
chr1:114641260
|
CA | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(197): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.-205+4187delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114641260 | ||||||
chr1:114641596
|
C | G | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-205+3852G>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114641596 | ||||||
chr1:114641847
|
G | A | 1 | a0004c0004t0004g0087 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-205+3601C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114641847 | ||||||
chr1:114641920
|
C | T | 1 | a0007c0010t0007g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-205+3528G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114641920 | ||||||
chr1:114641963
|
A | T | 17 | a0001c0001t0002g0004a0001c0001t0002g0172a0001c0006t0004g0060others(14): Show | 18 | HG01192.hp1 HG01261.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.-205+3485T>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114641963 | ||||||
chr1:114642198
|
G | A | 1 | a0009c0009t0002g0209 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-205+3250C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114642198 | ||||||
chr1:114643085
|
T | C | 2 | a0001c0001t0001g0155a0001c0001t0001g0157 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-205+2363A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114643085 | ||||||
chr1:114643302
|
G | A | 31 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0032others(28): Show | 32 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.-205+2146C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114643302 | ||||||
chr1:114643547
|
A | G | 1 | a0001c0001t0023g0048 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-205+1901T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114643547 | ||||||
chr1:114643850
|
T | TA | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-205+1597dupT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114643850 | ||||||
chr1:114644344
|
A | G | 14 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-205+1104T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114644344 | ||||||
chr1:114644420
|
T | C | 1 | a0001c0001t0043g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-205+1028A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114644420 | ||||||
chr1:114644472
|
C | T | 1 | a0001c0001t0029g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-205+976G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114644472 | ||||||
chr1:114644740
|
C | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-205+708G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114644740 | ||||||
chr1:114644763
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-205+685G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114644763 | ||||||
chr1:114644867
|
T | C | 1 | a0001c0001t0024g0223 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-205+581A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114644867 | ||||||
chr1:114644962
|
A | C | 37 | a0001c0001t0012g0046a0001c0001t0012g0052a0001c0001t0012g0054others(34): Show | 38 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.-205+486T>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114644962 | ||||||
chr1:114645020
|
A | G | 1 | a0001c0001t0029g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-205+428T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114645020 | ||||||
chr1:114645025
|
T | C | 2 | a0001c0001t0002g0196a0001c0001t0002g0197 | 2 | NA18957.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.-205+423A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114645025 | ||||||
chr1:114645067
|
A | T | 1 | a0001c0001t0001g0135 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-205+381T>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114645067 | ||||||
chr1:114645176
|
G | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(148): Show | 155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.-205+272C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114645176 | ||||||
chr1:114645261
|
G | A | 2 | a0002c0002t0001g0291a0002c0002t0001g0292 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-205+187C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 3/20 | chr1 | 114645261 | ||||||
chr1:114645866
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-316-307A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114645866 | ||||||
chr1:114645994
|
T | C | 35 | a0002c0002t0001g0041a0002c0002t0001g0233a0002c0002t0001g0234others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(32): Show |
intron_variant | MODIFIER | c.-316-435A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114645994 | ||||||
chr1:114646019
|
C | T | 1 | a0001c0011t0044g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-316-460G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114646019 | ||||||
chr1:114646071
|
C | T | 8 | a0003c0003t0003g0007a0003c0003t0003g0270a0003c0003t0003g0271others(5): Show | 9 | HG00733.hp2 HG00741.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.-316-512G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114646071 | ||||||
chr1:114646098
|
T | G | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-316-539A>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114646098 | ||||||
chr1:114646256
|
C | T | 1 | a0002c0002t0001g0246 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-316-697G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114646256 | ||||||
chr1:114646287
|
T | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-316-728A>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114646287 | ||||||
chr1:114646296
|
G | C | 2 | a0001c0001t0001g0110a0001c0001t0001g0229 | 2 | NA18612.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-316-737C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114646296 | ||||||
chr1:114646519
|
T | C | 1 | a0003c0003t0003g0273 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-316-960A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114646519 | ||||||
chr1:114646594
|
G | A | 8 | a0001c0001t0012g0046a0001c0001t0012g0052a0001c0001t0012g0054others(5): Show | 8 | HG01099.hp1 HG02258.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-316-1035C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114646594 | ||||||
chr1:114646863
|
A | G | 4 | a0002c0002t0001g0259a0002c0002t0015g0244a0002c0002t0015g0245others(1): Show | 4 | HG00733.hp1 HG00735.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.-316-1304T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114646863 | ||||||
chr1:114646986
|
CCT | C | 4 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0228others(1): Show | 4 | HG02622.hp2 HG02818.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-316-1429_-316-142 others(6): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114646986 | ||||||
chr1:114647161
|
T | TA | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(131): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.-316-1603dupT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114647161 | ||||||
chr1:114647172
|
AG | A | 4 | a0001c0001t0002g0174a0001c0001t0002g0215a0001c0001t0047g0206others(1): Show | 4 | HG01975.hp2 HG01993.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-316-1614delC | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114647172 | ||||||
chr1:114647173
|
G | A | 281 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(278): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.-316-1614C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114647173 | ||||||
chr1:114647177
|
G | A | 5 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(2): Show | 6 | HG00323.hp1 HG02280.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-316-1618C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114647177 | ||||||
chr1:114647345
|
T | C | 2 | a0002c0002t0001g0242a0002c0002t0041g0258 | 2 | HG00140.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-316-1786A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114647345 | ||||||
chr1:114647359
|
AT | A | 9 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0132others(6): Show | 10 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-316-1801delA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114647359 | ||||||
chr1:114647409
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(148): Show | 155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.-316-1850C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114647409 | ||||||
chr1:114647493
|
T | C | 2 | a0001c0001t0019g0011a0001c0001t0019g0012 | 2 | HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-316-1934A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114647493 | ||||||
chr1:114647542
|
C | T | 1 | a0001c0001t0047g0206 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-316-1983G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114647542 | ||||||
chr1:114647712
|
C | A | 1 | a0001c0006t0004g0060 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-316-2153G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114647712 | ||||||
chr1:114648302
|
A | G | 14 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0032others(11): Show | 14 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.-316-2743T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114648302 | ||||||
chr1:114648308
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-316-2749T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114648308 | ||||||
chr1:114648390
|
C | A | 1 | a0001c0001t0002g0199 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-316-2831G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114648390 | ||||||
chr1:114648407
|
G | C | 1 | a0001c0001t0008g0143 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-316-2848C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114648407 | ||||||
chr1:114648595
|
C | T | 14 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0032others(11): Show | 14 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.-316-3036G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114648595 | ||||||
chr1:114648868
|
T | A | 1 | a0001c0001t0001g0084 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-316-3309A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114648868 | ||||||
chr1:114649010
|
A | G | 1 | a0001c0001t0011g0045 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-316-3451T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114649010 | ||||||
chr1:114649079
|
C | T | 1 | a0001c0001t0024g0056 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-316-3520G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114649079 | ||||||
chr1:114649100
|
G | A | 1 | a0003c0003t0007g0286 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-316-3541C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114649100 | ||||||
chr1:114649120
|
A | G | 1 | a0001c0011t0044g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-316-3561T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114649120 | ||||||
chr1:114649146
|
G | C | 37 | a0001c0001t0012g0046a0001c0001t0012g0052a0001c0001t0012g0054others(34): Show | 38 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.-316-3587C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114649146 | ||||||
chr1:114649216
|
A | G | 1 | a0007c0010t0007g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-316-3657T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114649216 | ||||||
chr1:114649282
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-316-3723A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114649282 | ||||||
chr1:114649366
|
G | C | 1 | a0007c0010t0007g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-316-3807C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114649366 | ||||||
chr1:114649419
|
T | C | 1 | a0001c0001t0002g0200 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-316-3860A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114649419 | ||||||
chr1:114649530
|
C | T | 1 | a0001c0001t0029g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-316-3971G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114649530 | ||||||
chr1:114649567
|
A | G | 1 | a0001c0001t0002g0212 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-316-4008T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114649567 | ||||||
chr1:114649810
|
A | T | 1 | a0001c0001t0001g0135 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-316-4251T>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114649810 | ||||||
chr1:114649818
|
G | A | 1 | a0001c0001t0001g0135 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-316-4259C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114649818 | ||||||
chr1:114649819
|
T | G | 1 | a0001c0001t0001g0135 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-316-4260A>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114649819 | ||||||
chr1:114649893
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-316-4334A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114649893 | ||||||
chr1:114650264
|
A | T | 1 | a0001c0001t0001g0135 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-317+4241T>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114650264 | ||||||
chr1:114650323
|
TA | T | 20 | a0001c0001t0001g0076a0001c0001t0002g0172a0001c0001t0017g0020others(17): Show | 20 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-317+4181delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114650323 | ||||||
chr1:114650354
|
T | C | 1 | a0007c0010t0007g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-317+4151A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114650354 | ||||||
chr1:114650403
|
G | A | 1 | a0001c0001t0024g0223 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-317+4102C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114650403 | ||||||
chr1:114650430
|
C | T | 56 | a0001c0001t0012g0046a0001c0001t0012g0052a0001c0001t0012g0054others(53): Show | 57 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.-317+4075G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114650430 | ||||||
chr1:114650567
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-317+3938T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114650567 | ||||||
chr1:114650630
|
C | T | 2 | a0001c0001t0001g0103a0001c0011t0044g0227 | 2 | HG00741.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-317+3875G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114650630 | ||||||
chr1:114650657
|
G | C | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-317+3848C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114650657 | ||||||
chr1:114650673
|
C | CA | 148 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(145): Show | 151 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.-317+3831dupT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114650673 | ||||||
chr1:114650673
|
C | CAA | 10 | a0001c0001t0001g0096a0001c0001t0001g0099a0001c0001t0001g0120others(7): Show | 10 | HG00140.hp2 HG00558.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.-317+3830_-317+383 others(6): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114650673 | ||||||
chr1:114650673
|
CA | C | 13 | a0001c0001t0002g0171a0001c0001t0002g0204a0001c0001t0002g0205others(10): Show | 14 | HG00733.hp2 HG00741.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.-317+3831delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114650673 | ||||||
chr1:114650759
|
T | C | 17 | a0001c0006t0004g0059a0001c0006t0004g0060a0004c0004t0004g0049others(14): Show | 17 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.-317+3746A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114650759 | ||||||
chr1:114650928
|
T | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-317+3577A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114650928 | ||||||
chr1:114650958
|
C | T | 3 | a0002c0002t0001g0242a0002c0002t0008g0241a0002c0002t0041g0258 | 3 | HG00140.hp2 HG01071.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-317+3547G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114650958 | ||||||
chr1:114650982
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(128): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.-317+3523C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114650982 | ||||||
chr1:114651057
|
C | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(204): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-317+3448G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114651057 | ||||||
chr1:114651174
|
A | C | 1 | a0001c0001t0001g0129 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-317+3331T>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114651174 | ||||||
chr1:114651276
|
T | TAC | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(127): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.-317+3227_-317+322 others(6): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114651276 | ||||||
chr1:114651276
|
T | TACAC | 52 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0101others(49): Show | 53 | HG00099.hp2 HG00544.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.-317+3225_-317+322 others(8): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114651276 | ||||||
chr1:114651276
|
T | TACACAC | 14 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0032others(11): Show | 14 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.-317+3223_-317+322 others(10): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114651276 | ||||||
chr1:114651276
|
T | TACACACA others(1): Show |
3 | a0001c0001t0013g0025a0001c0014t0006g0026a0003c0003t0003g0272 | 3 | HG00323.hp2 HG01123.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.-317+3221_-317+322 others(12): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114651276 | ||||||
chr1:114651276
|
T | TACACACA others(3): Show |
1 | a0001c0001t0021g0021 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-317+3219_-317+322 others(14): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114651276 | ||||||
chr1:114651276
|
T | TACACACA others(9): Show |
8 | a0001c0001t0009g0014a0001c0001t0009g0017a0001c0001t0009g0018others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-317+3213_-317+322 others(20): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114651276 | ||||||
chr1:114651276
|
T | TACACACA others(11): Show |
4 | a0001c0001t0009g0016a0001c0001t0019g0011a0001c0001t0019g0012others(1): Show | 4 | HG01884.hp2 HG02145.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-317+3211_-317+322 others(22): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114651276 | ||||||
chr1:114651305
|
A | G | 1 | a0001c0001t0029g0055 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-317+3200T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114651305 | ||||||
chr1:114651455
|
A | T | 1 | a0001c0001t0001g0089 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-317+3050T>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114651455 | ||||||
chr1:114651671
|
G | A | 1 | a0001c0001t0002g0164 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-317+2834C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114651671 | ||||||
chr1:114651753
|
G | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-317+2752C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114651753 | ||||||
chr1:114651817
|
T | G | 1 | a0001c0001t0001g0091 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-317+2688A>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114651817 | ||||||
chr1:114651818
|
A | C | 1 | a0001c0001t0001g0091 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-317+2687T>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114651818 | ||||||
chr1:114651871
|
T | C | 1 | a0002c0002t0001g0255 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-317+2634A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114651871 | ||||||
chr1:114652036
|
G | T | 39 | a0001c0001t0012g0046a0001c0001t0012g0052a0001c0001t0012g0054others(36): Show | 40 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-317+2469C>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114652036 | ||||||
chr1:114652240
|
T | C | 1 | a0001c0001t0013g0034 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-317+2265A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114652240 | ||||||
chr1:114652605
|
A | T | 1 | a0001c0001t0001g0135 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-317+1900T>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114652605 | ||||||
chr1:114652608
|
T | A | 1 | a0001c0001t0001g0135 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-317+1897A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114652608 | ||||||
chr1:114652609
|
G | T | 1 | a0001c0001t0001g0135 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-317+1896C>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114652609 | ||||||
chr1:114652613
|
T | G | 1 | a0001c0001t0001g0135 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-317+1892A>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114652613 | ||||||
chr1:114652661
|
CT | C | 15 | a0001c0001t0001g0101a0001c0001t0002g0006a0001c0001t0002g0204others(12): Show | 16 | HG00558.hp2 HG03834.hp1 HG04115.hp1 others(13): Show |
intron_variant | MODIFIER | c.-317+1843delA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114652661 | ||||||
chr1:114652661
|
CTT | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(121): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.-317+1842_-317+184 others(6): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114652661 | ||||||
chr1:114652661
|
CTTT | C | 50 | a0001c0001t0001g0085a0001c0001t0001g0117a0001c0001t0001g0118others(47): Show | 51 | HG00323.hp1 HG00323.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.-317+1841_-317+184 others(7): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114652661 | ||||||
chr1:114652661
|
CTTTTTTT others(3): Show |
C | 36 | a0001c0001t0012g0052a0001c0001t0012g0054a0001c0001t0012g0224others(33): Show | 37 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.-317+1834_-317+184 others(14): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114652661 | ||||||
chr1:114652661
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0012g0046 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-317+1833_-317+184 others(15): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114652661 | ||||||
chr1:114652711
|
C | A | 3 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045 | 4 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-317+1794G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114652711 | ||||||
chr1:114652766
|
T | G | 1 | a0001c0001t0001g0080 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-317+1739A>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114652766 | ||||||
chr1:114652782
|
A | G | 1 | a0004c0004t0004g0049 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-317+1723T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114652782 | ||||||
chr1:114652854
|
C | T | 1 | a0007c0010t0007g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-317+1651G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114652854 | ||||||
chr1:114653003
|
A | T | 1 | a0001c0001t0001g0135 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-317+1502T>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114653003 | ||||||
chr1:114653033
|
C | T | 1 | a0007c0010t0007g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-317+1472G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114653033 | ||||||
chr1:114653087
|
A | T | 1 | a0001c0001t0001g0135 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-317+1418T>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114653087 | ||||||
chr1:114653088
|
T | A | 1 | a0001c0001t0001g0135 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-317+1417A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114653088 | ||||||
chr1:114653089
|
A | T | 1 | a0001c0001t0001g0135 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-317+1416T>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114653089 | ||||||
chr1:114653204
|
G | T | 4 | a0001c0001t0002g0167a0001c0001t0002g0212a0001c0001t0005g0168others(1): Show | 4 | NA18988.hp1 NA18989.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.-317+1301C>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114653204 | ||||||
chr1:114653394
|
C | A | 9 | a0004c0004t0004g0051a0004c0004t0004g0061a0004c0004t0004g0062others(6): Show | 9 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.-317+1111G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114653394 | ||||||
chr1:114653400
|
C | T | 15 | a0004c0004t0004g0049a0004c0004t0004g0050a0004c0004t0004g0051others(12): Show | 15 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.-317+1105G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114653400 | ||||||
chr1:114653453
|
A | T | 1 | a0001c0001t0001g0135 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-317+1052T>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114653453 | ||||||
chr1:114653533
|
C | T | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-317+972G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114653533 | ||||||
chr1:114653545
|
A | G | 39 | a0001c0001t0016g0237a0001c0001t0016g0238a0001c0001t0026g0264others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(36): Show |
intron_variant | MODIFIER | c.-317+960T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114653545 | ||||||
chr1:114654008
|
A | G | 1 | a0001c0001t0011g0043 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-317+497T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114654008 | ||||||
chr1:114654026
|
T | C | 1 | a0001c0001t0021g0021 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-317+479A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114654026 | ||||||
chr1:114654258
|
C | A | 1 | a0001c0001t0001g0138 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-317+247G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114654258 | ||||||
chr1:114654271
|
A | C | 1 | a0001c0001t0001g0135 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-317+234T>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114654271 | ||||||
chr1:114654293
|
G | A | 2 | a0001c0001t0020g0008a0001c0001t0020g0009 | 2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-317+212C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114654293 | ||||||
chr1:114654495
|
G | T | 1 | a0001c0001t0020g0008 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-317+10C>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 2/20 | chr1 | 114654495 | ||||||
chr1:114654763
|
T | C | 1 | a0001c0001t0002g0211 | 1 | HG01168.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.-573-2A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114654763 | ||||||
chr1:114654763
|
T | TA | 24 | a0001c0001t0001g0084a0001c0001t0001g0119a0001c0001t0011g0002others(21): Show | 25 | HG00735.hp2 HG01192.hp1 HG01257.hp1 others(22): Show |
splice_region_variant&intron_variant | LOW | c.-573-3dupT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114654763 | ||||||
chr1:114654763
|
TA | T | 7 | a0001c0001t0001g0097a0001c0001t0001g0135a0001c0001t0001g0146others(4): Show | 7 | HG01496.hp1 HG03704.hp2 NA18942.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.-573-3delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114654763 | ||||||
chr1:114654763
|
TAA | T | 10 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.-573-4_-573-3delTT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114654763 | ||||||
chr1:114654780
|
A | T | 2 | a0001c0001t0019g0011a0001c0001t0019g0012 | 2 | HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-573-19T>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114654780 | ||||||
chr1:114654967
|
T | G | 1 | a0002c0002t0041g0258 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-573-206A>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114654967 | ||||||
chr1:114655016
|
T | A | 1 | a0001c0001t0001g0135 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-573-255A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655016 | ||||||
chr1:114655024
|
C | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0145 | 2 | HG02486.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-573-263G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655024 | ||||||
chr1:114655104
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-573-343A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655104 | ||||||
chr1:114655264
|
C | G | 1 | a0002c0002t0001g0239 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-573-503G>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655264 | ||||||
chr1:114655609
|
G | A | 2 | a0001c0001t0020g0008a0001c0001t0020g0009 | 2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-573-848C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655609 | ||||||
chr1:114655867
|
TATATATA others(9): Show |
T | 22 | a0003c0003t0003g0007a0003c0003t0003g0270a0003c0003t0003g0271others(19): Show | 23 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.-573-1122_-573-110 others(20): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655867 | ||||||
chr1:114655875
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-573-1114A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655875 | ||||||
chr1:114655877
|
T | A | 2 | a0001c0001t0009g0017a0001c0001t0009g0018 | 2 | HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-573-1116A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655877 | ||||||
chr1:114655878
|
G | A | 2 | a0001c0001t0009g0017a0001c0001t0009g0018 | 2 | HG02886.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-573-1117C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655878 | ||||||
chr1:114655878
|
G | GTA | 3 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0034g0139 | 3 | HG00609.hp1 NA19055.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-573-1119_-573-111 others(6): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655878 | ||||||
chr1:114655878
|
G | GTATATAT others(3): Show |
3 | a0001c0001t0001g0085a0001c0001t0001g0099a0001c0001t0001g0229 | 3 | HG04199.hp1 NA18986.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-573-1118_-573-111 others(14): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655878 | ||||||
chr1:114655878
|
G | GTATATAT others(5): Show |
30 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0084others(27): Show | 30 | HG00544.hp1 HG01081.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.-573-1118_-573-111 others(16): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655878 | ||||||
chr1:114655878
|
G | GTATATAT others(7): Show |
20 | a0001c0001t0001g0001a0001c0001t0001g0080a0001c0001t0001g0090others(17): Show | 22 | HG00642.hp2 HG01074.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.-573-1118_-573-111 others(18): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655878 | ||||||
chr1:114655878
|
G | GTATATAT others(9): Show |
17 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0081others(14): Show | 18 | HG01070.hp1 HG01071.hp2 HG02723.hp2 others(15): Show |
intron_variant | MODIFIER | c.-573-1118_-573-111 others(20): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655878 | ||||||
chr1:114655878
|
G | GTATATAT others(13): Show |
4 | a0001c0001t0001g0129a0001c0001t0001g0154a0001c0001t0001g0157others(1): Show | 4 | HG00438.hp2 HG02055.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-573-1118_-573-111 others(24): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655878 | ||||||
chr1:114655878
|
G | GTATATAT others(15): Show |
1 | a0001c0001t0001g0155 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-573-1118_-573-111 others(26): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655878 | ||||||
chr1:114655878
|
G | GTGTATAT others(17): Show |
1 | a0001c0001t0001g0130 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-573-1118_-573-111 others(28): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655878 | ||||||
chr1:114655883
|
A | AATAT | 4 | a0001c0001t0019g0011a0001c0001t0019g0012a0001c0001t0021g0021others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-573-1126_-573-112 others(8): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655883 | ||||||
chr1:114655883
|
A | AATATAT | 39 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0032others(36): Show | 40 | HG00323.hp2 HG00735.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.-573-1128_-573-112 others(10): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655883 | ||||||
chr1:114655883
|
A | AATATATA others(1): Show |
36 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0008g0143others(33): Show | 36 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(33): Show |
intron_variant | MODIFIER | c.-573-1130_-573-112 others(12): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655883 | ||||||
chr1:114655883
|
A | AATATATA others(3): Show |
19 | a0001c0001t0001g0086a0001c0001t0001g0131a0001c0001t0001g0132others(16): Show | 19 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.-573-1132_-573-112 others(14): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655883 | ||||||
chr1:114655883
|
A | AATATATA others(5): Show |
6 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0159others(3): Show | 6 | HG01884.hp1 HG02145.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-573-1134_-573-112 others(16): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655883 | ||||||
chr1:114655883
|
A | AATATATA others(7): Show |
6 | a0001c0001t0001g0225a0001c0001t0012g0054a0001c0001t0012g0224others(3): Show | 6 | HG01099.hp1 HG02257.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.-573-1136_-573-112 others(18): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655883 | ||||||
chr1:114655883
|
A | AATATATA others(9): Show |
1 | a0001c0001t0023g0047 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-573-1138_-573-112 others(20): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655883 | ||||||
chr1:114655883
|
A | AATATATA others(11): Show |
1 | a0001c0001t0012g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-573-1123_-573-112 others(22): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655883 | ||||||
chr1:114655883
|
A | T | 83 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(80): Show | 86 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.-573-1122T>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114655883 | ||||||
chr1:114656198
|
A | G | 2 | a0001c0001t0001g0228a0001c0001t0008g0147 | 2 | HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-573-1437T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114656198 | ||||||
chr1:114656303
|
G | A | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-573-1542C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114656303 | ||||||
chr1:114656368
|
T | A | 1 | a0001c0001t0002g0212 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-573-1607A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114656368 | ||||||
chr1:114656401
|
C | CT | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(137): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.-573-1641dupA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114656401 | ||||||
chr1:114656401
|
C | CTT | 16 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0006g0027others(13): Show | 16 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.-573-1642_-573-164 others(6): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114656401 | ||||||
chr1:114656466
|
G | A | 1 | a0007c0010t0007g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-573-1705C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114656466 | ||||||
chr1:114656647
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0157 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-573-1886G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114656647 | ||||||
chr1:114656683
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-573-1922C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114656683 | ||||||
chr1:114656691
|
C | T | 17 | a0001c0006t0004g0059a0001c0006t0004g0060a0004c0004t0004g0049others(14): Show | 17 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.-573-1930G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114656691 | ||||||
chr1:114656917
|
A | C | 1 | a0001c0001t0043g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-573-2156T>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114656917 | ||||||
chr1:114656968
|
C | A | 1 | a0001c0013t0009g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-573-2207G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114656968 | ||||||
chr1:114657029
|
GCCTGAGC others(7): Show |
G | 2 | a0001c0001t0013g0025a0001c0014t0006g0026 | 2 | HG00323.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.-573-2282_-573-226 others(18): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114657029 | ||||||
chr1:114657195
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-573-2434G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114657195 | ||||||
chr1:114657249
|
T | G | 2 | a0001c0001t0020g0008a0001c0001t0020g0009 | 2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-573-2488A>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114657249 | ||||||
chr1:114657255
|
TTTTG | T | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-573-2498_-573-249 others(8): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114657255 | ||||||
chr1:114657280
|
C | T | 2 | a0001c0001t0002g0167a0001c0001t0005g0168 | 2 | NA18988.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-573-2519G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114657280 | ||||||
chr1:114657309
|
G | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-573-2548C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114657309 | ||||||
chr1:114657338
|
T | A | 1 | a0007c0010t0007g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-573-2577A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114657338 | ||||||
chr1:114657538
|
C | A | 1 | a0001c0001t0008g0134 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-573-2777G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114657538 | ||||||
chr1:114658020
|
A | G | 1 | a0001c0011t0044g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-573-3259T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114658020 | ||||||
chr1:114658187
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-573-3426T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114658187 | ||||||
chr1:114658436
|
G | A | 13 | a0001c0001t0012g0046a0001c0001t0012g0052a0001c0001t0012g0054others(10): Show | 13 | HG01099.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-573-3675C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114658436 | ||||||
chr1:114658502
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-573-3741C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114658502 | ||||||
chr1:114658602
|
C | T | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-573-3841G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114658602 | ||||||
chr1:114658604
|
A | C | 1 | a0007c0010t0007g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-573-3843T>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114658604 | ||||||
chr1:114658665
|
A | G | 1 | a0001c0012t0010g0092 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-573-3904T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114658665 | ||||||
chr1:114658771
|
A | ACAGTTCT others(297): Show |
21 | a0003c0003t0003g0007a0003c0003t0003g0270a0003c0003t0003g0271others(18): Show | 22 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.-573-4011_-573-401 others(308): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114658771 | ||||||
chr1:114658771
|
A | ACAGTTCT others(298): Show |
1 | a0003c0003t0003g0276 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-573-4011_-573-401 others(309): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114658771 | ||||||
chr1:114658884
|
A | T | 37 | a0001c0001t0012g0046a0001c0001t0012g0052a0001c0001t0012g0054others(34): Show | 38 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.-573-4123T>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114658884 | ||||||
chr1:114659076
|
T | C | 1 | a0002c0002t0001g0260 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-573-4315A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114659076 | ||||||
chr1:114659110
|
A | G | 1 | a0001c0011t0044g0227 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-573-4349T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114659110 | ||||||
chr1:114659319
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0157 | 2 | HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-573-4558C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114659319 | ||||||
chr1:114659429
|
G | A | 15 | a0004c0004t0004g0049a0004c0004t0004g0050a0004c0004t0004g0051others(12): Show | 15 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.-573-4668C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114659429 | ||||||
chr1:114659594
|
A | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(131): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.-573-4833T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114659594 | ||||||
chr1:114659619
|
A | G | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-573-4858T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114659619 | ||||||
chr1:114659738
|
T | C | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-573-4977A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114659738 | ||||||
chr1:114659757
|
C | T | 5 | a0001c0001t0012g0046a0001c0001t0012g0052a0001c0001t0012g0054others(2): Show | 5 | HG01099.hp1 HG02886.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-573-4996G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114659757 | ||||||
chr1:114659781
|
TTCCC | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(216): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.-573-5024_-573-502 others(8): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114659781 | ||||||
chr1:114659881
|
T | C | 1 | a0007c0010t0007g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-573-5120A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114659881 | ||||||
chr1:114659893
|
C | T | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-573-5132G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114659893 | ||||||
chr1:114659916
|
G | A | 10 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-573-5155C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114659916 | ||||||
chr1:114659963
|
T | TG | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-573-5203_-573-520 others(5): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114659963 | ||||||
chr1:114660049
|
C | T | 1 | a0001c0001t0033g0024 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-573-5288G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114660049 | ||||||
chr1:114660614
|
G | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0140 | 2 | NA18978.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.-573-5853C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114660614 | ||||||
chr1:114660774
|
A | T | 1 | a0001c0001t0005g0166 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-573-6013T>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114660774 | ||||||
chr1:114660842
|
G | A | 1 | a0001c0001t0002g0214 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-573-6081C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114660842 | ||||||
chr1:114660887
|
C | G | 1 | a0003c0003t0003g0007 | 2 | HG00733.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.-573-6126G>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114660887 | ||||||
chr1:114661106
|
C | A | 1 | a0003c0003t0003g0007 | 2 | HG00733.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.-573-6345G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114661106 | ||||||
chr1:114661106
|
CA | C | 54 | a0001c0001t0001g0138a0001c0001t0009g0014a0001c0001t0009g0016others(51): Show | 55 | HG00741.hp2 HG01099.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.-573-6346delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114661106 | ||||||
chr1:114661106
|
CAA | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(121): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.-573-6347_-573-634 others(6): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114661106 | ||||||
chr1:114661165
|
G | C | 1 | a0004c0004t0004g0067 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-573-6404C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114661165 | ||||||
chr1:114661189
|
C | T | 1 | a0001c0001t0036g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-573-6428G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114661189 | ||||||
chr1:114661190
|
G | C | 1 | a0001c0001t0032g0141 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-573-6429C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114661190 | ||||||
chr1:114661392
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-573-6631G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114661392 | ||||||
chr1:114661422
|
C | T | 1 | a0001c0001t0036g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-573-6661G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114661422 | ||||||
chr1:114661466
|
T | C | 1 | a0006c0005t0022g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-573-6705A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114661466 | ||||||
chr1:114661525
|
T | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0142 | 4 | NA18941.hp2 NA18964.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.-573-6764A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114661525 | ||||||
chr1:114661846
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-573-7085G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114661846 | ||||||
chr1:114662011
|
GATTAA | G | 37 | a0001c0001t0012g0046a0001c0001t0012g0052a0001c0001t0012g0054others(34): Show | 38 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.-573-7255_-573-725 others(9): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114662011 | ||||||
chr1:114662102
|
T | A | 1 | a0001c0001t0001g0232 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-573-7341A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114662102 | ||||||
chr1:114662483
|
G | T | 1 | a0001c0001t0005g0165 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-574+7500C>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114662483 | ||||||
chr1:114662641
|
G | GA | 13 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0008g0143others(10): Show | 13 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-574+7341dupT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114662641 | ||||||
chr1:114662641
|
GA | G | 25 | a0001c0001t0001g0084a0001c0001t0001g0090a0001c0001t0001g0148others(22): Show | 26 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.-574+7341delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114662641 | ||||||
chr1:114662728
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-574+7255A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114662728 | ||||||
chr1:114662952
|
C | G | 1 | a0001c0001t0024g0223 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-574+7031G>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114662952 | ||||||
chr1:114663000
|
G | A | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-574+6983C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114663000 | ||||||
chr1:114663035
|
A | G | 2 | a0003c0003t0003g0277a0003c0003t0003g0278 | 2 | HG02818.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-574+6948T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114663035 | ||||||
chr1:114663136
|
A | G | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-574+6847T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114663136 | ||||||
chr1:114663137
|
T | C | 1 | a0001c0001t0026g0264 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-574+6846A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114663137 | ||||||
chr1:114663588
|
G | A | 1 | a0001c0001t0013g0034 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-574+6395C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114663588 | ||||||
chr1:114663832
|
A | C | 1 | a0001c0001t0002g0164 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-574+6151T>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114663832 | ||||||
chr1:114663951
|
C | CT | 15 | a0001c0001t0001g0222a0001c0001t0002g0163a0001c0001t0005g0161others(12): Show | 16 | HG01257.hp1 HG01257.hp2 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.-574+6031dupA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114663951 | ||||||
chr1:114663951
|
CT | C | 8 | a0001c0001t0002g0215a0001c0001t0002g0216a0001c0001t0002g0217others(5): Show | 8 | HG01081.hp2 HG01928.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.-574+6031delA | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114663951 | ||||||
chr1:114664076
|
C | A | 17 | a0001c0006t0004g0059a0001c0006t0004g0060a0004c0004t0004g0049others(14): Show | 17 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.-574+5907G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114664076 | ||||||
chr1:114664077
|
C | A | 17 | a0001c0006t0004g0059a0001c0006t0004g0060a0004c0004t0004g0049others(14): Show | 17 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.-574+5906G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114664077 | ||||||
chr1:114664253
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-574+5730C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114664253 | ||||||
chr1:114664279
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-574+5704G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114664279 | ||||||
chr1:114664306
|
G | C | 1 | a0001c0001t0028g0269 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-574+5677C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114664306 | ||||||
chr1:114664324
|
G | A | 13 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-574+5659C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114664324 | ||||||
chr1:114664608
|
G | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-574+5375C>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114664608 | ||||||
chr1:114664611
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-574+5372G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114664611 | ||||||
chr1:114664798
|
T | C | 10 | a0001c0001t0009g0014a0001c0001t0009g0016a0001c0001t0009g0017others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-574+5185A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114664798 | ||||||
chr1:114664921
|
C | T | 17 | a0001c0006t0004g0059a0001c0006t0004g0060a0004c0004t0004g0049others(14): Show | 17 | HG01192.hp1 HG01257.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.-574+5062G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114664921 | ||||||
chr1:114664938
|
CA | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-574+5044delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114664938 | ||||||
chr1:114665115
|
A | G | 1 | a0002c0002t0001g0234 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-574+4868T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114665115 | ||||||
chr1:114665148
|
A | G | 1 | a0002c0002t0008g0265 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-574+4835T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114665148 | ||||||
chr1:114665252
|
G | C | 1 | a0001c0001t0045g0082 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-574+4731C>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114665252 | ||||||
chr1:114665271
|
GA | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(213): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.-574+4711delT | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114665271 | ||||||
chr1:114665542
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-574+4441G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114665542 | ||||||
chr1:114665543
|
G | A | 12 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(9): Show | 12 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-574+4440C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114665543 | ||||||
chr1:114665631
|
T | G | 1 | a0001c0001t0040g0057 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-574+4352A>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114665631 | ||||||
chr1:114665843
|
A | C | 2 | a0001c0001t0020g0008a0001c0001t0020g0009 | 2 | HG01891.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-574+4140T>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114665843 | ||||||
chr1:114665883
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-574+4100C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114665883 | ||||||
chr1:114665885
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-574+4098G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114665885 | ||||||
chr1:114666132
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-574+3851A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114666132 | ||||||
chr1:114666429
|
T | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-574+3554A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114666429 | ||||||
chr1:114666521
|
C | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-574+3462G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114666521 | ||||||
chr1:114666532
|
C | G | 1 | a0001c0001t0001g0084 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-574+3451G>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114666532 | ||||||
chr1:114666621
|
A | T | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-574+3362T>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114666621 | ||||||
chr1:114667121
|
G | A | 1 | a0001c0001t0005g0220 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-574+2862C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114667121 | ||||||
chr1:114667134
|
A | G | 1 | a0001c0001t0017g0022 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-574+2849T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114667134 | ||||||
chr1:114667330
|
C | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-574+2653G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114667330 | ||||||
chr1:114667496
|
A | G | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-574+2487T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114667496 | ||||||
chr1:114667540
|
T | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-574+2443A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114667540 | ||||||
chr1:114667575
|
A | C | 1 | a0004c0004t0004g0049 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-574+2408T>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114667575 | ||||||
chr1:114667613
|
T | C | 1 | a0007c0010t0007g0058 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-574+2370A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114667613 | ||||||
chr1:114667945
|
G | A | 2 | a0001c0006t0004g0059a0001c0006t0004g0060 | 2 | HG02698.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-574+2038C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114667945 | ||||||
chr1:114667946
|
C | A | 2 | a0001c0006t0004g0059a0001c0006t0004g0060 | 2 | HG02698.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-574+2037G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114667946 | ||||||
chr1:114667957
|
C | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0075others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-574+2026G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114667957 | ||||||
chr1:114668037
|
T | G | 1 | a0003c0003t0007g0288 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-574+1946A>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114668037 | ||||||
chr1:114668053
|
G | A | 1 | a0001c0001t0021g0021 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-574+1930C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114668053 | ||||||
chr1:114668054
|
A | C | 1 | a0001c0001t0021g0021 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-574+1929T>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114668054 | ||||||
chr1:114668055
|
A | C | 1 | a0001c0001t0012g0046 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-574+1928T>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114668055 | ||||||
chr1:114668125
|
T | C | 14 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0032others(11): Show | 14 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.-574+1858A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114668125 | ||||||
chr1:114668520
|
A | AAC | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0084others(119): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.-574+1461_-574+146 others(6): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114668520 | ||||||
chr1:114668520
|
A | AACAC | 15 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(12): Show | 15 | HG01891.hp1 HG02083.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-574+1459_-574+146 others(8): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114668520 | ||||||
chr1:114668520
|
A | AACACAC | 29 | a0001c0001t0019g0011a0001c0001t0019g0012a0001c0013t0009g0013others(26): Show | 30 | HG00099.hp2 HG00733.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.-574+1457_-574+146 others(10): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114668520 | ||||||
chr1:114668520
|
A | AACACACA others(1): Show |
18 | a0001c0001t0012g0052a0001c0001t0012g0054a0001c0001t0020g0008others(15): Show | 18 | HG01099.hp1 HG01099.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.-574+1455_-574+146 others(12): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114668520 | ||||||
chr1:114668520
|
A | AACACACA others(3): Show |
4 | a0001c0001t0012g0046a0001c0001t0023g0047a0001c0001t0023g0048others(1): Show | 4 | HG02258.hp2 HG02897.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-574+1453_-574+146 others(14): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114668520 | ||||||
chr1:114668520
|
AAC | A | 20 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(17): Show | 20 | HG00323.hp2 HG01070.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.-574+1461_-574+146 others(6): Show |
DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114668520 | ||||||
chr1:114668710
|
G | A | 1 | a0003c0003t0003g0290 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-574+1273C>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114668710 | ||||||
chr1:114668756
|
G | T | 4 | a0001c0001t0011g0002a0001c0001t0011g0043a0001c0001t0011g0045others(1): Show | 5 | HG02280.hp1 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-574+1227C>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114668756 | ||||||
chr1:114668786
|
T | C | 39 | a0001c0001t0016g0237a0001c0001t0016g0238a0001c0001t0026g0264others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(36): Show |
intron_variant | MODIFIER | c.-574+1197A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114668786 | ||||||
chr1:114668983
|
A | G | 3 | a0003c0003t0003g0270a0003c0003t0003g0271a0003c0003t0003g0272 | 3 | HG00741.hp1 HG01109.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.-574+1000T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114668983 | ||||||
chr1:114669000
|
G | T | 1 | a0001c0001t0002g0042 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-574+983C>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114669000 | ||||||
chr1:114669052
|
C | G | 1 | a0002c0002t0001g0041 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-574+931G>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114669052 | ||||||
chr1:114669112
|
T | C | 1 | a0001c0001t0028g0269 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-574+871A>G | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114669112 | ||||||
chr1:114669152
|
T | A | 22 | a0003c0003t0003g0007a0003c0003t0003g0270a0003c0003t0003g0271others(19): Show | 23 | HG00099.hp2 HG00733.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.-574+831A>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114669152 | ||||||
chr1:114669781
|
C | T | 1 | a0001c0001t0002g0040 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-574+202G>A | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114669781 | ||||||
chr1:114669782
|
C | A | 2 | a0002c0002t0001g0291a0002c0002t0001g0292 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-574+201G>T | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114669782 | ||||||
chr1:114669904
|
A | G | 5 | a0001c0001t0002g0035a0001c0001t0002g0036a0001c0001t0002g0037others(2): Show | 5 | HG01123.hp1 HG01358.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.-574+79T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114669904 | ||||||
chr1:114669951
|
A | G | 27 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0032others(24): Show | 27 | HG00323.hp2 HG01167.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.-574+32T>C | DENND2C | ENSG00000175984.16 | transcript | ENST00000393274.6 | protein_coding | 1/20 | chr1 | 114669951 |